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,
Departments of
*
Microbiology and Immunology and
Medicine, and
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
Ab. CD134-deficient
mice controlled infection with Leishmania major,
Nippostrongylus brasiliensis, and Theilers 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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