Vβ repertoire in rats and implications for endogenous superantigens
Lawrence R. Smith, Dwight H. Kono, Michael E. Kammuller, ROBERT S. BALDERAS, Argyrios N. Theofilopoulos
Abstract
Lawrence R. Smith, Dwight H. Kono, Michael E. Kammuller, ROBERT S. BALDERAS, Argyrios N. Theofilopoulos
Abstract
Endogenous superantigens of mice, encoded by mammary tumor virus proviral integrants, induce intrathymic deletion of entire T cell populations that express specific V beta gene products, a phenomenon proposed to be important in self-tolerance and prevention of toxic responses to exogenous microbial superantigens. Evidence for the presence of V beta selecting/deleting endogenous superantigens in other species is lacking. We report here that rats do not exhibit endogenous superantigen-induced V beta clonal deletions despite their strong response to bacterial superantigens. These findings indicate that endogenous superantigens are not obligatory in V beta repertoire shaping.
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Endogenous superantigens of mice, encoded by mammary tumor virus proviral integrants, induce intrathymic deletion of entire T cell populations that express specific V beta gene products, a phenomenon proposed to be important in self-tolerance and prevention of toxic responses to exogenous microbial superantigens. Evidence for the presence of V beta selecting/deleting endogenous superantigens in other species is lacking. We report here that rats do not exhibit endogenous superantigen-induced V beta clonal deletions despite their strong response to bacterial superantigens. These findings indicate that endogenous superantigens are not obligatory in V beta repertoire shaping.
Key concepts: Superantigen, Biology, Repertoire, Endogeny, Immunology, Computational biology, Cell biology, Evolutionary biology