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Modulation of regulatory T cell immunity by the neuropeptide alpha-melanocyte stimulating hormone.

机译:神经肽α-黑素细胞刺激激素对调节性T细胞免疫的调节。

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摘要

Although many immunosuppressive factors have been identified in the eye, one of these factors, alpha-melanocyte stimulating hormone (alpha-MSH), both suppresses the activation of inflammatory activity by primed T cells and induces the activation of regulatory T cells (Treg cells). This neuropeptide alone at its ocular physiological concentration can account for most of the immunosuppressive activity of aqueous humor (the fluid filing the anterior chamber of the eye). Aqueous humor made devoid of alpha-MSH no longer suppresses IFN-gamma production by Th1 cells. It is alpha-MSH that mediates aqueous humor induction of regulatory T cells. What we have found is that alpha-MSH mediates the induction of C4+ CD25+ Treg cells, and that if the alpha-MSH Treg cells are specific to an autoantigen they can be used to suppress autoimmune disease. It is the objective of this review to demonstrate how we came to discover that alpha-MSH could have such an important role in the extreme regional immunity of the immune privileged eye and how this discovery could be applied to create or reestablish tolerance to prevent autoimmune disease.
机译:尽管在眼中已经发现了许多免疫抑制因子,但是这些因子之一,即α-黑素细胞刺激激素(α-MSH),既可以抑制初免T细胞的炎症活性的激活,又可以诱导调节性T细胞(Treg细胞)的激活。 。单独的这种神经肽在其眼部生理浓度下可以解释房水(液体进入眼前房)的大部分免疫抑制活性。不含α-MSH的房水不再抑制Th1细胞产生的IFN-γ。 α-MSH介导房水诱导调节性T细胞。我们发现,α-MSH介导了C4 + CD25 + Treg细胞的诱导,如果α-MSHTreg细胞对自身抗原具有特异性,那么它们可用于抑制自身免疫性疾病。这篇综述的目的是证明我们如何发现α-MSH在免疫特权眼睛的极端区域免疫中具有如此重要的作用,以及如何将这一发现应用于建立或重建对自身免疫疾病的耐受性。

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