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用单克隆抗T细胞抗体对大鼠进行体内治疗。正常大鼠和实验性变应性神经炎的免疫组织化学及功能分析。

In vivo treatment of rats with monoclonal anti-T-cell antibodies. Immunohistochemical and functional analysis in normal rats and in experimental allergic neuritis.

作者信息

Holmdahl R, Olsson T, Moran T, Klareskog L

出版信息

Scand J Immunol. 1985 Aug;22(2):157-69. doi: 10.1111/j.1365-3083.1985.tb01868.x.

Abstract

The effects of intraperitoneal injection of monoclonal anti-rat T-lymphocyte antibodies were evaluated immunohistochemically and functionally in normal rats and in rats with experimental allergic neuritis. In the normal animals a single injection of OX8 antibodies, reactive with suppressor/cytotoxic T cells, completely eliminated OX8-reactive cells from peripheral lymphoid organs and from circulation, whereas the 'pan' T-cell-reactive W3/13 antibodies and the helper T-cell-reactive W3/25 antibodies only caused a partial elimination of their respective target cells. Injection of the W3/13 and W3/25 antibodies but not of OX8 antibodies led to a diminished responsiveness to allogeneic stimulation in vitro for spleen cells obtained from the treated rats, whereas the OX8 injection caused a complete elimination of the in vitro cytotoxic response to allogeneic cells in the mixed lymphocyte reaction-activated spleen cell population. When Lewis rats were injected with peripheral nerve myelin and Freund's adjuvant for the induction of EAN, treatment with W3/13 antibodies completely prevented the onset of disease, whereas treatment with the OX8 antibodies exaggerated the disease symptoms.

摘要

通过免疫组织化学和功能分析,评估腹腔注射单克隆抗大鼠T淋巴细胞抗体对正常大鼠和实验性变应性神经炎大鼠的影响。在正常动物中,单次注射与抑制性/细胞毒性T细胞反应的OX8抗体,可使外周淋巴器官和循环中的OX8反应性细胞完全消失;而“泛”T细胞反应性的W3/13抗体和辅助性T细胞反应性的W3/25抗体只能部分清除各自的靶细胞。注射W3/13和W3/25抗体而非OX8抗体,会导致处理后大鼠脾脏细胞对体外同种异体刺激的反应性降低;而注射OX8抗体则会使混合淋巴细胞反应激活的脾细胞群体对同种异体细胞的体外细胞毒性反应完全消失。当给Lewis大鼠注射周围神经髓鞘和弗氏佐剂以诱导实验性变应性神经炎时,用W3/13抗体治疗可完全预防疾病发作,而用OX8抗体治疗则会加重疾病症状。

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