Depletion of CD8+ T cells suppresses growth of Trypanosoma brucei brucei and interferon-gamma) production in infected rats

Author:

BAKHIET M1,OLSSON T1,VAN DER MEIDE P2,KRISTENSSON K3

Affiliation:

1. Department of Neurology, Karolinska Institute, Huddinge Hospital, Huddinge, Sweden

2. Department of Cellular Neuropathology, Karolinska Institute, Huddinge Hospital, Huddinge, Sweden

3. TNO Primate Centre, Rijswiik, The Netherlands

Abstract

SUMMARY Sprague-Dawley rats infected with Trypanosoma brucei brucei showed a strong and rapid induction of splenocyte IFN-γ (within 12 h post-infection) as measured by a single cell assay for IFN-γ secretion. Depiction of CD8+ cells in infected rats abrogated the IFN-γ production, suppressed parasite growth and increased survival of the animals. Induction of MHC class I antigens in the paraventricular and supra-optic hypothalamic nuclei caused by the trypanosome infection was also inhibited by the CD8+ cell depletion. It is suggested that the CD8+ cells are involved directly or indirectly in growth regulation of the parasite and that IFN-γ induced by the parasite may be one of the factors that trigger MHC expression and immunosuppression.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Reference21 articles.

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4. Two subsets of rat T-lymphocytes defined with monoclonal antibodies;Brideau;Fur. J. Immunol,1980

5. Reverse ELI-SPOT assay for clonal analysis of cytokine production. I. Enumeration of gamma-interferon-scecreting cells;Czerkinsky;J immunol. Methods,1988

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