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High IFN-γ Production of Individual CD8 T Lymphocytes Is Controlled by CD152 (CTLA-4)
Author(s) -
Pushpa Pandiyan,
Johannes Kolja Hegel,
Manuela Krueger,
Dagmar Quandt,
Monika C. BrunnerWeinzierl
Publication year - 2007
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.178.4.2132
Subject(s) - cytotoxic t cell , cd8 , cytokine , microbiology and biotechnology , immunology , t cell , biology , immune system , proinflammatory cytokine , chemistry , inflammation , biochemistry , in vitro
CD8 T cell expansion and cytokine production is needed to generate an effective defense against viral invasion of the host. These features of CD8 T lymphocytes are regulated, especially during primary responses, by positive and negative costimulation. We show in this study that surface expression of CD152 is highly up-regulated on activated CD8 T lymphocytes during primary immune responses, suggesting a prominent regulatory role. Indeed, production of the proinflammatory cytokine IFN-gamma, but not TNF-alpha, by CD8 T cells was inhibited by CD152 engagement. The inhibition was regulated independent of proliferation and IL-2 production, but dependent on the quality of the TCR signaling. We show that signals induced by CD152 on activated CD8 T lymphocytes reduce the frequency of IFN-gamma(high)-expressing cells. Our data also show that in activated CD8 T cells, the CD152-mediated inhibition of cytokine production is more pronounced than inhibition of their proliferation.

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