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用钥孔戚血蓝蛋白免疫后,不同人类IgG亚类的抗体表现出不同的亲和力成熟模式。

Antibodies of different human IgG subclasses show distinct patterns of affinity maturation after immunization with keyhole limpet haemocyanin.

作者信息

Devey M E, Bleasdale-Barr K M, Bird P, Amlot P L

机构信息

Department of Clinical Sciences, L.S.H.T.M., University of London.

出版信息

Immunology. 1990 Jun;70(2):168-74.

Abstract

The functional affinities of antibodies of different IgG subclasses were measured in normal individuals during the primary, secondary and tertiary immune responses to keyhole limpet haemocyanin (KLH). IgG1 responses showed marked affinity maturation between Days 7 and 21 after primary and by Day 7 after secondary and subsequent immunizations, correlating with an expansion of high-affinity antibody populations. When present, IgG2 responses were of low titre but high functional affinity with no change in response to immunization and may represent a T-independent cross-reacting response with a carbohydrate epitope of KLH. IgG3 responses were variable but generally of low titre and low functional affinity, although those of higher titre and affinity were associated with secondary delayed-type hypersensitivity (DTH) and clinical reactions to KLH. In contrast to IgG1, IgG4 antibodies were not detected until 1 year after primary immunization, when they were found at low titre but high functional affinity. Following secondary immunization, IgG4 titres increased rapidly but without any further increase in affinity. The emergence of high-affinity IgG4 antibodies coincided with a loss of the high-affinity IgG1 populations, suggesting a preferential switch with time from high-affinity IgG1 antibodies to IgG4.

摘要

在对钥孔戚血蓝蛋白(KLH)的初次、二次和三次免疫应答期间,测定了正常个体中不同IgG亚类抗体的功能亲和力。IgG1应答在初次免疫后第7天至21天之间以及二次及后续免疫后第7天显示出明显的亲和力成熟,这与高亲和力抗体群体的扩增相关。当存在时,IgG2应答滴度低但功能亲和力高,对免疫无反应变化,可能代表与KLH碳水化合物表位的非T细胞依赖性交叉反应应答。IgG3应答各不相同,但通常滴度低且功能亲和力低,尽管那些滴度和亲和力较高的应答与二次迟发型超敏反应(DTH)及对KLH的临床反应相关。与IgG1相反,IgG4抗体直到初次免疫后1年才被检测到,当时其滴度低但功能亲和力高。二次免疫后,IgG4滴度迅速升高,但亲和力没有进一步增加。高亲和力IgG4抗体的出现与高亲和力IgG1群体的丧失同时发生,表明随着时间的推移,优先从高亲和力IgG1抗体转换为IgG4。

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