Literature DB >> 2113314

A cell culture model for T lymphocyte clonal anergy.

R H Schwartz1.   

Abstract

T lymphocytes respond to foreign antigens both by producing protein effector molecules known as lymphokines and by multiplying. Complete activation requires two signaling events, one through the antigen-specific receptor and one through the receptor for a costimulatory molecule. In the absence of the latter signal, the T cell makes only a partial response and, more importantly, enters an unresponsive state known as clonal anergy in which the T cell is incapable of producing its own growth hormone, interleukin-2, on restimulation. Our current understanding at the molecular level of this modulatory process and its relevance to T cell tolerance are reviewed.

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Year:  1990        PMID: 2113314     DOI: 10.1126/science.2113314

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  367 in total

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5.  Lack of costimulation by both sphingomyelinase and C2 ceramide in resting human T cells.

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Journal:  Immunology       Date:  2000-06       Impact factor: 7.397

6.  Enhancement of cALL immunogenicity by co-culture with a CD154 expressing 293 cell line.

Authors:  A J Lee; C Haworth; R M Hutchinson; R Patel; R Carter; R F James
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Review 7.  T cell signal transduction and the role of CD7 in costimulation.

Authors:  R Stillwell; B E Bierer
Journal:  Immunol Res       Date:  2001       Impact factor: 2.829

8.  Signaling through CD28 and CTLA-4 controls two distinct forms of T cell anergy.

Authors:  A D Wells; M C Walsh; J A Bluestone; L A Turka
Journal:  J Clin Invest       Date:  2001-09       Impact factor: 14.808

9.  T cell activation up-regulates cyclic nucleotide phosphodiesterases 8A1 and 7A3.

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Review 10.  CD28, CTLA-4 and their ligands: who does what and to whom?

Authors:  D M Sansom
Journal:  Immunology       Date:  2000-10       Impact factor: 7.397

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