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人工智能鉴定的细胞分裂蛋白候选淋病疫苗的临床前疗效。

Preclinical efficacy of a cell division protein candidate gonococcal vaccine identified by artificial intelligence.

机构信息

Department of Medicine, Division of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

EVAXION Biotech, Hørsholm, Denmark.

出版信息

mBio. 2023 Dec 19;14(6):e0250023. doi: 10.1128/mbio.02500-23. Epub 2023 Oct 31.

Abstract

Vaccines to curb the global spread of multidrug-resistant gonorrhea are urgently needed. Here, 26 vaccine candidates identified by an artificial intelligence-driven platform (Efficacy Discriminative Educated Network[EDEN]) were screened for efficacy in the mouse vaginal colonization model. Complement-dependent bactericidal activity of antisera and the EDEN protective scores both correlated positively with the reduction in overall bacterial colonization burden. NGO1549 (FtsN) and NGO0265, both involved in cell division, displayed the best activity and were selected for further development. Both antigens, when fused to create a chimeric protein, elicited bactericidal antibodies against a wide array of gonococcal isolates and significantly attenuated the duration and burden of gonococcal colonization of mouse vaginas. Protection was abrogated in mice that lacked complement C9, the last step in the formation of the membrane attack complex pore, suggesting complement-dependent bactericidal activity as a mechanistic correlate of protection of the vaccine. FtsN and NGO0265 represent promising vaccine candidates against gonorrhea.

摘要

急需疫苗来遏制全球耐多药淋病的传播。在这里,通过人工智能驱动的平台(Efficacy Discriminative Educated Network[EDEN])鉴定了 26 种疫苗候选物,并在小鼠阴道定植模型中对其功效进行了筛选。抗血清的补体依赖性杀菌活性和 EDEN 保护评分均与总细菌定植负担的减少呈正相关。参与细胞分裂的 NGO1549(FtsN)和 NGO0265 显示出最佳活性,并被选择进一步开发。当这两种抗原融合形成嵌合蛋白时,均可诱导针对多种淋病奈瑟菌分离株的杀菌抗体,并显著减轻小鼠阴道淋病奈瑟菌定植的持续时间和负担。在缺乏补体 C9 的小鼠中(补体形成膜攻击复合物孔的最后一步),保护作用被消除,这表明补体依赖性杀菌活性是疫苗保护的机制相关因素。FtsN 和 NGO0265 是针对淋病的有前途的疫苗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a09b/10746169/700fcfbd57f3/mbio.02500-23.f001.jpg

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