Antibody-mediated enhancement aggravates chikungunya virus infection and disease severity

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作者
Fok-Moon Lum
Thérèse Couderc
Bing-Shao Chia
Ruo-Yan Ong
Zhisheng Her
Angela Chow
Yee-Sin Leo
Yiu-Wing Kam
Laurent Rénia
Marc Lecuit
Lisa F. P. Ng
机构
[1] Technology and Research (A*STAR),Singapore Immunology Network, Agency for Science
[2] National University of Singapore (NUS),Department of Biochemistry, Yong Loo Lin School of Medicine
[3] Institut Pasteur,Biology of Infection Unit
[4] Inserm U1117,Paris Descartes University, Sorbonne Paris Cité, Institut Imagine, Necker
[5] Institute of Infectious Disease and Epidemiology,Enfants Malades University Hospital
[6] Division of Infectious Diseases and Tropical Medicine,Institute of Infection and Global Health
[7] APHP,Department of Microbiology and Immunobiology
[8] University of Liverpool,School of Life Sciences
[9] Harvard Medical School,Institute of Molecular and Cell Biology, Agency for Science
[10] University of Dundee,undefined
[11] Technology and Research (A*STAR),undefined
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摘要
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.
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