Abstract

Immunotherapy has revolutionized cancer treatment and rejuvenated the field of tumor immunology. Several types of immunotherapy, including adoptive cell transfer (ACT) and immune checkpoint inhibitors (ICIs), have obtained durable clinical responses, but their efficacies vary, and only subsets of cancer patients can benefit from them. Immune infiltrates in the tumor microenvironment (TME) have been shown to play a key role in tumor development and will affect the clinical outcomes of cancer patients. Comprehensive profiling of tumor-infiltrating immune cells would shed light on the mechanisms of cancer–immune evasion, thus providing opportunities for the development of novel therapeutic strategies. However, the highly heterogeneous and dynamic nature of the TME impedes the precise dissection of intratumoral immune cells. With recent advances in single-cell technologies such as single-cell RNA sequencing (scRNA-seq) and mass cytometry, systematic interrogation of the TME is feasible and will provide insights into the functional diversities of tumor-infiltrating immune cells. In this review, we outline the recent progress in cancer immunotherapy, particularly by focusing on landmark studies and the recent single-cell characterization of tumor-associated immune cells, and we summarize the phenotypic diversities of intratumoral immune cells and their connections with cancer immunotherapy. We believe such a review could strengthen our understanding of the progress in cancer immunotherapy, facilitate the elucidation of immune cell modulation in tumor progression, and thus guide the development of novel immunotherapies for cancer treatment.

Highlights

  • The secretory products of plasmacytoid DCs (pDCs), especially type I IFN, were reported to have both immunogenic and tolerogenic functions in tumor immunity.[157,158]. These cytokines contribute to an immunostimulatory tumor microenvironment (TME) by promoting the maturation and activation of dendritic cells (DCs) and proinflammatory macrophages, by increasing the cytotoxicity of natural killer (NK) and T cells, and by facilitating the differentiation of activated B cells into plasma cells;[52,159,160] they drive an immunosuppressive TME by recruiting Tregs or by inducing the expression of immunomodulatory molecules such as those involved in negative regulatory pathways.[158,160,161]

  • A systematic review of the landmark studies in the progress of cancer immunotherapy could facilitate a better understanding of the basic principles, advantages and limitations of various types of immunotherapies, and will help promote the development of novel strategies to circumvent their drawbacks and achieve optimal clinical efficacy

  • Tumor-infiltrating immune cells, in particular T cells, serve as the cellular underpinnings of cancer immunotherapies, and a better understanding of immune cells in the TME is essential for deciphering mechanisms of immunotherapies, defining predictive biomarkers, and identifying novel therapeutic targets

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Summary

REVIEW ARTICLE

The history and advances in cancer immunotherapy: understanding the characteristics of tumor-infiltrating immune cells and their therapeutic implications. We outline the recent progress in cancer immunotherapy, by focusing on landmark studies and the recent single-cell characterization of tumor-associated immune cells, and we summarize the phenotypic diversities of intratumoral immune cells and their connections with cancer immunotherapy. We believe such a review could strengthen our understanding of the progress in cancer immunotherapy, facilitate the elucidation of immune cell modulation in tumor progression, and guide the development of novel immunotherapies for cancer treatment.

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Adoptive cell transfer
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