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人类B细胞无法通过其FcγRII或FcεRII受体被触发来杀伤靶细胞。

Human B cells cannot be triggered to kill target cells through their Fc gamma RII or Fc epsilon RII receptors.

作者信息

MacKenzie L E, Erbe D V, Pulford K A, Lydyard P M, Fanger M W

机构信息

Department of Immunology, U.C.M.S.M., London, U.K.

出版信息

Immunol Lett. 1991 Jun;28(3):245-50. doi: 10.1016/0165-2478(91)90011-x.

Abstract

There has been some controversy as to whether or not B cells can kill target cells through their Fc receptors. To address this, we have examined the ability of human B cells from a variety of sources to lyse hybridoma cells with specificity for either the B cell Fc gamma RII or Fc epsilon RII using a reverse killing assay, as well as their ability to lyse opsonized chicken erythrocytes using a classic ADCC assay. Tonsil B cells, chronic lymphocytic leukemia B cells, and Epstein-Barr virus-induced B cells, even after preactivation with a cocktail of cytokines, all failed to lyse any of these targets. We conclude that Fc gamma RII and Fc epsilon RII on human B cells are not cytotoxic trigger molecules.

摘要

关于B细胞是否能通过其Fc受体杀伤靶细胞一直存在一些争议。为了解决这个问题,我们使用反向杀伤试验检测了来自各种来源的人B细胞对具有B细胞FcγRII或FcεRII特异性的杂交瘤细胞进行裂解的能力,以及使用经典的抗体依赖的细胞介导的细胞毒性(ADCC)试验检测其裂解调理的鸡红细胞的能力。扁桃体B细胞、慢性淋巴细胞白血病B细胞和爱泼斯坦-巴尔病毒诱导的B细胞,即使在用细胞因子混合物预激活后,也都未能裂解任何这些靶细胞。我们得出结论,人B细胞上的FcγRII和FcεRII不是细胞毒性触发分子。

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