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抗小鼠γ干扰素的单克隆抗体可抑制T淋巴细胞对巨噬细胞的杀肿瘤激活作用。

Monoclonal antibodies against mouse gamma-interferon inhibit tumoricidal macrophage activation by T lymphocytes.

作者信息

Landolfo S, Cofano F, Gandino L, Gribaudo G, Prat M

出版信息

Exp Cell Biol. 1985;53(5):265-9. doi: 10.1159/000163321.

Abstract

A monoclonal antibody, AN-18.17.24, specific for murine interferon-gamma (IFN-gamma) was produced by immunizing Wistar rats with IFN-gamma secreted by a T-cell lymphoma, L12-R4, upon stimulation with phorbol myristic acetate (PMA). Antiviral activity as well as tumoricidal activation induced by PMA-stimulated L12-R4 cell supernatant or by Con A-stimulated normal spleen cells were neutralized at the same extent by AN-18 monoclonal antibody. Moreover, depletion experiments showed that inhibition of tumoricidal macrophage activation must be ascribed to the direct binding of the IFN-gamma molecule by AN-18 MAb and not to the interference of the monoclonal antibody with the cell surface IFN-gamma receptor. These studies conclusively demonstrate that in supernatants of T lymphocytes stimulated with polyclonal activators IFN-gamma was the only molecule responsible for macrophage activation in tumor cell killing.

摘要

用佛波酯(PMA)刺激T细胞淋巴瘤L12 - R4分泌的干扰素 - γ(IFN - γ)免疫Wistar大鼠,产生了一种对鼠IFN - γ具有特异性的单克隆抗体AN - 18.17.24。PMA刺激的L12 - R4细胞上清液或刀豆蛋白A刺激的正常脾细胞诱导的抗病毒活性以及杀肿瘤活性,均被AN - 18单克隆抗体以相同程度中和。此外,去除实验表明,杀肿瘤巨噬细胞激活的抑制作用必定归因于AN - 18单克隆抗体与IFN - γ分子的直接结合,而非单克隆抗体对细胞表面IFN - γ受体的干扰。这些研究确凿地证明,在多克隆激活剂刺激的T淋巴细胞上清液中,IFN - γ是唯一负责肿瘤细胞杀伤中巨噬细胞激活的分子。

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