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培养的人、小牛和大鼠少突胶质细胞上未检测到OKT8抗原的表达。

Absence of expression of OKT8 antigen on cultured human, calf and rat oligodendrocytes.

作者信息

Hirayama M, Lisak R P, Kim S U, Pleasure D E, Silberberg D H

出版信息

Nature. 1983 Jan 13;301(5896):152-4. doi: 10.1038/301152a0.

Abstract

Monoclonal antibodies which recognize human suppressor T cells (OKT8) have been reported by Oger and co-workers to bind to cultured sheep oligodendrocytes. These authors speculated that an immune response directed at determinants shared by suppressor lymphocytes and oligodendrocytes could explain the decrease in both circulating blood suppressor T cells and oligodendrocytes in patients with multiple sclerosis. In view of the vital issue of potential cross-reactivity between oligodendrocytes and lymphocytes, we studied the binding of viable cultured calf, rat and human oligodendrocytes using monoclonal antibodies to human T cells and monocytes. We report here that we were unable to confirm the presence of shared determinants among oligodendrocytes and any leukocytes, including human T cells or monocytes. As the reported observations of lymphocyte-oligodendrocyte shared determinants could not be identified in three other species, including man, we found no evidence to support the hypothesis that such shared determinants are of importance in the pathogenesis of multiple sclerosis.

摘要

奥热尔及其同事报告称,识别人类抑制性T细胞的单克隆抗体(OKT8)能与培养的绵羊少突胶质细胞结合。这些作者推测,针对抑制性淋巴细胞和少突胶质细胞共有的决定簇的免疫反应,或许可以解释多发性硬化症患者循环血液中抑制性T细胞和少突胶质细胞数量均减少的现象。鉴于少突胶质细胞与淋巴细胞之间潜在交叉反应这一关键问题,我们使用针对人类T细胞和单核细胞的单克隆抗体,研究了存活的培养小牛、大鼠和人类少突胶质细胞的结合情况。我们在此报告,我们无法证实在少突胶质细胞与任何白细胞(包括人类T细胞或单核细胞)之间存在共同的决定簇。由于在包括人类在内的其他三个物种中均未发现已报道的淋巴细胞 - 少突胶质细胞共同决定簇的观察结果,我们没有找到证据支持此类共同决定簇在多发性硬化症发病机制中起重要作用这一假说。

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