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Path_ggf_8i
Path_ggf_8i

... Other cellular receptors bind microbes for phagocytosis; these include receptors for mannose residues, which are typical of microbial but not host glycoproteins, and receptors for opsonins such as antibodies and complement proteins that coat microbes. ...
The Innate Immune Response
The Innate Immune Response

... Other cellular receptors bind microbes for phagocytosis; these include receptors for mannose residues, which are typical of microbial but not host glycoproteins, and receptors for opsonins such as antibodies and complement proteins that coat microbes. ...
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Saskatchewan Immunization Manual

... 1.8  Adaptive Immunity ‐ Cell Mediated Immunity (CMI)  Cell mediated immunity describes any immune response where T cells have the main role.  The  activation of T cells is an essential first stage in virtually all adaptive immune responses.  This is  called the “T cell‐dependent immune response”.   ...
Immunological Tolerance PP - The University of Arizona
Immunological Tolerance PP - The University of Arizona

... surface IgM and become anergic. These cells also up-regulate the Fas molecules on their surface. An interaction of these B cells with Fas-ligand-bearing cells results in their death via apoptosis. ...
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... HIV may infect dendritic cells and trigger TLR 7 or other sensors. Type I IFN is produced to help fight infection. However, the virus can also upregulate TRAIL (TNF-related apoptic ligand) on the DC’s. This can bind to TRAIL receptors on CD4 cells and induce CD4 depletion! ...
Chapter 7: Circulation and Blood
Chapter 7: Circulation and Blood

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The Adaptive Immune Response: T lymphocytes
The Adaptive Immune Response: T lymphocytes

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... Eosinophils have a bilobed nucleus and stain pink with the dye eosin. In panel b, the arrows note eosinophils that are partially degranulated. Their degranulation results in the release of rather ...
Acute Pain and Immune Impairment
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Ovarian Cancer Translational Research Initiative Planning Workshop
Ovarian Cancer Translational Research Initiative Planning Workshop

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Chapter 17
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...  Immediate protection against recent infection or ongoing disease  Antisera have several limitations ○ Contain antibodies against many antigens ...
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... body, in which cells and different mediators respond to tissue injury.[1] Inflammation, the response of tissue to injury, is characterized in the acute phase by increased blood flow and vascular permeability along with the accumulation of fluid, leukocytes, and inflammatory mediators such as cytokin ...
Chapter 16: Lymphatic System and Immunity
Chapter 16: Lymphatic System and Immunity

... harmful particles from lymph and to monitor body fluids. 2. Along with the red bone marrow, lymph nodes are centers for lymphocyte production. 3. Lymphocytes attack viruses, bacteria, and other parasitic cells. 4. The functions of macrophages are to engulf and destroy foreign substances, damaged cel ...
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Major Histocompability Complex (MHC)
Major Histocompability Complex (MHC)

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Dysregulation of Intestinal Mucosal Immunity
Dysregulation of Intestinal Mucosal Immunity

here. - Genomax Technologies Malaysia
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... Robert Weinberg and defines a distinct set of acquired capabilities that distinguish cancer from normal tissue. The Hallmarks help explain the complexities of cancer by describing a common set of capabilities present in cancer cells. These processes that, if unstopped, will allow cancer cells to thr ...
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Physics - BC Open Textbooks
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... alternate pathway does not involve antibody activation. Rather, C3 convertase spontaneously breaks down C3. Endogenous regulatory proteins prevent the complement complex from binding to host cells. Pathogens lacking these regulatory proteins are lysed. (credit: modification of work by NIH) ...
Tuberculosis tricks the body`s immune system to allow it to spread
Tuberculosis tricks the body`s immune system to allow it to spread

... suggesting that an autoimmunity process develops in TB. Professor Paul Elkington, of the University of Southampton, who led the project, said "We are not disputing that the immune system mainly targets the bacteria to fight it off, but we are suggesting that there is more to the story. "It seems tha ...
Outline 17
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...  They have a thin outer tunica externa o Lymphatic vessels converge along their path and become larger and larger o Lymphatic capillaries converge to form collecting vessels  These travel alongside veins and arteries o Collecting vessels alternate with lymph nodes  Lymph trickles through the node ...
TATA Molecular Immunology
TATA Molecular Immunology

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Characterization of the mycobacterial lipids presented by

... Several mycobacterial lipid antigens have been found to be associated with group I CD1 molecules - non-polymorphic, MHC class I-like glycoproteins. Mtb glycolipids presented in the context of CD1 molecules can get recognized by the T cells, which in turn triggers their activation and contributes to ...
1st seminar Ag, Ig, monoclonal 2016
1st seminar Ag, Ig, monoclonal 2016

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Cancer immunotherapy



Cancer immunotherapy (immuno-oncology) is the use of the immune system to treat cancer. Immunotherapies fall into three main groups: cellular, antibody and cytokine. They exploit the fact that cancer cells often have subtly different molecules on their surface that can be detected by the immune system. These molecules, known as cancer antigens, are most commonly proteins, but also include molecules such as carbohydrates. Immunotherapy is used to provoke the immune system into attacking the tumor cells by using these antigens as targets.Antibody therapies are the most successful immunotherapy, treating a wide range of cancers. Antibodies are proteins produced by the immune system that bind to a target antigen on the cell surface. In normal physiology the immune system uses them to fight pathogens. Each antibody is specific to one or a few proteins. Those that bind to cancer antigens are used to treat cancer. Cell surface receptors are common targets for antibody therapies and include the CD20, CD274, and CD279. Once bound to a cancer antigen, antibodies can induce antibody-dependent cell-mediated cytotoxicity, activate the complement system, or prevent a receptor from interacting with its ligand, all of which can lead to cell death. Multiple antibodies are approved to treat cancer, including Alemtuzumab, Ipilimumab, Nivolumab, Ofatumumab, and Rituximab.Cellular therapies, also known as cancer vaccines, usually involve the removal of immune cells from the blood or from a tumor. Immune cells specific for the tumor are activated, cultured and returned to the patient where the immune cells attack the cancer. Cell types that can be used in this way are natural killer cells, lymphokine-activated killer cells, cytotoxic T cells and dendritic cells. The only cell-based therapy approved in the US is Dendreon's Provenge, for the treatment of prostate cancer.Interleukin-2 and interferon-α are examples of cytokines, proteins that regulate and coordinate the behaviour of the immune system. They have the ability to enhance anti-tumor activity and thus can be used as cancer treatments. Interferon-α is used in the treatment of hairy-cell leukaemia, AIDS-related Kaposi's sarcoma, follicular lymphoma, chronic myeloid leukaemia and malignant melanoma. Interleukin-2 is used in the treatment of malignant melanoma and renal cell carcinoma.
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