Cardoso Kimberly Freitas, de Souza Lara Regina Alves, Martins Débora Silva, da Silva Santos Beatriz Senra Álvares, de Carvalho Ketyllen Reis Andrade, da Silva Messias Sarah Giarola, de Faria Gonçalves Ana Paula, Do Nascimento Macário Rayanne Rosa, de Jesus Deyse Julia Ferreira, De Mendonça Ângelo Ana Luiza Pessoa, de Paula Pereira Leonardo, Nascimento Sâmick Layene Moreira, Kano Flora Satiko, Alves Pedro Augusto, Xavier Marcelo Antonio Pascoal, Martins-Filho Olindo Assis, Russo Remo Castro, Gazzinelli Ricardo Tostes, Miyaji Eliane Namie, Garcia Cristiana Couto, de Magalhães Vieira Machado Alexandre, Araújo Márcio Sobreira Silva
Grupo Integrado de Pesquisa em Biomarcadores, Instituto René Rachou - Fundação Oswaldo Cruz, Avenida Augusto de Lima nº 1715, Barro Preto, Belo Horizonte, Minas Gerais, Brasil.
Laboratório de Imunologia de Doenças Virais, Instituto René Rachou - Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, 30190-009, Brasil.
Med Microbiol Immunol. 2025 Aug 29;214(1):39. doi: 10.1007/s00430-025-00848-w.
Influenza virus and Streptococcus pneumoniae are major respiratory pathogens responsible for significant global mortality. While influenza causes seasonal flu, pneumococcus is associated with pneumonia, meningitis, sepsis, and otitis, often worsening influenza cases through secondary infections. Aiming to develop a bivalent vaccine against these two pathogens, we used reverse genetics to construct a recombinant influenza virus that carries the gene of the pneumococcal PspA protein (Flu-PspA). This study assessed the safety and efficacy of a heterologous prime-boost vaccine protocol consisting of Flu-PspA prime and followed by a boost with recombinant PspA plus alum (Flu-PspA/PspA4 + Alum), administered intramuscularly in C57BL/6 mice. Following immunization, anti-PspA and anti-influenza antibody titers in serum and bronchoalveolar lavage fluid (BALF) were quantified by ELISA. The breadth of the immune response was evaluated by measuring complement deposition across multiple pneumococcal strains. Vaccine protection and efficacy were evaluated 21 days after final immunization by challenging mice with a lethal dose of 7 × LD50 of S. pneumoniae (strain ATCC6303) or 100 × LD50 of influenza A/PR8/34 virus. Mid-term pneumococcal protection was assessed similarly 90 days post-boost. Three days post-pneumococcal challenge, bacterial loads in BALF and blood were quantified. Additionally, bacterial colonization and secondary infection dynamics were evaluated and quantified after nasal colonization challenge (strain EF3030), infection with influenza H3N2 virus and secondary infection with pneumococcus and after nasal colonization with strain EF3030 and H3N2 virus infection. The results demonstrated that the vaccination regimen elicited a robust humoral immune response, conferring broad protection against diverse pneumococcal strains. Following lethal challenge with either pathogen, the vaccine provided 100% survival, by significantly reducing bacterial burden in blood and lungs. Notably, even 90 days post-boost, mice retained partial protection with minimal weight loss. Furthermore, the protocol reduced bacteremia following secondary infections and mitigated weight loss in H3N2-infected colonized mice. These findings demonstrate that the vaccine confers robust protection with broad-spectrum efficacy when administered intramuscularly, highlighting its potential as a viable preventive strategy against both influenza and pneumococcal infections, including co-infection scenarios.
流感病毒和肺炎链球菌是导致全球大量死亡的主要呼吸道病原体。流感引发季节性流感,而肺炎球菌与肺炎、脑膜炎、败血症和中耳炎相关,常通过继发感染使流感病情恶化。为研发针对这两种病原体的二价疫苗,我们利用反向遗传学构建了一种携带肺炎球菌PspA蛋白基因的重组流感病毒(Flu-PspA)。本研究评估了一种异源初免-加强疫苗方案的安全性和有效性,该方案包括以Flu-PspA进行初免,随后用重组PspA加明矾(Flu-PspA/PspA4+明矾)进行加强免疫,通过肌肉注射给予C57BL/6小鼠。免疫后,通过ELISA定量血清和支气管肺泡灌洗液(BALF)中的抗PspA和抗流感抗体滴度。通过测量多种肺炎球菌菌株的补体沉积来评估免疫反应的广度。在末次免疫21天后,用致死剂量的7×LD50肺炎链球菌(菌株ATCC6303)或100×LD50甲型流感病毒A/PR8/34攻击小鼠,评估疫苗的保护作用和效力。加强免疫90天后,以类似方式评估中期肺炎球菌保护作用。肺炎球菌攻击后三天,定量BALF和血液中的细菌载量。此外,在鼻腔定植攻击(菌株EF3030)、感染H3N2流感病毒以及继发肺炎球菌感染后,以及在鼻腔定植菌株EF3030和感染H3N2病毒后,评估并定量细菌定植和继发感染动态。结果表明,该疫苗接种方案引发了强烈的体液免疫反应,对多种肺炎球菌菌株提供了广泛保护。在用任何一种病原体进行致死性攻击后,疫苗通过显著降低血液和肺部的细菌负荷,提供了100%的存活率。值得注意的是,即使在加强免疫90天后,小鼠仍保留部分保护作用,体重减轻最小。此外,该方案减少了继发感染后的菌血症,并减轻了H3N2感染定植小鼠的体重减轻。这些发现表明,该疫苗通过肌肉注射给药时具有强大的保护作用和广谱效力,突出了其作为预防流感和肺炎球菌感染(包括共感染情况)的可行策略的潜力。