A pathway of costimulation that prevents anergy in CD28- T cells: B7-independent costimulation of CD1-restricted T cells

S. M. Behar, Steven A. Porcelli, E. M. Beckman, M. B. Brenner

Research output: Contribution to journalArticle

74 Citations (Scopus)

Abstract

A class of molecules that is expressed on antigen presenting cells, exemplified by CD80 (B7), has been found to provide a necessary costimulatory signal for T cell activation and proliferation. CD28 and CTLA4 are the B7 counterreceptors and are expressed on the majority of human CD4+ T cells and many CD8+ T cells. The signal these molecules mediate is distinguished from other costimulatory signals by the finding that T cell recognition of antigen results in a prolonged state of T cell unresponsiveness or anergy, unless these costimulatory molecules are engaged. However, nearly half of the CD8+ and CD4-CD8- T cells lack CD28, and the costimulatory signals required for the activation of such cells are unknown. To understand the pathways of activation used by CD28- T cells, we have examined the costimulatory requirements of antigen-specific CD4-CD8- TCR+-α/β circulating T cells that lack the expression of CD28. We have characterized two T cell lines, DN1 and DN6, that recognize a mycobacterial antigen, and are restricted not by major histocompatibility complex class I or II, but by CD1b or CD1c, two members of a family of major histocompatibility complex - related molecules that have been recently implicated in a distinct pathway for antigen presentation. Comparison of antigen-specific cytolytic responses of the DN1 and DN6 T cell lines against antigen-pulsed CD1+ monocytes or CD1+ B lymphoblastoid cell lines (B-LCL) demonstrated that these T cells recognized antigen presented by both types of cells. However, T cell proliferation occurred only when antigen was presented by CD1+ monocytes, indicating that the CD1+ monocytes expressed a costimulatory molecule that the B-LCL transfectants lacked. This hypothesis was confirmed by demonstrating that the T cells became anergic when incubated with the CD1+-transfected B-LCL in the presence of antigen, but not in the absence of antigen. The required costimulatory signal occurred by a CD28-independent mechanism since both the CD1+ monocytes and CD1+ B-LCL transfectants expressed B7-1 and B7-2, and DN1 and DN6 lacked surface expression of CD28. We propose that these data define a previously unrecognized pathway of costimulation for T cells distinct from that involving CD28 and its counterreceptors. We suggest that this B7-independent pathway plays a crucial role in the activation and maintenance of tolerance of at least a subset of CD28- T cells.

Original languageEnglish (US)
Pages (from-to)2007-2018
Number of pages12
JournalJournal of Experimental Medicine
Volume182
Issue number6
StatePublished - Dec 1 1995
Externally publishedYes

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T-Lymphocytes
Antigens
Cell Line
Monocytes
Major Histocompatibility Complex
CD1 Antigens
Cell Proliferation
CD4 Antigens
Antigen Presentation
T-Lymphocyte Subsets
Antigen-Presenting Cells
Maintenance

ASJC Scopus subject areas

  • Immunology

Cite this

A pathway of costimulation that prevents anergy in CD28- T cells : B7-independent costimulation of CD1-restricted T cells. / Behar, S. M.; Porcelli, Steven A.; Beckman, E. M.; Brenner, M. B.

In: Journal of Experimental Medicine, Vol. 182, No. 6, 01.12.1995, p. 2007-2018.

Research output: Contribution to journalArticle

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