Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/8075
Title: Anti-Severe Acute Respiratory Syndrome Coronavirus Spike Antibodies Trigger Infection of Human Immune Cells via a pH-and Cysteine Protease-Independent Fc gamma R Pathway
Authors: Jaume, M
Yip, MS
Cheung, CY
Leung, HL
Li, PH
Kien, F
Dutry, I
Callendret, B
Escriou, N
Altmeyer, R
Nal, B
Daeron, M
Bruzzone, R
Peiris, JSM
Keywords: Life Sciences & Biomedicine;Virology;Human-Immunodeficiency-Virus;Sars-Coronavirus;Dependent enhancement;Peritonitis-Virus;Functional receptor;Protective immunity;Feline Coronavirus;Mononuclear-Cells;Cathepsin-L;TNF-Alpha
Issue Date: 2011
Publisher: American Society for Microbiology
Citation: Journal of Virology, 85(20), 10582 - 10597, 2011
Abstract: Public health measures successfully contained outbreaks of the severe acute respiratory syndrome coronavirus (SARS-CoV) infection. However, the precursor of the SARS-CoV remains in its natural bat reservoir, and re-emergence of a human-adapted SARS-like coronavirus remains a plausible public health concern. Vaccination is a major strategy for containing resurgence of SARS in humans, and a number of vaccine candidates have been tested in experimental animal models. We previously reported that antibody elicited by a SARS-CoV vaccine candidate based on recombinant full-length Spike-protein trimers potentiated infection of human B cell lines despite eliciting in vivo a neutralizing and protective immune response in rodents. These observations prompted us to investigate the mechanisms underlying antibody-dependent enhancement (ADE) of SARS-CoV infection in vitro. We demonstrate here that anti-Spike immune serum, while inhibiting viral entry in a permissive cell line, potentiated infection of immune cells by SARS-CoV Spike-pseudotyped lentiviral particles, as well as replication-competent SARS coronavirus. Antibody-mediated infection was dependent on Fc_ receptor II but did not use the endosomal/lysosomal pathway utilized by angiotensin I converting enzyme 2 (ACE2), the accepted receptor for SARS-CoV. This suggests that ADE of SARS-CoV utilizes a novel cell entry mechanism into immune cells. Different SARS vaccine candidates elicit sera that differ in their capacity to induce ADE in immune cells despite their comparable potency to neutralize infection in ACE2-bearing cells. Our results suggest a novel mechanism by which SARS-CoV can enter target cells and illustrate the potential pitfalls associated with immunization against it. These findings should prompt further investigations into SARS pathogenesis.
Description: Copyright © 2011, American Society for Microbiology. All Rights Reserved.
URI: http://jvi.asm.org/content/85/20/10582.full.pdf+html
http://bura.brunel.ac.uk/handle/2438/8075
DOI: http://dx.doi.org/10.1128/JVI.00671-11
ISSN: 0022-538X
Appears in Collections:Biological Sciences
Dept of Life Sciences Research Papers

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