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The Journal of Immunology, 1999, 163: 6520-6529.
Copyright © 1999 by The American Association of Immunologists

Robust B Cell Immunity but Impaired T Cell Proliferation in the Absence of CD134 (OX40)1

Susanne D. Pippig2,3,*, Claudia Peña-Rossi2,4,*, James Long*, Wayne R. Godfrey*, Deborah J. Fowell{dagger}, Steven L. Reiner§, Marian L. Birkeland, Richard M. Locksley*,{dagger},{ddagger}, A. Neil Barclay and Nigel Killeen5,*

Departments of * Microbiology and Immunology and {dagger} Medicine, and {ddagger} Howard Hughes Medical Institute, University of California, San Francisco, CA 94143; § Department of Medicine, Committee on Immunology and the Gwenn Knapp Center for Lupus and Immunology Research, University of Chicago, Chicago, IL 60637; and Medical Research Council Cellular Immunology Unit, Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom

CD134 (OX40) is a member of the TNF receptor family that is expressed on activated T lymphocytes. T cells from mice that lack expression of CD134 made strong responses to a range of challenges, but they showed impaired proliferation in response to direct stimulation through the TCR with monoclonal anti-CD3{epsilon} Ab. CD134-deficient mice controlled infection with Leishmania major, Nippostrongylus brasiliensis, and Theiler’s murine encephalomyelitis virus, and they made overtly normal Ab responses to a variety of antigens. Thus, CD134 is not essential for many T cell responses in vivo, nor is it required for the provision of help to B cells. Nonetheless, a subtle role in the regulation of T cell reactivity is suggested by the effect of CD134 deficiency on in vitro T cell responses.




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