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首页> 外文期刊>Journal of the Royal Society Interface >A simple mechanistic explanation for original antigenic sin and its alleviation by adjuvants
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A simple mechanistic explanation for original antigenic sin and its alleviation by adjuvants

机译:原始抗原性犯罪及其佐剂缓解的简单机制解释

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A large number of published studies have shown that adaptive immunity to a particular antigen, including pathogen-derived, can be boosted by another, cross-reacting antigen while inducing suboptimal immunity to the latter. Although this phenomenon, called original antigenic sin (OAS), was first reported approximately 70 years ago (Francis et al. 1947 Am. J. Public Health 37, 1013-1016 (doi:10.2105/AJPH.37.8.1013)), its underlying biological mechanisms are still inadequately understood (Kim et al. Proc. Natl Acad. Sci. USA 109, 13 751-13 756 (doi: 10.1073/pnas.0912458109)). Here, focusing on the humoral aspects of adaptive immunity, I propose a simple and testable mechanism: that OAS occurs when T regulatory cells induced by the first antigen decrease the dose of the second antigen that is loaded by dendritic cells and available to activate naive lymphocytes. I use both a parsimonious mathematical model and experimental data to confirm the deductive validity of this proposal. This model also explains the puzzling experimental observation that administering certain dendritic cell-activating adjuvants during antigen exposure alleviates OAS. Specifically, the model predicts that such adjuvants will attenuate T regulatory suppression of naive lymphocyte activation. Together, these results suggest additional strategies for redeeming adaptive immunity from the destructive consequences of antigenic 'sin'.
机译:大量已发表的研究表明,对另一种抗原(包括病原体衍生的抗原)的适应性免疫可以被另一种交叉反应的抗原增强,同时诱导对该抗原的次优免疫。尽管大约70年前首次报道了这种称为原始抗原罪(OAS)的现象(Francis等,1947 Am。J. Public Health 37,1013-1016(doi:10.2105 / AJPH.37.8.1013)),仍未充分理解潜在的生物学机制(Kim等人,Proc.Natl Acad.Sci.USA 109,13751-13756(doi:10.1073 / pnas.0912458109))。在这里,我着眼于适应性免疫的体液方面,我提出了一个简单且可检验的机制:当由第一种抗原诱导的T调节细胞降低树突状细胞负载的可用于激活幼稚淋巴细胞的第二种抗原的剂量时,就会发生OAS 。我同时使用简化的数学模型和实验数据来确认该提议的推论有效性。该模型还解释了令人费解的实验观察,即在抗原暴露期间给予某些树突状细胞激活佐剂可缓解OAS。具体而言,该模型预测此类佐剂将减弱T细胞对幼稚淋巴细胞活化的调节性抑制。总之,这些结果提出了从抗原性“罪恶”的破坏性后果中挽救适应性免疫力的其他策略。

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