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猿猴免疫缺陷病毒SIVsmmPBj 1.9可诱导人外周血单核细胞形成多核巨细胞。

Simian immunodeficiency virus SIVsmmPBj 1.9 induces multinucleated giant cell formation in human peripheral blood monocytes.

作者信息

Baskar P, Narayan O, McClure H M, Hildreth J E

机构信息

Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

AIDS Res Hum Retroviruses. 1994 Jan;10(1):73-80. doi: 10.1089/aid.1994.10.73.

Abstract

SIVsmmPBJ 1.9 is an extremely virulent clone of the simian immunodeficiency virus SIVsmmPBj 14 that causes an acute lethal disease in pigtail macaques, with death occurring 6 to 8 days after infection. The disease is characterized by bloody mucoid diarrhea, lymphoid hyperplasia, and giant cell pneumonia. We have developed an in vitro model for the production of multinucleated giant cells (MGCs) in which peripheral blood monocytes rapidly fuse to form MGCs when cultured in lymphocyte-conditioned medium and antibody against class II MHC. We have tested the effect of SIVsmmPBj on monocytes in our MGC model system. Peripheral blood mononuclear cells (PBMCs) from normal healthy human subjects, when cultured in the presence of anti-class II MHC monoclonal antibody and SIVsmmPBj 1.9, but not either alone, resulted in the formation of MGCs within 4 days. Experiments using Transwell chambers indicated that such MGCs are formed by fusion of monocytes, not by virus-induced fusion of lymphocytes. SIVsmmPBj 1.9 is unique in inducing MGC formation in that other SIV and HIV isolates do not induce MGCs. Whereas SIVsmmPBj 1.9 grown in PBMCs was a potent inducer of MGCs in the presence of anti-class II MHC antibody, SIVsmmPBj 1.9 grown in CEMx174 failed to do so. Antibodies against IFN-gamma and TNF-alpha significantly inhibited SIVsmmPBj/anti-class II-induced formation of MGCs. These results indicate that cytokines released in response to SIVsmmPBj 1.9, in conjunction with antibodies to class II MHC, caused fusion of monocytes.

摘要

SIVsmmPBJ 1.9是猿猴免疫缺陷病毒SIVsmmPBj 14的一个极具毒性的克隆株,它可在猪尾猕猴中引发急性致死性疾病,感染后6至8天就会导致死亡。该疾病的特征为血性黏液性腹泻、淋巴组织增生和巨细胞肺炎。我们开发了一种体外模型用于产生多核巨细胞(MGCs),在外周血单核细胞于淋巴细胞条件培养基和抗II类主要组织相容性复合体(MHC)抗体中培养时,它们会迅速融合形成MGCs。我们在MGC模型系统中测试了SIVsmmPBj对单核细胞的影响。来自正常健康人类受试者的外周血单个核细胞(PBMCs),在抗II类MHC单克隆抗体和SIVsmmPBj 1.9共同存在但单独一种不存在时培养,会在4天内形成MGCs。使用Transwell小室的实验表明,此类MGCs是由单核细胞融合形成的,而非病毒诱导的淋巴细胞融合。SIVsmmPBj 1.9在诱导MGC形成方面具有独特性,因为其他SIV和HIV分离株不会诱导MGCs形成。虽然在PBMCs中培养的SIVsmmPBj 1.9在抗II类MHC抗体存在时是MGCs的强力诱导剂,但在CEMx174中培养的SIVsmmPBj 1.9却无法做到。抗γ干扰素(IFN-γ)和肿瘤坏死因子-α(TNF-α)的抗体显著抑制了SIVsmmPBj/抗II类MHC诱导的MGCs形成。这些结果表明,响应SIVsmmPBj 1.9释放的细胞因子,与抗II类MHC抗体一起,导致了单核细胞的融合。

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