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Part of the book series: Current Topics in Microbiology and Immunology ((CT MICROBIOLOGY,volume 231))

Abstract

Effector T cells constitute a critical component in the immune response to most viral infections (Doherty et al. 1992). Consequently, understanding the mechanisms regulating the generation and function of effector T cells is central to the study of viral pathogenesis. It is characteristic that T cells — as opposed to B cells — are only able to exert their effector function within a very limited distance. Therefore, once effector T cells are generated, they must be able to migrate to relevant sites of infection. This requires a set of surface receptors which direct the migration of effector cells to infected areas. However, not only must fully differentiated effector T cells be able to reach any part of the organism, but, it is also nescessary for naive T cells to continually recirculate in order for the immune system to optimally utilize the limited number of cells with T cell receptors (TCRs) relevant to a given antigen.

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Thomsen, A.R., Nansen, A., Christensen, J.P. (1998). Virus-Induced T Cell Activation and the Inflammatory Response. In: Holzmann, B., Wagner, H. (eds) Leukocyte Integrins in the Immune System and Malignant Disease. Current Topics in Microbiology and Immunology, vol 231. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71987-5_7

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