By J. H. L. Playfair
Immunology at a look is designed to be a concise, comfortably available creation and revision reduction for undergraduate scientific and technological know-how scholars. Following the now established, easy-to-use structure, every one subject is gifted as a double-page unfold with key evidence followed through clear,informative line diagrams illustrating the basic points.The 7th version of this well known immunology textbook has been thoroughly up-to-date to make sure that middle wisdom approximately immunology is summarized within the 'at a look' format.Immunology At a look will proceed to attract all scholars of biomedical technology and medication who need a speedy, but thorough take hold of of immunology. Condenses the topic into forty-one double-page spreads, every one corresponding approximately to a 50 minute lecture. provides a schematic diagram at the left web page and a concise clarification at the correct displaying the mechanisms fascinated with immunological approaches. Has been thoroughly up-to-date with specific emphasis on fresh figuring out of the genetic foundation of immune responses Immunology at a look will proceed to attract all scholars of biomedical technology and drugs who need a fast, but thorough, snatch of immunology.
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Extra info for Immunology at a glance
One key step in T cells is the activation of the transcription factor NF-AT, and it is this step which is inhibited by cyclosporin, an important immunosuppressant used clinically to block transplant rejection (see Fig. 37). IL2 One of the main events which follow recognition of antigen by T cells is that the responding T cells undergo several rounds of cell division (a phenomenon known as clonal expansion). T cell proliferation is driven largely by the secretion from the T cells themselves of the cytokine interleukin 2.
Hypervariable regions Three parts of each of the variable regions of heavy and light chains, spaced roughly equally apart in the amino acid sequence (see figure, lower left) but brought close together as the chain folds into a P-pleated sheet, form the antigen-combining site. It is because of the enormous degree of variation in the DNA coding for these regions that the total number of combinations is so high. The hypervariable regions are also unusually susceptible to further somatic mutation, which occurs during B cell proliferation within the germinal centre of lymph nodes or spleen.
CD 19 One of the molecules (the complement receptor CR2 is another) that need to be bound in order to fully activate the B cell, thus playing a 'coreceptor' role somewhat analogous to CD4, CD8 and CD28 on theT cell. CD 19 is also a convenient 'marker' for B cells, since it is not expressed on other types of cell. Origins of diversity Four features of antibody contribute to the enormous number of possible antigen-binding sites, and thus of antibody specificities: (1) gene rearrangement allows any V, D and J genes to become associated; (2) a heavy chain can pair with either a K or h light chain; (3) V-D and D-J joining is not always at precisely the same point; (4) mutations can occasionally occur in the V genes of an individual B cell (this would be a case of somatic mutation) and the resulting small change in the antigen-binding site may sometimes prove advantageous, for example by increasing the affinity of an antibody for the inducing antigen.