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肿瘤坏死因子对体内免疫反应的增强作用。

Enhancement of in vivo immune response by tumor necrosis factor.

作者信息

Ghiara P, Boraschi D, Nencioni L, Ghezzi P, Tagliabue A

机构信息

Laboratorio di Immunofarmacologia, Centro Ricerche Sclavo, Stena, Italy.

出版信息

J Immunol. 1987 Dec 1;139(11):3676-9.

PMID:3500228
Abstract

Interleukin 1 (IL-1) has been shown to regulate several immunologic functions. Since tumor necrosis factor (TNF) shares many biologic properties with IL-1, we have investigated here the role of TNF in the modulation of the immune response. We have thus tested low doses of human recombinant TNF-alpha (hu rTNF-alpha) for its capacity to enhance the in vivo antibody responses evaluated at the cellular level in the hemolytic plaque assay. It was found that hu rTNF-alpha, like human IL-1 beta, is able to enhance the immune response to a T cell-dependent antigen (sheep red blood cells). Interestingly, at variance with human recombinant IL-1 beta, hu rTNF-alpha was not able to enhance the in vivo antibody response to a T cell-independent antigen (type III pneumococcal polysaccharide). These results suggest that low levels of TNF may have a role in the modulation of the immune response in vivo and shed new light on the biologic significance of this mediator.

摘要

白细胞介素1(IL-1)已被证明可调节多种免疫功能。由于肿瘤坏死因子(TNF)与IL-1具有许多生物学特性,我们在此研究了TNF在调节免疫反应中的作用。因此,我们测试了低剂量的重组人肿瘤坏死因子-α(hu rTNF-α)在溶血空斑试验中增强体内抗体反应的能力,该反应在细胞水平上进行评估。结果发现,hu rTNF-α与人白细胞介素-1β一样,能够增强对T细胞依赖性抗原(绵羊红细胞)的免疫反应。有趣的是,与重组人白细胞介素-1β不同,hu rTNF-α不能增强对T细胞非依赖性抗原(III型肺炎球菌多糖)的体内抗体反应。这些结果表明,低水平的TNF可能在体内免疫反应的调节中发挥作用,并为这种介质的生物学意义提供了新的线索。

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