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Cloning of B7-2: a CTLA-4 Counter-Receptor That Costimulates Human T Cell Proliferation

Freeman, Gordon J., Gribben, John G., Boussiotis, Vassiliki A., Ng, Judy W., Restivo, Vincent A., Lombard, Lisa A., Gray, Gary S., Nadler, Lee M.·1993·Science

Abstract

Although presentation of antigen to the T cell receptor is necessary for the initiation of an immune response, additional molecules expressed on antigen-presenting cells deliver essential costimulatory signals. T cell activation, in the absence of costimulation, results in T cell anergy. The B7-1 protein is a costimulator molecule that regulates interleukin-2 (IL-2) secretion by signaling through the pathway that uses CD28 and CTLA-4 (hereafter referred to as the CD28 pathway). We have cloned a counter-receptor of CD28 and CTLA-4, termed B7-2. Although only 26 percent identical to B7-1, B7-2 also costimulates IL-2 production and T cell proliferation. Unlike B7-1, B7-2 messenger RNA is constitutively expressed in unstimulated B cells. It is likely that B7-2 provides a critical early costimulatory signal determining if the T cell will contribute to an immune response or become anergic.

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Metadata

Authors
Freeman, G. J., Gribben, J. G., Boussiotis, V. A., Ng, J. W., Restivo, V. A., Lombard, L. A., Gray, G. S., & Nadler, L. M.
Venue
Science
Published
1993-11-05
Volume
262
Issue
5135
Pages
909-911
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2062029576
Cited by
902
References
1
FWCI
36.87
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Cloning of B7-2: a CTLA-4 Counter-Receptor That Costimulates Human T Cell Proliferation. https://app.cochat.ai/papers/10.1126/science.7694363
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Freeman, G. J., Gribben, J. G., Boussiotis, V. A., Ng, J. W., Restivo, V. A., Lombard, L. A., Gray, G. S., & Nadler, L. M. (1993). Cloning of B7-2: a CTLA-4 Counter-Receptor That Costimulates Human T Cell Proliferation. Science. https://doi.org/10.1126/science.7694363

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.