## Activation1 of virus-specific major histocompatibility complex class 11-restricted CD8+ cytotoxic T cells in CD4-deficient mice Acute enteritic or respiratory disease is a consequence of coronavirus infection in man and rodents. Mouse hepatitis virus, stain A59 (MHV-A59) causes acute hepatitis
Increased number of cytotoxic T cells within CD4+8− T cells in β2-microglobulin, major histocompatibility complex class I-deficient mice
✍ Scribed by Suzana Marušić-Galešić; Keiko Udaka; Peter Walden
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 509 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
✦ Synopsis
Increased number of cytotoxic T cells within CD4+8-T cells in P2-microglobulin, major histocompatibility complex class I-deficient mice*
Targeted disruption of fi2-microgobulin gene results in deficient major histocompatibility complex class I expression and failure to develop CD4-V T cells. Despite this, fi2M-/-mice reject skin grafts and cope with most viral infections tested. We asked whether CD4+8-cytotoxic T cells could play a role in compensating for the defect in CD4-8+ cytotoxic T cell function. We found that the cytotoxic activity against class 11+ targets is significantly higher among CD4+8-T cells of fi2M-I-than among those of fizM+I+ mice. In the limiting dilution experiment, we showed that the precursor frequency for the cytotoxic, CD4+8-, class 11-specific T cells is at least fivefold higher in P2M-I-than in P2M+/+ mice. These results suggest that CD4+8-cytotoxic T cells could play a major role in carrying out cytotoxic function in fi2M-I-mice.
📜 SIMILAR VOLUMES
## Class I1 major histocompatibility complex-restricted T cell function in CD4deficient mice* Previously, we and others have demonstrated that CD4-deficient mice have a normal number of Tcells and B cells with a significant population of CD4-8-TcRaP+ T cells. Surprisingly, however, these mice lack
This report shows that lymphoid tissues of mice which have resolved a primary infection with Leishmania major contain parasite-specific major histocompatibility complex (MHC) class I-restricted cytolytic CD8+ T cell precusors that can be expanded after specific restimulation in vitro with syngeneic