Human monoclonal antibodies targeting subdominant meningococcal antigens confer cross-protection against gonococcus

抗原 病毒学 生物 抗体 微生物学 单克隆抗体 脑膜炎奈瑟菌 淋病 免疫学 细菌 遗传学 人类免疫缺陷病毒(HIV)
作者
Marco Troisi,Monica Fabbrini,Samuele Stazzoni,Viola Viviani,Filippo Carboni,Valentina Abbiento,Lucia Eleonora Fontana,Sara Tomei,Martina Audagnotto,Laura Santini,Angela Spagnuolo,Giada Antonelli,Ida Paciello,Fabiola Vacca,Dario Cardamone,Eleonora Marini,Pardis Mokhtary,Francesca Finetti,Fabiola Giusti,Margherita Bodini
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:17 (799)
标识
DOI:10.1126/scitranslmed.adv0969
摘要

Gonococcus, a bacterium resistant to most antibiotics, causes more than 80 million cases of gonorrhea annually and is considered a high-priority pathogen by the World Health Organization. Recently, vaccine development prospects were boosted by reports that licensed meningococcus serogroup B (MenB) vaccines provided partial protection against gonococcal infection. To determine antigens responsible for cross-protection, memory B cells isolated from 4CMenB-vaccinated volunteers were single cell–sorted to identify antibodies that kill gonococcus in a bactericidal assay. Nine different antibodies, all deriving from the IGHV4-34 germline and carrying an unusually long heavy-chain complementarity-determining region 3, recognized the PorB protein; four others recognized the lipooligosaccharide; and another four had unknown specificity. One of the PorB-specific antibodies provided protection in a mouse model of gonococcus infection. The identification of PorB and lipooligosaccharide as key antigens of gonococcal and meningococcal immunity provides a mechanistic explanation of the cross-protection observed in the clinic and shows that isolating human monoclonal antibodies from vaccinees can be instrumental for bacterial antigen discovery.

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