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针对肺炎球菌多糖的抗体的IgG2亚类限制

IgG2 subclass restriction of antibody to pneumococcal polysaccharides.

作者信息

Barrett D J, Ayoub E M

出版信息

Clin Exp Immunol. 1986 Jan;63(1):127-34.

Abstract

Studies in experimental animals suggest that antibody responses to certain polysaccharide antigens may be restricted in IgG subclass distribution. To determine if human antibodies to pneumococcal polysaccharides are similarly restricted we measured the IgG subclass specific response to immunization with purified polyvalent pneumococcal polysaccharide vaccine. For the type 3 pneumococcal antigen, the geometric mean titre of IgG2 antibody was significantly greater than that of IgG1, IgG3 or IgG4, in both pre-immunization and post-immunization sera. A significant rise in mean titre, comparing pre- to post-immunization sera was observed only for IgG2 antibody. Similar predominance of IgG2 antibody was found for pneumococcal polysaccharides types 6, 18, 19 and 23. In contrast, antibody to the protein antigen tetanus toxoid was exclusively of the IgG1 subclass. Patients with IgA/IgG2 deficiency demonstrated a normal IgG response to tetanus, a normal IgM response to pneumococcal polysaccharides, but no IgG antibody to pneumococcal antigens. IgG2 subclass restriction of antibody to pneumococcal polysaccharides suggest that these antigens may elicit an immune response analogous to the murine type 2 T-cell independent immunogens which show IgG subclass restriction and the requirement of a mature B cell subset defined by the Lyb5+ alloantiserum. Our findings support the possibility of subclass-specific inducing or regulating mechanisms for human responses to carbohydrate or polysaccharide antigens.

摘要

对实验动物的研究表明,针对某些多糖抗原的抗体反应可能在IgG亚类分布上受到限制。为了确定人类针对肺炎球菌多糖的抗体是否也受到类似限制,我们测定了用纯化的多价肺炎球菌多糖疫苗免疫后IgG亚类的特异性反应。对于3型肺炎球菌抗原,在免疫前和免疫后的血清中,IgG2抗体的几何平均滴度均显著高于IgG1、IgG3或IgG4。仅观察到IgG2抗体在免疫前和免疫后血清中的平均滴度有显著升高。对于6、18、19和23型肺炎球菌多糖,也发现了类似的IgG2抗体优势。相比之下,针对蛋白质抗原破伤风类毒素的抗体仅为IgG1亚类。IgA/IgG2缺乏的患者对破伤风表现出正常的IgG反应,对肺炎球菌多糖表现出正常的IgM反应,但对肺炎球菌抗原没有IgG抗体。针对肺炎球菌多糖的抗体的IgG2亚类限制表明,这些抗原可能引发类似于小鼠2型T细胞非依赖性免疫原的免疫反应,后者表现出IgG亚类限制以及由Lyb5 +同种抗血清定义的成熟B细胞亚群的需求。我们的研究结果支持了人类对碳水化合物或多糖抗原反应存在亚类特异性诱导或调节机制的可能性。

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