Yoshino Naoto, Yokoyama Takuya, Sakai Hironori, Sugiyama Ikumi, Odagiri Takashi, Kimura Masahiro, Hojo Wataru, Saino Tomoyuki, Muraki Yasushi
Division of Infectious Diseases and Immunology, Department of Microbiology, School of Medicine, Iwate Medical University, 1-1-1 Idaidori, Yahaba 028-3694, Iwate, Japan.
Department of Anatomy (Cell Biology), Iwate Medical University, 1-1-1 Idaidori, Yahaba 028-3694, Iwate, Japan.
Vaccines (Basel). 2023 Nov 18;11(11):1727. doi: 10.3390/vaccines11111727.
Polymyxin B (PMB) is an antibiotic that exhibits mucosal adjuvanticity for ovalbumin (OVA), which enhances the immune response in the mucosal compartments of mice. Frequent breakthrough infections of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants indicate that the IgA antibody levels elicited by the mRNA vaccines in the mucosal tissues were insufficient for the prophylaxis of this infection. It remains unknown whether PMB exhibits mucosal adjuvanticity for antigens other than OVA. This study investigated the adjuvanticity of PMB for the virus proteins, hemagglutinin (HA) of influenza A virus, and the S1 subunit and S protein of SARS-CoV-2. BALB/c mice immunized either intranasally or subcutaneously with these antigens alone or in combination with PMB were examined, and the antigen-specific antibodies were quantified. PMB substantially increased the production of antigen-specific IgA antibodies in mucosal secretions and IgG antibodies in plasma, indicating its adjuvanticity for both HA and S proteins. This study also revealed that the PMB-virus antigen complex diameter is crucial for the induction of mucosal immunity. No detrimental effects were observed on the nasal mucosa or olfactory bulb. These findings highlight the potential of PMB as a safe candidate for intranasal vaccination to induce mucosal IgA antibodies for prophylaxis against mucosally transmitted infections.
多粘菌素B(PMB)是一种抗生素,对卵清蛋白(OVA)具有黏膜佐剂活性,可增强小鼠黏膜部位的免疫反应。严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体频繁出现突破性感染,表明mRNA疫苗在黏膜组织中引发的IgA抗体水平不足以预防这种感染。PMB对OVA以外的抗原是否具有黏膜佐剂活性尚不清楚。本研究调查了PMB对甲型流感病毒的病毒蛋白血凝素(HA)以及SARS-CoV-2的S1亚基和S蛋白的佐剂活性。对单独或与PMB联合经鼻或皮下免疫这些抗原的BALB/c小鼠进行了检测,并对抗原特异性抗体进行了定量。PMB显著增加了黏膜分泌物中抗原特异性IgA抗体和血浆中IgG抗体的产生,表明其对HA和S蛋白均具有佐剂活性。本研究还表明,PMB-病毒抗原复合物的直径对于诱导黏膜免疫至关重要。未观察到对鼻黏膜或嗅球有有害影响。这些发现突出了PMB作为鼻内疫苗接种安全候选物的潜力,可诱导黏膜IgA抗体以预防黏膜传播感染。