细胞毒性人淋巴细胞:从体外试验(1970年代)到免疫治疗(1990年代)。

Acta microbiologica Hungarica Pub Date : 1993-01-01
J Sinkovics, J Horvath
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引用次数: 0

摘要

资深作者是美国国家癌症研究所(NCI)在20世纪70年代早期的一份合同(1-CP3-3292)的接受者。NCI的目标研究计划的目的是建立肿瘤特异性人淋巴细胞介导的细胞毒性测定。没有淋巴细胞生长因子和单克隆抗体用于淋巴细胞分型。肿瘤特异性淋巴细胞群不能维持,但它们在血黄皮的ficoll-hypaque制剂或肿瘤原代培养物中的存在被清楚地识别出来。另一种不加区分的细胞毒性淋巴细胞群通常覆盖肿瘤特异性淋巴细胞群。与当时的统治理论相反,在荷瘤患者和健康个体的血液中很容易发现不分青红皂白的细胞毒性淋巴细胞(1971年,这位资深作者的淋巴细胞被证明具有不分青红皂白的细胞毒性,这一观察结果最初被解释为每天接触转移性癌症患者的个体的“免疫监视在起作用”)。NCI没有将合同的主题从肿瘤特异性转化为非特异性细胞毒性试验,而是过早地“逐步淘汰”(但将该项目作为内部研究继续进行)。尽管如此,细胞毒性淋巴细胞的许多功能现在已经得到了很好的证实,在1970年代早期,在NCI合同的有限支持和其他来源的资金的支持下,这些功能被预示了出来。在这里,我们叙述这些早期的观察;介绍各种自体淋巴细胞群的过继免疫治疗大纲,并在本卷的单独报告中给出这些淋巴细胞群如何在实验室准备用于治疗性再输注到患者体内的技术描述。
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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Cytotoxic human lymphocytes: from in vitro testing (1970s) to immunotherapy (1990s).

The senior author was the recipient of a contract (1-CP3-3292) from the National Cancer Institute, USA (NCI) in the early 1970s. The aim of NCI's targeted research program was the establishment of a tumour-specific human lymphocyte-mediated cytotoxicity assay. Neither lymphocyte growth factors nor monoclonal antibodies for lymphocyte typing were available. Tumour-specific populations of lymphocytes could not be maintained but their presence in ficoll-hypaque preparations of blood buffy coats or in primary cultures of tumours was clearly recognized. Another indiscriminately cytotoxic population of lymphocytes had usually overridden the tumour-specific population. In contradistinction to the ruling doctrine of the era, indiscriminately cytotoxic lymphocytes were readily found in the blood of tumour-bearing patients and healthy individuals (the senior author's lymphocytes were shown to practice indiscriminate cytotoxicity in 1971, an observation first interpreted as "immune surveillance at work" in an individual daily exposed to patients with metastatic cancers). Instead of converting the subject matter of the contract from a tumour-specific to a non-specific cytotoxicity assay, the NCI prematurely "phased it out" (but continued the project as intramural research). Nevertheless, many functions of cytotoxic lymphocytes that had become by now well established were foreshadowed during the early 1970s with the limited support of that NCI contract and funds from other sources. Here we recount those early observations; present the outlines of adoptive immunotherapy with various autologous lymphocyte populations and in a separate report in this volume give a technical description how these lymphocyte populations are prepared in the laboratory for therapeutic reinfusions into the patient.

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