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艾滋病疫苗转化研究迷你综述系列:T淋巴细胞转运与疫苗诱导的黏膜免疫

Translational Mini-Review Series on Vaccines for HIV: T lymphocyte trafficking and vaccine-elicited mucosal immunity.

作者信息

Kaufman D R, Barouch D H

机构信息

Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.

出版信息

Clin Exp Immunol. 2009 Aug;157(2):165-73. doi: 10.1111/j.1365-2249.2009.03927.x.

Abstract

Many pathogens use mucosal surfaces to enter and propagate within the host, making particularly desirable vaccines that target immune responses specifically to mucosal compartments. The majority of mucosal vaccine design strategies to date have been empirical in nature. However, an emerging body of basic immunological knowledge is providing new insights into the regulation of tissue-specific lymphocyte trafficking and differentiation. These insights afford the opportunity for the rational design of vaccines that focus immune responses at mucosal surfaces. Mucosal cellular immunity may prove critical for protection in the context of HIV infection, and thus there has been considerable interest in developing vaccines that target HIV-specific cellular immune responses to the gastrointestinal and vaginal mucosa. However, the optimal strategies for eliciting mucosal cellular immune responses through vaccination remain to be determined. Here, we review both recent vaccine studies and emerging paradigms from the basic immunological literature that are relevant to the elicitation of potent and protective mucosal cellular immune memory. Increasing the synergy between these avenues of research may afford new opportunities for mucosal vaccine design.

摘要

许多病原体利用粘膜表面进入宿主并在其中繁殖,因此特别需要能够特异性针对粘膜区室引发免疫反应的疫苗。迄今为止,大多数粘膜疫苗设计策略本质上都是经验性的。然而,新出现的一系列基础免疫学知识为组织特异性淋巴细胞运输和分化的调控提供了新的见解。这些见解为合理设计将免疫反应聚焦于粘膜表面的疫苗提供了机会。粘膜细胞免疫在HIV感染的情况下可能对保护作用至关重要,因此人们对开发针对胃肠道和阴道粘膜的HIV特异性细胞免疫反应的疫苗产生了浓厚兴趣。然而,通过疫苗接种引发粘膜细胞免疫反应的最佳策略仍有待确定。在此,我们综述了近期的疫苗研究以及基础免疫学文献中与引发强效和保护性粘膜细胞免疫记忆相关的新兴范例。增强这些研究途径之间的协同作用可能为粘膜疫苗设计带来新机遇。

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