CD1-Restricted T Cell Recognition of Microbial Lipoglycan Antigens

P. A. Sieling(University of California, Los Angeles), Delphi Chatterjee(Colorado State University), Steven A. Porcelli(Brigham and Women's Hospital), Theodore I. Prigozy(University of California, Los Angeles), Richard J. Mazzaccaro(Albert Einstein College of Medicine), Teresa Soriano(University of California, Los Angeles), Barry R. Bloom(Albert Einstein College of Medicine), Michael B. Brenner(Brigham and Women's Hospital), Mitchell Kronenberg(University of California, Los Angeles), Patrick J. Brennan(Colorado State University), Robert L. Modlin(University of California, Los Angeles)
Science
July 14, 1995
Cited by 738

Abstract

It has long been the paradigm that T cells recognize peptide antigens presented by major histocompatibility complex (MHC) molecules. However, nonpeptide antigens can be presented to T cells by human CD1b molecules, which are not encoded by the MHC. A major class of microbial antigens associated with pathogenicity are lipoglycans. It is shown here that human CD1b presents the defined mycobacterial lipoglycan lipoarabinomannan (LAM) to alpha beta T cell receptor-bearing lymphocytes. Presentation of these lipoglycan antigens required internalization and endosomal acidification. The T cell recognition required mannosides with alpha(1-->2) linkages and a phosphotidylinositol unit. T cells activated by LAM produced interferon gamma and were cytolytic. Thus, an important class of microbial molecules, the lipoglycans, is a part of the universe of foreign antigens recognized by human T cells.


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