Vascular abnormalities in tumors have a major impact on the immune microenvironment in tumors. The consequences of abnormal vasculature include increased hypoxia, acidosis, high intra-tumoral fluid pressure, and angiogenesis. This introduces an immunosuppressive microenvironment that alters immune cell maturation, activation, and trafficking, which supports tumor immune evasion and dissemination of tumor cells. Increasing data suggests that cancer endothelium is a major barrier for traveling leukocytes, ranging from a partial blockade resulting in a selective endothelial barrier, to a complete immune infiltration blockade associated with immune exclusion and immune desert cancer phenotypes. Failed immune cell trafficking as well as immunosuppression within the tumor microenvironment limits the efficacy of immunotherapeutic approaches. As such, targeting proteins with key roles in angiogenesis may potentially reduce immunosuppression and might restore infiltration of anti-tumor immune cells, creating a therapeutic window for successful immunotherapy. In this review, we provide a comprehensive overview of established as well as more controversial endothelial pathways that govern selective immune cell trafficking across cancer endothelium. Additionally, we discuss recent insights and strategies that target tumor vasculature in order to increase infiltration of cytotoxic immune cells during the therapeutic window of vascular normalization hereby improving the efficacy of immunotherapy.
机构:
Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu, Peoples R China
Sichuan Univ, West China Hosp, Canc Ctr, Chengdu, Peoples R China
Sichuan Univ, West China Hosp, Frontiers Sci Ctr Dis Related Mol Network, Chengdu, Peoples R ChinaSichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu, Peoples R China
机构:
Inst Canc Res, Div Clin Studies, London SM2 5NG, England
Royal Marsden Hosp, Prostate Canc Targeted Therapy Grp, London SM2 5PT, EnglandInst Canc Res, Div Clin Studies, London SM2 5NG, England
Westaby, Daniel
Jimenez-Vacas, Juan M.
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Inst Canc Res, Div Clin Studies, London SM2 5NG, EnglandInst Canc Res, Div Clin Studies, London SM2 5NG, England
Jimenez-Vacas, Juan M.
Padilha, Ana
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Inst Canc Res, Div Clin Studies, London SM2 5NG, EnglandInst Canc Res, Div Clin Studies, London SM2 5NG, England
Padilha, Ana
Varkaris, Andreas
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机构:
Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02215 USAInst Canc Res, Div Clin Studies, London SM2 5NG, England
Varkaris, Andreas
Balk, Steven P.
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Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02215 USAInst Canc Res, Div Clin Studies, London SM2 5NG, England
Balk, Steven P.
de Bono, Johann S.
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机构:
Inst Canc Res, Div Clin Studies, London SM2 5NG, England
Royal Marsden Hosp, Prostate Canc Targeted Therapy Grp, London SM2 5PT, EnglandInst Canc Res, Div Clin Studies, London SM2 5NG, England
de Bono, Johann S.
Sharp, Adam
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h-index: 0
机构:
Inst Canc Res, Div Clin Studies, London SM2 5NG, England
Royal Marsden Hosp, Prostate Canc Targeted Therapy Grp, London SM2 5PT, EnglandInst Canc Res, Div Clin Studies, London SM2 5NG, England
机构:
Inst Pasteur, Dept Atherosclerosis, F-59019 Lille, France
Univ Lille 2, Fac Pharm, Lille, France
Univ Lille 2, Fac Med, Lille, France
INSERM, U545, F-59045 Lille, FranceInst Pasteur, Dept Atherosclerosis, F-59019 Lille, France