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人淋巴细胞在体外的细胞毒性活性。

The cytotoxic activity of lymphocytes from human lymph in vitro.

作者信息

Holm G, Franksson C, Campbell A C, Maclennan I C

出版信息

Clin Exp Immunol. 1974 Jul;17(3):361-9.

Abstract

The cytotoxicity and DNA synthesis of thoracic duct and blood lymphocytes from four patients have been studied on the 1st day of drainage. Three patients were being drained as a pretreatment for kidney transplantation and one had myasthenia gravis. In one patient lymphocytes were obtained from a lymphatic fistula in the groin and from the blood 5 weeks after drainage began. Lysis of tissue culture cells (Chang cells) in the presence of PHA or antiserum to target cell antigens was quantitated by [Cr]chromate release. Lymphocytes from lymph were at best poorly cytotoxic to antibody-treated target cells under conditions where purified blood lymphocytes from the same donors had normal lytic activity. PHA-induced cytotoxicity by lymph-borne lymphocytes was noted but was considerably weaker than that of blood lymphocytes. In contrast, incorporation of [C]thymidine into DNA of thoracic duct lymphocytes after stimulation with PHA was about 60% of that of the patients' blood lymphocytes. The DNA synthesis of thoracic duct lymphocytes induced by PPD or allogeneic lymphocytes was as good as that of blood lymphocytes. The mitotic response to PHA by lymphocytes from the lymph was reduced after two weeks drainage. It is assumed that the number of effector cells and/or supporting cells in antibody-induced cytotoxicity in thoracic duct lymph is too small to induce target cell lysis under the present experimental conditions. Moreover, our data indicate that PHA-induced and antibody-mediated cytotoxicity are at least partly mediated by different lymphocyte subpopulations.

摘要

对4例患者引流第1天胸导管和血液淋巴细胞的细胞毒性及DNA合成进行了研究。3例患者作为肾移植的预处理进行引流,1例患有重症肌无力。1例患者在引流开始5周后从腹股沟淋巴瘘和血液中获取淋巴细胞。通过[铬]铬酸盐释放定量测定在PHA或针对靶细胞抗原的抗血清存在下组织培养细胞(Chang细胞)的裂解情况。在相同供体的纯化血液淋巴细胞具有正常裂解活性的条件下,来自淋巴的淋巴细胞对抗体处理的靶细胞的细胞毒性充其量很差。观察到淋巴源性淋巴细胞的PHA诱导的细胞毒性,但比血液淋巴细胞的细胞毒性弱得多。相比之下,PHA刺激后胸导管淋巴细胞中[碳]胸苷掺入DNA的量约为患者血液淋巴细胞的60%。PPD或同种异体淋巴细胞诱导的胸导管淋巴细胞的DNA合成与血液淋巴细胞的DNA合成一样好。引流两周后,来自淋巴的淋巴细胞对PHA的有丝分裂反应降低。据推测,在目前的实验条件下,胸导管淋巴中抗体诱导的细胞毒性中的效应细胞和/或支持细胞数量太少,无法诱导靶细胞裂解。此外,我们的数据表明,PHA诱导的和抗体介导的细胞毒性至少部分由不同的淋巴细胞亚群介导。

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