首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Antibody-dependent eosinophil-mediated damage to 51Cr-labeled schistosomula of Schistosoma mansoni: damage by purieid eosinophils
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Antibody-dependent eosinophil-mediated damage to 51Cr-labeled schistosomula of Schistosoma mansoni: damage by purieid eosinophils

机译:依赖抗体的嗜酸性粒细胞介导的曼氏血吸虫对51Cr标记的血吸虫的损​​害:嘌呤类嗜酸性粒细胞的损害

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摘要

After earlier observations that antibody-dependent, cell-mediated damage to 51Cr-labeled schistosomula can be ablated by pretreatment of a mixed preparation of human peripheral blood leukocytes with an anti- eosinophil serum and complement, we investigated the cytotoxic effects of eosinophil-enriched cell preparations. Preparations containing up to 98.5% eosinophils and devoid of neutrophils were effective in mediating antibody-dependent damage to schistosomula. Preparations enriched in mononuclear cells or in neutrophils, and devoid of eosinophils, were inactive. Eosinophils from some patients with eosinophilia induced by schistosomiasis were less active on a cell-to-cell basis than cells from normal individuals. The possibility that such cells were initially blocked by immune complexes was considered, and it was found that reasonable cytotoxicity by purified eosinophils from patients with eosinophilia could be generated by overnight cultures. A possible requirement for cooperation between eosinophils and other cell types was also studied. Lymphocytes, neutrophils and monocytes failed to enhance eosinophil-mediated cytotoxicity. These results provide further evidence that the eosinophil is the only cell in man responsible for antibody-dependent, complement-independent damage to schistosomula in vitro. Eosinophils from individuals, however, differ in their cytotoxic potential by a mechanism yet to be elucidated. The possible relationship of these findings to immunity in vivo is discussed.
机译:在较早的观察中,可以通过用抗嗜酸性粒细胞血清和补体预处理人外周血白细胞的混合制剂来消除抗体依赖性的细胞介导的对51Cr标记的血吸虫的损​​害,我们研究了嗜酸性粒细胞丰富的细胞的细胞毒性作用准备。含有多达98.5%嗜酸性粒细胞且不含嗜中性粒细胞的制剂可有效介导对血吸虫的抗体依赖性损伤。富含单核细胞或嗜中性粒细胞且不含嗜酸性粒细胞的制剂没有活性。来自血吸虫病诱发的一些嗜酸性粒细胞增多症患者的嗜酸性粒细胞在细胞间的活性低于正常个体的细胞。考虑了这种细胞最初被免疫复合物阻断的可能性,并且发现通过过夜培养可以从来自嗜酸性粒细胞增多症患者的纯化嗜酸性粒细胞中产生合理的细胞毒性。还研究了嗜酸性粒细胞与其他细胞类型之间合作的可能要求。淋巴细胞,嗜中性粒细胞和单核细胞未能增强嗜酸性粒细胞介导的细胞毒性。这些结果提供了进一步的证据,表明嗜酸性粒细胞是人类中唯一对血吸虫的抗体依赖性,补体依赖性损伤负责的细胞。然而,来自个体的嗜酸性粒细胞的细胞毒性潜力因尚待阐明的机制而不同。讨论了这些发现与体内免疫的可能关系。

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