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Updated: Jul 27, 2025

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Three neutralizing mAbs induced by MPXV A29L protein recognizing different epitopes act synergistically against
Mengjun Li1, Zuning Ren1,2, Yuelin Wang1
1BSL-3 Laboratory (Guangdong), Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health; Department of Laboratory Medicine, Zhujiang Hospital; Southern Medical University, Guangzhou, People's Republic of China.
Abstract:
The worldwide outbreak of the monkeypox virus (MPXV) has become a "Public Health Emergency of International Concern" (PHEIC). Severe monkeypox virus infection can be fatal, however, effective therapeutic methods are yet to be developed. Mice were immunized with A35R protein and A29L protein of MPXV, and the binding and neutralizing activities of the immune sera against poxvirus-associated antigens and viruses were identified. A29L protein and A35R protein-specific monoclonal antibodies (mAbs) were generated and their antiviral activities of these mAbs were characterized in vitro and in vivo. Immunization with the MPXV A29L protein and A35R protein induced neutralizing antibodies against the orthopoxvirus in mice. None of the mAbs screened in this study against A35R could effectively neutralize the vaccinia virus (VACV), while three mAbs against A29L protein, 9F8, 3A1 and 2D1 were confirmed to have strong broad binding and neutralizing activities against orthopoxvirus, among which 9F8 showed the best neutralizing activity. 9F8, 3A1, and 2D1 recognized different epitopes on MPXV A29L protein, showing synergistic antiviral activity in vitro against the VACV Tian Tan and WR strains; the best activity was observed when the three antibodies were combined. In the vivo antiviral prophylactic and therapeutic experiments, 9F8 showed complete protective activity, whereas 3A1 and 2D1 showed partial protective activity. Similarly, the three antibodies showed synergistic antiviral protective activity against the two VACVs. In conclusion, three mAbs recognized different epitopes on MPXV A29L protein were developed and showed synergistic effects against orthopoxvirus.
Insights
New monoclonal antibodies (mAbs) targeting the monkeypox virus (MPXV) A29L protein show potent neutralizing activity against orthopoxviruses. These MPXV-derived antibodies demonstrate synergistic effects, offering promising therapeutic potential for poxvirus infections.
Area of Science:
- Virology
- Immunology
- Therapeutics
Background:
- The global monkeypox virus (MPXV) outbreak is a significant public health concern.
- Effective treatments for severe MPXV infections are currently lacking.
Purpose of the Study:
- To develop and characterize monoclonal antibodies (mAbs) against MPXV proteins for potential therapeutic use.
- To evaluate the in vitro and in vivo antiviral activities of these mAbs against orthopoxviruses.
Main Methods:
- Mice were immunized with MPXV A35R and A29L proteins to generate immune sera.
- Monoclonal antibodies targeting A29L and A35R proteins were generated and screened.
- Antiviral activities of mAbs were assessed in vitro and in vivo against vaccinia virus (VACV) strains.
Main Results:
- Immunization induced neutralizing antibodies against orthopoxviruses.
- Three mAbs (9F8, 3A1, 2D1) against A29L protein exhibited strong binding and neutralizing activity against orthopoxviruses.
- These A29L-specific mAbs demonstrated synergistic antiviral effects in vitro and in vivo, with 9F8 showing the highest neutralizing potency.
Conclusions:
- Novel mAbs targeting distinct epitopes on MPXV A29L protein were successfully developed.
- These mAbs exhibit significant synergistic antiviral activity against orthopoxviruses, highlighting their therapeutic potential.
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