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非洲猪瘟病毒特异性猪细胞毒性T细胞活性

African swine fever virus specific porcine cytotoxic T cell activity.

作者信息

Martins C L, Lawman M J, Scholl T, Mebus C A, Lunney J K

机构信息

Pathobiology Laboratory, Plum Island Animal Disease Center, ARS, U.S. Department of Agriculture, Greenport, New York.

出版信息

Arch Virol. 1993;129(1-4):211-25. doi: 10.1007/BF01316896.

Abstract

African swine fever virus (ASFV) specific, cytotoxic T lymphocyte (CTL) activity has been studied in a protection model in which SLA inbred miniature swine are experimentally inoculated with a naturally occurring, non-fatal ASFV isolate (NHV). Peripheral blood mononuclear cells (PBMC) from such infected swine show significant activity in CTL assays, using cultured ASFV-infected porcine blood derived macrophages as target cells. This CTL activity is elicited from PBMC by in vitro restimulation of effector cells with low doses (multiplicity of infection = 0.1) of the homologous virus isolate for 48 to 72 h. For SLAc/c effectors, this CTL activity appears to be SLA class I restricted because (1) blocking target cell antigens with monoclonal antibodies (mAb) against SLA class I antigens causes a major reduction in CTL activity; (2) there is preferential lysis of SLA class I matched, ASFV infected targets; and (3) depletion of effector cells with CD8 specific mAb and complement causes a reduction in CTL activity. The CTL activity is ASFV specific for all pigs tested in that infected macrophages are preferentially lysed as compared to normal (non-infected) cultured macrophages or macrophages infected with hog cholera virus (HCV). Lysis of macrophages infected with different ASFV isolates revealed that there is marked lysis of macrophages infected with the virulent L60 isolate but less lysis of macrophages infected with the DR-II and Tengani isolates. In summary, our data show that ASFV specific CTL activity is triggered in swine infected with the NHV ASFV isolate.

摘要

在一个保护模型中,对非洲猪瘟病毒(ASFV)特异性细胞毒性T淋巴细胞(CTL)活性进行了研究。在该模型中,将SLA近交小型猪用一种自然发生的、非致死性的ASFV分离株(NHV)进行实验性接种。来自此类感染猪的外周血单核细胞(PBMC)在CTL检测中表现出显著活性,该检测使用培养的ASFV感染的猪源巨噬细胞作为靶细胞。这种CTL活性是通过用低剂量(感染复数=0.1)的同源病毒分离株对效应细胞进行体外再刺激48至72小时,从PBMC中诱导产生的。对于SLAc/c效应细胞,这种CTL活性似乎受SLA I类分子限制,原因如下:(1)用抗SLA I类抗原的单克隆抗体(mAb)阻断靶细胞抗原会导致CTL活性大幅降低;(2)对SLA I类分子匹配的、ASFV感染的靶细胞有优先裂解作用;(3)用CD8特异性mAb和补体去除效应细胞会导致CTL活性降低。对于所有测试的猪,CTL活性均具有ASFV特异性,因为与正常(未感染)培养的巨噬细胞或感染猪霍乱病毒(HCV)的巨噬细胞相比,感染的巨噬细胞优先被裂解。对感染不同ASFV分离株的巨噬细胞进行裂解实验发现,感染强毒株L60的巨噬细胞有明显裂解,而感染DR-II和滕加尼分离株的巨噬细胞裂解较少。总之,我们的数据表明,在感染NHV ASFV分离株的猪中会触发ASFV特异性CTL活性。

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