Immunization with recombinant Streptococcus pneumoniae PgdA protects mice against lung invasion

• Published in: Experimental biology and medicine (Maywood, N.J.) Vol. 249; p. 10119
• Main Authors: Xiao, Jiangming, Liu, Bichen, Yin, Yibing, Zhang, Xuemei
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 14.10.2024
• Subjects: Animals; Antibodies, Bacterial - blood; Antibodies, Bacterial - immunology; Bacterial Proteins - immunology; colonization; Experimental Biology and Medicine; Female; Humans; Immunization - methods; Lung - immunology; Lung - microbiology; Lung - pathology; Mice; Mice, Inbred BALB C; novel strategy; PgdA; Pneumococcal Infections - immunology; Pneumococcal Infections - microbiology; Pneumococcal Infections - prevention & control; Pneumococcal Vaccines - administration & dosage; Pneumococcal Vaccines - immunology; Recombinant Proteins - immunology; Streptococcus pneumoniae; Streptococcus pneumoniae - immunology; vaccine candidate; PgdA; colonization; novel strategy; vaccine candidate; Streptococcus pneumoniae
• ISSN: 1535-3699; 1535-3702; 1535-3699
• DOI: 10.3389/ebm.2024.10119

Current pneumococcal vaccines, including the pneumococcal polysaccharide (PPV23) and conjugate (PCV13) vaccines, offer protection against specific serotypes but pose risks of serotype replacement that can alter the composition of the nasopharyngeal microbiota. To address this challenge, a novel strategy has been proposed to provide effective protection without disrupting the colonization of other bacterial populations. In our study, we found that subcutaneous immunization with recombinant peptidoglycan N-acetylglucosamine deacetylase A (rPgdA) elicited robust humoral and cellular immune responses, significantly reducing the invasion of pneumoniae in the lungs without affecting nasopharyngeal carriage. Furthermore, rPgdA antisera were shown to diminish bacterial invasion of lung epithelial cells . Notably, sera from patients with invasive pneumococcal infections exhibited higher levels of antibodies against the PgdA protein compared to sera from healthy adults, suggesting that a natural immune response to this protein occurs during infection. These results suggest a promising new target for the development of pneumococcal vaccines.