A humanized neutralizing antibody protects against human adenovirus type 7 infection in humanized desmoglein-2 and CD46 double-receptor transgenic mice

Human adenovirus type 7 (HAdV7) has become a major public health threat due to its widespread transmission, severe associated pneumonia, and a lack of effective anti-HAdV7 drugs. The aim of the current study is to design a humanized monoclonal antibody (mAb) demonstrating efficacy against HAdV-7 inf...

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Veröffentlicht in:Virology journal 2024-11, Vol.21 (1), p.294-294, Article 294
Hauptverfasser: Zhou, Chengxing, Liao, Xiaohong, Zhou, Zhichao, Mo, Chuncong, Yang, Yujie, Liao, Hui, Liu, Minglei, Zhang, Qiong, Li, Qiuru, Tian, Xingui, Zhou, Rong, Cao, Hong
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Sprache:eng
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Zusammenfassung:Human adenovirus type 7 (HAdV7) has become a major public health threat due to its widespread transmission, severe associated pneumonia, and a lack of effective anti-HAdV7 drugs. The aim of the current study is to design a humanized monoclonal antibody (mAb) demonstrating efficacy against HAdV-7 infections in vitro and in vivo. The humanized neutralizing antibody, 3G5-hu, was derived from the murine mAb 3G5. Antibody activity was evaluated using a flow cytometry-based neutralization (FCN) assay to identify humanized mAbs retaining potent neutralizing activity. Additionally, a humanized hDSG2/hCD46 dual-receptor transgenic mouse model was developed to simulate HAdV-7 infection. Using recombinant HAdV-7 expressing enhanced green fluorescent protein and clinically isolated wild-type HAdV-7, the half-maximal effective concentration of 3G5-hu against HAdV-7 was determined to be
ISSN:1743-422X
1743-422X
DOI:10.1186/s12985-024-02572-y