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Multivalent structure of an αβT cell receptor

1999; National Academy of Sciences; Volume: 96; Issue: 4 Linguagem: Inglês

10.1073/pnas.96.4.1547

1091-6490

Gemma Fernández-Miguel, Balbino Alarcón, Antonio Iglesias, Horst Bluethmann, Melchor Álvarez‐Mon, Eva Sanz, Antonio de la Hera,

Immunotherapy and Immune Responses

Whether there is one or multiple αβT cell antigen receptor (TCR) recognition modules in a given TCR/CD3 complex is a long-standing controversy in immunology. We show that T cells from transgenic mice that coexpress comparable amounts of two distinct TCRβ chains incorporate at least two αβTCRs in a single TCR/CD3 complex. Evidence for bispecific αβTCRs was obtained by immunoprecipitation and immunoblotting and confirmed on the surface of living cells both by fluorescence resonance energy transfer and comodulation assays by using antibodies specific for TCRβ-variable regions. Such (αβ) 2 TCR/CD3 or higher-order complexes were evident in T cells studied either ex vivo or after expansion in vitro . T cell activation is thought by many, but not all, to require TCR cross-linking by its antigen/major histocompatibility complex ligand. The implications of a multivalent (αβ) 2 TCR/CD3 complex stoichiometry for the ordered docking of specific antigen/major histocompatibility complex, CD4, or CD8 coreceptors and additional TCRs are discussed.