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CD38 and CD157 as Receptors of the Immune System: A Bridge Between Innate and Adaptive Immunity

机译:CD38和CD157作为免疫系统的受体:天生和适应性免疫之间的桥梁

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摘要

This paper reviews some of the results and the speculations presented at the Torino CD38 Meeting in June, 2006 and focused on CD38 and CD157 seen as a family of molecules acting as surface receptors of immune cells. This partisan view was adopted in the attempt to combine the enzymatic functions with what the immunologists consider key functions in different cell models. At the moment, it is unclear whether the two functions are correlated, indifferent, or independent. Here we present conclusions inferred exclusively on human cell models, namely T and B lymphocytes, dendritic cells, and granulocytes. As an extra analytical tool, we try to follow in the history of life when the enzymatic and receptorial functions were generated, mixing ontogeny, membrane localization, and cell anchorage.
机译:本文回顾了在2006年6月的都灵CD38会议上提出的一些结果和推测,并将重点放在了CD38和CD157上,它们被视为是免疫细胞表面受体的一个分子家族。这种党派观点是为了将酶功能与免疫学家认为在不同细胞模型中的关键功能结合在一起而尝试的。目前,尚不清楚这两个功能是相关的,无差异的还是独立的。在这里,我们提出的结论完全基于人类细胞模型,即T和B淋巴细胞,树突状细胞和粒细胞。作为一种额外的分析工具,我们尝试遵循生命的历史,其中产生了酶和受体功能,混合了个体发育,膜定位和细胞锚定。

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