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体外通过细胞和体液机制协同调节人T细胞对日本血吸虫卵抗原的反应

Regulation of the human T-cell response to Schistosoma japonicum egg antigen by concomitant cellular and humoral mechanisms in vitro.

作者信息

Ohta N, Asahi H, Hosaka Y, Minai M, Ishii A

机构信息

Department of Parasitology, Okayama University Medical School, Japan.

出版信息

Parasitol Res. 1991;77(1):54-8. doi: 10.1007/BF00934386.

Abstract

Serum-mediated regulation of T-cell responses specific for soluble egg antigen (SEA) of Schistosoma japonicum was tested in human hosts. When we added autologous serum to SEA-specific human T-cell lines (CD3+, 4+, 8-), we observed suppression of T-cell proliferation, and this suppressive activity was detected in the immunoglobulin-G2 (IgG2) subclass. Suppression was dose-dependent and antigen-specific. T-cell proliferation induced by only one SEA fraction of greater than 18 kDa was modulated in the presence of 100 micrograms/ml autologous as well as allogeneic infected IgG2. This SEA fraction-driven proliferation was also regulated by suppressor T-cells through distinct suppressive mechanisms. Our results suggest that T-cell responses to a particular component(s) of SEA are strictly regulated through both cellular and humoral mechanisms in human chronic S. japonicum infection.

摘要

在人类宿主中测试了血清介导的对日本血吸虫可溶性虫卵抗原(SEA)特异性T细胞反应的调节作用。当我们将自体血清添加到SEA特异性人T细胞系(CD3 +、4 +、8 -)中时,观察到T细胞增殖受到抑制,并且这种抑制活性在免疫球蛋白G2(IgG2)亚类中被检测到。抑制作用呈剂量依赖性且具有抗原特异性。在存在100微克/毫升自体以及同种异体感染的IgG2的情况下,仅由大于18 kDa的一种SEA组分诱导的T细胞增殖受到调节。这种SEA组分驱动的增殖也由抑制性T细胞通过不同的抑制机制进行调节。我们的结果表明,在人类慢性日本血吸虫感染中,针对SEA特定成分的T细胞反应通过细胞和体液机制受到严格调节。

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