|
||
Articles |


Department of Pathology, Stanford University School of Medicine, Stanford, California 94305-5111
T cells with T cell receptor (TCR) transgenes that recognized CD1 on syngeneic B cells stimulated B cells to secrete immunoglobulins in vitro. The CD4+, CD8+, or CD4–CD8– T cells from the spleen of the TCR transgenic BALB/c donors induced lupus with anti–double stranded DNA antibodies, proteinuria, and immune complex glomerulonephritis in irradiated BALB/c nude mice reconstituted with nude bone marrow. Injection of purified CD4–CD8– T cells from the marrow of transgenic donors prevented the induction of lupus by the transgenic T cells. Transgenic T cells that induced lupus secreted large amounts of interferon (IFN)-
and little interleukin (IL)-4, and those that prevented lupus secreted large amounts of IL-4 and little IFN-
or IL-10.
Address correspondence to Samuel Strober, Division of Immunology and Rheumatology, Rm. S105B, Stanford University School of Medicine, 300 Pasteur Dr., Stanford, CA 94305-5111. Phone: 650-723-6500; Fax: 650-725-6104; E-mail: sstrober{at}leland.stanford.edu
1 Abbreviations used in this paper: BCL, B cell lymphoma; BM, bone marrow; cGy, centiGray; DN, double-negative; ds, double-stranded; SP, single-positive.
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Facebook
Reddit
Technorati
Twitter What's this?
| TABLE OF CONTENTS |
|