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Immunostimulatory Properties of Chemotherapy in Breast Cancer: From Immunogenic Modulation Mechanisms to Clinical Practice

期刊

FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.819405

关键词

breast cancer; chemotherapy; immunotherapy; immunogenic modulation; clinic trial

资金

  1. Science and Technology Program of Anhui Province [1804 h08020259]
  2. Scientific Research Start-up Funds of The First Affiliated Hospital of USTC [RC2021122]

向作者/读者索取更多资源

Breast cancer is the most common malignancy among females, and chemotherapy drugs have been the mainstay of treatment. The advent of immunotherapy has provided new hope for breast cancer treatment. Chemotherapy drugs have shown to stimulate the immune system in multiple ways, including inducing immunogenic cell death and activating immune effector cells while depleting immunosuppressive cells. This review summarizes recent clinical trials on the combination of chemotherapy and immunotherapy in breast cancer and discusses the molecular mechanisms of the immunostimulatory properties of chemotherapy.
Breast cancer (BC) is the most common malignancy among females. Chemotherapy drugs remain the cornerstone of treatment of BC and undergo significant shifts over the past 100 years. The advent of immunotherapy presents promising opportunities and constitutes a significant complementary to existing therapeutic strategies for BC. Chemotherapy as a cytotoxic treatment that targets proliferation malignant cells has recently been shown as an effective immune-stimulus in multiple ways. Chemotherapeutic drugs can cause the release of damage-associated molecular patterns (DAMPs) from dying tumor cells, which result in long-lasting antitumor immunity by the key process of immunogenic cell death (ICD). Furthermore, Off-target effects of chemotherapy on immune cell subsets mainly involve activation of immune effector cells including natural killer (NK) cells, dendritic cells (DCs), and cytotoxic T cells, and depletion of immunosuppressive cells including Treg cells, M2 macrophages and myeloid-derived suppressor cells (MDSCs). Current mini-review summarized recent large clinical trials regarding the combination of chemotherapy and immunotherapy in BC and addressed the molecular mechanisms of immunostimulatory properties of chemotherapy in BC. The purpose of our work was to explore the immune-stimulating effects of chemotherapy at the molecular level based on the evidence from clinical trials, which might be a rationale for combinations of chemotherapy and immunotherapy in BC.

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