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在肿瘤排斥反应过程中,体内特异性巨噬细胞武装因子的产生先于细胞毒性T淋巴细胞的活性。

Production of specific macrophage-arming factor precedes cytotoxic T lymphocyte activity in vivo during tumor rejection.

作者信息

Dullens H F, De Weger R A, Van der Maas M, Den Besten P J, Vandebriel R J, Den Otter W

机构信息

Department of Experimental Pathology, University of Utrecht, The Netherlands.

出版信息

Cancer Immunol Immunother. 1989;30(1):28-33. doi: 10.1007/BF01665027.

Abstract

Recently we published a hypothesis on the immunological events occurring during tumor rejection. One of the implications of this hypothesis is that specific macrophage-arming factor (SMAF) is produced early during the initiation of the immune response, whereas the "classical" cell-mediated immune response components, such as cytotoxic T lymphocytes (CTL), are produced later, that is, during the amplifier-effector phase. In this paper we establish the kinetics of the induction of (a) lymphocytes producing SMAF and (b) CTL. Groups of DBA/2 mice were injected i.p. once, twice or three times with irradiated and/or non-irradiated syngeneic SL2 tumor cells, the injections being given at intervals of 10 days. After each of these injections the production of SMAF and the expression of CTL activity were established. The results showed that in the peritoneal cavity SMAF-producing lymphocytes appeared earlier than cytotoxic lymphocytes (CTL). In addition, it was shown (a) that SMAF does not interfere with the in vitro cytotoxicity expressed by CTL and (b) that in addition to CTL memory cells, SMAF-producing memory cells were also induced after injection of syngeneic tumor cells. These data support the hypothesis that SMAF is involved in the early phase of the cellular immune response against tumors, whereas CTL are induced later.

摘要

最近我们发表了一个关于肿瘤排斥过程中发生的免疫事件的假说。该假说的一个含义是,特异性巨噬细胞武装因子(SMAF)在免疫反应启动的早期产生,而“经典”的细胞介导免疫反应成分,如细胞毒性T淋巴细胞(CTL),则在后期产生,即在放大-效应阶段产生。在本文中,我们确定了(a)产生SMAF的淋巴细胞和(b)CTL诱导的动力学。将DBA/2小鼠分组,腹腔注射一次、两次或三次经照射和/或未经照射的同基因SL2肿瘤细胞,注射间隔为10天。每次注射后,确定SMAF的产生和CTL活性的表达。结果表明,在腹腔中,产生SMAF的淋巴细胞比细胞毒性淋巴细胞(CTL)出现得早。此外,研究表明:(a)SMAF不干扰CTL在体外表达的细胞毒性;(b)除了CTL记忆细胞外,注射同基因肿瘤细胞后还诱导产生了产生SMAF的记忆细胞。这些数据支持了以下假说:SMAF参与了针对肿瘤的细胞免疫反应的早期阶段,而CTL则在后期被诱导产生。

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A macrophage factor enhancing the systemic anti-tumour effect of T lymphocytes.
Immunobiology. 1984 Mar;166(2):118-30. doi: 10.1016/S0171-2985(84)80031-5.

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