Equine Polyclonal Antibodies Prevent Acute Chikungunya Virus Infection in Mice

被引:1
|
作者
Barker, Douglas [1 ]
Han, Xiaobing [1 ]
Wang, Eryu [2 ]
Dagley, Ashley [3 ]
Anderson, Deborah M. [1 ]
Jha, Aruni [1 ]
Weaver, Scott C. [2 ]
Julander, Justin [3 ]
Nykiforuk, Cory [1 ]
Kodihalli, Shantha [1 ]
机构
[1] Emergent BioSolut Canada Inc, Winnipeg, MB R3T 5Y3, Canada
[2] Univ Texas Med Branch Galveston, Inst Human Infect & Immun, Dept Microbiol & Immunol, Galveston, TX 77555 USA
[3] Utah State Univ, Inst Antiviral Res, Logan, UT 84322 USA
来源
VIRUSES-BASEL | 2023年 / 15卷 / 07期
关键词
chikungunya; pharmacodynamics; mouse model; PARTICLE VACCINE; MONOCLONAL-ANTIBODIES; NONHUMAN-PRIMATES; CELL-CULTURE; DISEASE; THERAPY; IMMUNOGENICITY; EPIDEMIOLOGY; TRANSMISSION; PROPHYLAXIS;
D O I
10.3390/v15071479
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chikungunya virus (CHIKV) is a mosquito-transmitted pathogen that causes chikungunya disease (CHIK); the disease is characterized by fever, muscle ache, rash, and arthralgia. This arthralgia can be debilitating and long-lasting, seriously impacting quality of life for years. Currently, there is no specific therapy available for CHIKV infection. We have developed a despeciated equine polyclonal antibody (CHIKV-EIG) treatment against CHIKV and evaluated its protective efficacy in mouse models of CHIKV infection. In immunocompromised (IFNAR(-/-)) mice infected with CHIKV, daily treatment for five consecutive days with CHIKV-EIG administered at 100 mg/kg starting on the day of infection prevented mortality, reduced viremia, and improved clinical condition as measured by body weight loss. These beneficial effects were seen even when treatment was delayed to 1 day after infection. In immunocompetent mice, CHIKV-EIG treatment reduced virus induced arthritis (including footpad swelling), arthralgia-associated cytokines, viremia, and tissue virus loads in a dose-dependent fashion. Collectively, these results suggest that CHIKV-EIG is effective at preventing CHIK and could be a viable candidate for further development as a treatment for human disease.
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页数:17
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