The role of the tumour microenvironment in immunotherapy
Роль микроокружения опухоли в иммунотерапии
2017-07-28
SCID: 54.1/n9hds95s
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cancer immunologycancer immunotherapyimmune evasionimmune tolerancetumour microenvironment
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Abstract (AI)
Recent success in immunomodulating strategies in lung cancer and melanoma has prompted much enthusiasm in their potential to treat other advanced solid malignancies. However, their applications have shown variable success and are even ineffective against some tumours. The efficiency of immunotherapies relies on an immunogenic tumour microenvironment. The current field of cancer immunology has focused on understanding the interaction of cancer and host immune cells to break the state of immune tolerance and explain how molecular patterns of cytokines and chemokines affect tumour progression. Here, we review our current knowledge of how inherent properties of tumours and their different tumour microenvironments affect therapeutic outcome. We also discuss insights into recent multimodal therapeutic approaches that target tumour immune evasion and suppression to restore anti-tumour immunity.
Key Findings
1
Immunotherapy has achieved notable success in lung cancer and melanoma but shows variable efficacy and can be ineffective in other advanced solid tumors.
2
Interactions between cancer cells and host immune cells, including cytokine and chemokine signaling patterns, influence immune tolerance and tumor progression.
3
Multimodal strategies targeting immune evasion and immunosuppression may restore antitumor immunity and improve treatment effectiveness.
4
Therapeutic efficacy depends substantially on the immunogenicity and characteristics of the tumor microenvironment.
5
Tumor-intrinsic properties and distinct tumor microenvironments help determine patient responses and therapeutic outcomes.
Research Object
tumour microenvironments in advanced solid malignancies
Research Subject
the effects of tumour-intrinsic properties and tumour microenvironmental immune interactions on immunotherapy outcomes, including immune evasion and suppression
Publication Details
Publication Date
2017-07-28
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