VIP modulation of immune cell functions

Mónica De la Fuente , Mario Delgado , Rosa P. Gomariz
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引用次数: 96

Abstract

Neuropeptides have recently been shown to modulate the immune response. Vasoactive intestinal peptide (VIP) released from nerve endings and from immune cells modulates the mobility and adherence of lymphocytes and macrophages, phagocytic cell functions (phagocytosis and free radical production), the lymphocyte proliferative response, lymphokine and immunoglobulin production and the natural killer cell activity, with opposite effects in vitro on these immune cell functions. The VIP receptor heterogeneity and the different action mechanisms of VIP-mediated immunoregulation could explain, at least in part, the different VIP effects observed on lymphoid and phagocytic cells. The evidence supports the theory that VIP acts not as an inhibitor, but as a modulator of immune functions, as previously thought, and that this neuropeptide may play a relevant role in vivo.

免疫细胞功能的VIP调节
神经肽最近被证明可以调节免疫反应。从神经末梢和免疫细胞释放的血管活性肠肽(VIP)调节淋巴细胞和巨噬细胞的流动性和粘附性、吞噬细胞功能(吞噬和自由基产生)、淋巴细胞增殖反应、淋巴因子和免疫球蛋白的产生以及自然杀伤细胞的活性,在体外对这些免疫细胞功能有相反的作用。VIP受体的异质性和VIP介导免疫调节的不同作用机制至少可以部分解释VIP对淋巴细胞和吞噬细胞的不同作用。这些证据支持VIP不是作为一种抑制剂,而是作为一种免疫功能调节剂的理论,正如之前所认为的那样,这种神经肽可能在体内发挥相关作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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