Very few cultured CD8+ T cell clones can normally be obtained from a single mouse and maintained in long-term culture. To improve the yield, we immunized p53 mutant mice with peptides of Sendai virus (FAPGNYPAL) and influenza virus (ASNENMETM) origin. Substantially more clones could be derived from p53−/− mice than from similarly treated wild-type mice (p53+/+); an intermediate yield was obtained from heterozygous mice (p53+/−). CTL lines or clones from p53−/− mice exhibited greater proliferative activity and resistance to γ-irradiation than those from p53+/+ mice, and were cytolytically potent.
CITATION STYLE
Zhou, X., Wong, S., Walter, J., Jacks, T., & Eisen, H. N. (1999). Increased Generation of CD8+ T Cell Clones in p53 Mutant Mice. The Journal of Immunology, 162(7), 3957–3960. https://doi.org/10.4049/jimmunol.162.7.3957
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