Mycoplasma Superantigen Is a CDR3-dependent Ligand for the T Cell Antigen Receptor

Author:

Hodtsev Andrew S.1,Choi Yongwon1,Spanopoulou Eugenia1,Posnett David N.1

Affiliation:

1. From the Ruttenberg Cancer Center, Mount Sinai School of Medicine, New York 10029; the Howard Hughes Medical Institute, The Rockefeller University, New York 10021; the Howard Hughes Medical Institute, Ruttenberg Cancer Center, Mount Sinai School of Medicine, New York 10029; and the Immunology Program, Graduate School of Medical Sciences, and the Department of Medicine, Cornell University Medical

Abstract

Superantigens are defined as proteins that activate a large number of T cells through interaction with the Vβ region of the T cell antigen receptor (TCR). Here we demonstrate that the superantigen produced by Mycoplasma arthritidis (MAM), unlike six bacterial superantigens tested, interacts not only with the Vβ region but also with the CDR3 (third complementarity-determining region) of TCR-β. Although MAM shares typical features with other superantigens, direct interaction with CDR3-β is a feature of nominal peptide antigens situated in the antigen groove of major histocompatibility complex (MHC) molecules rather than superantigens. During peptide recognition, Vβ and Vα domains of the TCR form contacts with MHC and the complex is stabilized by CDR3–peptide interactions. Similarly, recognition of MAM is Vβ-dependent and is apparently stabilized by direct contacts with the CDR3-β region. Thus, MAM represents a new type of ligand for TCR, distinct from both conventional peptide antigens and other known superantigens.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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