Abstract |
The course of infection after injection of small doses of bacillus Calmette-Guérin (BCG) was studied in mice which were depleted in vivo of T cell subsets by administration of either anti-L3T4 or anti-Lyt-2 mAb. The results presented herein strongly suggest that the L3T4+ subpopulation play a pivotal role in the immunologic control of BCG infection because the depletion of L3T4+ cells led to a dramatic increase in the number of viable bacteria. Depletion of Lyt-2+ cells had no significant effect on the course of infection. These results were confirmed by using adoptive transfer experiments which showed that protective immunity was mediated by L3T4+ cells generated in the spleen as a result of infection. Moreover, T cells capable of controlling the recurrence of BCG multiplication from residual bacteria remaining in organs after the recovery from infection were shown to belong to the L3T4+ subpopulation.
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Authors | T Pedrazzini, K Hug, J A Louis |
Journal | Journal of immunology (Baltimore, Md. : 1950)
(J Immunol)
Vol. 139
Issue 6
Pg. 2032-7
(Sep 15 1987)
ISSN: 0022-1767 [Print] United States |
PMID | 3114383
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal
- Antigens, Differentiation, T-Lymphocyte
- Antigens, Ly
- Antigens, Surface
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Topics |
- Animals
- Antibodies, Monoclonal
- Antigens, Differentiation, T-Lymphocyte
- Antigens, Ly
(immunology)
- Antigens, Surface
(immunology)
- Immunization, Passive
- Mice
- Mycobacterium bovis
(immunology)
- Spleen
(immunology)
- T-Lymphocytes
(classification, immunology)
- Time Factors
- Tuberculosis
(veterinary)
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