Abstract |
Spleen cells taken from mice soon after infection with Trypanosoma brucei S 42 enhance the primary in vitro antibody response of normal spleen cells to sheep red blood cells (SRBC), but do not affect their response to DNP-Ficoll. Spleen cells harvested later in the infection (day 6 onwards) suppress the antibody response of normal spleen cells to both SRBC and DNP-Ficoll. The enhancing and suppressive effects of "infected" spleen cells are sensitive to treatment with anti-Thy 1.2 anti-serum and complement, and can be mediated by nylon wool-purified populations of T cells. The enhancing T cell is sensitive to ALS, not lost within 4 weeks of adult thymectomy, and bears the Ly-1+, 23- phenotype. The suppressor T cell is insensitive to ALS, lost within 20 weeks of adult thymectomy, and bears the Ly-1+, 23+ phenotype. The significance of the activation of distinct helper and suppressor T cells is discussed in relation to the pathogenesis of trypanosomiasis.
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Authors | A N Jayawardena, B H Waksman, D D Eardley |
Journal | Journal of immunology (Baltimore, Md. : 1950)
(J Immunol)
Vol. 121
Issue 2
Pg. 622-8
(Aug 1978)
ISSN: 0022-1767 [Print] United States |
PMID | 355549
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Animals
- Antilymphocyte Serum
(pharmacology)
- Cattle
- Hemolytic Plaque Technique
- Immunosuppression Therapy
- Lymphocyte Cooperation
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Inbred CBA
- T-Lymphocytes
(immunology)
- Thymectomy
- Trypanosoma brucei brucei
(immunology)
- Trypanosomiasis, Bovine
(immunology)
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