Positive Selection of Natural Autoreactive B Cells

Author:

Hayakawa Kyoko1,Asano Masanao1,Shinton Susan A.1,Gui Ming1,Allman David1,Stewart Colin L.2,Silver Jack3,Hardy Richard R.1

Affiliation:

1. Institute for Cancer Research, Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, PA 19111, USA.

2. Laboratory of Cancer and Developmental Biology, ABL-Basic Research Program, National Cancer Institute–Fredrick Cancer Research and Development Center, Fredrick, MD 21702, USA.

3. Division of Molecular Medicine, North Shore University Hospital, Cornell University Medical College, Manhasset, NY 11030, USA.

Abstract

Lymphocyte development is critically influenced by self-antigens. T cells are subject to both positive and negative selection, depending on their degree of self-reactivity. Although B cells are subject to negative selection, it has been difficult to test whether self-antigen plays any positive role in B cell development. A murine model system of naturally generated autoreactive B cells with a germ line gene–encoded specificity for the Thy-1 (CD90) glycoprotein was developed, in which the presence of self-antigen promotes B cell accumulation and serum autoantibody secretion. Thus, B cells can be subject to positive selection, generated, and maintained on the basis of their autoreactivity.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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4. S. Boyden ibid. 201 200 (1964); M. Schlesinger ibid. 207 429 (1965); A. J. Cunningham ibid. 252 749 (1974).

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