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.

PubMed

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.