Access study material, solved assignments, essays, and dissertations on Immunology. Learn about cells, immune system receptors, antigen processing, T cell activation, cytokines, cancer immunotherapy, immune deficiencies, transplantation immunology, vaccines, and more.
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Running head: IMMUNOLOGY IMMUNOLOGY Name of the Student Name of the University Author Note
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1IMMUNOLOGY Week 1 Cellsare generally called as the building blocks of life. A group of cells together forms tissue and tissue system. Now, the tissue system is accumulated to form a particular organ. A group of organs, which function together to perform one or more physiological actions called asorgan system. Immune system receptors, actually present on the cell membrane and binds to a substance, like cytokines and give responses. Cells involved in the natural or native immunity are skin and outer epithelial barrier cells, scavenger cells, like neutrophils, mast cells, basophils, eosinophils, macrophages, dendrite cells and natural killer cells. Also, cells involved in the specific immunity or acquired immunity are B- Lymphocytes and T- Lymphocytes and effecters T-cells. Week2 There are two types of receptors involved in recognition of antigen. One is B cell receptors and another one is T cell receptors. B cell receptors exclusively recognize unprocessed antigen binds to B cell receptors, like protein, lipids, polysaccharides and nucleic acids. T cell receptors recognizes processed peptides presented by major histocompatibility complex( MHC)molecule on the surface of other cells.
2IMMUNOLOGY Week 3 Antigens are deteriorated into small antigenic peptides that form substances in association with class I or class II MHC molecules. There are two types of antigen processings. One is exogenous processing and other is endogenous processing. Exogenous antigens are produced outside the cells. In case of exogenous processing exogenous antigens are ingested by phagocytises or endocytosis and fragmented in to small peptides by macrophages, dendrite cells and B cells. Now this degraded antigen fragments bind to the cleft within the class II MHC molecules. However, endogenous antigens are produced inside the host cells. In endogenous pathway fragmented antigens bind with the class l MHC molecules. The peptide-class I MHC complex is allowed to pass into the cell membrane. All cells producing endogenous toxin use this route to process the antigen. The main difference between the presentation of peptides by MHC class l and class ll is that, class I MHC complexes are formed in case of exogenous pathway and class II MHC complexes are formed in endogenous processing of antigen . The machinery involved in the processing of antigens is antigen processing and presenting machinery (APM). The purpose of antigen processing is to recognition of antigen presenting cells by T cell depending upon their expression of a spectrum of peptides combine to class I or Class II MHC complexes.
3IMMUNOLOGY Week 4 T cells get stimulated on identification of peptide-MHC complexes with T cell receptors and become proliferated. Then T cells form clonal expantion and split into memory cells and effecter T cells. It is used to recognition of antigens both in lymphoid organs and peripheral non-lymphoid tissues. The promptness of T cells needs identification of antigens shown over APCs. Its activation also requires cytokines manufactured by the APCs and by T cells. Activation of native T cells need dendrite cells and macrophages or B cells. However, both the signals are eventually important for highest activation of T cell stimulation. Signal 1 is produced because of the interaction of TCR-CD3 complex with MHC peptide. Signal 2 is propagated by the interaction of CD28 on the T cells and members of the B7 family on the APC, which is also known as co-stimulatory signal. Week 5 Cytokinesarethelargepolypeptidesorglycoproteins,whicharesecretedby particular cells of immune system. Cytokines are signalling molecules that regulate both immunity and inflammation. Cytokines regulate proliferation, differentiation, and function of immune system cells. Cytokine has very less molecular weight and it is secreted by white blood cells and other cells in response to a number of stimuli. Cytokine combines with specific receptors present on the membrane of target cells. Cytokines and cytokine receptors show very high bracing to each other. A specific cytokine can attach to a particular receptor on the membrane of the same cell that secreted it, which is termed as autocrine action. Sometimes binding occurs in nearer vicinity to the producer cell, which is termed as paracrine action.
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4IMMUNOLOGY Th1-Th2 dichotomy- The immunology of pregnancy is a complex issue, here the mothermusttoleratethe“foreign”foetus,andhencerequiresadegreeof immunosuppression. However, on the other hand it is necessary to maintain immune function to destroy infection. The specific mechanism which is engaged in successful pregnancy maintenance is the proposed switch from the T helper 1 (Th1) cytokine profile to the T helper 2 (Th2) profile.Therefore, maintaining the pregnancy and prevent the infection of the fetus Th1-Th2 dichotomy is required. Evolution strategies of pathogens to avoid host immune system- There is a way in which a pathogen or an infectious agent may elude immune surveillance is by altering its antigens. There are three ways by which antigenic variation can be performed. The most common process is hiding from immune cells by change or shed antigens and remain inaccessible to the host immune system. Second method is resisting innate immune defences, like carbohydrate capsule resists phagocytosis, replication within phagocytes, and inhibition to antimicrobial peptides. The third one is the activating and interfering with signalling pathways and resist antigen presentation. Pathogens are overcome by the following four mechanisms. First process is phagocyte signalling, which describes the binding of antibodies to antigens on the surface of pathogens, that makes it easier for phagocytes to find the pathogens and kill them. Second process is associated with the antigen clumping.
5IMMUNOLOGY The third process based on the prevention of cell entry by coating the surface of the pathogens. As a result, pathogens are incapable of entering body cells. In the last method, antibodies secret some complementary proteins, like perforin, that pokes holes in pathogen membranes. It causes burst of the pathogen cells. Immunotherapyis a type of therapeutic medication to prevent or treat certain disease with substances that stimulate the immune response. It can generally be applied to various disorders by boosting the immune system of the body. Also help to instruct the body’s immune system to attack cancer cells specifically. Sometimes man-made immune system proteins will be very helpful to fight against certain pathogens. Immunotherapy works by both passive and active therapies. Passive immune-therapy are based on the administration of monoclonal antibodies that aim either tumour-specific or over-expressed antigens. On the other hand active immunotherapy are crucially controlled by cytokines, cancer vaccines, cell-based therapies, tumour-specific CTL, tumour-derived APC and DC priming. Week 6 Canceris mainly developed by abnormal cell multiplication. It only happens by damaged gene or activated oncogene , which is called mutation of genes. Mutation can be happened by exposure to toxic chemicals, low dose radiation and infection with certain virus. The main characteristics of the cancer cells isunrestrained proliferation,unnatural nucleus,reduction of anchorage,chaotic multilayer,tumour or undifferentiated cell
6IMMUNOLOGY massproduction,undergoes metastasisandangiogenesis,lack of differentiation into specialized cellsandenhance the rate of anaerobic glycolysis. Oncogenesare the genes that earlier was proto oncogenes. That means, proto- oncogenes , when mutated may develop into oncogene. Oncogene are all those genes, which produces certain proteins that will lastly result cancer to grow into the body of an individual. Now oncogene when translated they will produce specific proteins known as onco-proteins. This oncoproteins are required for developing cancer. Because, it induces the cell division and proliferation pathway. Secondly, it averts the cell death, which is known as apoptosis or program cell death. Becauseofabnormalcelldivisionthecellwillmanufactureaenormousmassof undifferentiated cells, which will form tumour. Now, that tumour will generate new features after every particular time gap, like angiogenesis feature, metastasis feature and slowly the tumour will turn in to malignant tumour or cancer. As a result, the tumour will cause the person to die. There are some molecules or proteins that help in regulating whether the cell will follow the living pathway or follow the death pathway. Those regulatory proteins are known as tumour suppressor protein and the gene that encodes those protein are known astumour suppressor genes. TATA- Major number of tumor particles are also present on our own cells and are considered as tumor associated transplantation antigens (TATA). They are shown only during the growth of cells and lost during mature phase of life however re-disclose in tumours.
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7IMMUNOLOGY Immunotherapy for cancercan be developed by cytokines. Cytokines generally act as a molecular messenger that permit the cells of the immune system to impart with one another to produce a strong, coordinated response to a specific antigen. Cytokines act by stimulating immune effector cells and stromal cells of certain tumours directly. These molecules also promote cancer cell recognition by cytotoxic effecter cells. In the present years certain number of cytokines, including GM-CSF, IL-7, and IL-21, use in the clinical trials for the patient having advanced type of cancer. In other hand IL-10 and TGF-beta promote anti-tumour immunity. FDA gives achievement to IL-2 for metastatic melanoma and renal carcinoma and IFN-alpha for adjuvant therapy of stage III melanoma. Week 7 Somecommon immune-deficienciesare B cell deficiencies, T-cell deficiencies, Phagocytise cell deficiencies and complement deficiencies. Among them B-cell and T-cell deficiencies are the most severe type of deficiencies. Immune deficiency can be treated either by transplantation of bone marrow, stem cell and thymus or by replacement of immunoglobulin. Sometimes gene therapy and preventive antibiotic strategies are highly beneficial in the management of specific immune defects. Week 8 Transplantation immunologydeals with removing injured tissues from one site to another and is a form of organ transplantation. There is one side effect in this process, which is rejection from the donor. This rejection is caused by the immune response, which fails to recognize, ultimately leading to destruction of the transplanted organ.
8IMMUNOLOGY Before the operation tests are considered like testing of blood groups and tissue type to decrease the chances of rejection. Immunosuppressive drugs are administered to mediate the risk of rejection. Immunosuppressive drug ensures dampening of immunity resistance. Week 10 Traditional vaccines- Lived virus vaccines are mumps, measles, rubella and varicella vaccine. Killed or inactivated vaccines, such as whooping cough vaccine. Toxoid vaccines, like tetanus and diphtheria vaccine. Biosynthetic vaccines are Hepatitis B vaccine. Vaccine induces effecter mechanism by which it rapidly controls the replication of pathogens or inactivates their toxic component. Vaccine mainly acts by triggering of B and T-cell responses. We can influence this by developing primary and secondary immunity. Some of the newer types of vaccines are pneumococcal conjugate vaccine (PCV), rota virus vaccine (RV) and haemophilias influenza type b (Hib) vaccine. Week 11 Immunological bioinformatics- The combination of immunology and bioinformatics is known as immunomics or computational immunology. Bioinformatics have been used to reveal how MHC heterozygosis influences individual’s interaction with bacteria and the influenza virus. Also shows the process of the stress level of host to affect the pathogenicity of pseudomonas aeruginosa in the gut of human. Immunomics again properly describes the reason ofloweringthevalueofthefrequencyofstaphylococcal-inducedtoxicstress response.
9IMMUNOLOGY Week 12- Mechanisms of allergic reaction can be described as follows: Figure 1 :Mechanism of Allergy Source:(https://link.springer.com/chapter/10.1007) Allergy can be diagnosedby the measurement of the level of IgE antibodies in blood by radio-allergosorbent test (RAST). Also skin prick test and patch test are generally used to diagnose allergy. The most effective treatments of allergy are medication and immunotherapy.
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10IMMUNOLOGY In the first case antihistamine, decongestants, leukotrine receptor antagonist and steroid sprays are used in the treatment and management of an allergic reaction in the body. SECTION B 1. There are four types of route of administration of vaccine. Those are oral vaccination,intramuscularvaccination,subcutaneousvaccinationandintradermal vaccination. Oral vaccination is given against OPV and Rotavirus. Intramuscular vaccine is administered against Hepatitis B, IPV, Hib, diphtheria pertussis and tetanus (DPT) virus. Subcutaneous vaccination is used for measles and yellow fever. Lastly, the intradermal vaccination is given against BCG. 2.Co-stimulationis secondarily generated signal which the immune system cells depend on to activate an immune response. In most of the immune responses, activation needs the presence of a co stimulator. An antigen and a co stimulator are required to generate the immune response, which ensures that healthy cells are not destroy. 4. The capability of recipient T cells to identify antigen from donor ( transplanted organ) or donor MHC molecules directly or indirectly, known as allorecognition, begins allograft rejection. Activated T -cells undergo clonal expansion and split into effector cells. These cells then place into graft, where those cells initiate tissue damage. Also B cells and anti-HLA antibodies play an major role in the acute allograft rejection. Mycophenolate mofetilis used as an immunosuppressive agents in combination with ciclosporin in transplantation surgery.
11IMMUNOLOGY 5. Dendrite cells convert antigens into immunogens for T cells. DCs act as catalysts for triggering and controlling immunity. On the other hand, DCs are located in the body where antigens gain access to body and maintain a vital role in the induction of antitumor responses. Figure 2:DCs mediated immunology Source:(https://www.frontiersin.org/articles/10.3389) 6.Therapeutic antibodiesare certain kind of proteins activated by the immune responses through immune system and neutralize specific or non-specific foreign antigens. These are two types : monoclonal and polyclonal antibodies. Monoclonalantibodiesare manufacturedby a single cloneof cells, examples: abciximab, basiliximab, cetuximab and ipilimumab. Whereas, polyclonal antibodies are produced by serum or B-lymphocytes by in-vivo method, examples: S-100. Another types of immunoglobulin are IgG, IgA, IgM, IgE, IgD. They all are composed of two heavy chain and two light chain.