TCR independent suppression of CD8(+) T cell cytokine production mediated by IFNγ in vivo.
Virology
; 498: 69-81, 2016 11.
Article
in En
| MEDLINE
| ID: mdl-27564543
ABSTRACT
CD8(+) memory T cells produce IFNγ within hours of secondary infection, but this is quickly terminated in vivo despite the presence of stimulatory viral antigen, suggesting that active suppression occurs. Herein, we investigated the in vivo effector function of CD8(+) memory T cells during successive encounters with viral antigen. CD8(+) T cells in immune mice receiving prior viral or peptide challenge failed to reproduce IFNγ during LCMV rechallenge. Surprisingly, this refractory state was induced even in memory cells that had not encountered their cognate antigen, indicating that the silencing of CD8(+) T cell responses is TCR-independent. Direct injection of IFNγ also suppressed the ability of virus-specific memory cells to respond to subsequent viral challenge. We propose the existence of a negative feedback loop whereby IFNγ, produced by memory CD8(+) T cells to combat viral challenge, acts - directly or indirectly - to limit its further production.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Receptors, Antigen, T-Cell
/
Cytokines
/
Interferon-gamma
/
CD8-Positive T-Lymphocytes
/
Immunomodulation
Limits:
Animals
Language:
En
Journal:
Virology
Year:
2016
Document type:
Article
Affiliation country:
United States