• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1038/s41598-018-20305-4
PMID:29382880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5789897/
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/e1a7/5789897/2c334a14c153/41598_2018_20305_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/446b83664fd3/41598_2018_20305_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/0c75b8be9fa5/41598_2018_20305_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/c918afc77986/41598_2018_20305_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/cc12c8ffe9cf/41598_2018_20305_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/3aa73676d6d6/41598_2018_20305_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/ce7f9d1dbc79/41598_2018_20305_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/ffef39b0cb5d/41598_2018_20305_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/2c334a14c153/41598_2018_20305_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/446b83664fd3/41598_2018_20305_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/0c75b8be9fa5/41598_2018_20305_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/c918afc77986/41598_2018_20305_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/cc12c8ffe9cf/41598_2018_20305_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/3aa73676d6d6/41598_2018_20305_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/ce7f9d1dbc79/41598_2018_20305_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/ffef39b0cb5d/41598_2018_20305_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a7/5789897/2c334a14c153/41598_2018_20305_Fig8_HTML.jpg

相似文献

1
Antibody-mediated enhancement aggravates chikungunya virus infection and disease severity.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。
Sci Rep. 2018 Jan 30;8(1):1860. doi: 10.1038/s41598-018-20305-4.
2
Loss of TLR3 aggravates CHIKV replication and pathology due to an altered virus-specific neutralizing antibody response.由于病毒特异性中和抗体反应改变,Toll样受体3(TLR3)的缺失会加重基孔肯雅病毒(CHIKV)的复制和病理变化。
EMBO Mol Med. 2015 Jan;7(1):24-41. doi: 10.15252/emmm.201404459.
3
A potent neutralizing IgM mAb targeting the N218 epitope on E2 protein protects against Chikungunya virus pathogenesis.一种靶向E2蛋白上N218表位的强效中和性IgM单克隆抗体可预防基孔肯雅病毒发病。
MAbs. 2015;7(6):1178-94. doi: 10.1080/19420862.2015.1083664. Epub 2015 Aug 25.
4
A high-dose inoculum size results in persistent viral infection and arthritis in mice infected with chikungunya virus.高剂量接种量会导致感染基孔肯雅病毒的小鼠持续病毒感染和关节炎。
PLoS Negl Trop Dis. 2022 Jan 31;16(1):e0010149. doi: 10.1371/journal.pntd.0010149. eCollection 2022 Jan.
5
Monoclonal Antibodies as Prophylactic and Therapeutic Agents Against Chikungunya Virus.单克隆抗体作为抗基孔肯雅病毒的预防和治疗药物
J Infect Dis. 2016 Dec 15;214(suppl 5):S506-S509. doi: 10.1093/infdis/jiw324.
6
A lipid-encapsulated mRNA encoding a potently neutralizing human monoclonal antibody protects against chikungunya infection.一种包裹脂质的 mRNA 编码了一种强效中和的人源单克隆抗体,可预防基孔肯雅热感染。
Sci Immunol. 2019 May 17;4(35). doi: 10.1126/sciimmunol.aaw6647.
7
Development of Vaccines for Chikungunya Fever.基孔肯雅热疫苗的研发
J Infect Dis. 2016 Dec 15;214(suppl 5):S488-S496. doi: 10.1093/infdis/jiw271.
8
Chikungunya-specific IgG and neutralizing antibody responses in natural infection of Chikungunya virus in children from India.印度儿童自然感染基孔肯雅病毒的特异性 IgG 和中和抗体应答。
Arch Virol. 2021 Jul;166(7):1913-1920. doi: 10.1007/s00705-021-05049-3. Epub 2021 Apr 27.
9
Molecular Mimicry between Chikungunya Virus and Host Components: A Possible Mechanism for the Arthritic Manifestations.基孔肯雅病毒与宿主成分之间的分子模拟:关节炎表现的一种可能机制。
PLoS Negl Trop Dis. 2017 Jan 26;11(1):e0005238. doi: 10.1371/journal.pntd.0005238. eCollection 2017 Jan.
10
Anti-Chikungunya Virus Monoclonal Antibody That Inhibits Viral Fusion and Release.抗基孔肯雅病毒单克隆抗体抑制病毒融合和释放。
J Virol. 2020 Sep 15;94(19). doi: 10.1128/JVI.00252-20.

引用本文的文献

1
Nonreciprocity in CHIKV and MAYV Vaccine-Elicited Protection.基孔肯雅病毒和马亚罗病毒疫苗诱导的保护作用中的非互惠性。
Vaccines (Basel). 2024 Aug 27;12(9):970. doi: 10.3390/vaccines12090970.
2
Mouse Models of Mayaro Virus.马亚罗病毒的鼠模型。
Viruses. 2023 Aug 24;15(9):1803. doi: 10.3390/v15091803.
3
Understanding the Biology and Immune Pathogenesis of Chikungunya Virus Infection for Diagnostic and Vaccine Development.了解基孔肯雅热病毒感染的生物学和免疫发病机制,用于诊断和疫苗开发。

本文引用的文献

1
Dengue virus sero-cross-reactivity drives antibody-dependent enhancement of infection with zika virus.登革病毒血清交叉反应性驱动寨卡病毒感染的抗体依赖性增强。
Nat Immunol. 2016 Sep;17(9):1102-8. doi: 10.1038/ni.3515. Epub 2016 Jun 23.
2
Innate and Adaptive Immune Regulation During Chronic Viral Infections.慢性病毒感染期间的固有和适应性免疫调节。
Annu Rev Virol. 2015 Nov;2(1):573-97. doi: 10.1146/annurev-virology-100114-055226. Epub 2015 Sep 2.
3
Dengue Antibody-Dependent Enhancement: Knowns and Unknowns.登革热抗体依赖增强作用:已知与未知。
Viruses. 2022 Dec 23;15(1):48. doi: 10.3390/v15010048.
4
Characterization and Involvement of Exosomes Originating from Chikungunya Virus-Infected Epithelial Cells in the Transmission of Infectious Viral Elements.源自基孔肯雅病毒感染上皮细胞的外泌体的特征和作用及其在传染性病毒元件传播中的作用。
Int J Mol Sci. 2022 Oct 11;23(20):12117. doi: 10.3390/ijms232012117.
5
A Brighton Collaboration standardized template with key considerations for a benefit/risk assessment for an inactivated viral vaccine against Chikungunya virus.一个针对基孔肯雅病毒灭活病毒疫苗的获益/风险评估的布莱顿协作标准化模板,其中考虑了关键因素。
Vaccine. 2022 Aug 19;40(35):5263-5274. doi: 10.1016/j.vaccine.2022.06.006. Epub 2022 Jun 15.
6
Comodulation of Dengue and Chikungunya Virus Infection During a Coinfection Scenario in Human Cell Lines.登革热和基孔肯雅热病毒在人细胞系中的共感染情况下的共调节。
Front Cell Infect Microbiol. 2022 Apr 28;12:821061. doi: 10.3389/fcimb.2022.821061. eCollection 2022.
7
Chikungunya Virus Exposure Partially Cross-Protects against Mayaro Virus Infection in Mice.基孔肯雅病毒暴露可部分交叉保护小鼠免受马亚罗病毒感染。
J Virol. 2021 Nov 9;95(23):e0112221. doi: 10.1128/JVI.01122-21. Epub 2021 Sep 22.
8
Mosquito-bite infection of humanized mice with chikungunya virus produces systemic disease with long-term effects.基孔肯雅病毒感染人源化小鼠可导致全身性疾病,并产生长期影响。
PLoS Negl Trop Dis. 2021 Jun 9;15(6):e0009427. doi: 10.1371/journal.pntd.0009427. eCollection 2021 Jun.
9
Requirement of Fc-Fc Gamma Receptor Interaction for Antibody-Based Protection against Emerging Virus Infections.抗体基于Fc-Fcγ 受体相互作用的新兴病毒感染的保护作用要求。
Viruses. 2021 May 31;13(6):1037. doi: 10.3390/v13061037.
10
Co-Immunization With CHIKV VLP and DNA Vaccines Induces a Promising Humoral Response in Mice.二价嵌合病毒样颗粒和 DNA 疫苗共免疫诱导小鼠产生有前景的体液免疫应答。
Front Immunol. 2021 Mar 24;12:655743. doi: 10.3389/fimmu.2021.655743. eCollection 2021.
Microbiol Spectr. 2014 Dec;2(6). doi: 10.1128/microbiolspec.AID-0022-2014.
4
Caribbean and La Réunion Chikungunya Virus Isolates Differ in Their Capacity To Induce Proinflammatory Th1 and NK Cell Responses and Acute Joint Pathology.加勒比地区和留尼汪岛的基孔肯雅病毒分离株在诱导促炎性Th1和NK细胞反应以及急性关节病变的能力上存在差异。
J Virol. 2015 Aug;89(15):7955-69. doi: 10.1128/JVI.00909-15. Epub 2015 May 20.
5
Expanding regulatory T cells alleviates chikungunya virus-induced pathology in mice.扩增调节性T细胞可减轻基孔肯雅病毒诱导的小鼠病理变化。
J Virol. 2015 Aug 1;89(15):7893-7904. doi: 10.1128/JVI.00998-15. Epub 2015 May 20.
6
Chikungunya: Evolutionary history and recent epidemic spread.基孔肯雅热:进化史与近期的流行传播。
Antiviral Res. 2015 Aug;120:32-9. doi: 10.1016/j.antiviral.2015.04.016. Epub 2015 May 12.
7
Sero-prevalence and cross-reactivity of chikungunya virus specific anti-E2EP3 antibodies in arbovirus-infected patients.基孔肯雅病毒特异性抗E2EP3抗体在虫媒病毒感染患者中的血清流行率及交叉反应性
PLoS Negl Trop Dis. 2015 Jan 8;9(1):e3445. doi: 10.1371/journal.pntd.0003445. eCollection 2015 Jan.
8
Loss of TLR3 aggravates CHIKV replication and pathology due to an altered virus-specific neutralizing antibody response.由于病毒特异性中和抗体反应改变,Toll样受体3(TLR3)的缺失会加重基孔肯雅病毒(CHIKV)的复制和病理变化。
EMBO Mol Med. 2015 Jan;7(1):24-41. doi: 10.15252/emmm.201404459.
9
Prime-boost immunization strategies against Chikungunya virus.针对基孔肯雅病毒的初免-加强免疫策略。
J Virol. 2014 Nov;88(22):13333-43. doi: 10.1128/JVI.01926-14. Epub 2014 Sep 10.
10
Infectious diseases. Crippling virus set to conquer Western Hemisphere.传染病。致残病毒即将征服西半球。
Science. 2014 May 16;344(6185):678-9. doi: 10.1126/science.344.6185.678.