Immunity adaptive

The two major components of the immune system are soluble factors and cells. The former include complement, cytokines and antibodies. The cells include lymphocytes, neutrophils macrophages and eosinophils (see Appendices 17.1 and 17.2). The most numerous are the lymphocytes. [Pg.380]

Two major classes of lymphocytes are T- and B-cells. Although both develop from the pluripotent stem cell in the bone marrow, B-ceUs remain in the marrow to mature, prior to release into the blood (hence their name, B-cells). In contrast, immature T-lymphocytes are released from the bone marrow and travel to the thymus, where they develop and mature prior to release into the blood (hence their [Pg.380]

Helper T-ceU 1 ThI CD4-H Coordination of immune response, particularly activation of phagocytosis by macrophages. [Pg.381]

Cytotoxic T-cells T CD8-H Killing of host cells infected with viruses. [Pg.381]

Humoral immunity depends on soluble, noncellular effector mechanisms of the immune system. These include defensins and complement components (proteins of the innate immune system) and antibodies (products of the adaptive immune system). They are capable of reacting with foreign substances (e.g., bacteria and viruses) to produce detoxification and elimination. [Pg.605]

Immune Defense. Figure 1 Innate immune responses after challenge of skin or mucosa Acute inflammation and priming of adaptive immunity. [Pg.613]

Parallel to orchestrating acute inflammatory processes by providing an optimal milieu of cytokines, mediators, and adhesion molecules in order to recruit and activate effector cells to the site of infection, dendritic cells also setve as professional antigen-presenting cells for cells of the adaptive immune system ( antigen presentation ... [Pg.614]

Cellular Components of Adaptive Immune Responses are T- and B-Lymphocytes whereas Humoral Components are Antibodies. [Pg.614]

Immune Defense. Figure 2 Cytokines involved in the development of adaptive immune responses in secondary lympoid tissues such as the lymph nodes or spleen. Abbreviations B B-lymphocyte, IFN interferon, Ig immunoglobulin, IL interleukin, NK natural killer cell, TE T-effector (cytotoxic) lymphocyte, TH T-helper lymphocyte... [Pg.615]

Immune Defense. Figure 3 Drugs involved in suppressing innate and adaptive immune response. Abbreviations mob monoclonal antibody, TCR T-cell antigen receptor, IL-2 interleukin-2, R receptor, CD cluster of differentiation. [Pg.617]

NF-kB regulates both innate and adaptive immune responses ( immune defense) [2]. Understanding the function of NF-kB in the development, maintenance, and activation of cells from the immune system (including hematopoietic cells, macrophages, dendritic cells, B and T lymphocytes) has greatly benefited from the analysis of knockout mice in which individual NF-kB family members were defective. [Pg.886]

NF-kB is also crucial for the proper functioning of the adaptive immune system not only by acting on the immune cells themselves but also by participating in the development and organization of the secondary lymphoid organs (lymph nodes, spleen, and Peyer s patches), in which both B and T lymphocytes undergo maturation and activation. NF-kB proteins have an important role in lymphocyte development and... [Pg.887]

The activation of DRF-3 through the TREF dependent pathway allows for chemokines such as RANTES to be produced. It also leads to the production of DFN-a and EFN-(3, which are involved in anti-viral immunity. The TREF pathway, activated by either TLR-3 or TLR-4, can also induce MHC class-II expression and costimulatory molecules, thus leading to T-cell activation. This provides an important link between innate and adaptive immunity. [Pg.1210]

Acyl-CoA Synthetase Adaptive Immunity Adaptor Proteins Addiction Addison s Disease Additive Interaction Adenosine Adenosine Receptors Adenoviruses Adenylate Cyclase Adenylyl Cyclases ADH ADHD... [Pg.1485]

IFNs are natural glycoproteins produced by the cells of most vertebrates in response to the challenge by foreign agents, such as infectious organisms (viruses, bacteria, fungi, and parasites), and by tumor cells. IFNs can be produced by cells of the innate and adaptive immune systems and by non-immune cells such as fibroblasts and epithelial cells. [Pg.205]

Gough DJ, Sabapathy K, Ko EY, Arthur HA, Schreiber RD, Trapani JA, Clarke CJ, Johnstone RW (2007) A novel c-Jun-dependent signal transduction pathway necessary for the transcriptional activation of interferon gamma response genes. J Biol Chem 282 938-946 Guidotti LG, Chisari EV (2001) Noncytolytic control of viral infections by the innate and adaptive immune response. Annu Rev Immunol 19 65-91... [Pg.234]

Trinchieri G Interleukin-12 and the regulation of irmate resistance and adaptive immunity. Nat Rev Immunol 2003 3 133-146. [Pg.38]

Kadowaki N. Antonenko S, Lau JY, Liu YJ Natural 45 interferon a/p-producing cells link irmate and adaptive immunity. J Exp Med 2000 192 219-226. [Pg.39]

Specific defence mechanisms (adaptive immune system)... [Pg.283]

Beyond roles of chemokine receptors in hematopoiesis and innate immunity, roles for chemokines in adaptive immunity emerged. Moreover, other nonleukocyte migration properties of chemokine receptors have been identified. These include roles in the biology of endothelial cells (Chapter 15), cancer (Chapter 16), smooth muscle (Chapter 11), fibroblasts (Chapter 14), stem cells (Chapter 8), and all cell types associated with nervous system tissues (Chapter 17). In many instances, broad functional overlap is evident as chemokines can direct the migration of these cells just as they do with leukocytes. In certain instances, the ability of chemokines to retain cell populations within a specific microenvironment is as important as their migration-promoting properties. However, it is also clear that migration and retention are not the sole end points. [Pg.6]

Yang D, Chertov O, Bykovskaia SN, et al. Beta-defensins linking innate and adaptive immunity through dendritic and T cell CCR6. Science 1999 286(5439) 525-528. [Pg.49]

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