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Factors controlling the turnover of T memory cells
Author(s): Sprent J, Tough DF, Sun SQ
Source: IMMUNOLOGICAL REVIEWS    Volume: 156    Pages: 79-85    Published: APR 1997  
Times Cited: 67     References: 57     
Abstract: Most of the T cells participating in the primary immune response are rapidly eliminated, but small numbers of these cells survive and differentiate into long-lived memory cells. Information on the life history of memory cells can be obtained by studying the component of memory-phenotype T cells found in normal animals; these cells are presumed to represent memory cells specific for various environmental antigens. For CD8(+) cells, in vivo exposure to viruses and certain other infectious agents causes a large proportion of memory-phenotype (CD44(hi)) cells to enter the cell cycle. In this situation, stimulation of CD44(hi) CD8(+) cells does not seem to require T-cell receptor ligation and appears to reflect release of various cytokines, especially type I interferon. The capacity of infectious agents to induce non-antigen-specific stimulation of T cells may play a role in boosting the survival of memory cells and perhaps also in providing an adjuvant function during the primary response.
Document Type: Review
Language: English
Reprint Address: Sprent, J (reprint author), Scripps Res Inst, DEPT IMMUNOL, IMM4, 10550 N TORREY PINES RD, LA JOLLA, CA 92037 USA
Publisher: MUNKSGAARD INT PUBL LTD, 35 NORRE SOGADE, PO BOX 2148, DK-1016 COPENHAGEN, DENMARK
Subject Category: Immunology
IDS Number: WY221
ISSN: 0105-2896
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