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Study on cellular events in post-thymectomy autoimmune oophoritis in mice. II. Requirement of Lyt-1 cells in normal female mice for the prevention of oophoritis.

Abstract
Autoimmune oophoritis that develops in A/J mice after neonatally thymectomy (NTx) was prevented by a single intraperitoneal injection of spleen cells or thymocytes from normal adult female mice. Prevention of oophoritis was achieved when spleen cells were given within 2 wk after Tx. When spleen cells were obtained from neonatally oophorectomized mice, four times more cells were required for the prevention of oophoritis, but those from the mice oophorectomized on day 7 after birth had equivalent capacity to prevent oophoritis to those from normal female mice. The spleen cells from normal A/J mice that prevented the development of oophoritis in NTx A/J mice were Thy-1+, Lyt-1+,23-, Ia-, Qa-1-, sensitive to in vitro irradiation with 400 rad, resistant to administration of cyclophosphamide or anti-thymocyte serum, and were not eliminated by adult thymectomy. Thymocytes with oophoritis-preventing capacity were also found to be Lyt-1+,23- and TL-1,2,3-. These results seem to correlate well with the finding that the Lyt-1 subpopulation is substantially decreased in NTx mice. The results suggest that, in this post-thymectomy autoimmune oophoritis, NTx abrogates the Lyt-1 T cell subpopulation that serves as suppressive or regulatory cells over developing self-reactive cells directed toward ovarian antigens, and eventually may cause autoimmune oophoritis.
AuthorsS Sakaguchi, T Takahashi, Y Nishizuka
JournalThe Journal of experimental medicine (J Exp Med) Vol. 156 Issue 6 Pg. 1577-86 (Dec 01 1982) ISSN: 0022-1007 [Print] United States
PMID6983558 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antigens, Ly
  • Cyclophosphamide
Topics
  • Aging
  • Animals
  • Antigens, Ly (immunology)
  • Autoimmune Diseases (etiology, immunology, therapy)
  • Cyclophosphamide (pharmacology)
  • Female
  • Immunity, Cellular (drug effects, radiation effects)
  • Lymphocyte Transfusion
  • Lymphocytes (drug effects, radiation effects)
  • Mice
  • Mice, Inbred A
  • Mice, Inbred C57BL
  • Oophoritis (etiology, immunology, therapy)
  • Phenotype
  • Spleen (cytology)
  • T-Lymphocytes (immunology, transplantation)
  • Thymectomy

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