Abstract

Leukocytes and their soluble mediators play important regulatory roles in all aspects of solid tumor development. While immunotherapeutic strategies have conceptually held clinical promise, with the exception of a small percentage of patients, they have failed to demonstrate effective, consistent, and durable anti-cancer responses. Several subtypes of leukocytes that commonly infiltrate solid tumors harbor immunosuppressive activity and undoubtedly restrict the effectiveness of these strategies. Several of these same immune cells also foster tumor development by expression of potent protumor mediators. Given recent evidence revealing that immune-based mechanisms regulate the response to conventional cytotoxic therapy, it seems reasonable to speculate that tumor progression could be effectively diminished by combining cytotoxic strategies with therapies that blunt protumor immune-based effectors and/or neutralize those that instead impede development of desired anti-tumor immunity, thus providing synergistic effects between traditional cytotoxic and immune-modulatory approaches.

Keywords

Immune systemBiologyCytotoxic T cellImmunologyEffectorImmunityImmunotherapyCancerCancer research

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Publication Info

Year
2011
Type
review
Volume
25
Issue
24
Pages
2559-2572
Citations
316
Access
Closed

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Stephen L. Shiao, Anusha-Preethi Ganesan, Hope S. Rugo et al. (2011). Immune microenvironments in solid tumors: new targets for therapy. Genes & Development , 25 (24) , 2559-2572. https://doi.org/10.1101/gad.169029.111

Identifiers

DOI
10.1101/gad.169029.111