A Nonhuman Primate Scrub Typhus Model: Protective Immune Responses Induced by pKarp47 DNA Vaccination in Cynomolgus Macaques

被引:33
|
作者
Paris, Daniel H. [1 ,2 ]
Chattopadhyay, Suchismita [3 ]
Jiang, Ju [3 ]
Nawtaisong, Pruksa [1 ]
Lee, John S. [4 ]
Tan, Esterlina [5 ]
Dela Cruz, Eduardo [5 ]
Burgos, Jasmin [5 ]
Abalos, Rodolfo [5 ]
Blacksell, Stuart D. [1 ,2 ]
Lombardini, Eric [6 ]
Turner, Gareth D. [1 ,2 ]
Day, Nicholas P. J. [1 ,2 ]
Richards, Allen L. [3 ,7 ]
机构
[1] Mahidol Univ, Fac Trop Med, Mahidol Oxford Trop Med Res Unit, Bangkok 10400, Thailand
[2] Univ Oxford, Nuffield Dept Clin Med, Ctr Trop Med & Global Hlth, Oxford OX3 7FZ, England
[3] Naval Med Res Ctr, Viral & Rickettsial Dis Dept, Silver Spring, MD 20910 USA
[4] Walter Reed Army Inst Res, Div Entomol, Silver Spring, MD 20910 USA
[5] Leonard Wood Mem Inst, Cebu 6000, Philippines
[6] Armed Forces Med Res Inst Sci, Dept Vet Med, Bangkok 10400, Thailand
[7] Uniformed Serv Univ Hlth Sci, Dept Prevent Med & Biometr, Bethesda, MD 20814 USA
来源
JOURNAL OF IMMUNOLOGY | 2015年 / 194卷 / 04期
基金
英国惠康基金;
关键词
ENCEPHALITIS-VIRUS REPLICON; SILVERED LEAF MONKEYS; RICKETTSIA-TSUTSUGAMUSHI; ORIENTIA-TSUTSUGAMUSHI; PRESBYTIS-CRISTATUS; MACACA-FASCICULARIS; GAMMA-INTERFERON; GUINEA-PIGS; INFECTION; VACCINES;
D O I
10.4049/jimmunol.1402244
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We developed an intradermal (ID) challenge cynomolgus macaque (Macaca fascicularis) model of scrub typhus, the leading cause of treatable undifferentiated febrile illness in tropical Asia, caused by the obligate intracellular bacterium, Orientia tsutsugamushi. A well-characterized animal model is required for the development of clinically relevant diagnostic assays and evaluation of therapeutic agents and candidate vaccines. We investigated scrub typhus disease pathophysiology and evaluated two O. tsutsugamushi 47-kDa, Ag-based candidate vaccines, a DNA plasmid vaccine (pKarp47), and a virus-vectored vaccine (Kp47/47-Venezuelan equine encephalitis virus replicon particle) for safety, immunogenicity, and efficacy against homologous ID challenge with O. tsutsugamushi Karp. Control cynomolgus macaques developed fever, classic eschars, lymphadenopathy, bacteremia, altered liver function, increased WBC counts, pathogen-specific Ab (IgM and IgG), and cell-mediated immune responses. Vaccinated macaques receiving the DNA plasmid pKarp47 vaccine had significantly increased O. tsutsugamushi-specific, IFN-gamma-producing PBMCs (p = 0.04), reduced eschar frequency and bacteremia duration (p <= 0.01), delayed bacteremia onset (p < 0.05), reduced circulating bacterial biomass (p = 0.01), and greater reduction of liver transaminase levels (p < 0.03) than controls. This study demonstrates a vaccine-induced immune response capable of conferring sterile immunity against high-dose homologous ID challenge of O. tsutsugamushi in a nonhuman primate model, and it provides insight into cell-mediated immune control of O. tsutsugamushi and dissemination dynamics, highlights the importance of bacteremia indices for evaluation of both natural and vaccine-induced immune responses, and importantly, to our knowledge, has determined the first phenotypic correlates of immune protection in scrub typhus. We conclude that this model is suitable for detailed investigations into vaccine-induced immune responses and correlates of immunity for scrub typhus.
引用
收藏
页码:1702 / 1716
页数:15
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