Recombinant proteins A29L, M1R, A35R, and B6R vaccination protects mice from mpox virus challenge

Front Immunol. 2023 Jun 26:14:1203410. doi: 10.3389/fimmu.2023.1203410. eCollection 2023.

Abstract

Since May 2022, mutant strains of mpox (formerly monkeypox) virus (MPXV) have been rapidly spreading among individuals who have not traveled to endemic areas in multiple locations, including Europe and the United States. Both intracellular and extracellular forms of mpox virus have multiple outer membrane proteins that can stimulate immune response. Here, we investigated the immunogenicity of MPXV structural proteins such as A29L, M1R, A35R, and B6R as a combination vaccine, and the protective effect against the 2022 mpox mutant strain was also evaluated in BALB/c mice. After mixed 15 μg QS-21 adjuvant, all four virus structural proteins were administered subcutaneously to mice. Antibody titers in mouse sera rose sharply after the initial boost, along with an increased capacity of immune cells to produce IFN-γ alongside an elevated level of cellular immunity mediated by Th1 cells. The vaccine-induced neutralizing antibodies significantly inhibited the replication of MPXV in mice and reduced the pathological damage of organs. This study demonstrates the feasibility of a multiple recombinant vaccine for MPXV variant strains.

Keywords: antibody response; mpox virus; recombinant protein; vaccination; virus challenge.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Mice
  • Mice, Inbred BALB C
  • Monkeypox virus
  • Mpox, Monkeypox* / prevention & control
  • Recombinant Proteins
  • Smallpox Vaccine*
  • Vaccination

Substances

  • Recombinant Proteins
  • Smallpox Vaccine

Grants and funding

This work was supported by The National Key Research and Development Program of China(2023YFC0871900).