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Allostimulation-induced tumor cytotoxic cells: from mouse to man
G Parmiani1, M Sensi, G Fossati
1Division of Experimental Oncology D, Istituto Nazionale Tumori, Via Venezian, 1-20133 Milan, Italy.
Immunology Today
|October 8, 2014
Summary
Immunizing animals with normal allogeneic tissues can induce resistance to syngeneic tumors, generating tumor-specific cytotoxic cells. This review explores the mechanisms and clinical potential of these cytotoxic cells in cancer research.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Experimental tumors can express cell surface antigens that cross-react with normal allogeneic tissues.
- This cross-reactivity, involving histocompatibility and differentiation antigens, can lead to immune responses against tumors.
- Previous studies show tumor rejection even without detectable cross-reacting antigens, indicating complex mechanisms.
Purpose of the Study:
- To review investigations on the generation of tumor-specific cytotoxic cells.
- To discuss the potential clinical applications of these cytotoxic cells in cancer therapy.
Main Methods:
- Review of existing experimental data on tumor rejection and cytotoxic cell generation.
- Analysis of studies involving immunization with allogeneic tissues and allostimulation of lymphocytes.
- Discussion of in vivo and in vitro experimental models in mice, rats, and humans.
Main Results:
- Immunization with allogeneic tissues bearing shared determinants can induce resistance to syngeneic tumors.
- Lymphocytes generated through allostimulation can exhibit cytotoxicity against syngeneic or autologous tumor cells.
- These processes result in the production of tumor-restricted cytotoxic cells, though underlying mechanisms vary.
Conclusions:
- The generation of tumor-restricted cytotoxic cells via allogeneic immunization or allostimulation is a significant finding.
- These cytotoxic cells hold potential for clinical utility in cancer treatment strategies.
- Further research is warranted to fully elucidate mechanisms and optimize therapeutic applications.

