{"title":"氨死亡:增强癌症免疫疗法的潜在新策略。","authors":"Zhi Li, Junyi Lin, Peihao Yin","doi":"10.1038/s41417-024-00851-y","DOIUrl":null,"url":null,"abstract":"The efficacy of immunotherapy is diminished by the low survival rate of effector CD8 + T cells after they have exerted their antitumor effects. Recent studies indicate that ammonia, generated from glutamine metabolism, accumulates in effector CD8 + T cells and triggers their apoptosis. These findings offer a comprehensive mechanistic understanding of effector T-cell mortality from a metabolic viewpoint, presenting novel opportunities for improving T-cell-mediated anticancer treatments.","PeriodicalId":9577,"journal":{"name":"Cancer gene therapy","volume":"31 12","pages":"1751-1753"},"PeriodicalIF":4.8000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s41417-024-00851-y.pdf","citationCount":"0","resultStr":"{\"title\":\"Ammonia death: a novel potential strategy to augment immunotherapy in cancer\",\"authors\":\"Zhi Li, Junyi Lin, Peihao Yin\",\"doi\":\"10.1038/s41417-024-00851-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The efficacy of immunotherapy is diminished by the low survival rate of effector CD8 + T cells after they have exerted their antitumor effects. Recent studies indicate that ammonia, generated from glutamine metabolism, accumulates in effector CD8 + T cells and triggers their apoptosis. These findings offer a comprehensive mechanistic understanding of effector T-cell mortality from a metabolic viewpoint, presenting novel opportunities for improving T-cell-mediated anticancer treatments.\",\"PeriodicalId\":9577,\"journal\":{\"name\":\"Cancer gene therapy\",\"volume\":\"31 12\",\"pages\":\"1751-1753\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2024-11-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.nature.com/articles/s41417-024-00851-y.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer gene therapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.nature.com/articles/s41417-024-00851-y\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer gene therapy","FirstCategoryId":"3","ListUrlMain":"https://www.nature.com/articles/s41417-024-00851-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Ammonia death: a novel potential strategy to augment immunotherapy in cancer
The efficacy of immunotherapy is diminished by the low survival rate of effector CD8 + T cells after they have exerted their antitumor effects. Recent studies indicate that ammonia, generated from glutamine metabolism, accumulates in effector CD8 + T cells and triggers their apoptosis. These findings offer a comprehensive mechanistic understanding of effector T-cell mortality from a metabolic viewpoint, presenting novel opportunities for improving T-cell-mediated anticancer treatments.
期刊介绍:
Cancer Gene Therapy is the essential gene and cellular therapy resource for cancer researchers and clinicians, keeping readers up to date with the latest developments in gene and cellular therapies for cancer. The journal publishes original laboratory and clinical research papers, case reports and review articles. Publication topics include RNAi approaches, drug resistance, hematopoietic progenitor cell gene transfer, cancer stem cells, cellular therapies, homologous recombination, ribozyme technology, antisense technology, tumor immunotherapy and tumor suppressors, translational research, cancer therapy, gene delivery systems (viral and non-viral), anti-gene therapy (antisense, siRNA & ribozymes), apoptosis; mechanisms and therapies, vaccine development, immunology and immunotherapy, DNA synthesis and repair.
Cancer Gene Therapy publishes the results of laboratory investigations, preclinical studies, and clinical trials in the field of gene transfer/gene therapy and cellular therapies as applied to cancer research. Types of articles published include original research articles; case reports; brief communications; review articles in the main fields of drug resistance/sensitivity, gene therapy, cellular therapy, tumor suppressor and anti-oncogene therapy, cytokine/tumor immunotherapy, etc.; industry perspectives; and letters to the editor.