Huang, F.-P., Xu, D., Esfandiari, E.-O., Sands, W., Wei, X.-q. and Liew, F. Y. (1998) Cutting edge: Mice defective in Fas are highly susceptible to Leishmania major infection despite elevated interleukin-12 synthesis, strong Th1 responses and enhanced nitric oxide production. Journal of Immunology, 160(9), pp. 4143-4147. (PMID:9574511)
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Publisher's URL: http://www.jimmunol.org/content/160/9/4143
Abstract
MRL/MP-lpr/lpr (MRL/lpr) mice have a single mutation (lpr) of the fasapoptosis gene. The mutant mice developed significantly smaller lesions than the wild-type mice at the earlier stage of infection with the intracellular protozoan parasite Leishmania major. However, while all the wild-type mice achieved complete lesion resolution, the disease in the mutant mice progressed inexorably. The mutant mice had more IL-12 and nitrite/nitrate in the serum than wild-type mice following infection. Lymphoid cells from infected MRL/lpr mice produced more IFN-γ but less IL-4 and IL-5 than cells from MRL-+/+ mice. Peritoneal macrophages from the mutant mice also produced more IL-12 and NO after stimulation with LPS. Thus, Fas expression is essential for resistance against leishmaniasis, and Fas-mediated apoptosis may form an integral part of the Th1-mediated microbicidal function.
Item Type: | Articles |
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Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Liew, Prof Foo and Xu, Dr Damo and Sands, Dr William |
Authors: | Huang, F.-P., Xu, D., Esfandiari, E.-O., Sands, W., Wei, X.-q., and Liew, F. Y. |
College/School: | College of Medical Veterinary and Life Sciences > School of Infection & Immunity |
Journal Name: | Journal of Immunology |
Publisher: | American Association of Immunologists |
ISSN: | 0022-1767 |
ISSN (Online): | 1550-6606 |
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