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#Autoimmunity
science-sculpt · 2 months
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The T Cell Landscape
T cells, a critical component of the adaptive immune system, stand as the body's elite force in combatting infections and diseases. These specialized lymphocytes boast remarkable diversity, each type playing a distinct role in orchestrating a targeted and effective immune response.
T cells, like all blood cells, originate from hematopoietic stem cells residing in the bone marrow. However, their training ground lies within the thymus, a specialized organ located in the chest. Here, they undergo a rigorous selection process known as thymocyte education. During this process, immature T cells, called thymocytes, are presented with self-antigens (molecules unique to the body) by special cells. Thymocytes that bind too strongly to these self-antigens are eliminated, preventing them from attacking healthy tissues later. Only thymocytes that demonstrate the ability to recognize foreign invaders while exhibiting tolerance to self are released into the bloodstream as mature T cells.
Following this rigorous training, mature T cells exit the thymus and embark on their patrol, circulating throughout the bloodstream and lymphatic system. They remain vigilant, constantly scanning for their specific targets – antigens. Antigens are foreign molecules, such as fragments of viruses, bacteria, or even cancerous cells, that trigger the immune response.
The hallmark of a T cell is its T cell receptor (TCR), a highly specialized protein complex embedded on its surface. This receptor acts like a lock, uniquely shaped to fit a specific antigen, the "key." Each T cell develops a unique TCR capable of recognizing only a single antigen, enabling a highly specific immune response.
But how do T cells encounter these hidden antigens lurking within infected or cancerous cells? This critical role is played by antigen-presenting cells (APCs). APCs, such as macrophages and dendritic cells, engulf pathogens or abnormal cells, break them down into smaller fragments (peptides), and present them on their surface complexed with major histocompatibility complex (MHC) molecules. MHC molecules act as identification tags, allowing T cells to distinguish between "self" and "non-self." When a T cell's TCR encounters its specific antigen bound to an MHC molecule on an APC, a dance of activation begins. The T cell becomes stimulated, and a cascade of signaling events is triggered. This leads to the T cell's proliferation, producing an army of clones specifically tailored to combat the recognized threat.
T cells are not a single, monolithic entity. They comprise a diverse population, each type with a specialized function:
Helper T Cells (Th Cells):
Helper T cells, often abbreviated as Th cells, play a central role in coordinating immune responses. They express the CD4 surface marker and can recognize antigens presented by major histocompatibility complex class II (MHC-II) molecules. Subtypes of helper T cells include Th1, Th2, Th17, and regulatory T cells (Tregs), each with distinct functions and cytokine profiles.
Th1 cells mediate cellular immunity by activating macrophages and cytotoxic T cells, crucial for defense against intracellular pathogens.
Th2 cells are involved in humoral immunity, promoting B cell activation and antibody production, thus aiding in defense against extracellular parasites.
Th17 cells contribute to the immune response against extracellular bacteria and fungi, producing pro-inflammatory cytokines. Regulatory T cells (Tregs) maintain immune tolerance and prevent autoimmunity by suppressing excessive immune responses.
Cytotoxic T Cells (Tc Cells):
Cytotoxic T cells, also known as Tc cells or CD8+ T cells, are effector cells responsible for directly killing infected or aberrant cells. They recognize antigens presented by MHC class I molecules on the surface of target cells. Upon activation, cytotoxic T cells release perforin and granzymes, inducing apoptosis in target cells and eliminating the threat.
Memory T Cells:
Memory T cells are a long-lived subset of T cells that persist after the clearance of an infection. They provide rapid and enhanced immune responses upon re-exposure to the same antigen, conferring immunological memory. Memory T cells can be either central memory T cells (TCM), residing in lymphoid organs, or effector memory T cells (TEM), circulating in peripheral tissues.
γδ T Cells:
Unlike conventional αβ T cells, γδ T cells express a distinct T cell receptor (TCR) composed of γ and δ chains. They recognize non-peptide antigens, such as lipids and metabolites, and are involved in immune surveillance at epithelial barriers and responses to stress signals.
Beyond the Battlefield: The Expanding Roles of T Cells: The remarkable capabilities of T cells have opened doors for several groundbreaking applications in medicine:
Vaccines: By presenting weakened or inactivated forms of pathogens, vaccines "train" the immune system to generate memory T cells. This prepares the body to recognize and rapidly eliminate the real pathogen upon future exposure, preventing disease.
Cancer immunotherapy: CAR T-cell therapy, a revolutionary approach, genetically engineers a patient's own T cells to express chimeric antigen receptors (CARs) that recognize and target specific cancer cells. These "supercharged" T cells are then reintroduced into the patient, unleashing a potent attack against the tumor.
Autoimmune disease treatment: Researchers are exploring ways to manipulate T cells to suppress harmful immune responses that underlie autoimmune diseases like rheumatoid arthritis and multiple sclerosis.
The diverse array of T cells underscores the immune system's complexity and adaptability in mounting tailored responses against a myriad of threats. From orchestrating immune reactions to maintaining tolerance and establishing long-term immunity, T cells play multifaceted roles in safeguarding the body's health. Understanding the intricacies of T cell biology not only sheds light on immune-mediated diseases but also paves the way for developing novel therapeutic strategies harnessing the power of the immune system.
T cells represent a fascinating aspect of immunology, with their diversity and specificity driving the complexity of immune responses. As research advances, further insights into T cell biology promise to revolutionize immunotherapy and enhance our ability to combat diseases ranging from infections to cancer. By understanding and harnessing their power, we can unlock new avenues for protecting and improving human health.
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thelupuslady · 20 days
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Recovering from a nasty nasty lupus flare! On steroids.
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the-diabolic-acid · 5 months
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gancanagh · 7 months
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...Some people know me as hope...
So cower at the man I've become when I sing from the top of my lungs
That I won't retire, I'll stand in your fire, inspire the meek to be strong
And when I am gone, I will rise in the music that I left behind
Ferocious, persistent, immortal like you, we’re a coin with two different sides
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nicolagriffith · 3 months
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Snippets—Women and autoimmune disease, the first wine, early Americans, and how cats purr
For Sunday: snippets of science news on some of my favourite things in life (well, the favourite things we can talk about in polite company): cats, wine, and humans in the Americas, plus one of my ongoing personal concerns, autoimmune disease. Some weight
Some of this stuff dates from late last year when I was too busy with Menewood stuff to comment. But as some of my favourite things in life (well, the favourite things we can talk about in polite company) are cats, wine, and history, and as one of my ongoing personal concerns is autoimmune disease, I thought, Eh, let’s combine them. We’ll start with the weighty stuff first then lighten up a…
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what-remains-of-wren · 10 months
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I think what people underestimate most about chronic and repeated childhood trauma is that it truly effects every single proportion of you.
There is some theory at the moment that a component of depression is inflammation. This isn’t just out of left field, since clinical encephalitis is well demonstrated to cause psychosis. Encephalitis is inflammation of the brain and it causes neuropsychiatric symptoms like you have never seen before- and is usually quite hard to detect on labs until someone starts having siezures- by which point you’re in shit.
This is partly why fibromyalgia symptoms are treated with antidepressants, and why depression can have some wicked somatic symptoms- they’re not two seperate things- treat the body to treat the brain, or if the brain is convinced the body is being hurt because you feel some sort of pain all the time- emotional or psychological- treat the brain.
It’s not as simple as one thing causing the other either. Inflammation is a mistaken immune response. One of the major effects of cortisol, the hormone released when you are chronically stressed, is that you stop producing things you don’t need to produce. Processes stop working where they should and can even affect your immune system. Recurrent trauma stops your body from producing it’s own natural inflammatories.
Stress also causes epigenetic changes. These are heritable. These can mute and activate genes- most notably those responsible for stopping cancer. It is possible for your mother or father to have a stressful period in life, epigenetic changes to happen, and then for you to be born with those already happening. 
The majority of autoimmune conditions have stress- acute or chronic- as a major trigger factor. Stress isn’t just in the head. You produce hormones, you make protiens, you make antibodies- sometimes ones you shouldn’t. Mental and physical health aren’t too seperate, especially not when it comes to this area.
 What I’m saying is that what you’ve gone through isn’t just in your head. Chances are it’s in your body as well. So don’t expect to just feel it in your head.
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ghostzussy · 3 months
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"Why are you wearing a mask again why are you afraid" BECAUSE I'M AUTOIMMUNE AND MY IMMUNE SYSTEM CAN'T TAKE ANOTHER L PLS
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longhaulerbear · 1 year
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Pathway analysis identified the strongest network interactions particularly for proteins involved in thrombogenicity and enhanced platelet activity, but also inflammation, cardiac contractility and hypertrophy, and increased adrenergic activity. Our observations generated by the first use a label-free unbiased quantification reveal the proteomic footprint of POTS in terms of a hypercoagulable state, proinflammatory state, enhanced cardiac contractility and hypertrophy, skeletal muscle expression, and adrenergic activity. These findings support the hypothesis that POTS may be an autoimmune, inflammatory and hyperadrenergic disorder.
Growing evidence points toward POTS being an autoimmune disease, oftentimes triggered by a viral or bacterial infection, Lumican (LUM) interacts with CD14 and CD18 on macrophage and neutrophils to promote innate immune response, and normally helps to restrict autoimmunity, antiviral, bacterial and inflammatory responses.
Increased expression of skeletal muscle myosin in POTS
We observed significantly increased expression of myosin light chain 1/3, skeletal muscle isoform (MYL1) expressed only in fast skeletal muscles in adults and required for proper formation and maintenance of myofibers, and muscle function.
POTS, differences in sympathetic nerve discharge and fiber loss from skeletal muscles is observed which could putatively explain muscle fatiguability and deconditioning associated with POTS.
Upregulated alpha-adrenergic activity in POTS
We noted significant upregulation of myosin regulatory light chain 12B (MYL12B) protein in POTS, which triggers polymerization of vascular smooth muscle.
Vascular smooth muscle cells are predominantly innervated by the sympathetic α1 adrenergic receptors and play an important role in maintaining cardiovascular homeostasis by regulating vascular tone, blood flow and blood pressure. In POTS, increased sympathetic activation causes activation of the adrenergic receptors and a surge in norepinephrine levels, and approximately 89% of patients with POTS exhibit elevated levels of autoantibodies against the adrenergic α1 receptor.
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Me: *wiping sweat off myself because I’m allergic to it*
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It is 33*c today 😭
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spooniestrong · 7 months
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theonlyladyt · 1 month
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Low Carb vs Insulin Sensitivity
Hello my lovelies I am having an autoimmune flare presently and this has triggered the symptoms of Reactive Hypoglycemia (RH for short) as well. So it took several days before I could continue this blog post today. The flare I think was on its way a few days ago as I started waking up more than usual. My blood glucose which was fairly stable, started waking me up with autoimmune symptoms and…
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thelupuslady · 1 year
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crimeronan · 8 months
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CDC finally fuckin' recommended the new COVID boosters for everyone in the US. letting my american followers who don't check the news know because i've been turned away for wanting to get an extra booster & now won't be anymore & it's Lovely. most americans are not going to get these and are going to grumble about them, which sucks as far as spread goes - but DOES mean u can schedule with ur local pharmacy sooner rather than later. please do so. ur immunocompromised friends and ur own body will thank u.
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k-star-holic · 6 months
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Na Young-seok, Endless AutoimmunityCloning?
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drshook · 9 months
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Can Turmeric Help With Managing Psoriasis
Turmeric, a traditional Ayurvedic herb, has been used for centuries to improve overall health and well-being. Recently, research suggests that turmeric may also be beneficial in helping with the management of psoriasis. Psoriasis is an autoimmune disease that causes red and scaly patches on the skin. Studies suggest that turmeric can help with reducing inflammation, which often plays a role in…
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ayeforscotland · 1 month
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Holy shit.
Researchers at the University of Chicago have been able to create an ‘inverse vaccine’ that can remove the immune systems memory of specific molecules.
Reading that, sounds like a horrendous bio weapon in the making. But the plan is for it to be used to treat autoimmune diseases like multiple sclerosis, type one diabetes and rheumatoid arthritis.
This was already proven to be able to prevent autoimmunity but the new work shows it can be used to treat ongoing autoimmune issues.
Source.
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