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In vivocytokine gene expression in T cell subsets of the autoimmune MRL/Mp‐lpr/lprmouse

机译:In vivocytokine gene expression in T cell subsets of the autoimmune MRL/Mp‐lpr/lprmouse

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AbstractExpression of cytokine genes in freshly isolated T cell subsets in the autoimmunelprmouse has been studied to determine what factors may be produced by these cellsin vivo.RNA prepared from T cell subsets from diseasedlprmice and from the normal congenic strain, MRL/n, was tested for the presence of cytokine‐specific message using the polymerase chain reaction. Cells of the expanded abnormal T cell subset were shown to express genes encoding interferon (IFN)‐γ, tumor necrosis factor (TNF)‐β,TNF‐α and interleukin (IL) 6, cytokines which are associated with inflammatory immune responses. These cells may thus play an important role in exacerbation of the pathological symptoms of the systemic autoimmune disease. These cells expressed no detectable IL 1, IL 2, IL 3, IL 4 or IL 5. Phenotypically normal CD4+ and CD8+T cells from bothlprand MRL/n also contained transcripts for IFN‐γ, TNF‐α, TNF‐β and IL 6. IL 2 mRNA was found almost exclusively in the CD4+ subset, indicating that the CD8+ T cells in thelprmouse are not highly activated through their class I major histocompatibility complex molecules to produce IL 2, as could occur if a virus infection was inducing autoimmunity in these mice. Similar levels of IL 2 mRNA were present in the CD4+ T cells oflprand MRL/n mice, demonstrating that these cells are not defective in IL

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