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对系统性红斑狼疮患者的研究将成为未来HIV疫苗设计的关键吗?

Will studies in individuals with systemic lupus erythematosus be the key to future HIV vaccine design?

作者信息

Bonsignori Mattia

机构信息

Duke Human Vaccine Institute, Duke University Medical Center, MSRB II - Room 4013, PO Box 103020, 2 Genome Court, Durham, NC 27710, USA.

出版信息

Expert Rev Vaccines. 2014 Nov;13(11):1271-3. doi: 10.1586/14760584.2014.938056. Epub 2014 Jul 12.

Abstract

The induction of HIV-1 broadly neutralizing antibodies (bnAbs) remains the primary goal of a preventive HIV-1 vaccine but no HIV-1 vaccine candidate has succeeded in inducing bnAbs. All the bnAbs isolated from chronically HIV-1 infected subjects display one or more traits associated with control by host tolerance and immunoregulatory mechanisms, including reactivity against self antigens. Recent studies on a HIV-1 patient with concurrent systemic lupus erythematosus have informed on how similar bnAbs are to typical autoantibodies controlled by immune tolerance mechanisms. Future studies aimed at elucidating the intersection between autoantibodies generated in the context of systemic lupus erythematosus and the development of HIV-1 bnAbs will further our knowledge of specific roadblocks that hamper the production of bnAbs and, ultimately, inform us on how to implement vaccine strategies to circumvent them.

摘要

诱导HIV-1广泛中和抗体(bnAbs)仍然是预防性HIV-1疫苗的主要目标,但尚无HIV-1疫苗候选物成功诱导出bnAbs。从长期感染HIV-1的受试者中分离出的所有bnAbs都表现出一种或多种与宿主耐受和免疫调节机制控制相关的特征,包括对自身抗原的反应性。最近对一名同时患有系统性红斑狼疮的HIV-1患者的研究揭示了类似的bnAbs与由免疫耐受机制控制的典型自身抗体的相似程度。旨在阐明系统性红斑狼疮背景下产生的自身抗体与HIV-1 bnAbs产生之间交集的未来研究,将进一步加深我们对阻碍bnAbs产生的特定障碍的认识,并最终告知我们如何实施疫苗策略来规避这些障碍。

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