Research summary
The cancer immunoediting framework is articulated, describing how the immune system both suppresses tumor growth by killing nascent cancer cells and promotes progression by selecting for resistant clones and shaping a permissive tumor microenvironment, integrating two decades of mouse and human evidence into a single elimination-equilibrium-escape model [1]. A companion review of innate and adaptive immunity to cancer details the immune cell types, effector molecules, and pathways that act as extrinsic tumor-suppressor mechanisms and the conditions under which the same components instead support tumor outgrowth [2]. Earlier work reviewed immune surveillance of tumors, summarizing mouse and human data that justified renewed interest in natural anti-tumor immunity as a foundation for combination immunotherapy [4]. A four-category stratification of the tumor microenvironment based on the presence or absence of tumor-infiltrating lymphocytes and PD-L1 expression is proposed as a rational framework for designing combination immunotherapy regimens, distinguishing tumors that need T-cell recruitment from those that need checkpoint blockade or other interventions [3]. Taken together, these contributions formalize the conceptual vocabulary of cancer immunology used to interpret PD-1/PD-L1 axis trials and to rationalize next-generation combination immunotherapy.
Recent publications
- Cancer Immunoediting: Integrating Immunity’s Roles in Cancer Suppression and PromotionDOI
- Natural Innate and Adaptive Immunity to CancerDOI
- Activation of the NLRP3 inflammasome in dendritic cells induces IL-1β–dependent adaptive immunity against tumorsDOI
- Cancer immunoediting and resistance to T cell-based immunotherapyDOI
- Classifying Cancers Based on T-cell Infiltration and PD-L1DOI
- New insights into cancer immunoediting and its three component phases — elimination, equilibrium and escapeDOI
- Immune surveillance of tumorsDOI
- Adaptive immunity maintains occult cancer in an equilibrium stateDOI
- Translational biology of osteosarcomaDOI
- Type I interferons in anticancer immunityDOI
The lab page does not clearly state student acceptance status. Email the professor directly to confirm.
How to apply
Email Mark J. Smyth 6-12 months before your application deadline. Read several recent papers and reference specific work in your message. Use our how to email a Japanese professor guide for the proven email structure.
For applications via MEXT scholarship: see our MEXT 2027 complete guide and university-specific University Recommendation track.
External profiles
- ORCID: https://orcid.org/0000-0001-7098-7240
- OpenAlex: openalex.org
Profile compiled from public sources (Researchmap, OpenAlex, Kyoto University faculty directory). Last refreshed 2026-05. Report incorrect information.