Use of adoptive transfer of T-cell-antigen-receptor-transgenic T cell for the study of T-cell activation in vivo.

Abstract:

:Adoptive transfer of TCR-transgenic T cells uniformly expressing an identifiable TCR of known peptide/MHC specificity can be used to monitor the in vivo behavior of antigen-specific T cells. We have used this system to show that naive T cells are initially activated within the T-cell zones of secondary lymphoid tissue to proliferate in a B7-dependent manner. If adjuvants or inflammatory cytokines are present during this period, enhanced numbers of T cells accumulate, migrate into B-cell-rich follicles, and acquire the capacity to produce IFN-gamma and help B cells produce IgG2a. If inflammation is absent, most of the initially activated antigen-specific T cells disappear without entering the follicles, and the survivors are poor producers of IL-2 and IFN-gamma. Our results indicate that inflammatory mediators play a key role in regulating the anatomic location, clonal expansion, survival and lymphokine production potential of antigen-stimulated T cells in vivo.

journal_name

Immunol Rev

journal_title

Immunological reviews

authors

Pape KA,Kearney ER,Khoruts A,Mondino A,Merica R,Chen ZM,Ingulli E,White J,Johnson JG,Jenkins MK

doi

10.1111/j.1600-065x.1997.tb00959.x

subject

Has Abstract

pub_date

1997-04-01 00:00:00

pages

67-78

eissn

0105-2896

issn

1600-065X

journal_volume

156

pub_type

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