PMID- 15448029 OWN - NLM STAT- MEDLINE DCOM- 20041201 LR - 20201212 IS - 1078-0432 (Print) IS - 1078-0432 (Linking) VI - 10 IP - 18 Pt 2 DP - 2004 Sep 15 TI - Dendritic cell-tumor fusion vaccines for renal cell carcinoma. PG - 6347S-52S AB - Renal cell carcinoma is a malignant disease that demonstrates resistance to standard chemotherapeutic agents. A promising area of investigation is the use of cancer vaccines to educate host immunity to specifically target and eliminate malignant cells. Dendritic cells (DCs) are potent antigen-presenting cells that are uniquely effective in generating primary immune responses. DCs that are manipulated to present tumor antigens induce antitumor immunity in animal models and preclinical human studies. A myriad of strategies have been developed to effectively load tumor antigen onto DCs, including the introduction of individual peptides, proteins, or tumor-specific genes, as well as the use of whole tumor cells as a source of antigen. A promising approach for the design of cancer vaccines involves the fusion of whole tumor cells with DCs. The DC-tumor fusion presents a spectrum of tumor-associated antigens to helper and cytotoxic T-cell populations in the context of DC-mediated costimulatory signals. In animal models, vaccination with DC-tumor fusions resulted in protection from tumor challenge and regression of established metastatic disease. We have conducted phase 1 dose escalation studies in which patients with metastatic breast and renal cancer underwent vaccination with DC-tumor fusions. Twenty-three patients underwent vaccination with autologous DC-tumor fusions. Vaccination was well tolerated without substantial treatment-related toxic effects. Immunologic responses and disease regression were observed in a subset of patients. Future studies will explore the effect of DC maturation and cytokine adjuvants on vaccine potency. FAU - Avigan, David AU - Avigan D AD - Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215, USA. davigan@caregroup.harvard.edu LA - eng GR - N01-C0-12400/PHS HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PT - Review PL - United States TA - Clin Cancer Res JT - Clinical cancer research : an official journal of the American Association for Cancer Research JID - 9502500 RN - 0 (Antigens, Neoplasm) RN - 0 (Cancer Vaccines) RN - 0 (Recombinant Fusion Proteins) SB - IM MH - Animals MH - Antigens, Neoplasm/*immunology MH - *Cancer Vaccines MH - Carcinoma, Renal Cell/*immunology MH - Dendritic Cells/*immunology MH - Disease Models, Animal MH - Humans MH - Kidney Neoplasms/*immunology MH - Recombinant Fusion Proteins/immunology RF - 62 EDAT- 2004/09/28 05:00 MHDA- 2004/12/16 09:00 CRDT- 2004/09/28 05:00 PHST- 2004/09/28 05:00 [pubmed] PHST- 2004/12/16 09:00 [medline] PHST- 2004/09/28 05:00 [entrez] AID - 10/18/6347S [pii] AID - 10.1158/1078-0432.CCR-050005 [doi] PST - ppublish SO - Clin Cancer Res. 2004 Sep 15;10(18 Pt 2):6347S-52S. doi: 10.1158/1078-0432.CCR-050005.