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The immunological synapse and CD28-CD80 interactions.

Authors
  • Bromley, S K
  • Iaboni, A
  • Davis, S J
  • Whitty, A
  • Green, J M
  • Shaw, A S
  • Weiss, A
  • Dustin, M L
Type
Published Article
Journal
Nature immunology
Publication Date
Dec 01, 2001
Volume
2
Issue
12
Pages
1159–1166
Identifiers
PMID: 11713465
Source
Medline
License
Unknown

Abstract

According to the two-signal model of T cell activation, costimulatory molecules augment T cell receptor (TCR) signaling, whereas adhesion molecules enhance TCR-MHC-peptide recognition. The structure and binding properties of CD28 imply that it may perform both functions, blurring the distinction between adhesion and costimulatory molecules. Our results show that CD28 on naïve T cells does not support adhesion and has little or no capacity for directly enhancing TCR-MHC-peptide interactions. Instead of being dependent on costimulatory signaling, we propose that a key function of the immunological synapse is to generate a cellular microenvironment that favors the interactions of potent secondary signaling molecules, such as CD28.

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