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自然感染恙虫病东方体抗体可抑制HIV CXCR4(X4)病毒。

Natural Scrub Typhus Antibody Suppresses HIV CXCR4(X4) Viruses.

作者信息

Watt George, Kantipong Pacharee, Burnouf Thierry, Shikuma Cecilia, Philpott Sean

机构信息

Department of Medicine, John A. Burns School of Medicine, University of Hawai'i at Manoa , Honolulu, HI, USA.

Department of Internal Medicine, Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.

出版信息

Infect Dis Rep. 2013 May 15;5(1):e8. doi: 10.4081/idr.2013.e8. eCollection 2013 Jan 22.

Abstract

Viral load generally rises in HIV-infected individuals with a concomitant infection, but falls markedly in some individuals with scrub typhus (ST), a common Asian rickettsial infection. ST infection appears to shift the viral population from CXCR4-using (X4) to CCR5-utilizing (R5) strains, and there is evidence of cross-reactivity between ST-specific antibodies and HIV-1. We examined the mechanism of ST suppression of HIV by measuring the effects of ST infection on X4 and R5 viruses in vivo and in vitro, and assessing the relative contributions of antibodies and chemokines to the inhibitory effect. In vivo, a single scrub typhus plasma infusion markedly reduced the subpopulation of HIV-1 viruses using the X4 co-receptor in all 8 recipients, and eliminated X4 viruses 6 patients. In vitro, the 14 ST sera tested all inhibited the replication of an X4 but not an R5 virus. This inhibitory effect was maintained if ST sera were depleted of chemokines but was lost upon removal of antibodies. Sera from STinfected mice recognized a target that co-localized with X4 HIV gp120 in immunofluorescent experiments. These in vivo and in vitro data suggest that acute ST infection generates cross-reactive antibodies that produce potent suppression of CXCR4- but not CCR5-using HIV-1 viruses. ST suppression of HIV replication could reveal novel mechanisms that could be exploited for vaccination strategies, as well as aid in the development of fusion inhibitors and other new therapeutic regimens. This also appears to be the first instance where one pathogen is neutralized by antibody produced in response to infection by a completely unrelated organism.

摘要

在合并感染的HIV感染者中,病毒载量通常会升高,但在一些感染恙虫病(一种常见的亚洲立克次体感染)的个体中,病毒载量会显著下降。恙虫病感染似乎会使病毒群体从使用CXCR4的(X4)毒株转变为使用CCR5的(R5)毒株,并且有证据表明恙虫病特异性抗体与HIV-1之间存在交叉反应。我们通过测量恙虫病感染对体内和体外X4和R5病毒的影响,并评估抗体和趋化因子对抑制作用的相对贡献,来研究恙虫病抑制HIV的机制。在体内,单次输注恙虫病血浆在所有8名接受者中均显著降低了使用X4共受体的HIV-1病毒亚群,并且在6名患者中清除了X4病毒。在体外,所检测的14份恙虫病血清均抑制了X4病毒而非R5病毒的复制。如果恙虫病血清中的趋化因子被去除,这种抑制作用仍然存在,但去除抗体后则丧失。在免疫荧光实验中,来自感染恙虫病小鼠的血清识别出一个与X4 HIV gp120共定位的靶点。这些体内和体外数据表明,急性恙虫病感染产生交叉反应性抗体,这些抗体对使用CXCR4而非CCR5的HIV-1病毒产生强效抑制作用。恙虫病对HIV复制的抑制作用可能揭示可用于疫苗接种策略的新机制,也有助于融合抑制剂和其他新治疗方案的开发。这似乎也是首例一种病原体被针对完全无关生物体感染产生的抗体中和的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7775/3892615/312f792d8258/idr-2013-1-e8-g001.jpg

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