J. Nemunaitis, Monika Devanaboyina, N. Ngo, Rakan Albalawy, L. Filipiak, H. Staats, L. Stanbery, Danae M. Hamouda
{"title":"血管生成抑制剂在免疫应答中的作用","authors":"J. Nemunaitis, Monika Devanaboyina, N. Ngo, Rakan Albalawy, L. Filipiak, H. Staats, L. Stanbery, Danae M. Hamouda","doi":"10.31487/J.COR.2021.02.01","DOIUrl":null,"url":null,"abstract":"Angiogenesis plays an important role in tumor growth. Established vasculature provides a supply of\nnutrients and other necessary survival factors for tumor cell maintenance. In addition, immune factors with\ncapacity to both decrease immune activity leading to cancer suppression and to increase anticancer response\nare provided via VEGF stimulated angiogenesis. However, VEGF provides more than angiogenesis\nstimulation; it is itself a growth factor with activity to also decrease the stimulation of dendritic cells (DCs)\nand T cells involved in anti-cancer mechanisms. As such inhibition of VEGF provides immune therapeutic\nadvantage. This was well demonstrated by IFN-ɣ ELISPOT assay in which T lymphocytes antitumor\nresponse was measured against multiple myeloma cells following exposure to myeloma lysate-loaded\ndendric cells. Block of VEGF lead to enhanced T lymphocyte anticancer immune response. Through\nstimulation of the immune system angiogenesis inhibitors can work in conjunction with immunotherapy,\nchemotherapy and/or radiation therapy. Recent clinical trials in advanced renal cell carcinoma, non-small\ncell lung cancer (NSCLC), and hepatocellular carcinoma have evidenced improved outcomes due to an\nimmune enhancing effect with angiogenesis inhibition and in particular immune checkpoint blockade\ntreatment.\n","PeriodicalId":10487,"journal":{"name":"Clinical Oncology and Research","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Immune Response Role of Angiogenesis Inhibitors\",\"authors\":\"J. Nemunaitis, Monika Devanaboyina, N. Ngo, Rakan Albalawy, L. Filipiak, H. Staats, L. Stanbery, Danae M. Hamouda\",\"doi\":\"10.31487/J.COR.2021.02.01\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Angiogenesis plays an important role in tumor growth. Established vasculature provides a supply of\\nnutrients and other necessary survival factors for tumor cell maintenance. In addition, immune factors with\\ncapacity to both decrease immune activity leading to cancer suppression and to increase anticancer response\\nare provided via VEGF stimulated angiogenesis. However, VEGF provides more than angiogenesis\\nstimulation; it is itself a growth factor with activity to also decrease the stimulation of dendritic cells (DCs)\\nand T cells involved in anti-cancer mechanisms. As such inhibition of VEGF provides immune therapeutic\\nadvantage. This was well demonstrated by IFN-ɣ ELISPOT assay in which T lymphocytes antitumor\\nresponse was measured against multiple myeloma cells following exposure to myeloma lysate-loaded\\ndendric cells. Block of VEGF lead to enhanced T lymphocyte anticancer immune response. Through\\nstimulation of the immune system angiogenesis inhibitors can work in conjunction with immunotherapy,\\nchemotherapy and/or radiation therapy. Recent clinical trials in advanced renal cell carcinoma, non-small\\ncell lung cancer (NSCLC), and hepatocellular carcinoma have evidenced improved outcomes due to an\\nimmune enhancing effect with angiogenesis inhibition and in particular immune checkpoint blockade\\ntreatment.\\n\",\"PeriodicalId\":10487,\"journal\":{\"name\":\"Clinical Oncology and Research\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Oncology and Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31487/J.COR.2021.02.01\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/J.COR.2021.02.01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Angiogenesis plays an important role in tumor growth. Established vasculature provides a supply of
nutrients and other necessary survival factors for tumor cell maintenance. In addition, immune factors with
capacity to both decrease immune activity leading to cancer suppression and to increase anticancer response
are provided via VEGF stimulated angiogenesis. However, VEGF provides more than angiogenesis
stimulation; it is itself a growth factor with activity to also decrease the stimulation of dendritic cells (DCs)
and T cells involved in anti-cancer mechanisms. As such inhibition of VEGF provides immune therapeutic
advantage. This was well demonstrated by IFN-ɣ ELISPOT assay in which T lymphocytes antitumor
response was measured against multiple myeloma cells following exposure to myeloma lysate-loaded
dendric cells. Block of VEGF lead to enhanced T lymphocyte anticancer immune response. Through
stimulation of the immune system angiogenesis inhibitors can work in conjunction with immunotherapy,
chemotherapy and/or radiation therapy. Recent clinical trials in advanced renal cell carcinoma, non-small
cell lung cancer (NSCLC), and hepatocellular carcinoma have evidenced improved outcomes due to an
immune enhancing effect with angiogenesis inhibition and in particular immune checkpoint blockade
treatment.