Evaluation of a novel severe combined immunodeficiency mouse model for antiviral drug evaluation against Chandipura virus infection

被引:6
|
作者
Kitaura, Satoshi [1 ,2 ]
Tobiume, Minoru [3 ]
Kawahara, Madoka [1 ]
Satoh, Masaaki [1 ]
Kato, Hirofumi [1 ]
Nakayama, Noriko [1 ]
Nakajima, Nozomi [4 ]
Komeno, Takashi [4 ]
Furuta, Yousuke [4 ]
Suzuki, Tadaki [3 ]
Moriya, Kyoji [5 ]
Saijo, Masayuki [1 ]
Ebihara, Hideki [1 ,7 ]
Takayama-Ito, Mutsuyo [1 ,6 ]
机构
[1] Natl Inst Infect Dis, Dept Virology1, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Internal Med, Tokyo, Japan
[3] Natl Inst Infect Dis, Dept Pathol, Tokyo, Japan
[4] FUJIFILM Toyama Chem Co Ltd, Toyama, Japan
[5] Univ Tokyo Hosp, Dept Infect Dis, Tokyo, Japan
[6] Natl Inst Infect Dis, Dept virol 1, Lab Neuroviruses, 1-23-1, SHINJYUKU-KU, Toyama, Tokyo, Japan
[7] Natl Inst Infect Dis, Dept virol, 1-23-1, SHINJYUKU-KU, Toyama, Tokyo, Japan
关键词
SCID; Favipiravir; CHPV; T-705; Vesiculovirus; Pediatric infectious disease; FAVIPIRAVIR T-705; ACUTE ENCEPHALITIS; ANDHRA-PRADESH; OUTBREAK; CHILDREN; MICE; SANDFLIES; CELLS; INDIA; FOCUS;
D O I
10.1016/j.antiviral.2023.105582
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chandipura virus (CHPV) is a negative-sense single-stranded RNA virus known to cause fatal encephalitis out-breaks in the Indian subcontinent. The virus displays tropism towards the pediatric population and holds sig-nificant public health concerns. Currently, there is no specific, effective therapy for CHPV encephalitis. In this study, we evaluated a novel C.B-17 severe combined immunodeficiency (SCID) mouse model which can be used for pre-clinical antiviral evaluation. Inoculation of CHPV developed a lethal infection in our model. Plaque assay and immunohistochemistry detected increased viral loads and antigens in various organs, including the brain, spinal cord, adrenal glands, and whole blood. We further conducted a proof-of-concept evaluation of favipiravir in the SCID mouse model. Favipiravir treatment improved survival with pre-symptomatic (days 5-14) and post-symptomatic (days 9-18) treatment. Reduced viral loads were observed in whole blood, kidney/adrenal gland, and brain tissue with favipiravir treatment. The findings in this study demonstrate the utility of SCID mouse for in vivo drug efficacy evaluation and the potential efficacy of favipiravir against CHPV infection.
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页数:10
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