Significant efforts over the last two decades have been made to better understand the factors that control DC maturation and activation and the impact of these processes on overall host immunity. In addition to the well-characterized role of DC in the induction of immunity to pathogens, a role for these cells as critical regulators of anti-tumor immune responses has more recently become apparent. These findings have generated interest in understanding how tumor/DC interactions impact the quality of anti-tumor immune responses, and they have contributed to increased enthusiasm for a variety of DC-based cancer immunotherapies. Such strategies have included DNA- or peptide-based vaccines that involve uptake and processing of tumor antigens by endogenous DC in cancer patients or the administration of tumor antigen-loaded exogenous DC-based vaccines. Additionally, many adjuvant, cytokine, and monoclonal antibody therapies aim either to enhance the immunostimulatory capacity of endogenous DC or to supplement the activity of these cells by targeting costimulatory receptors on T cells. Despite the promise of such therapeutic approaches for cancer treatment, their success is often limited, and much remains to be understood about how tumors influence DC function and the quality of DC-mediated immune responses. Tumor/DC interactions have therefore become an increasingly active area of investigation, and many studies have described effects of tumors on DC phenotype and function that include an accumulation of immature DC within tumors, tumor-altered differentiation of DC precursors into myeloid-derived suppressor cells, and the generation of tumor-associated DC with immunoregulatory properties. As this field moves forward, it will be important to gain mechanistic insights into the basis for both tumor-mediated DC dysfunction as well as the induction of either suboptimal or immunosuppressive adaptive anti-tumor immune responses by tumor-associated DC. Progress in these areas of tumor immunology will greatly improve our understanding of the factors that contribute to effective DC-mediated anti-tumor immune control versus DC-associated anti-tumor immune dysfunction and subsequent tumor immune escape. Such information is vital for improving current and developing novel immunotherapeutic strategies for interfering with tumor-associated DC dysfunction and enhancing the functional quality of endogenous DC in cancer patients as well as the efficacy of exogenous DC-based anti-tumor vaccines. Topics of interest for this collection of articles will promote this understanding and include, but are not limited to:
1. DC maturation/activation and tumor-associated “danger signals”/damage-associated molecular patterns (DAMPs)
2. cross-presentation of tumor antigen
3. the role of DC in tumor inflammation
4. the role of DC in the induction of anti-tumor T cell responses
5. DC-induced imprinting of T cell migration and the role of DC-derived chemokines in the recruitment of tumor-infiltrating lymphocytes
6. tumor-associated DC dysfunction and the influence of tumor-derived factors on DC differentiation, maturation, activation, and function
7. tumor-associated immunosuppression by myeloid-derived suppressor cells (MDSC)
8. immunoregulatory DC and cancer
9. DC-associated and DC-targeted anti-cancer vaccines and immunotherapies
10. emerging technologies and model systems for studying the influence of tumors on DC immunobiology
11. diagnostic and prognostic phenotyping of DC in cancer patients and tumor-bearing animals
Significant efforts over the last two decades have been made to better understand the factors that control DC maturation and activation and the impact of these processes on overall host immunity. In addition to the well-characterized role of DC in the induction of immunity to pathogens, a role for these cells as critical regulators of anti-tumor immune responses has more recently become apparent. These findings have generated interest in understanding how tumor/DC interactions impact the quality of anti-tumor immune responses, and they have contributed to increased enthusiasm for a variety of DC-based cancer immunotherapies. Such strategies have included DNA- or peptide-based vaccines that involve uptake and processing of tumor antigens by endogenous DC in cancer patients or the administration of tumor antigen-loaded exogenous DC-based vaccines. Additionally, many adjuvant, cytokine, and monoclonal antibody therapies aim either to enhance the immunostimulatory capacity of endogenous DC or to supplement the activity of these cells by targeting costimulatory receptors on T cells. Despite the promise of such therapeutic approaches for cancer treatment, their success is often limited, and much remains to be understood about how tumors influence DC function and the quality of DC-mediated immune responses. Tumor/DC interactions have therefore become an increasingly active area of investigation, and many studies have described effects of tumors on DC phenotype and function that include an accumulation of immature DC within tumors, tumor-altered differentiation of DC precursors into myeloid-derived suppressor cells, and the generation of tumor-associated DC with immunoregulatory properties. As this field moves forward, it will be important to gain mechanistic insights into the basis for both tumor-mediated DC dysfunction as well as the induction of either suboptimal or immunosuppressive adaptive anti-tumor immune responses by tumor-associated DC. Progress in these areas of tumor immunology will greatly improve our understanding of the factors that contribute to effective DC-mediated anti-tumor immune control versus DC-associated anti-tumor immune dysfunction and subsequent tumor immune escape. Such information is vital for improving current and developing novel immunotherapeutic strategies for interfering with tumor-associated DC dysfunction and enhancing the functional quality of endogenous DC in cancer patients as well as the efficacy of exogenous DC-based anti-tumor vaccines. Topics of interest for this collection of articles will promote this understanding and include, but are not limited to:
1. DC maturation/activation and tumor-associated “danger signals”/damage-associated molecular patterns (DAMPs)
2. cross-presentation of tumor antigen
3. the role of DC in tumor inflammation
4. the role of DC in the induction of anti-tumor T cell responses
5. DC-induced imprinting of T cell migration and the role of DC-derived chemokines in the recruitment of tumor-infiltrating lymphocytes
6. tumor-associated DC dysfunction and the influence of tumor-derived factors on DC differentiation, maturation, activation, and function
7. tumor-associated immunosuppression by myeloid-derived suppressor cells (MDSC)
8. immunoregulatory DC and cancer
9. DC-associated and DC-targeted anti-cancer vaccines and immunotherapies
10. emerging technologies and model systems for studying the influence of tumors on DC immunobiology
11. diagnostic and prognostic phenotyping of DC in cancer patients and tumor-bearing animals
