Antibodies Quotes

It is not difficult to deceive the first time, for the deceived possesses no antibodies; unvaccinated by suspicion, she overlooks lateness, accepts absurd excuses, permits the flimsiest patching to repair great rents in the quotidian.

I am a child of the poisonous wind that copulated with the East River on an oil-slick, garbage infested midnight. I turn about on my own parentage. I inoculate against those very biles that brought me to light. I am a serum born of venoms. I am the antibody of all Time. I am the Cure. You do of the City, do you not? Manhattan is your punisher, let me be you shield.

I now have anti-bodies to assholes after working for so many.

A Witch is born out of the true hungers of her time. I am a child of the poisonous wind that copulated with the river on an oil-slick, garbage infested midnight. I turn about on my own parentage. I inoculate against those very biles that brought me to light. I am a serum born of venoms. I am the antibody of all time.

Perhaps it was a knack that humans had, for cleaning up their untidy existences - a hidden survival weapon, like antibodies in the bloodstream.

On April 2, the nurses started my first round of five intravenous immunoglobulin (IVIG) infusions. The clear IV bags hung on a metal pole above my head, their liquid trickling down into my vein. Each of those ordinary-looking bags contained the healthy antibodies of over a thousand blood donors and cost upwards of $20,000 per infusion. One thousand tourniquets, one thousand nurses, one thousand veins, one thousand blood-sugar regulating cookies, all just to help one patient.

A faith without some doubts is like a human body without any antibodies in it. People who blithely go through life too busy or indifferent to ask hard questions about why they believe as they do will find themselves defenseless against either the experience of tragedy or the probing questions of a smart skeptic. A person's faith can collapse almost overnight if she has failed over the years to listen patiently to her own doubts, which should only be discarded after long reflection. Believers should acknowledge and wrestle with doubts — not only their own but their friends' and neighbors'. It is no longer sufficient to hold beliefs just because you inherited them. Only if you struggle long and hard with objections to your faith will you be able to provide the grounds for your beliefs to skeptics, including yourself, that are plausible rather than ridiculous or offensive. And, just as important for our current situation, such a process will lead you, even after you come to a position of strong faith, to respect and understand those who doubt.

About one-third of COVID deaths occurred in the nursing homes and ALFs across the US during the pandemic.46 Dr. Fauci should have equipped both nursing homes and quarantine hospitals with monoclonal antibodies,” said Risch. Instead, he obstructed these institutions from administering that medicine.

It was as if a virus had been injected into our school, but Macey'd known about a thousand boys before she'd come here. And I'd known Josh. The two of us had been exposed to boys before, so we had built up antibodies. We were, in a word, immune.

If, as a child, you are struck or hit, you will never forget that sense of your own powerlessness and vulnerability, of how a situation can turn from benign to brutal in the blink of an eye, in the space of a breath. That sensibility will run in your veins, like an antibody. You learn fairly quickly to recognise the approach of these sudden acts against you: that particular pitch or vibration in the atmosphere. You develop antennae for violence and, in turn, you devise a repertoire of means to divert it.

Reminiscing in the drizzle of Portland, I notice the ring that’s landed on your finger, a massive insect of glitter, a chandelier shining at the end of a long tunnel. Thirteen years ago, you hid the hurt in your voice under a blanket and said there’s two kinds of women—those you write poems about and those you don’t. It’s true. I never brought you a bouquet of sonnets, or served you haiku in bed. My idea of courtship was tapping Jane’s Addiction lyrics in Morse code on your window at three A.M., whiskey doing push-ups on my breath. But I worked within the confines of my character, cast as the bad boy in your life, the Magellan of your dark side. We don’t have a past so much as a bunch of electricity and liquor, power never put to good use. What we had together makes it sound like a virus, as if we caught one another like colds, and desire was merely a symptom that could be treated with soup and lots of sex. Gliding beside you now, I feel like the Benjamin Franklin of monogamy, as if I invented it, but I’m still not immune to your waterfall scent, still haven’t developed antibodies for your smile. I don’t know how long regret existed before humans stuck a word on it. I don’t know how many paper towels it would take to wipe up the Pacific Ocean, or why the light of a candle being blown out travels faster than the luminescence of one that’s just been lit, but I do know that all our huffing and puffing into each other’s ears—as if the brain was a trick birthday candle—didn’t make the silence any easier to navigate. I’m sorry all the kisses I scrawled on your neck were written in disappearing ink. Sometimes I thought of you so hard one of your legs would pop out of my ear hole, and when I was sleeping, you’d press your face against the porthole of my submarine. I’m sorry this poem has taken thirteen years to reach you. I wish that just once, instead of skidding off the shoulder blade’s precipice and joyriding over flesh, we’d put our hands away like chocolate to be saved for later, and deciphered the calligraphy of each other’s eyelashes, translated a paragraph from the volumes of what couldn’t be said.

We have gone sick by following a path of untrammelled rationalism, male dominance, attention to the visible surface of things, practicality, bottom-line-ism. We have gone very, very sick. And the body politic, like any body, when it feels itself to be sick, it begins to produce antibodies, or strategies for overcoming the condition of dis-ease. And the 20th century is an enormous effort at self-healing. Phenomena as diverse as surrealism, body piercing, psychedelic drug use, sexual permissiveness, jazz, experimental dance, rave culture, tattooing, the list is endless. What do all these things have in common? They represent various styles of rejection of linear values. The society is trying to cure itself by an archaic revival, by a reversion to archaic values. So when I see people manifesting sexual ambiguity, or scarifying themselves, or showing a lot of flesh, or dancing to syncopated music, or getting loaded, or violating ordinary canons of sexual behaviour, I applaud all of this; because it's an impulse to return to what is felt by the body -- what is authentic, what is archaic -- and when you tease apart these archaic impulses, at the very centre of all these impulses is the desire to return to a world of magical empowerment of feeling. And at the centre of that impulse is the shaman: stoned, intoxicated on plants, speaking with the spirit helpers, dancing in the moonlight, and vivifying and invoking a world of conscious, living mystery. That's what the world is. The world is not an unsolved problem for scientists or sociologists. The world is a living mystery: our birth, our death, our being in the moment -- these are mysteries. They are doorways opening on to unimaginable vistas of self-exploration, empowerment and hope for the human enterprise. And our culture has killed that, taken it away from us, made us consumers of shoddy products and shoddier ideals. We have to get away from that; and the way to get away from it is by a return to the authentic experience of the body -- and that means sexually empowering ourselves, and it means getting loaded, exploring the mind as a tool for personal and social transformation. The hour is late; the clock is ticking; we will be judged very harshly if we fumble the ball. We are the inheritors of millions and millions of years of successfully lived lives and successful adaptations to changing conditions in the natural world. Now the challenge passes to us, the living, that the yet-to-be-born may have a place to put their feet and a sky to walk under; and that's what the psychedelic experience is about, is caring for, empowering, and building a future that honours the past, honours the planet and honours the power of the human imagination. There is nothing as powerful, as capable of transforming itself and the planet, as the human imagination. Let's not sell it straight. Let's not whore ourselves to nitwit ideologies. Let's not give our control over to the least among us. Rather, you know, claim your place in the sun and go forward into the light. The tools are there; the path is known; you simply have to turn your back on a culture that has gone sterile and dead, and get with the programme of a living world and a re-empowerment of the imagination. Thank you very, very much.

Arrows you may dodge and fever you may antibody for, but mortal grief is a misfortune you cannot escape.

This, then, is the dread that seems to lie beneath the fear of equalizing. Equity is seen as dispossession. Local autonomy is seen as liberty--even if the poverty of those in nearby cities robs them of all meaningful autonomy by narrowing their choices to the meanest and the shabbiest of options. In this way, defendants in these cases seem to polarize two of the principles that lie close to the origins of this republic. Liberty and equity are seen as antibodies to each other.

Male, female, gay, straight, legal, illegal, country of origin—who cares? You can either cook an omelet or you can’t. You can either cook five hundred omelets in three hours—like you said you could, and like the job requires—or you can’t. There’s no lying in the kitchen. The restaurant kitchen may indeed be the last, glorious meritocracy—where anybody with the skills and the heart is welcomed. But if you’re old, or out of shape—or were never really certain about your chosen path in the first place—then you will surely and quickly be removed. Like a large organism’s natural antibodies fighting off an invading strain of bacteria, the life will slowly push you out or kill you off. Thus it is. Thus it shall always be. The ideal progression for a nascent culinary career would be to, first, take a jump straight into the deep end of the pool. Long before student loans and culinary school, take the trouble to find out who you are.

Kissing a stranger you'd never see again, kissing someone whose name you didn't even know, just to feel a little high in that moment. Just to feel the warmth of someone's skin on yours. Just, for a while, to feel purely alive. God. I wished I could do that. But the idea of trying to get with any of these people--no matter their gender--was, honestly, unnerving. It made me feel itchy. Shivery, maybe. It filled my stomach with a weird, horrible dread, and a warning siren went off in my brain. It felt like my antibodies were fighting it off.

The immune system is also thought to be behind sex-specific responses to vaccines: women develop higher antibody responses and have more frequent and severe adverse reactions to vaccines,19 and a 2014 paper proposed developing male and female versions of influenza vaccines.20

Authority has been the ideological disease of humankind. And finally, a mass of anarchists has been injected into the artery of society as antibodies geared to combat this illness.

When my world gets reset to zero, my starting post is blood. Specifically, the elements of it, the working compounds that make it what it is. Red cells, white cells, DNA, plasma full of proteins, enzymes, antibodies, minerals, electrolytes—all the things that when poked and prodded right tell you just about everything you want to know about a person. Fascinating stuff, and a little freaky, when you think about it. Blood was where I returned to after the accident that smashed my knee. It was where I went when I got out of prison. It was where I was when Mercy fell into my lap. Now it seemed, blood was my whole reason for being.

Unlike an antibody, a gunslinging sheriff itching for a showdown with a gang of molecular criminals in the center of town, a T cell is the gumshoe detective going door to door to look for perpetrators hiding inside.

A grotesque thought struck Benji: Humankind was a disease. The earth was the body. Climate change was the fever. And in that fever, in that rising of global temperature, the earth was able to release new defenses. White Mask was not here to kill the world. It was here to kill the people—the fungus would serve as a vicious defense mechanism to eradicate the infection of humanity. This epidemic represented antibodies to restore balance to the body. Kill the parasite and save the host.

What we ourselves have fallen victim to -- and by no means allegorically -- is a virus destructive of otherness. And we may predict that -- even more than in the case of AIDS -- no science will be able to protect us from this viral pathology which, by dint of antibodies and immune strategies, aims at the extinction, pure and simple, of the other. Though, for the moment, this virus does not affect the biological reproduction of the species, it affects an even more fundamental function, that of the symbolic reproduction of the other, favouring, rather, a cloned, asexual reproduction of the species-less individual. For to be deprived of the other is to be deprived of sex, and to be deprived of sex is to be deprived of symbolic belonging to any species whatsoever.

Freedom is not as free as is generally thought: it produces antibodies which rebel against it. Truth, too, is threatened from within, like a state battling with its own police force. If values enjoyed total immunity, they would be as lethal as a scientific truth.

Researchers at the Heidelberg University Hospital conducted a study in which they subjected a young doctor to a job interview, which they made even more stressful by forcing him to solve complex math problems for thirty minutes. Afterward, they took a blood sample. What they discovered was that his antibodies had reacted to stress the same way they react to pathogens, activating the proteins that trigger an immune response. The problem is that this response not only neutralizes harmful agents, it also damages healthy cells, leading them to age prematurely.

But maybe it would have been better if I’d experienced this while I was still young,” Tokai said. “Then I would have developed love antibodies.” I didn’t think things were that simple. I knew a few people who, far from developing love antibodies, carried around a dormant but vicious disease.

..and of AIDS. The virus too small to imagine travelling through our fluids, even a drop or two of saliva or cunt slime, and unlocking our antibodies with its little picks, so that our insides lose their balance and we topple into pneumonia, into starvation. Love and death, they can't be pried apart anymore.

For some reason there is a tendency to assume that one wild animal is a suitable model for another related species, whereas similar evidence would not be acceptable in human or veterinary medicine. For example, Shulaw etal. (1986) developed a serologic test to detect antibodies to Mycobacterium aviumssp. paratuberculosisin white-tailed deer, but determined the validity of the test “in deer” by using samples from infected sika and fallow deer. It is doubtful that a test developed to detect disease in humans would be accepted for use in public health circles, if its validity had been established by using squirrel monkeys and baboons!

Against other illnesses, though—including measles, mumps, rubella, pertussis, and the now defeated smallpox—our antibodies stimulated by one infection confer lifelong immunity. That’s the principle of vaccination: to stimulate our antibody production without our having to go through the actual experience of the disease, by inoculating us with a dead or weakened strain of microbe.

99.4% communicability, he thought. It played insanely over and over in his mind. And that meant 99.4% excess mortality, because the human body couldn’t produce the antibodies necessary to stop a constantly shifting antigen virus. Every time the body did produce the right antibody, the virus simply shifted to a slightly new form. For the same reason a vaccine was going to be almost impossible to create.

To understand what ended up happening in the 2016 presidential election, you have to understand this: When protests toppled the Ukrainian government, Putin interpreted that as the United States coming into Russia, akin to an act of war; when he launched his counterattack—annexing Crimea, creeping into eastern Ukraine—he weaponized information and showed a willingness to lie, using traditional media like television, and new media platforms like Twitter, Facebook, and YouTube, to spread disinformation into open, Western societies like a virus. Eventually, the Russians would come into America, as they believed we’d gone into Ukraine. They took advantage of the fact that we were worn down by decades of political polarization and the balkanization of our media. America’s antibodies to the sickness of Russian disinformation were weak, if they were there at all.

More about the selection theory: Jerne meant that the Socratic idea of learning was a fitting analogy for 'the logical basis of the selective theories of antibody formation': Can the truth (the capability to synthesize an antibody) be learned? If so, it must be assumed not to pre-exist; to be learned, it must be acquired. We are thus confronted with the difficulty to which Socrates calls attention in Meno [ ... ] namely, that it makes as little sense to search for what one does not know as to search for what one knows; what one knows, one cannot search for, since one knows it already, and what one does not know, one cannot search for, since one does not even know what to search for. Socrates resolves this difficulty by postulating that learning is nothing but recollection. The truth (the capability to synthesize an antibody) cannot be brought in, but was already inherent.

Every time we practice mindful living, we plant healthy seeds and strengthen the healthy seeds already in us. Healthy seeds function similarly to antibodies. When a virus enters our bloodstream, our body reacts and antibodies come and surround it, take care of it, and transform it. This is true with our psychological seeds as well. If we plant wholesome, healing, refreshing seeds, they will take care of the negative seeds, even without our asking them. To succeed, we need to cultivate a good reserve of refreshing seeds.

Yale law professor Dan Kahan, the lead author on this study, attributes the tight correlation between “worldview” and acceptance of climate science to “cultural cognition,” the process by which all of us—regardless of political leanings—filter new information in ways that will protect our “preferred vision of the good society.” If new information seems to confirm that vision, we welcome it and integrate it easily. If it poses a threat to our belief system, then our brain immediately gets to work producing intellectual antibodies designed to repel the unwelcome invasion.

If white supremacy applies only to the KKK and its ilk, the logic runs, even an abstract condemnation of these extremist groups is the equivalent of a rejection of white supremacy. White responses to the problem of white supremacy too often begin with “Of course.” But this inoculation of white consciences is actually as big a problem as the documented rise of fringe white supremacist groups. It creates within mainstream white Christians moral antibodies that preemptively neutralize thornier questions about the current power of white supremacy in our institutions, culture, and psyches.

The word chimeric comes from Greek mythology, in which a chimera was a fire-breathing monster with the head of a lion, the body of a goat, and the tail of a snake. CAR T-cells are called “chimeric” because they begin with ordinary T-cells taken from a person’s blood (the so-called “killer” white blood cells that recognize and attack a broad range of bacteria or viruses) and attach a kind of lion’s head: a molecular signal that guides the T-cells to seek and destroy cancer. The T-cell part of the chimera is a powerful killer, and the antibody at the head makes the attack more specific, reducing side effects.

A recent 2013 randomized, placebo-controlled study in hypothyroid patients demonstrated that in people who got near-infrared light therapy, thyroid function dramatically improved, and remarkably, that thyroid antibody (TPOAb) levels were massively reduced. Amazingly, 47% of patients were able to stop medication completely! Moreover, the researchers also followed up 9 months after treatment and found that the effects were still evident!116 They even published a 6-year follow-up, which basically said that even at 6 years, some of the benefits still remained, but periodic sessions were recommended to maintain all benefits.117

The patient would prick her finger to draw a small sample of blood and place it in a cartridge that looked like a thick credit card. The cartridge would slot into a bigger machine called a reader. Pumps inside the reader would push the blood through tiny channels in the cartridge and into little wells coated with proteins known as antibodies. On its way to the wells, a filter would separate the blood’s solid elements, its red and white blood cells, from the plasma and let only the plasma through. When the plasma came into contact with the antibodies, a chemical reaction would produce a signal that would be “read” by the reader and translated into a result.

using a virus that could glue cells together, they fused the B cell with a cancer cell. I am still awestruck by the idea. How did they even think of using the undead to resuscitate the dying? The result was one of the strangest cells in biology. The plasma cell retained its antibody-secreting property, while the cancer cell conferred its immortality. They called their peculiar cell a hybridoma—a, well, hybrid of hybrid and oma, the suffix of carcinoma. The immortal plasma cell was now capable of perpetually secreting only one kind of antibody. We call this antibody of a single type (in other words, a clone), a monoclonal antibody. Milstein and Köhler’s paper was published in Nature in 1975.

It is dynamic. In some cells, it reshuffles its own sequence to make novel variants of itself. Cells of the immune system secrete "anti-bodies"-missilelike proteins designed to attach themselves to invading pathogens. But since pathogens are constantly evolving, antibodies must also be capable of changing; an evolving pathogen demands an evolving host. The genome accomplishes this counter-evolution by reshuffling its genetic elements-thereby achieving astounding diversity)s...tru...c...t...ure and g...en...ome can be reshuffled to form an entirely new word c...ome...t). The reshuffled genes generate the diversity of antibodies. In these cells, every genome is capable of giving rise to an entirely different genome.

Did you know that in 90% of cases, hypothyroidism is an autoimmune disease? Did you know that autoimmune thyroid disease is linked to a gluten intolerance? Hashimoto’s and Graves’ disease are most likely caused by a gluten intolerance. What happens is that the molecular structure of gliadin (the protein in gluten) resembles the thyroid gland. If you don’t have a healthy intestinal lining, you can create holes; enter leaky gut syndrome. To review, leaky gut happens because food leaks into the bloodstream, and since your blood doesn’t know what the substances are, it puts your immune system into overdrive to kill the foreign substance (this is why I have my clients get a thyroid “antibody” test; it helps determine if there is a food allergy).

antibody, which she administered via their nasal passages. The problem was, her therapy didn’t effectively cross the blood-brain barrier and reach the plaques in the parts of the brain affected by Alzheimer’s. In what might go down as one of the greatest twists of scientific luck, Solomon decided to attach her antibody to a virus called M13 to transport it across the blood-brain barrier. M13 was a special type of virus called a bacteriophage—a virus that infected only bacteria. And M13 infected only one type of bacteria: Escherichia coli, or E. coli. To Solomon’s surprise, the antibody, when attached to M13, showed great success in her trials. But what was truly surprising was that the group of mice treated with the M13 virus alone—without Solomon’s antibody therapy—

According to Yale’s Cultural Cognition Project, for example, one’s “cultural worldview”—that would be political leanings or ideological outlook to the rest of us—explains “individuals’ beliefs about global warming more powerfully than any other individual characteristic.”16 More powerfully, that is, than age, ethnicity, education, or party affiliation. The Yale researchers explain that people with strong “egalitarian” and “communitarian” worldviews (marked by an inclination toward collective action and social justice, concern about inequality, and suspicion of corporate power) overwhelmingly accept the scientific consensus on climate change. Conversely, those with strong “hierarchical” and “individualistic” worldviews (marked by opposition to government assistance for the poor and minorities, strong support for industry, and a belief that we all pretty much get what we deserve) overwhelmingly reject the scientific consensus.17 The evidence is striking. Among the segment of the U.S. population that displays the strongest “hierarchical” views, only 11 percent rate climate change as a “high risk,” compared with 69 percent of the segment displaying the strongest “egalitarian” views.18 Yale law professor Dan Kahan, the lead author on this study, attributes the tight correlation between “worldview” and acceptance of climate science to “cultural cognition,” the process by which all of us—regardless of political leanings—filter new information in ways that will protect our “preferred vision of the good society.” If new information seems to confirm that vision, we welcome it and integrate it easily. If it poses a threat to our belief system, then our brain immediately gets to work producing intellectual antibodies designed to repel the unwelcome invasion.19 As Kahan explained in Nature, “People find it disconcerting to believe that behavior that they find noble is nevertheless detrimental to society, and behavior that they find base is beneficial to it. Because accepting such a claim could drive a wedge between them and their peers, they have a strong emotional predisposition to reject it.” In other words, it is always easier to deny reality than to allow our worldview to be shattered, a fact that was as true of die-hard Stalinists at the height of the purges as it is of libertarian climate change deniers today. Furthermore, leftists are equally capable of denying inconvenient scientific evidence. If conservatives are inherent system justifiers, and therefore bridle before facts that call the dominant economic system into question, then most leftists are inherent system questioners, and therefore prone to skepticism about facts that come from corporations and government. This can lapse into the kind of fact resistance we see among those who are convinced that multinational drug companies have covered up the link between childhood vaccines and autism. No matter what evidence is marshaled to disprove their theories, it doesn’t matter to these crusaders—it’s just the system covering up for itself.20 This kind of defensive reasoning helps explain the rise of emotional intensity that surrounds the climate issue today. As

There is a classic observation that rings true across all of biology. The observation concerns whether organisms learn and take instruction from the environment or whether the reactions that organisms have to environmental stimuli are managed by systems already built into the organism. The “selection versus instruction” debate has raged for years and has especially caught the limelight in the field of immunology. Put simply, when something foreign enters the body and there is an immune response to it, are the antibodies formed then and there around the foreign body, and do they then multiply (instruction)? Or does the antibody already exist, and is the immune response time the time it takes to find the preexisting antibody (selection) and jerk it into action? In the previous century, biology learned it is the latter situation, a finding that illustrates that a whole lot of stuff comes with the package—standard equipment for our bodies and brains.

It is not only through their complexity that the immune systems confuse their owners' longing for security; they cause even more perplexity through their immanent paradox, as their successes, if they become too thorough, are perverted to become their own kind of reasons for illness: the growing universe of auto-immune pathologies illustrates the dangerous tendency of the own to win itself to death in the battle against the other. It is no coincidence that recent interpretations of the immunity phenomenon exhibit a tendency to assign far greater significance to the presence of the foreign amidst the own than was intended in traditional identitary understandings of a monolithically closed organismic self - one could almost speak of a post-structuralist turn in biology. In the light of this, the patrol of antibodies in an organism seems less like a police force applying a rigid immigration policy than a theater troupe parodying its invaders and performing as their transvestites.

1. Oral Involvement 2. Laryngeal Involvement 3. Cardiovascular Involvement 4. Skin: rashes, vitiligo, Raynaud’s 5. Constitutional symptoms: including fever, fatigue, and muscle wasting (cachexia), infections 6. Rheumatoid vasculitis and blood vessel disease 7. Lung Involvement 8. Kidney involvement 9. Eye involvement 10. Other organs: including spleen, liver, lymph system, gut KEY POINTS 1. Some symptoms and antibodies can precede diagnosis over 10 years. 2. Many studies indicate RD begins in the lungs, before joint symptoms are diagnosable. 3. RD is often called an “invisible”illness because symptoms are not obvious to casual observers. 4. Doctors must be more aware that systemic symptoms like fatigue may indicate serious problems. 5. Extra-articular disease has been proven to affect most PRD, but is still not widely recognized. 6. Acknowledging rheumatoid disease that exists beyond and before joint inflammation (arthritis) could bring a) Improved care for lower mortality b) Improved research for better treatments c) Improved diagnosis for increased remissions

When Dr. Ramasamy first lectured to their class in the century-old Donovan Auditorium, even the murmuring backbenchers were silenced when the tall, confident woman in a short-sleeved lab coat floated in. She had launched right into inflammation, the body’s first response to any threat, the common denominator of all disease. In minutes she had drawn them into the thick of a battle: the invaders (typhoid bacteria) are spotted by the hilltop sentries (macrophages), who send signals back to the castle (the bone marrow and lymph nodes). The few aging veterans of previous battles with typhoid (memory T-lymphocytes) are roused from their beds, summoned to hastily teach untested conscripts the specific typhoid-grappling skills needed, and then to arm them with custom lances designed solely to latch onto and pierce the typhoid shield—in essence, the veterans clone their younger selves. The same veterans of prior typhoid campaigns also assemble a biological-warfare platoon (B lymphocytes) who hastily manufacture a one-of-a-kind boiling oil (antibodies) to pour over the castle wall; it will melt the typhoid intruders’ shields, while not harming others. Meanwhile, having heard the call to battle, the rogue mercenaries (neutrophils), armed to the teeth,

Autoimmune Disease—the “Leak” in Your Gut Autoimmune diseases are a disaster and there are no good medicines available (steroids work, but the treatment is worse than the disease). They’ve been around for centuries, but there’s been a clear uptick in the last fifty years. Why? Two hypotheses have been proffered to explain it: the barrier hypothesis (our skin or lungs are letting in antigens) and the hygiene hypothesis (we don’t eat dirt and are too hygienic). But in fact, in the gut, they’re the same thing; because the gut is the dirtiest place in the world—one hundred trillion bacteria to have to fend off at all times—you don’t need an intestine, you need a fortress. We’ve known for a while that leaky gut is akin to chinks in the walls of that fortress. Antigens, like enemy soldiers, escape through those chinks into the bloodstream, where T cells and antibodies react against them. But in a case of mistaken identity, these immune cells then accidentally identify parts of your body as foreign invaders and generate an immune response to kill them off, a process termed molecular mimicry. Then there are two new twists. First, it appears that one autoimmune disease, called ankylosing spondylitis, produces antibodies to a gut bacterium called Klebsiella pneumoniae. Conversely, a different autoimmune disease called rheumatoid arthritis produces antibodies to a second gut bacterium called Proteus mirabilis. Now, this might not seem that earth-shattering, but recent work has shown that the refined carbohydrates in processed food feed those two bacteria in particular, and that carbohydrate restriction improves both of these diseases. Indeed, a low-sugar, high-fiber Mediterranean diet has been shown to be efficacious at prevention and treatment of rheumatoid arthritis. Furthermore, introduction of fiber to the diet appears to improve asthma (frequently an autoimmune disease), likely by improving gut function and reducing inflammation.

Gejala HIV HIV (human immunodeficiency virus) adalah virus yang merusak sistem kekebalan tubuh, dengan menginfeksi dan menghancurkan sel CD4. Semakin banyak sel CD4 yang dihancurkan, kekebalan tubuh akan semakin lemah, sehingga rentan diserang berbagai penyakit. Untuk Info Segera Hubungi Kami HP/WA 081 329 878 999 Infeksi HIV yang tidak segera ditangani akan berkembang menjadi kondisi serius yang disebut AIDS (Acquired Immune Deficiency Syndrome). AIDS adalah stadium akhir dari infeksi virus HIV. Pada tahap ini, kemampuan tubuh untuk melawan infeksi sudah hilang sepenuhnya. Sampai saat ini belum ada obat untuk menangani HIV dan AIDS. Akan tetapi, ada obat untuk memperlambat perkembangan penyakit tersebut, dan dapat meningkatkan harapan hidup penderita. Tipe HIV Virus HIV terbagi menjadi 2 tipe utama, yaitu HIV-1 dan HIV-2. Masing-masing tipe terbagi lagi menjadi beberapa subtipe. Pada banyak kasus, infeksi HIV disebabkan oleh HIV-1, 90% di antaranya adalah HIV-1 subtipe M. Sedangkan HIV-2 diketahui hanya menyerang sebagian kecil individu, terutama di Afrika Barat. Infeksi HIV dapat disebabkan oleh lebih dari 1 subtipe virus, terutama bila seseorang tertular lebih dari 1 orang. Kondisi ini disebut dengan superinfeksi. Meski kondisi ini hanya terjadi kurang dari 4% penderita HIV, risiko superinfeksi cukup tinggi pada 3 tahun pertama setelah terinfeksi. Untuk Info Segera Hubungi Kami HP/WA 081 329 878 999 HIV dan AIDS di Indonesia Berdasarkan data Kementerian Kesehatan RI, selama tahun 2016 terdapat lebih dari 40 ribu kasus infeksi HIV di Indonesia. Dari jumlah tersebut, HIV paling sering terjadi pada heteroseksual, diikuti lelaki seks lelaki (LSL), dan pengguna NAPZA suntik (penasun). Di tahun yang sama, lebih dari 7000 orang menderita AIDS, dengan jumlah kematian lebih dari 800 orang. Data terakhir Kemenkes RI menunjukkan, pada rentang Januari hingga Maret 2017 saja sudah tercatat lebih dari 10.000 laporan infeksi HIV, dan tidak kurang dari 650 kasus AIDS di Indonesia. Gejala HIV dibagi dalam beberapa tahap. Tahap pertama adalah tahap infeksi akut, dan terjadi pada beberapa bulan pertama setelah seseorang terinfeksi HIV. Pada tahap ini, sistem kekebalan tubuh orang yang terinfeksi membentuk antibodi untuk melawan virus HIV. Pada banyak kasus, gejala pada tahap ini muncul 1-2 bulan setelah infeksi terjadi. Penderita umumnya tidak menyadari telah terinfeksi HIV. Hal ini karena gejala yang muncul mirip dengan gejala penyakit flu, serta dapat hilang dan kambuh kembali. Perlu diketahui, pada tahap ini jumlah virus di aliran darah cukup tinggi. Oleh karena itu, penyebaran infeksi lebih mudah terjadi pada tahap ini.

A True Story Let me tell you about Wendy. For more than ten years, Wendy struggled unsuccessfully with ulcerative colitis. A thirty-six-year-old grade school teacher and mother of three, she lived with constant cramping, diarrhea, and frequent bleeding, necessitating occasional blood transfusions. She endured several colonoscopies and required the use of three prescription medications to manage her disease, including the highly toxic methotrexate, a drug also used in cancer treatment and medical abortions. I met Wendy for an unrelated minor complaint of heart palpitations that proved to be benign, requiring no specific treatment. However, she told me that, because her ulcerative colitis was failing to respond to medications, her gastroenterologist advised colon removal with creation of an ileostomy. This is an artificial orifice for the small intestine (ileum) at the abdominal surface, the sort to which you affix a bag to catch the continually emptying stool. After hearing Wendy’s medical history, I urged her to try wheat elimination. “I really don’t know if it’s going to work,” I told her, “but since you’re facing colon removal and ileostomy, I think you should give it a try.” “But why?” she asked. “I’ve already been tested for celiac and my doctor said I don’t have it.” “Yes, I know. But you’ve got nothing to lose. Try it for four weeks. You’ll know if you’re responding.” Wendy was skeptical but agreed to try. She returned to my office three months later, no ileostomy bag in sight. “What happened?” I asked. “Well, first I lost thirty-eight pounds.” She ran her hand over her abdomen to show me. “And my ulcerative colitis is nearly gone. No more cramps or diarrhea. I’m off everything except my Asacol.” (Asacol is a derivative of aspirin often used to treat ulcerative colitis.) “I really feel great.” In the year since, Wendy has meticulously avoided wheat and gluten and has also eliminated the Asacol, with no return of symptoms. Cured. Yes, cured. No diarrhea, no bleeding, no cramps, no anemia, no more drugs, no ileostomy. So if Wendy’s colitis tested negative for celiac antibodies, but responded to—indeed, was cured by—wheat gluten elimination, what should we label it? Should we call it antibody-negative celiac disease? Antibody-negative wheat intolerance? There is great hazard in trying to pigeonhole conditions such as Wendy’s into something like celiac disease. It nearly caused her to lose her colon and suffer the lifelong health difficulties associated with colon removal, not to mention the embarrassment and inconvenience of wearing an ileostomy bag. There is not yet any neat name to fit conditions such as Wendy’s, despite its extraordinary response to the elimination of wheat gluten. Wendy’s experience highlights the many unknowns in this world of wheat sensitivities, many of which are as devastating as the cure is simple.

The substrates within each CDR that are frequently seen mutated are defined as “hotspots”. They are described by preferences for purines, rather than pyrimidines, as well as for particular codons, or codon motifs within the sequence. The fact that mutation in a hotspot can create or delete other hotspots indicates a higher order structure to the mutation process than that which is currently observable. McKay Brown, Mary Stenzel-Poore, Susan Stevens, Sophia K. Kondoleon, James Ng, Hans Peter Bachinger, and Marvin B. Rittenberg. Immunologic memory to phosphocholine keyhole limpet hemocyanin. Journal of Immunology, 148(2):339–346, January 1992.

You will recall from chapter 8 that getting four to six hours of sleep a night in the week before your flu shot means that you will produce less than half of the normal antibody response required, while seven or more hours of sleep consistently returns a powerful and comprehensive immunization response.

IgA can protect mucous membranes (like the lining of the digestive tract and the lining of the respiratory tract) from bacteria and viruses. That’s why breastfed babies are less likely to have diarrheal illnesses or colds in the first year. Most other diseases can be prevented with other types of antibodies. These protective antibodies can cross the placenta from the mother to the baby, but they cannot be passed in breast milk. That’s why breastfeeding can’t replace vaccination. Even if the mother is immune to whooping cough, for example, she can’t pass that immunity to her baby through breast milk. She can pass it through the placenta during pregnancy, but those antibodies will last in the baby’s bloodstream for only six months at the longest.

Instead of injecting an antigen & adjuvant as with traditional vaccines, Moderna plugs a small piece of coronavirus genetic code into human cells, altering DNA throughout the human body and reprograming our cells to produce antibodies to fight the virus. MRNA vaccines are a form

it may cause. Useful as they are to a virus, though, the spikes also represent points of vulnerability. They are the primary targets of immune response by an infected host. Antibodies, produced by white blood cells, are molecules that glom onto the spikes and prevent a virion from grabbing a cell.

Statistics also confirmed what every physician, indeed every person, already knew. In the civilian population as well, young adults had died at extraordinary, and frightening, rates. The elderly, normally the group most susceptible to influenza, not only survived attacks of the disease but were attacked far less often. This resistance of the elderly was a worldwide phenomenon. The most likely explanation is that an earlier pandemic (later analysis of antibodies proved it was not the 1889–90 one), so mild as to not attract attention, resembled the 1918 virus closely enough that it provided protection.

Inasmuch as the individual no longer confronts the other, he finds himself face to face with himself. On account of an aggressive backlash on the part of his immune system, a dislocation of his own code and the destruction of his own defences, the individual becomes in a sense an antibody to himself. Our society is entirely dedicated to neutralizing otherness, to destroying the other as a natural point of reference in a vast flood of aseptic communication and interaction, of illusory exchange and contact. By dint of communication, our society develops an allergy to itself. By becoming transparent in its genetic, biological and cybernetic being, the body even develops an allergy to its own shadow. Otherness denied becomes a spectre and returns in the form of a selfdestructive process. This, too, is the transparency of Evil.

The antibody, now a potential drug, would soon be renamed Herceptin, fusing the words Her-2, intercept, and inhibitor.

Drama mamas,” the homeless man interrupted again. “That’s what I call men and women who’ve caught the virus of victimitis excusitis. All they do is complain about how bad things are for them instead of applying their primal power to make things better. They take instead of give, criticize instead of create and worry instead of work. Build antibodies to combat any form of average from getting anywhere near your professional days at the office and your private life at home. Never be a drama mama.

You pride yourself on not knowing who employs you. Rather behind the curve, in that. I might pride myself, were I so inclined, on not knowing what it is I do.” “Literally?” “If one has a sufficiently open mind about it, certainly. I was an intelligence officer, early in my career. In a sense I suppose I still am, but today I find myself enabled to undertake investigations, as I see fit. Into, should I so deem them, matters of state security. Simultaneously, I’m a law enforcement officer, or whatever that means in as frank a kleptocracy as ours. I sometimes feel like an antibody, Mr. Netherton. One protecting a disease.

The tests fit the production code like an antibody fits an antigen.

patients with initially negative tests will develop positive results if retested six weeks later.) Proof of Lyme disease among these individuals who are negative on the two-tiered approach to testing may be hard to obtain, but occasionally one may get confirmation from other positive tests such as other antibody-based tests (C6 peptide ELISA or an IgG Western blot [even though the ELISA is negative]), a PCR assay for Borrelia DNA, or growth of the organism in culture. Experimental or newer tests (for example, tests of immune complexes or of Borrelia specific proteins) may also prove informative

They became demi-heroes, and were moved to respond with special sales, reduced prices, and a carnival atmosphere. The ghetto was a living organism: to counter external threats, it responded with the antibodies of courage, solidarity, and that desperate, magnificent love we usually call the survival instinct.

autoimmunity. “A person becomes allergic to his own tissue,” he explains, “and produces antibodies that attack healthy cells.

Under normal circumstances, the cytokines—soluble, hormonelike proteins—acted as messengers among the cells of the immune system, helping to target microbial infections like viruses, bacteria, parasites, and fungi, and directing the antibodies and killer cells to attack them. But with the Spanish flu, the whole system went into overdrive, the cytokines targeting everything in sight, the antibodies sticking like glue to anything they came into contact with, the killer cells blasting everything in range. It was like a wild shoot ’em up, devastating every cell in the body, compromising every defense mechanism, until the victim ultimately drowned in an overwhelming tide of his own mucus and virus-choked blood.

When a silverback gorilla dies of Ebola, he does it beyond the eyes of science and medicine. No one is there in the forest to observe the course of his agony, with the possible exception of other gorillas. No one takes his temperature or peers down his throat. When a female gorilla succumbs to Ebola, no one measures the rate of her breathing or checks for a telltale rash. Thousands of gorillas may have been killed by the virus but no human has ever attended one of those deaths - not even Billy Karesh, not even Alain Ondzie. A small number of carcasses have been found, some of which have tested positive for Ebola antibodies. A large number of carcasses have been seen and reported by casual witnesses, in Ebola territory at Ebola times, but because the forest is a hungry place, most of those carcasses could never be inspected and sampled by scientific researchers.

Then there are two new twists. First, it appears that one autoimmune disease, called ankylosing spondylitis, produces antibodies to a gut bacterium called Klebsiella pneumoniae. Conversely, a different autoimmune disease called rheumatoid arthritis produces antibodies to a second gut bacterium called Proteus mirabilis. Now, this might not seem that earth-shattering, but recent work has shown that the refined carbohydrates in processed food feed those two bacteria in particular, and that carbohydrate restriction improves both of these diseases. Indeed, a low-sugar, high-fiber Mediterranean diet has been shown to be efficacious at prevention and treatment of rheumatoid arthritis. Furthermore, introduction of fiber to the diet appears to improve asthma (frequently an autoimmune disease), likely by improving gut function and reducing inflammation.

With every other disease, the presence of antibodies is the signal that the patient has vanquished the disease. With AIDS, Fauci and Gallo, and now Gates, claim it’s a sign you’re about to die. Think about it; if the objective of an AIDS vaccine is to stimulate antibody production, then success would mean that every vaccinated person would also have an AIDS diagnosis.

not supplying the nursing homes with monoclonal antibodies where they might have saved thousands of lives.

used deceptive protocols to inflate the body counts. The CDC’s mortality numbers include anyone with an HIV positive antibody “status,” even if the deceased had no “AIDS defining illness,” and instead succumbed to suicide, a drug overdose, a car accident, or a heart attack.

Neither Gallo’s test nor any of the later-developed antibody tests have ever proven that these proteins they identify as HIV antibodies have anything to do with HIV, or any other retrovirus. The antibody test manufacturers recognize this deficiency with a caveat on their inserts:

There is no recognized standard for establishing the presence or absence of antibodies to HIV-1 and HIV-2 in human blood.”64

There’s nothing worse than the virus of politics. Especially when it infects someone without the antibodies to combat it.

The scientific basis for separating neocortical from limbic brain matter rests on solid neuroanatomical, cellular, and empirical grounds. As viewed through the microscope, limbic areas exhibit a far more primitive cellular organization than their neocortical counterparts. Certain radiographic dyes selectively stain limbic structures, thus painting the molecular dissimilarity between the two brains in clean, vivid strokes. One researcher made an antibody that binds to cells of the hippocampus—a limbic component—and found that those same fluorescent markers stuck to all parts of the limbic brain, lighting it up like a biological Christmas tree, without coloring the neocortex at all. Large doses of some medications destroy limbic tissue while leaving the neocortex unscathed, a sharp-shooting feat enabled by evolutionary divergence in the chemical composition of limbic and neocortical cell membranes.

Every life experience and all creativity come from the clash of opposing forces—the collision of the energy of polar opposites. It’s healthy to laugh and it’s healthy to cry—the brightest stars eventually become black holes—the good person without accountability becomes the evil one. Steroids take away skin redness, but if used too long, they redden the skin. The germaphobe cleans her hands to avoid germs, but cleaning too much destroys antibodies, allowing for infection. Lying down for a headache helps, but if you stay down too long it gives you a headache. The desire of total control results in the loss of all control. The greater the love you feel the deeper the pain of loss. If you help your child, she learns; if you do everything for her, she never learns…

Every life experience and all creativity come from the clash of opposing forces—the collision of the energy of polar opposites. It’s healthy to laugh and it’s healthy to cry—the brightest stars eventually become black holes—the good person without accountability becomes the evil one. Steroids take away skin redness, but if used too long, they redden the skin. The germaphobe cleans her hands to avoid germs, but cleaning too much destroys antibodies, allowing for infection. Lying down for a headache helps, but if you stay down too long it gives you a headache. The desire of total control results in the loss of all control. The greater the love you feel the deeper the pain of loss. If you help your child, she learns; if you do everything for her, she never learns…

With Operation Warp Speed, we had monoclonal antibodies that were high tech and fully FDA-approved by November 2020—long before the vaccines,” says Dr. McCullough.

It is important to realize that while vaccines are considered “smart bombs” that work by stimulating antibodies to just one microbe such as influenza or pertussis, in reality vaccines contain adjuvants that can stimulate widespread immune activation. In other words, vaccines can precipitate a cytokine cascade and systemic inflammation. This may result in a relapse or exacerbation of symptoms in patients with Lyme disease complex.21 I have witnessed several patients relapse after routine vaccinations.

Generous, pro-social behavior seems to strengthen these relationships across cultures. Generosity is even associated with better health and longer life expectancy. Generosity seems to be so powerful that, according to researchers David McClelland and Carol Kirshnit, just thinking about it “significantly increases the protective antibody salivary immunoglobulin A, a protein used by the immune system.

This is how we know that Anthony Fauci was well aware of remdesivir’s toxicity when he orchestrated its approval for COVID patients. NIAID sponsored that project. Dr. Fauci had another NIAID-incubated drug, ZMapp, in the same clinical trial, testing efficacy against Ebola alongside two experimental monoclonal antibody drugs. Researchers planned to administer all four drugs to Ebola patients across Africa over a period of four to eight months.10,11 However, six months into the Ebola study, the trial’s Safety Review Board suddenly pulled both remdesivir and ZMapp from the trial.12 Remdesivir, it turned out, was hideously dangerous. Within 28 days, subjects taking remdesivir had lethal side effects including multiple organ failure, acute kidney failure, septic shock, and hypotension, and 54 percent of the remdesivir group died—the highest mortality rate among the four experimental drugs.13 Anthony Fauci’s drug, ZMapp, ran up the second-highest body count at 44 percent. NIAID was the primary funder of this study, and its researchers published the bad news about remdesivir in the New England Journal of Medicine in December 2019.

Much like a vaccine inoculates our physical immune system against a virus, the act of resistance fortifies our psychological immune system. Refuting a point of view produces antibodies against future influence attempts.

Finally, he’d treated some of what he saw as the clearer prints with gold nanoparticles and attached cotinine antibodies; this could tell him if the individual who left the prints was a smoker.

Antibodies can continue to circulate in our blood for many months, but not all antibodies are equally effective in neutralizing a virus.

But a good vaccine maximizes its ability to kindle all of our immune system’s machinery, not only stimulating the production of antibodies but also spurring the activity of T cells and B cells that have memory, and are able to churn out new antibodies and other mediators of our immune response after they come into contact with a virus months or years later.

It was always likely that, in the event that a new virus emerged, the first therapeutics that could be made available would be antibody drugs fashioned to attack proteins on the virus’s surface. Yet we didn’t have a plan on the shelf for how we would maximize their use.

An October 3, 2021 study in the peer-reviewed journal BioRxiv by Stanford and Emory University scientists suggests that antibody levels generated by the Pfizer-BioNTech vaccine can suffer a ten-fold decrease seven months after the second vaccination.93 The scientists warn that the precipitous drop in antibody levels will compromise the body’s ability to defend itself against COVID-19 if the individual is exposed to COVID.

In the ten days after getting a flu shot, the blood levels of antibodies against the flu virus can increase fifty-fold. But to get the optimal benefit from the vaccination, its recipient must get enough sleep. In one study, participants were allowed only 4 hours of sleep a night for six nights, starting four nights before the vaccination. A week later, their antibody levels were only half those of participants who had slept normally.5 In another study, participants deprived of just a single night of sleep after receiving a hepatitis vaccination similarly produced only half the antibody levels of controls.

The so-called Hygiene Hypothesis, first voiced by Strachan, is that our immune system needs a certain amount of bacteria on which to flex its muscles. Deprived of it, the white cells that are designed to fight bacteria, called Th1 lymphocytes, fail to develop, and the other white cells, Th2 lymphocytes—those designed to make antibodies to defend the body against microbial dangers as well as to produce allergic reaction—will take over.

The characteristic of the influenza virus that makes it so dangerous and gives rise to epidemic after epidemic is its extreme mutability. It perpetually is changing the nature of its outer surface, which antibodies, the body’s most important defense system, must zero in on to be effective.

if they’ve managed to isolate any antibodies. In Mexico, no one survived long enough to produce them,

The virus leaves behind tiny pieces of itself after the body breaks it down. These pieces, similar to fragments of the virus’s outer shell, can clump together into structures that trick the body into thinking there’s a bigger threat. This triggers an intense immune response, like sounding a massive alarm over a few leftover virus bits, which can contribute to severe inflammation and symptoms seen in serious COVID-19 cases. It's like the virus has a ghostly afterlife, continuing to affect the body even after the majority of it has been destroyed. In the battle against the virus, our body initiates a defense mechanism that, while protective, also causes inflammation in critical areas, particularly where our stem cells are nurtured including the bone marrow, gut, and brain. For instance, the mitochondria in our blood cells—often referred to as the cellular powerhouses responsible for energy production — are compromised. Their functionality is impaired; they either push themselves too hard or don’t work as efficiently as they should, leading to a notable decrease in the body's energy levels. This energy deficit is more than just feeling tired; it's a systemic issue affecting the body's ability to fight off the virus effectively. The T cells, which are supposed to eliminate any remaining virus, find themselves restrained rendering their arsenal less effective and their capacity to multiply weakened. Despite these limitations, they release copious amounts of interferon-gamma (IFN-γ), a signaling molecule that rallies the body's defenses to fight vigorously. This intense response may play a role in the virus's stubborn persistence and ongoing immune response. Meanwhile, the B cells are on overdrive, producing an excessive amount of antibodies in this heightened state of alert. This heightened immune response complicates the path to recovery, posing challenges for individuals striving to reclaim their sense of health and wellness.

Fight Hashimoto’s Hypothyroidism with Red and Near-Infrared Light Therapy Several studies have shown profound benefits of red and near-infrared light therapy for autoimmune hypothyroidism. This is one of the only treatments that has been shown to potentially reverse (or at least greatly slow the progression of) autoimmune hypothyroidism. A recent 2013 randomized, placebo-controlled study in hypothyroid patients demonstrated that in people who got near-infrared light therapy, thyroid function dramatically improved, and remarkably, that thyroid antibody (TPOAb) levels were massively reduced. Amazingly, 47% of patients were able to stop medication completely! Moreover, the researchers also followed up 9 months after treatment and found that the effects were still evident!116 They even published a 6-year follow-up, which basically said that even at 6 years, some of the benefits still remained, but periodic sessions were recommended to maintain all benefits.117 (To be honest, I don’t suggest red/NIR light as a one-time treatment that is expected to last long-term. For optimal benefits, most research indicates that sessions be done with red/NIR therapy at least once a week consistently.) A 2010 study found that red light therapy helped 38% of study participants reduce their hypothyroid medication dose, with a whopping 17% being able to stop taking the medication altogether!118 A 1997 study done in Russia included some data on people with autoimmune hypothyroidism who underwent a thyroid surgery. They found that red/NIR light therapy improved thyroid hormone levels enough that they required, on average, roughly half as much thyroid hormone medication.119 A 2003 study done in the Ukraine showed that red light therapy can decrease thyroid medication needs by 50-75% in people with postsurgical hypothyroidism.120 A 2010 Russian dissertation study gave red light therapy on the thyroid gland to a group of people with hypothyroidism and found that 17% of people could completely get off thyroid medication and 38% could decrease the dose by 25-50µg.121 A 2014 study used the light therapy for 10 sessions with 347 women with subclinical hypothyroidism. At baseline, the average TSH (thyroid stimulating hormone) was 9.1 mIU/L. (Note: Higher TSH is a sign of hypothyroidism). After ten sessions of light therapy, the TSH was normalized in 337 (97%) of these women. Their TSH averaged at 2.2 mIU/L after just 10 light treatments.

Although unappreciated, Maurice Brodie advanced the field of polio research. He was one of the first to show that formaldehyde could kill polio virus; he was the first to figure out that formaldehyde-treated virus induced polio antibodies in children; he was the first to advance the notion that overtreatment with formaldehyde rendered the virus incapable of inducing polio antibodies; and he was the first to claim that a killed polio virus vaccine might induce long-lived protection.

Saad Jalal Toronto Canada - Boost Your Immune System with Healthy Eating A robust immune system is your body's first line of defense against illnesses and infections. While genetics plays a role in immunity, your diet plays a crucial part in supporting and strengthening it. By making mindful choices in your eating habits, you can boost your immune system and enhance your overall health. Saad Jalal said water is crucial for overall health. It helps with digestion, regulates body temperature, and supports various bodily functions. Aim to drink plenty of water throughout the day, and consider reducing sugary drinks and excessive caffeine consumption. Nutrient-Rich Foods: Incorporating a variety of nutrient-rich foods into your diet is key. Vitamins like C and D, minerals like zinc, and antioxidants found in fruits, vegetables, and whole grains help fortify your immune system. Citrus fruits, broccoli, spinach, and berries are excellent choices. Saad Jalal Toronto Canada - Protein for Immunity: Protein is essential for the production of antibodies and immune cells. Lean sources of protein, such as poultry, fish, beans, and tofu, provide the building blocks your body needs to fight off infections.

According to the CDC, in the fifth full year of AIDS, 1986, 12,205 people “with” AIDS died in the United States. At that time, CDC—in a now-familiar scheme to stoke pandemic fears—used deceptive protocols to inflate the body counts. The CDC’s mortality numbers include anyone with an HIV positive antibody “status,” even if the deceased had no “AIDS defining illness,” and instead succumbed to suicide, a drug overdose, a car accident, or a heart attack.

During the three years that the Pilgrims had been organizing their voyage to America, the Indians of southern New England had been hit by what scientists refer to as a virgin soil epidemic—a contagion against which they had no antibodies. From 1616 to 1619, what may have been bubonic plague introduced by European fishermen in modern Maine spread south along the Atlantic seaboard to the eastern shore of Narragansett Bay, killing in some cases as many as 90 percent of the region’s inhabitants.

Thyroid Panel (blood test)—Abnormal thyroid hormone levels are a common cause of anxiety, depression, forgetfulness, confusion, and lethargy. Having low thyroid levels decreases overall brain activity, which can impair your thinking, judgment, and self-control and make it very hard for you to feel good. Low thyroid functioning can make it nearly impossible to manage weight effectively. To know your thyroid levels, you need to know these figures: thyroid-stimulating hormone (TSH) Free T3 Free T4 Thyroid antibodies (thyroid peroxidase and thyroglobulin antibodies)

According to famed Silicon Valley investor Paul Graham, we haven’t had time to develop societal “antibodies to addictive new things.”[cxvii] Graham places responsibility on the user: “Unless we want to be canaries in the coal mine of each new addiction — the people whose sad example becomes a lesson to future generations — we’ll have to figure out for ourselves what to avoid and how.

The presence of anti-IF antibodies is highly specific for pernicious anemia.

suffer from rheumatoid arthritis and find that fasting so effectively removes the antigen/antibody complexes from your body's tissues that you may he pain-free, possibly for the first time in

Somatic hypermutation gives rise to B cells bearing mutant immunoglobulin molecules on their surface. Some of these mutant immunoglobulins have substitutions in the antigen-binding site that increase its affinity for the antigen. B cells bearing these mutant high-affinity immunoglobulin receptors compete most effectively for binding to antigen and are preferentially selected to mature into antibody-secreting plasma cells. The mutant antibodies that emerge from the selection do not have a random distribution of amino-acid substitutions. The changes are concentrated at positions in the heavy-chain and light-chain CDR loops that form the antigen-binding site and directly contact antigen. As the adaptive immune response to infection proceeds, antibodies of progressively higher affinity for the infecting pathogen are produced – a phenomenon called affinity maturation. Affinity maturation is a process of evolution in which variant immunoglobulins generated in a random manner are subjected to selection for improved binding to a pathogen. It achieves in a few days what would require thousands, if not millions, of years of classical Darwinian evolution in a conventional gene. This capacity for extraordinarily rapid evolution in pathogen-binding immunoglobulins is a major factor in allowing the human immune system to keep up with the generally faster-evolving pathogens.