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抗体介导的增强作用会加重基孔肯雅病毒感染和疾病严重程度。

Antibody-mediated enhancement aggravates chikungunya virus infection and disease severity.

机构信息

Singapore Immunology Network, Agency for Science, Technology and Research (A*STAR), Singapore, 138648, Singapore.

Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore (NUS), Singapore, 117596, Singapore.

出版信息

Sci Rep. 2018 Jan 30;8(1):1860. doi: 10.1038/s41598-018-20305-4.

Abstract

The arthropod-transmitted chikungunya virus (CHIKV) causes a flu-like disease that is characterized by incapacitating arthralgia. The re-emergence of CHIKV and the continual risk of new epidemics have reignited research in CHIKV pathogenesis. Virus-specific antibodies have been shown to control virus clearance, but antibodies present at sub-neutralizing concentrations can also augment virus infection that exacerbates disease severity. To explore this occurrence, CHIKV infection was investigated in the presence of CHIKV-specific antibodies in both primary human cells and a murine macrophage cell line, RAW264.7. Enhanced attachment of CHIKV to the primary human monocytes and B cells was observed while increased viral replication was detected in RAW264.7 cells. Blocking of specific Fc receptors (FcγRs) led to the abrogation of these observations. Furthermore, experimental infection in adult mice showed that animals had higher viral RNA loads and endured more severe joint inflammation in the presence of sub-neutralizing concentrations of CHIKV-specific antibodies. In addition, CHIKV infection in 11 days old mice under enhancing condition resulted in higher muscles viral RNA load detected and death. These observations provide the first evidence of antibody-mediated enhancement in CHIKV infection and pathogenesis and could also be relevant for other important arboviruses such as Zika virus.

摘要

节肢动物传播的基孔肯雅病毒(CHIKV)引起类似流感的疾病,其特征是使人丧失能力的关节炎。CHIKV 的再次出现以及新的流行病的持续风险重新激发了对 CHIKV 发病机制的研究。已表明病毒特异性抗体可控制病毒清除,但存在于亚中和浓度的抗体也可增强病毒感染,从而加重疾病严重程度。为了探索这种发生情况,在原发性人细胞和鼠巨噬细胞系 RAW264.7 中研究了 CHIKV 特异性抗体存在时的 CHIKV 感染。观察到 CHIKV 与原代人单核细胞和 B 细胞的附着增强,而在 RAW264.7 细胞中检测到病毒复制增加。特异性 Fc 受体(FcγRs)的阻断导致这些观察结果被消除。此外,在成年小鼠中的实验感染表明,在存在亚中和浓度的 CHIKV 特异性抗体的情况下,动物的病毒 RNA 载量更高,关节炎症更严重。此外,在增强条件下,11 天大的小鼠中的 CHIKV 感染导致肌肉中检测到更高的病毒 RNA 载量并导致死亡。这些观察结果提供了 CHIKV 感染和发病机制中抗体介导增强的第一个证据,并且对于其他重要的虫媒病毒(如寨卡病毒)也可能相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/446b83664fd3/41598_2018_20305_Fig1_HTML.jpg

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