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热灭活的人淋巴细胞在混合淋巴细胞培养中的功能缺陷

Functional defect of heat-inactivated human lymphocytes in mixed-lymphocyte culture.

作者信息

Boyer C M, Kostyu D D, Brissette C S, Amos D B

出版信息

Cell Immunol. 1986 Sep;101(2):440-53. doi: 10.1016/0008-8749(86)90156-5.

Abstract

Possible causes were examined for the inability of heat-inactivated lymphocytes to induce proliferative responses in mixed-lymphocyte cultures (MLC). Cells heated at 45 degrees C for 60 min lost greater than 90% of their capacity to stimulate in primary (1 degree) or secondary (2 degrees) MLC. This was not due to accelerated or delayed proliferation, nor to a simple quantitative loss of antigen since a 10-fold increase in stimulators or sequential addition of heated stimulators at 4-hr intervals was ineffective. Heated B lymphocytes had approximately 80% expression of HLA-DR and DQ antigens compared to unheated B cells when measured by flow cytometry using monoclonal antibodies detecting both monomorphic and polymorphic antigens. Contrary to some reports, there was no evidence of direct suppression or induction of suppression by heated stimulators or their supernatants. Reconstitution of 1 degree and 2 degrees MLC with crude MLC supernatants or more purified interleukin 1 (Il-1) or interleukin 2 (Il-2) was unsuccessful. The results indicate the heat-induced defect occurs immediately and is not due to direct or indirect suppression, insufficient amounts of Il-1 or Il-2, nor loss of polymorphic Class II HLA determinants. Heat inactivation of stimulator function may result from failure to present an "immunogenic grid" or loss of accessory molecules required in lymphocyte interactions.

摘要

研究了热灭活淋巴细胞在混合淋巴细胞培养(MLC)中无法诱导增殖反应的可能原因。在45摄氏度加热60分钟的细胞在初次(1°)或二次(2°)MLC中刺激能力丧失超过90%。这并非由于增殖加速或延迟,也不是由于抗原简单的定量损失,因为刺激细胞增加10倍或每隔4小时依次添加加热的刺激细胞均无效。当使用检测单态和多态抗原的单克隆抗体通过流式细胞术测量时,与未加热的B淋巴细胞相比,加热的B淋巴细胞HLA-DR和DQ抗原的表达约为80%。与一些报道相反,没有证据表明加热的刺激细胞或其上清液有直接抑制作用或诱导抑制作用。用粗制的MLC上清液或更纯化的白细胞介素1(Il-1)或白细胞介素2(Il-2)重建初次和二次MLC均未成功。结果表明,热诱导的缺陷立即出现,并非由于直接或间接抑制、Il-1或Il-2数量不足,也不是由于多态性II类HLA决定簇的丧失。刺激细胞功能的热灭活可能是由于无法呈现“免疫原性网格”或淋巴细胞相互作用所需的辅助分子丧失所致。

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