Synergistic OX40 and CD30 signals sustain CD8+ T cells during antigenic challenge.

Abstract:

:Prior to acquiring a memory phenotype, antigen-activated CD8(+) T cells need to expand and then undergo a contraction phase. Utilizing two different antigenic stimuli, we provide evidence that the tumor necrosis factor receptors OX40 and CD30 integrate synergistic signals during the expansion phase to help maintain CD8(+) effectors. Thus, double deficiency in OX40 and CD30 leads to CD8(+) cell loss during expansion after immunization either with OVA or with murine CMV. Following their contraction, OX40- and CD30-deficient CD8(+) T cells persist normally in CMV-infected mice. In contrast, persistence after OVA challenge is dependent on OX40 and CD30. Collectively, our data define the important role of both OX40 and CD30 during CD8(+) T-cell activation, and show that long-term CD8 persistence after contraction is regulated not only by stimulatory receptors but also by the nature of the antigen or how the antigen is presented.

journal_name

Eur J Immunol

authors

Bekiaris V,Gaspal F,Kim MY,Withers DR,Sweet C,Anderson G,Lane PJ

doi

10.1002/eji.200939424

subject

Has Abstract

pub_date

2009-08-01 00:00:00

pages

2120-5

issue

8

eissn

0014-2980

issn

1521-4141

journal_volume

39

pub_type

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