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一种不符合传统超敏反应分类的抗原特异性超敏反应。

An antigen-specific hypersensitivity which does not fit into traditional classification of hypersensitivity.

作者信息

Lei H Y, Huang K J, Shen C L, Huang J L

机构信息

Department of Microbiology, National Cheng Kung University, Tainan, Taiwan, R.O.C.

出版信息

J Immunol. 1989 Jul 15;143(2):432-8.

PMID:2472437
Abstract

A unique type of Ag-specific hypersensitivity was induced by challenging the Ag-sensitized mice at the ear. It was elicited within 1 h after the Ag challenge, and thus was distinct from either the delayed-type hypersensitivity (DTH) which developed in 24 h or the immune complex-mediated hypersensitivity which evolved in 4 to 6 h. This hypersensitivity was referred to as early-type hypersensitivity (ETH). The time required for these types of hypersensitivity to develop after immunization was also different; DTH required 4 to 6 days, ETH 9 to 11 days, whereas plasma protein-induced immune complex-mediated hypersensitivity needed 18 to 21 days. The ETH could be induced by a smaller amount of Ag than DTH, and unlike DTH could be transferred by either immune sera or T cell-derived culture factor which was small m.w. Although the ETH developed later than DTH after sensitization, it lasted longer once developed and the pattern of response was inversely related to DTH. Furthermore, the denatured hepatitis B surface Ag induced DTH but not ETH, in contrast to native hepatitis B surface Ag that induced both, suggesting that the epitopes recognized by TETH cells were distinct from those recognized by TDTH cells. The ETH could be induced by most Ag tested including poly(Glu60Ala10Tyr10, L-lactic dehydrogenase, insulin, chicken egg white lysozyme, polymerized human serum albumin, horse gamma-globulin, transferrin, fibrinogen, and plasminogen, but not by purified protein derivative. Because poly(Glu60Ala10Tyr10, L-lactic dehydrogenase, egg white lysozyme and insulin were under the Ir gene control and the inducibility of ETH was Ag dependent and was closely correlated with that of DTH, the expression of ETH also must be regulated by Ir gene. The histopathologic changes in ETH consisted of capillary congestion and edema. The vasopermeability was increased and there was the leakage of plasma proteins into the tissue. Based on these data, we concluded that the ETH reported in this study was a novel type of Ag-specific hypersensitivity.

摘要

通过在耳部对已致敏小鼠进行抗原激发,诱导出了一种独特的抗原特异性超敏反应。它在抗原激发后1小时内出现,因此与24小时后出现的迟发型超敏反应(DTH)或4至6小时内发生的免疫复合物介导的超敏反应不同。这种超敏反应被称为早发型超敏反应(ETH)。这些类型的超敏反应在免疫后发生所需的时间也不同;DTH需要4至6天,ETH需要9至11天,而血浆蛋白诱导的免疫复合物介导的超敏反应需要18至21天。与DTH相比,诱导ETH所需的抗原量更少,并且与DTH不同,ETH可以由免疫血清或低分子量的T细胞衍生培养因子转移。尽管致敏后ETH比DTH出现得晚,但一旦出现持续时间更长,且反应模式与DTH呈负相关。此外,与天然乙型肝炎表面抗原能同时诱导DTH和ETH相反,变性乙型肝炎表面抗原诱导DTH但不诱导ETH,这表明TETH细胞识别的表位与TDTH细胞识别的表位不同。包括聚(Glu60Ala10Tyr10)、L-乳酸脱氢酶、胰岛素、鸡卵清溶菌酶、聚合人血清白蛋白、马γ球蛋白、转铁蛋白、纤维蛋白原和纤溶酶原在内的大多数测试抗原都能诱导ETH,但纯化蛋白衍生物不能。由于聚(Glu60Ala10Tyr10)、L-乳酸脱氢酶、卵清溶菌酶和胰岛素受Ir基因控制,且ETH的诱导性取决于抗原并与DTH密切相关,因此ETH的表达也必定受Ir基因调控。ETH的组织病理学变化包括毛细血管充血和水肿。血管通透性增加,血浆蛋白渗漏到组织中。基于这些数据,我们得出结论,本研究中报道的ETH是一种新型的抗原特异性超敏反应。

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