Jackson D. Harris , Yun Chang , Ramizah Syahirah , Xiaojun Lance Lian , Qing Deng , Xiaoping Bao
{"title":"来自人类多能干细胞的工程化抗前列腺癌症CAR-营养因子","authors":"Jackson D. Harris , Yun Chang , Ramizah Syahirah , Xiaojun Lance Lian , Qing Deng , Xiaoping Bao","doi":"10.1016/j.regen.2023.100074","DOIUrl":null,"url":null,"abstract":"<div><p><span><span><span><span>Immunotherapy is a powerful technique where </span>immune cells<span><span> are modified to improve cytotoxicity against cancerous cells to treat cancers that do not respond to surgery, chemotherapy, or radiotherapy. Expressing </span>chimeric antigen receptor<span> (CAR) in immune cells, typically T lymphocytes, is a practical modification that drives an immune response against cancerous tissue. CAR-T efficacy is suboptimal in </span></span></span>solid tumors<span><span> due to the tumor microenvironment (TME) that limits T lymphocyte cytotoxicity. In this study, we demonstrate that </span>neutrophils<span> differentiated from human pluripotent stem cells modified with AAVS1-inserted CAR constructs showed a robust cytotoxic effect against prostate-specific membrane antigen (PSMA) expressing LNCaP cells as a model for </span></span></span>prostate cancer </span><em>in vitro</em>. Our results suggest that engineered CARs can significantly enhance the neutrophil anti-tumor effect, providing a new avenue in treating prostate cancers.</p></div>","PeriodicalId":94333,"journal":{"name":"Journal of immunology and regenerative medicine","volume":"20 ","pages":"Article 100074"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121188/pdf/","citationCount":"4","resultStr":"{\"title\":\"Engineered anti-prostate cancer CAR-neutrophils from human pluripotent stem cells\",\"authors\":\"Jackson D. Harris , Yun Chang , Ramizah Syahirah , Xiaojun Lance Lian , Qing Deng , Xiaoping Bao\",\"doi\":\"10.1016/j.regen.2023.100074\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span><span><span>Immunotherapy is a powerful technique where </span>immune cells<span><span> are modified to improve cytotoxicity against cancerous cells to treat cancers that do not respond to surgery, chemotherapy, or radiotherapy. Expressing </span>chimeric antigen receptor<span> (CAR) in immune cells, typically T lymphocytes, is a practical modification that drives an immune response against cancerous tissue. CAR-T efficacy is suboptimal in </span></span></span>solid tumors<span><span> due to the tumor microenvironment (TME) that limits T lymphocyte cytotoxicity. In this study, we demonstrate that </span>neutrophils<span> differentiated from human pluripotent stem cells modified with AAVS1-inserted CAR constructs showed a robust cytotoxic effect against prostate-specific membrane antigen (PSMA) expressing LNCaP cells as a model for </span></span></span>prostate cancer </span><em>in vitro</em>. Our results suggest that engineered CARs can significantly enhance the neutrophil anti-tumor effect, providing a new avenue in treating prostate cancers.</p></div>\",\"PeriodicalId\":94333,\"journal\":{\"name\":\"Journal of immunology and regenerative medicine\",\"volume\":\"20 \",\"pages\":\"Article 100074\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121188/pdf/\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of immunology and regenerative medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468498823000057\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of immunology and regenerative medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468498823000057","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Engineered anti-prostate cancer CAR-neutrophils from human pluripotent stem cells
Immunotherapy is a powerful technique where immune cells are modified to improve cytotoxicity against cancerous cells to treat cancers that do not respond to surgery, chemotherapy, or radiotherapy. Expressing chimeric antigen receptor (CAR) in immune cells, typically T lymphocytes, is a practical modification that drives an immune response against cancerous tissue. CAR-T efficacy is suboptimal in solid tumors due to the tumor microenvironment (TME) that limits T lymphocyte cytotoxicity. In this study, we demonstrate that neutrophils differentiated from human pluripotent stem cells modified with AAVS1-inserted CAR constructs showed a robust cytotoxic effect against prostate-specific membrane antigen (PSMA) expressing LNCaP cells as a model for prostate cancer in vitro. Our results suggest that engineered CARs can significantly enhance the neutrophil anti-tumor effect, providing a new avenue in treating prostate cancers.