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热处理的外周血单个核细胞和爱泼斯坦-巴尔病毒转化的淋巴母细胞系(EBV-LCL)的差异抗原呈递:加热的EBV-LCL呈递同种异体抗原和可溶性抗原,但在刺激自体EBV-LCL致敏的T细胞方面存在缺陷。

Differential antigen presentation by heat-treated peripheral blood mononuclear cells and Epstein-Barr virus-transformed lymphoblastoid cell lines (EBV-LCL): heated EBV-LCL present alloantigen and soluble antigen but are deficient in the stimulation of autologous EBV-LCL primed T cells.

作者信息

Mandell R B, Hank J A, Chen B P, Robins H I, Sondel P M

出版信息

Hum Immunol. 1987 Jul;19(3):163-77. doi: 10.1016/0198-8859(87)90067-x.

Abstract

Heat-treated PBM (1 hr at 45 degrees C) cannot present soluble Candida albicans antigens (CAN) or stimulate in the mixed lymphocyte culture (MLC) reaction. This is despite their continued expression of serologically defined class II MHC antigens. In contrast, heat-treated EBV-LCL present soluble CAN and stimulate allogeneic T cells in the MLC. Heated EBV-LCL stimulate strong secondary responses from allogeneic alloprimed T-cell lines in the primed lymphocyte test (PLT), while heated PBM stimulate only weak secondary allogeneic responses. To test whether this difference was due to a subtle difference in the thermal stability of the functional expression of class II MHC antigens on PBM and EBV-LCL cells, the EBV-LCL cells were heated for 1 hr at temperatures from 45 degrees C to 60 degrees C. Even after treatment at 60 degrees C, the heated EBV-LCL strongly stimulated alloreactive T cells in MLC and PLT reactions. Heated EBV-LCL are not nonspecifically mitogenic, as they do not stimulate autologous T-cell lines primed to alloantigens. However, the weak response of alloprimed T-cell lines to heated allogeneic PBM can be augmented by coculturing with autologous heated EBV-LCL, suggesting heated EBV-LCL maintain a metabolic activity necessary for allogeneic stimulation that is deficient in heated PBM. While heated EBV-LCL stimulate allogeneic alloprimed T-cell lines, they no longer stimulate autologous EBV-LCL primed T-cell lines; irradiated EBV-LCL stimulate both strongly. This suggests the involvement of a heat labile antigenic or metabolic factor in the T-cell recognition of autologous but not allogenic EBV-LCL.

摘要

经热处理的外周血单核细胞(45℃处理1小时)无法呈现可溶性白色念珠菌抗原(CAN),也不能在混合淋巴细胞培养(MLC)反应中发挥刺激作用。尽管它们仍持续表达血清学定义的II类主要组织相容性复合体抗原。相比之下,经热处理的EB病毒转化的B淋巴细胞系(EBV-LCL)呈现可溶性CAN,并在MLC中刺激同种异体T细胞。加热的EBV-LCL在致敏淋巴细胞试验(PLT)中能刺激同种异体预致敏T细胞系产生强烈的二次反应,而加热的外周血单核细胞仅能刺激微弱的同种异体二次反应。为了测试这种差异是否是由于外周血单核细胞和EBV-LCL细胞上II类主要组织相容性复合体抗原功能表达的热稳定性存在细微差异所致,将EBV-LCL细胞在45℃至60℃的温度下加热1小时。即使在60℃处理后,加热的EBV-LCL在MLC和PLT反应中仍能强烈刺激同种异体反应性T细胞。加热的EBV-LCL并非非特异性促有丝分裂,因为它们不会刺激针对同种异体抗原预致敏的自体T细胞系。然而,通过与自体加热的EBV-LCL共培养,同种异体预致敏T细胞系对加热的同种异体外周血单核细胞的微弱反应可以增强,这表明加热的EBV-LCL维持了同种异体刺激所需的代谢活性,而加热的外周血单核细胞则缺乏这种活性。虽然加热的EBV-LCL刺激同种异体预致敏T细胞系,但它们不再刺激自体EBV-LCL预致敏T细胞系;经辐照的EBV-LCL对两者均有强烈刺激作用。这表明在T细胞识别自体而非同种异体EBV-LCL过程中涉及一种热不稳定的抗原性或代谢因子。

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