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Updated: Jan 17, 2026

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Generation of Murine Monoclonal Antibodies by Hybridoma Technology
Published on: January 2, 2017
43.5K
Antibody Development Strategies for SFTSV: From Hybridoma to Emerging Technologies
Wanqing Lu1, Yan Liu1,2, Boyu Zhang3
1Department of Microbiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, China.
Viral Immunology
|September 24, 2025
Summary
Severe fever with thrombocytopenia syndrome (SFTS) is a deadly tick-borne illness. This review explores neutralizing monoclonal antibodies (mAbs) as a promising therapeutic strategy against SFTS virus (SFTSV).
Area of Science:
- Virology
- Immunology
- Drug Discovery
Background:
- Severe fever with thrombocytopenia syndrome (SFTS) is an emerging zoonotic disease caused by the SFTS virus (SFTSV).
- SFTSV infection has a high case fatality rate (16.2-32.6%) in East Asia.
- No approved vaccines or antiviral treatments are currently available for SFTSV.
Purpose of the Study:
- To review advances in the development of neutralizing monoclonal antibodies (mAbs) against SFTSV.
- To discuss conventional and innovative methods for mAb generation and design.
- To highlight challenges and propose strategies for developing effective SFTSV therapeutics.
Main Methods:
- Review of current literature on SFTSV neutralizing mAb research.
- Exploration of mAb generation techniques including hybridoma, phage display, and single B cell sequencing.
- Discussion of computational tools for epitope prediction and *in silico* mAb design.
Main Results:
- Advances in generating SFTSV-neutralizing mAbs using various methods.
- Insights into structure-function relationships of mAbs targeting SFTSV Gn and Gc glycoproteins.
- Identification of challenges like epitope accessibility and antibody-dependent enhancement.
Conclusions:
- Monoclonal antibody (mAb) therapy is a promising strategy for SFTSV treatment.
- Integrating structure-guided engineering and high-throughput screening can accelerate therapeutic development.
- Further research is needed to overcome challenges and develop safe, effective SFTSV mAbs.

