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Original Article |
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T Cells in Antierythrocyte Immunoglobulin Transgenic Mice
honjo{at}mfour.med.kyoto-u.ac.jp
Using normal and transgenic (Tg) mice, we have shown that peritoneal B-1 cells are activated by administration of cytokines or lipopolysaccharide and migrate to other lymphoid organs where they differentiate into antibody-secreting cells. However, little is known about the process of B-1 cell migration and differentiation in vivo. We developed a mouse line by crossing the antierythrocyte antibody Tg mice (HL mice) with TCR-
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Tg mice specific for a self-thymus leukemia (TL) antigen in the recombination activating gene (RAG)2–/– background. In the presence of the self-antigen, Tg
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T cells increased in number and manifested activated phenotypes. Peritoneal B-1 cells in these mice migrated into mesenteric lymph nodes and differentiated into autoantibody-secreting cells, resulting in strong autoimmune hemolytic anemia. Furthermore, transfer of RAG2–/– x HL bone marrow or peritoneal cells into the peritoneal cavity of RAG2–/– x TCR-
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Tg mice gave rise to donor-derived B-1 cells in mesenteric lymph nodes, and these cells produced the autoantibody. Thus, this study demonstrates that the migration of B-1 cells and differentiation into the antibody-secreting cells can be induced by noncognate T cell help and implies the possibility that
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T cells may induce B-1 cell differentiation in vivo.
Key Words: RAG2 deficient
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TCR transgenic germinal center peritoneal cavity hemolytic anemia
© 2000 The Rockefeller University Press
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