M. Shibata, A. Inukai, Daigo Yoshimori, M. Ashizawa, T. Nakajima, Makoto Takada, T. Yazawa, K. Mimura, N. Inoue, Takafumi Watanabe, Kazunos .
{"title":"Metabolic Impact of Immune-Suppressor Cells in Cancer Patients","authors":"M. Shibata, A. Inukai, Daigo Yoshimori, M. Ashizawa, T. Nakajima, Makoto Takada, T. Yazawa, K. Mimura, N. Inoue, Takafumi Watanabe, Kazunos .","doi":"10.26502/jsr.10020207","DOIUrl":null,"url":null,"abstract":"Immune checkpoint inhibitors (ICIs) are not equally effective for all patients, regardless type of cancer. Immune-suppressor cells, including regulatory T tumor and their metabolic microenvironment (TME) play important roles in resistance to ICIs. Although Treg cells, TAMs and MDSCs play significant roles in immunosuppression in the TME, these cells are very important in the orchestration of metabolism such as angiogenesis and production of indoleamine 2,3-dioxygenase (IDO) and nitric oxide (NO) towards tumor escape, progression and expansion. Cancer immunotherapies tailored with metabolic characterizations such as parameters of angiogenesis, inflammation or obesity may be needed for the establishment of a successful treatment modality in the immunotherapy era.","PeriodicalId":73961,"journal":{"name":"Journal of surgery and research","volume":"24 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of surgery and research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26502/jsr.10020207","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Immune checkpoint inhibitors (ICIs) are not equally effective for all patients, regardless type of cancer. Immune-suppressor cells, including regulatory T tumor and their metabolic microenvironment (TME) play important roles in resistance to ICIs. Although Treg cells, TAMs and MDSCs play significant roles in immunosuppression in the TME, these cells are very important in the orchestration of metabolism such as angiogenesis and production of indoleamine 2,3-dioxygenase (IDO) and nitric oxide (NO) towards tumor escape, progression and expansion. Cancer immunotherapies tailored with metabolic characterizations such as parameters of angiogenesis, inflammation or obesity may be needed for the establishment of a successful treatment modality in the immunotherapy era.