CD4-independent T cells impair TCR triggering of CD4-dependent T cells: a putative mechanism for T cell affinity maturation.

Abstract:

:In vivo, T cells expressing low-affinity TCR predominate in primary, but not in secondary responses, a process referred to as T cell affinity maturation. Using CD4 dependence as a measure of the avidity of the interaction between the allospecific TCR and the alloantigen, we show that a similar process occurs in mixed lymphocyte cultures in vitro. Moreover, in coculture experiments high-avidity (CD4-independent) T cell clones inhibited the TCR internalization of low-avidity (CD4-dependent) T cell clones, whereas low-avidity T cell clones had no such effect on high-avidity T cell clones. The extent of inhibition of TCR internalization was dependent on both the avidity of the competing clone and the number of competing cells. Thus, there was a cell dose- and avidity-dependent effect on TCR internalization, an early parameter in T cell activation. These results suggest that low- and high-avidity T cell clones compete for the availability of antigen-presenting cells and that this favors the selective outgrowth of high-avidity T cell clones.

journal_name

Eur J Immunol

authors

van Bergen J,Kooy Y,Koning F

doi

10.1002/1521-4141(200102)31:2<646::aid-immu646>3.0

keywords:

subject

Has Abstract

pub_date

2001-02-01 00:00:00

pages

646-52

issue

2

eissn

0014-2980

issn

1521-4141

pii

10.1002/1521-4141(200102)31:2<646::AID-IMMU646>3.0

journal_volume

31

pub_type

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