Maternal immunization with pneumococcal surface protein A provides the immune memories of offspring against pneumococcal infection

Front Cell Infect Microbiol. 2023 Mar 23:13:1059603. doi: 10.3389/fcimb.2023.1059603. eCollection 2023.

Abstract

Introduction: Streptococcus pneumoniae (S. pneumoniae) is one of the most widespread pathogens in the world and one of the largest infectious causes of infant mortality. Although current vaccines have various benefits, antibiotic resistance and the inability to vaccinate infants less than one year old demands the development of new protective strategies. One strategy, 'maternal immunization', is to protect infants by passive immunity from an immunized mother, although its mechanism is still not fully understood.

Materials and methods: The current study aimed to acquire immunity against S. pneumoniae in infants by maternal immunization with pneumococcal common antigen, pneumococcal surface protein A (PspA). Four-week-old female mice were immunized with recombinant PspA intranasally twice a week for three weeks. Females were mated with age-matched males after immunization, and delivered offspring.

Results: The week-old offspring derived from and fostered by immunized mothers had more anti-PspA-specific antibody producing cells in the spleen than those derived from sham-immunized mothers. The offspring were raised up to four weeks old and were subcutaneously stimulated with recombinant PspA. The levels of anti-PspA IgG in sera after stimulation were significantly higher in the offspring derived from the immunized mothers and the induced specific antibody to PspA showed protective efficacy against systemic pneumococcal infection.

Discussion: Maternal immunization is suggested to be able to provide a sustained immune memory to offspring. The current study would be a milestone in the field of maternal immunization toward a universal pneumococcal vaccine.

Keywords: PspA; Streptococcus pneumoniae; immunological memory; invasive infection; maternal immunization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bacterial
  • Antigens, Bacterial
  • Bacterial Proteins
  • Female
  • Immunization
  • Immunoglobulin G
  • Immunologic Memory*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Pneumococcal Infections* / prevention & control
  • Pneumococcal Vaccines
  • Streptococcus pneumoniae
  • Vaccination

Substances

  • pneumococcal surface protein A
  • Immunoglobulin G
  • Bacterial Proteins
  • Antigens, Bacterial
  • Pneumococcal Vaccines
  • Antibodies, Bacterial

Grants and funding

This work was supported by JSPS KAKENHI Grant Number 15K10758 to MH and JSPS KAKENHI Grant Number 21K20976 to TI.