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The Journal of Immunology, 1998, 161: 6189-6197.
Copyright © 1998 by The American Association of Immunologists

Experimental Murine Trypanosoma congolense Infections. II. Role of Splenic Adherent CD3+ Thy1.2+ TCR-{alpha}ß- {gamma}{delta}- CD4+8- and CD3+ Thy1.2+ TCR-{alpha}ß- {gamma}{delta}- CD4-8- Cells in the Production of IL-4, IL-10, and IFN-{gamma} and in Trypanosome-Elicited Immunosuppression1

Jude E. Uzonna, Radhey S. Kaushik, Ying Zhang, John R. Gordon and Henry Tabel2

Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Canada

Trypanosome-induced suppression of T and B cell responses to parasite-related and -unrelated Ags is considered a major mechanism of evasion of the host’s immune defenses by the parasite. Reduced T and B cell responses have been attributed to suppressor T cells, suppressor macrophages, or both. We have previously shown that endogenously produced IL-10 and IFN-{gamma} mediate the suppression of T cell responses in Trypanosoma congolense-infected mice. Here, we show for the first time that splenic CD3+ Thy1.2+ {alpha}ß- {gamma}{delta}- CD4+8- and CD3+ Thy1.2+ {alpha}ß- {gamma}{delta}- CD4-8- cells that copurify with plastic-, nylon wool-, or Sephadex G-10-adherent cell populations, in synergy with adherent Thy1.2- cells, are the major producers of IL-4, IL-10, and IFN-{gamma} in T. congolense-infected mice. We further demonstrate the involvement of these cells in the suppression of T cell proliferative responses to mitogen and in B cell responses to a parasite-unrelated Ag.




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