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. 1991 Oct 1;174(4):891-900.
doi: 10.1084/jem.174.4.891.

Characterization of human T cells reactive with the Mycoplasma arthritidis-derived superantigen (MAM): generation of a monoclonal antibody against V beta 17, the T cell receptor gene product expressed by a large fraction of MAM-reactive human T cells

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Characterization of human T cells reactive with the Mycoplasma arthritidis-derived superantigen (MAM): generation of a monoclonal antibody against V beta 17, the T cell receptor gene product expressed by a large fraction of MAM-reactive human T cells

S M Friedman et al. J Exp Med. .

Abstract

While all known microbial superantigens are mitogenic for human peripheral blood lymphocytes (PBL), the functional response induced by Mycoplasma arthritidis-derived superantigen (MAM) is unique in that MAM stimulation of PBL consistently results in T cell-dependent B cell activation characterized by polyclonal IgM and IgG production. These immunostimulatory effects of MAM on the humoral arm of the human immune system warranted a more precise characterization of MAM-reactive human T cells. Using an uncloned MAM reactive human T cell line as immunogen, we have generated a monoclonal antibody (mAb) (termed C1) specific for the T cell receptor V beta gene expressed by the major fraction of MAM-reactive human T cells, V beta 17. In addition, a V beta 17- MAM-reactive T cell population exists, assessed by MAM, induced T cell proliferation and cytotoxic T cell activity. mAb C1 will be useful in characterizing the functional properties of V beta 17+ T cells and their potential role in autoimmune disease.

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References

    1. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2466-70 - PubMed
    1. Immunol Today. 1989 Aug;10(8):262-4 - PubMed
    1. J Immunol. 1991 Jun 15;146(12):4392-7 - PubMed
    1. Nature. 1991 Feb 7;349(6309):531-2 - PubMed
    1. Nature. 1991 Feb 7;349(6309):529-30 - PubMed

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