Evaluation of Dengue Virus strains for human challenge studies

被引:35
|
作者
Mammen, M. P. [1 ,2 ,3 ,4 ]
Lyons, A. [1 ,2 ,3 ,4 ]
Innis, B. L. [1 ,2 ,3 ,4 ]
Sun, W. [1 ,2 ,3 ,4 ]
McKinney, D. [1 ,2 ,3 ,4 ]
Chung, R. C. Y. [5 ]
Eckels, K. H. [7 ]
Putnak, R. [1 ,2 ,3 ,4 ]
Kanesa-thasan, N. [1 ,2 ,3 ,4 ]
Scherer, J. M. [1 ,2 ,3 ,4 ]
Statler, J. [6 ]
Asher, L. V. [7 ]
Thomas, S. J. [1 ,2 ,3 ,4 ]
Vaughn, D. W. [1 ,2 ,3 ,4 ]
机构
[1] Walter Reed Army Inst Res, Div Viral Dis, Silver Spring, MD 20910 USA
[2] Walter Reed Army Inst Res, Div Regulated Act, Silver Spring, MD 20910 USA
[3] Walter Reed Army Inst Res, Div Vet Serv Program, Silver Spring, MD 20910 USA
[4] Walter Reed Army Inst Res, Div Pathol, Silver Spring, MD 20910 USA
[5] Walter Reed Army Med Ctr, Infect Dis Serv, Washington, DC 20307 USA
[6] Walter Reed Army Med Ctr, Serv Radiol, Washington, DC 20307 USA
[7] WRAIR, Translat Med Branch, Silver Spring, MD 20910 USA
关键词
Dengue; Virus; Vaccine; Challenge; DOG KIDNEY-CELLS; HEMORRHAGIC-FEVER; PROTECTIVE EFFICACY; ATTENUATED DENGUE; SERIAL PASSAGE; VACCINE; CANDIDATE; IMMUNIZATION; RECOMBINANT; VOLUNTEERS;
D O I
10.1016/j.vaccine.2013.12.040
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Discordance between the measured levels of dengue virus neutralizing antibody and clinical outcomes in the first-ever efficacy study of a dengue tetravalent vaccine (Lancet, Nov 2012) suggests a need to re-evaluate the process of pre-screening dengue vaccine candidates to better predict clinical benefit prior to large-scale vaccine trials. In the absence of a reliable animal model and established correlates of protection for dengue, a human dengue virus challenge model may provide an approach to down-select vaccine candidates based on their ability to reduce risk of illness following dengue virus challenge. We report here the challenge of flavivirus-naive adults with cell culture-passaged dengue viruses (DENV) in a controlled setting that resulted in uncomplicated dengue fever (DF). This sets the stage for proof-of-concept efficacy studies that allow the evaluation of dengue vaccine candidates in healthy adult volunteers using qualified DENV challenge strains well before they reach field efficacy trials involving children. Fifteen flavivirus-naive adult volunteers received 1 of 7 DENV challenge strains (n = 12) or placebo (n = 3). Of the twelve volunteers who received challenge strains, five (two DENV-1 45AZ5 and three DENV-3 CH53489 cl24/28 recipients) developed DF, prospectively defined as >= 2 typical symptoms, >= 48 h of sustained fever (> 100.4 degrees F) and concurrent viremia. Based on our study and historical data, we conclude that the DENV-1 and DENV-3 strains can be advanced as human challenge strains. Both of the DENV-2 strains and one DENV-4 strain failed to meet the protocol case definition of DF. The other two DENV-4 strains require additional testing as the illness approximated but did not satisfy the case definition of DF. Three volunteers exhibited effusions (1 pleural/ascites, 2 pericardial) and 1 volunteer exhibited features of dengue (rash, lymphadenopathy, neutropenia and thrombocytopenia), though in the absence of fever and symptoms. The occurrence of effusions in milder DENV infections counters the long-held belief that plasma leakage syndromes are restricted to dengue hemorrhagic fever/dengue shock syndromes (DHF/DSS). Hence, the human dengue challenge model may be useful not only for predicting the efficacy of vaccine and therapeutic candidates in small adult cohorts, but also for contributing to our further understanding of the mechanisms behind protection and virulence. Published by Elsevier Ltd.
引用
收藏
页码:1488 / 1494
页数:7
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