Pandey J P
Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425-2230, USA.
Vaccine. 2000 Nov 8;19(6):613-7. doi: 10.1016/s0264-410x(00)00255-3.
Immunoglobulin (Ig) GM and KM allotypes are genetic markers of gamma and kappa-type light chains, respectively. The striking qualitative and quantitative differences in the distribution of these determinants among different races raise questions concerning the nature of the evolutionary selective mechanism that maintains this variation. Associations between Ig allotypes and specific antibody responses could be a selective force for the maintenance of various haplotypes and their frequencies. Data from several studies reporting significant associations between certain GM and KM allotypes and immune responsiveness to polysaccharide vaccines and to particular infectious pathogens support this hypothesis. Possible ways in which constant (C)-region allotypes could contribute to the antibody specificity include the following: (i) certain alleles coding for allotypes may be in linkage disequilibrium with particular variable (V)-region determinants associated with immune responsiveness; (ii) they could directly contribute to the formation of specific idiotypes, as shown for the T15 system in mice; and (iii) allotype-associated structural variability in the C-region could modulate the kinetic competence of the antigen binding sites.
免疫球蛋白(Ig)GM和KM同种异型分别是γ型和κ型轻链的遗传标记。这些决定簇在不同种族间分布存在显著的质和量的差异,这引发了关于维持这种变异的进化选择机制本质的问题。Ig同种异型与特定抗体反应之间的关联可能是维持各种单倍型及其频率的一种选择力量。几项研究的数据报告了某些GM和KM同种异型与对多糖疫苗及特定感染性病原体的免疫反应性之间存在显著关联,这支持了这一假设。恒定(C)区同种异型可能影响抗体特异性的可能方式如下:(i)编码同种异型的某些等位基因可能与与免疫反应性相关的特定可变(V)区决定簇处于连锁不平衡状态;(ii)它们可能直接有助于形成特定的独特型,如小鼠中的T15系统所示;(iii)C区中与同种异型相关的结构变异性可能调节抗原结合位点的动力学活性。