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抗原驱动的T细胞克隆可在体内增殖,根除播散性白血病,并提供特异性免疫记忆。

Antigen-driven T cell clones can proliferate in vivo, eradicate disseminated leukemia, and provide specific immunologic memory.

作者信息

Klarnet J P, Matis L A, Kern D E, Mizuno M T, Peace D J, Thompson J A, Greenberg P D, Cheever M A

出版信息

J Immunol. 1987 Jun 1;138(11):4012-7.

PMID:3108381
Abstract

The aim of the current study was to determine the ability of antigen-driven cloned helper cell independent cytotoxic T lymphocytes (HITc) to proliferate and to survive in vivo and to mediate tumor therapy. The HITc clone utilized (denoted 1.B6) was specifically cytolytic to FBL-3, a syngeneic Friend virus-induced murine leukemia. Activation in vitro (48 hr) with FBL-3 induced secretion of interleukin 2 (IL 2), expression of IL 2 receptors (IL 2R), and in vitro proliferation. These cells could be "rested" for several weeks without stimulation, which resulted in reduced expression of IL 2R; however, restimulation with antigen resulted in reinduction of IL 2R and proliferation. The ability of cloned HITc to proliferate and to survive in vivo was examined in cyclophosphamide (CY) pretreated donor mice congenic for the Thy-1 gene. Adoptively transferred cloned HITc could be found in large numbers, and were widely distributed in vivo 1 wk after transfer. In tumor therapy, 1.B6 cells when injected into a site of tumor (i.p.) and used as an adjunct to CY were effective against disseminated FBL-3. In this circumstance, cloned 1.B6 cells could be recovered from cured mice 125 days after transfer and were shown to specifically lyse tumor and proliferate in vitro in response to FBL-3. Thus as an adjunct to CY, tumor-specific cloned HITc are capable of eradicating disseminated leukemia, persisting long-term in vivo, and providing specific immunologic memory.

摘要

本研究的目的是确定抗原驱动的克隆辅助细胞非依赖性细胞毒性T淋巴细胞(HITc)在体内增殖、存活以及介导肿瘤治疗的能力。所使用的HITc克隆(命名为1.B6)对同基因Friend病毒诱导的小鼠白血病FBL-3具有特异性细胞溶解作用。用FBL-3在体外激活(48小时)可诱导白细胞介素2(IL-2)分泌、IL-2受体(IL-2R)表达以及体外增殖。这些细胞在无刺激的情况下可“静止”数周,这导致IL-2R表达降低;然而,用抗原再次刺激会导致IL-2R重新诱导和增殖。在经环磷酰胺(CY)预处理的Thy-1基因同基因供体小鼠中检测克隆的HITc在体内增殖和存活的能力。过继转移的克隆HITc在转移后1周可在体内大量发现,并广泛分布。在肿瘤治疗中,将1.B6细胞注射到肿瘤部位(腹腔内)并作为CY的辅助手段,对播散性FBL-3有效。在这种情况下,转移后125天可从治愈的小鼠中回收克隆的1.B6细胞,并且显示它们可特异性裂解肿瘤并在体外对FBL-3作出反应而增殖。因此,作为CY的辅助手段,肿瘤特异性克隆HITc能够根除播散性白血病,在体内长期存活,并提供特异性免疫记忆。

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