Human Antibody Neutralizes Severe Fever with Thrombocytopenia Syndrome Virus, an Emerging Hemorrhagic Fever Virus

Author:

Guo Xiling1,Zhang Li1,Zhang Wenshuai1,Chi Ying1,Zeng Xiaoyan1,Li Xian1,Qi Xian1,Jin Qiu2,Zhang Xiao3,Huang Mingming4,Wang Hua1,Chen Yin1,Bao Changjun1,Hu Jianli1,Liang Shuyi5,Bao Lin5,Wu Tao1,Zhou Minghao1,Jiao Yongjun1

Affiliation:

1. Institute of Pathogenic Microbiology, Jiangsu Provincial Center for Disease Prevention and Control, Key Laboratory of Enteric Pathogenic Microbiology, Ministry Health, Nanjing, China

2. Huaiyin Advanced Vocational and Technical School of Health, Huaian, China

3. Key Laboratory of Antibody Technology, Ministry Health, Nanjing Medical University, Nanjing, China

4. School of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China

5. School of Public Health, Nanjing Medical University, Nanjing, China

Abstract

ABSTRACT Severe fever with thrombocytopenia syndrome virus (SFTSV), a newly discovered member of the Bunyaviridae family, is the causative agent of an emerging hemorrhagic fever, SFTS, in China. Currently, there are no vaccines or effective therapies against SFTS. In this study, a combinatorial human antibody library was constructed from the peripheral lymphocytes of 5 patients who had recovered from SFTS. The library was screened against purified virions for the production of single-chain variable-region fragments (ScFv). Of the 6 positive clones, one clone (monoclonal antibody [MAb] 4-5) showed neutralizing activity against SFTSV infection in Vero cells. MAb 4-5 was found to effectively neutralize all of the clinical isolates of SFTSV tested, which were isolated from patients in China from 2010 to 2012. MAb 4-5 was found to bind a linear epitope in the ectodomain of glycoprotein Gn. Its neutralizing activity is attributed to blockage of the interactions between the Gn protein and the cellular receptor, indicating that inhibition of virus-cell attachment is its main mechanism. These data suggest that MAb 4-5 can be used as a promising candidate molecule for immunotherapy against SFTSV infection.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

Reference35 articles.

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