Kelly Ann Mahool,Emily Nguyen,Victoria Godfrey,Ann Marie Stanley,Tyler Brady,Adam Gamson,Kim Rosenthal,Justin Green,Ondrej Podlaha,Bret Sellman,Christine Tkaczyk,Vancheswaran Gopalakrishnan
{"title":"广泛中和抗毒素B单克隆抗体AZD5148在不同和全球当代艰难梭菌分离株中的表位保守性","authors":"Kelly Ann Mahool,Emily Nguyen,Victoria Godfrey,Ann Marie Stanley,Tyler Brady,Adam Gamson,Kim Rosenthal,Justin Green,Ondrej Podlaha,Bret Sellman,Christine Tkaczyk,Vancheswaran Gopalakrishnan","doi":"10.1093/infdis/jiaf423","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nC. difficile Toxin B is a virulence factor for C. difficile infections (CDI), and a clinically validated target for prevention of CDI recurrence. AZD5148 is a Toxin B neutralizing human monoclonal antibody that binds to an epitope on the Toxin B glucosyltransferase domain. Herein, we aim to evaluate the conservation of this binding epitope using a collection of 9,134 global C. difficile genomes obtained from a public repository to confirm that residues that are crucial for neutralization are conserved.\r\n\r\nMETHODS\r\nUsing isolates collected between 2015-2023 from two independent sources, we performed variant calling, sequence typing and phylogenetic analysis. We tested in vitro neutralization of cytotoxicity by AZD5148 using two different cell-lines.\r\n\r\nRESULTS\r\nHerein, we showed that the AZD5148 epitope is highly conserved across all geographic regions and sequence types (STs) and has a higher average conservation frequency in its binding site (99.58%) when compared to bezlotoxumab (82.47%). AZD5148 also exhibited broad neutralization in vitro against 8 recently circulating ribotypes.\r\n\r\nCONCLUSIONS\r\nOur comprehensive analysis of global sequences found the AZD5148 epitope to be highly conserved, and thus unlikely to be impacted by most of the genotypic variations in recently circulating C. difficile ribotypes and STs.","PeriodicalId":501010,"journal":{"name":"The Journal of Infectious Diseases","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Epitope conservation of AZD5148, a broadly neutralizing anti-Toxin B monoclonal antibody, among diverse and global contemporary Clostridioides difficile isolates.\",\"authors\":\"Kelly Ann Mahool,Emily Nguyen,Victoria Godfrey,Ann Marie Stanley,Tyler Brady,Adam Gamson,Kim Rosenthal,Justin Green,Ondrej Podlaha,Bret Sellman,Christine Tkaczyk,Vancheswaran Gopalakrishnan\",\"doi\":\"10.1093/infdis/jiaf423\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\r\\nC. difficile Toxin B is a virulence factor for C. difficile infections (CDI), and a clinically validated target for prevention of CDI recurrence. AZD5148 is a Toxin B neutralizing human monoclonal antibody that binds to an epitope on the Toxin B glucosyltransferase domain. Herein, we aim to evaluate the conservation of this binding epitope using a collection of 9,134 global C. difficile genomes obtained from a public repository to confirm that residues that are crucial for neutralization are conserved.\\r\\n\\r\\nMETHODS\\r\\nUsing isolates collected between 2015-2023 from two independent sources, we performed variant calling, sequence typing and phylogenetic analysis. We tested in vitro neutralization of cytotoxicity by AZD5148 using two different cell-lines.\\r\\n\\r\\nRESULTS\\r\\nHerein, we showed that the AZD5148 epitope is highly conserved across all geographic regions and sequence types (STs) and has a higher average conservation frequency in its binding site (99.58%) when compared to bezlotoxumab (82.47%). AZD5148 also exhibited broad neutralization in vitro against 8 recently circulating ribotypes.\\r\\n\\r\\nCONCLUSIONS\\r\\nOur comprehensive analysis of global sequences found the AZD5148 epitope to be highly conserved, and thus unlikely to be impacted by most of the genotypic variations in recently circulating C. difficile ribotypes and STs.\",\"PeriodicalId\":501010,\"journal\":{\"name\":\"The Journal of Infectious Diseases\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-08-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Infectious Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/infdis/jiaf423\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Infectious Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/infdis/jiaf423","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Epitope conservation of AZD5148, a broadly neutralizing anti-Toxin B monoclonal antibody, among diverse and global contemporary Clostridioides difficile isolates.
BACKGROUND
C. difficile Toxin B is a virulence factor for C. difficile infections (CDI), and a clinically validated target for prevention of CDI recurrence. AZD5148 is a Toxin B neutralizing human monoclonal antibody that binds to an epitope on the Toxin B glucosyltransferase domain. Herein, we aim to evaluate the conservation of this binding epitope using a collection of 9,134 global C. difficile genomes obtained from a public repository to confirm that residues that are crucial for neutralization are conserved.
METHODS
Using isolates collected between 2015-2023 from two independent sources, we performed variant calling, sequence typing and phylogenetic analysis. We tested in vitro neutralization of cytotoxicity by AZD5148 using two different cell-lines.
RESULTS
Herein, we showed that the AZD5148 epitope is highly conserved across all geographic regions and sequence types (STs) and has a higher average conservation frequency in its binding site (99.58%) when compared to bezlotoxumab (82.47%). AZD5148 also exhibited broad neutralization in vitro against 8 recently circulating ribotypes.
CONCLUSIONS
Our comprehensive analysis of global sequences found the AZD5148 epitope to be highly conserved, and thus unlikely to be impacted by most of the genotypic variations in recently circulating C. difficile ribotypes and STs.