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- A H Lichtman
- Department of Pathology, Brigham and Women's Hospital, Boston, MA.
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- J Chin
- Department of Pathology, Brigham and Women's Hospital, Boston, MA.
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- J A Schmidt
- Department of Pathology, Brigham and Women's Hospital, Boston, MA.
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- A K Abbas
- Department of Pathology, Brigham and Women's Hospital, Boston, MA.
説明
<jats:p>The activation of T lymphocytes requires their stimulation via clonotypic antigen receptors as well as nonantigen-specific costimulators, the best defined of which is the cytokine interleukin 1 (IL-1). Recent studies have shown that murine CD4+ helper T lymphocytes consist of two nonoverlapping subsets that selectively utilize interleukin 2 (IL-2) or interleukin 4 as their autocrine growth factors and are called Th1 and Th2 cells, respectively. We now show that IL-1 functions as a costimulator for the proliferation of Th2 but not of Th1 clones and only Th2 cells express high-affinity receptors for IL-1. Secretion of autocrine growth-promoting lymphokines by Th1 and Th2 cells occurs after stimulation via the antigen receptor-CD3 complex and is neither dependent on nor affected by IL-1. These findings suggest that the activation of T lymphocytes can be divided into two stages, lymphokine secretion and proliferation, and only proliferation requires costimulators such as IL-1. Moreover, the prevailing view that IL-1 functions as a costimulator by inducing secretion of IL-2 or expression of IL-2 receptors may not be generally applicable, because IL-2-producing Th1 clones do not express receptors for IL-1 and are insensitive to this cytokine.</jats:p>
収録刊行物
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- Proceedings of the National Academy of Sciences
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Proceedings of the National Academy of Sciences 85 (24), 9699-9703, 1988-12
Proceedings of the National Academy of Sciences
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詳細情報 詳細情報について
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- CRID
- 1362544421039680256
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- NII論文ID
- 30016284078
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- ISSN
- 10916490
- 00278424
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- データソース種別
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- Crossref
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