Cross-reactive antibodies enhance live attenuated virus infection for increased immunogenicity

被引:0
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作者
Chan K.R. [1 ]
Wang X. [1 ]
Saron W.A.A. [1 ]
Gan E.S. [1 ]
Tan H.C. [1 ]
Mok D.Z.L. [2 ]
Zhang S.L.-X. [1 ]
Lee Y.H. [3 ,4 ]
Liang C. [3 ]
Wijaya L. [5 ]
Ghosh S. [6 ]
Cheung Y.B. [1 ]
Tannenbaum S.R. [7 ,8 ,9 ]
Abraham S.N. [1 ,10 ]
St John A.L. [5 ]
Low J.G.H. [1 ,2 ,3 ]
Ooi E.E. [2 ]
机构
[1] Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore
[2] Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
[3] Interdisciplinary Research Group in Infectious Diseases, Singapore-MIT Alliance for Research and Technology (SMART), Singapore
[4] KK Research Centre, KKWomen's and Children's Hospital, Singapore
[5] Department of Infectious Diseases, Singapore General Hospital, Singapore
[6] Centre for Computational Biology, Duke-NUS Medical School, Singapore
[7] Center for Quantitative Medicine, Duke-NUS Medical School, Singapore
[8] Department for International Health, University of Tampere
[9] Department of Biological Engineering and Chemistry, Massachusetts Institute of Technology, Cambridge, 02139, MA
[10] Department of Immunology and the Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham
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D O I
10.1038/nmicrobiol.2016.164
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摘要
Vaccination has achieved remarkable successes in the control of childhood viral diseases. To control emerging infections, however, vaccines will need to be delivered to older individuals who, unlike infants, probably have had prior infection or vaccination with related viruses and thus have cross-reactive antibodies against the vaccines. Whether and how these cross-reactive antibodies impact live attenuated vaccination efficacy is unclear. Using an open-label randomized trial design, we show that subjects with a specific range of cross-reactive antibody titres from a prior inactivated Japanese encephalitis vaccination enhanced yellow fever (YF) immunogenicity upon YF vaccination. Enhancing titres of cross-reactive antibodies prolonged YF vaccine viraemia, provoked greater pro-inflammatory responses, and induced adhesion molecules intrinsic to the activating Fc-receptor signalling pathway, namely immune semaphorins, facilitating immune cell interactions and trafficking. Our findings clinically demonstrate antibody-enhanced infection and suggest that vaccine efficacy could be improved by exploiting cross-reactive antibodies.
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