Abstract
1. A SARS vaccine was produced based on recombinant native full-length Spike-protein trimers (triSpike) and efficient establishment of a vaccination procedure in rodents. 2. Antibody-mediated enhancement of SARS-CoV infection with anti-SARS-CoV Spike immune-serum was observed in vitro. 3. Antibody-mediated infection of SARS-CoV triggers entry into human haematopoietic cells via an FcγR-dependent and ACE2-, pH-, cysteine-protease-independent pathways. 4. The antibody-mediated enhancement phenomenon is not a mandatory component of the humoral immune response elicited by SARS vaccines, as pure neutralising antibody only could be obtained. 5. Occurrence of immune-mediated enhancement of SARS-CoV infection raises safety concerns regarding the use of SARS-CoV vaccine in humans and enables new ways to investigate SARS pathogenesis (tropism and immune response deregulation).
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Authors
Jaume M, Yip MS, Kam YW, Cheung CY, Kien F, Roberts A, Li PH, Dutry I, Escriou N, Daeron M, Bruzzone R, Subbarao K, Peiris JS, Nal B, Altmeyer R
Institution
HKU-Pasteur Research Centre, 8 Sassoon Road, Hong Kong SAR, China. breizh@hku.hk
Source
Hong Kong medical journal = Xianggang yi xue za zhi / Hong Kong Academy of Medicine 18 Suppl 2: 2012 Feb pg 31-6MeSH
AnimalsAntibodies, Neutralizing
Antibodies, Viral
Antibody-Dependent Enhancement
Cell Line, Tumor
Cysteine Proteases
Humans
Hydrogen-Ion Concentration
Membrane Glycoproteins
Mice
Mice, Inbred BALB C
Monocytes
Peptidyl-Dipeptidase A
Receptors, Fc
SARS Virus
Severe Acute Respiratory Syndrome
Vaccines
Viral Envelope Proteins
Virus Internalization
Pub Type(s)
Journal ArticleResearch Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22311359
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