» Articles » PMID: 15185011

Dendritic Cell-tumor Cell Hybrid Vaccination for Metastatic Cancer

Abstract

Dendritic cells are the most potent antigen-presenting cells, and the possibility of their use for cancer vaccination has renewed the interest in this therapeutic modality. Nevertheless, the ideal immunization protocol with these cells has not been described yet. In this paper we describe the preliminary results of a protocol using autologous tumor and allogeneic dendritic hybrid cell vaccination every 6 weeks, for metastatic melanoma and renal cell carcinoma (RCC) patients. Thirty-five patients were enrolled between March 2001 and March 2003. Though all patients included presented with large tumor burdens and progressive diseases, 71% of them experienced stability after vaccination, with durations up to 19 months. Among RCC patients 3/22 (14%) presented objective responses. The median time to progression was 4 months for melanoma and 5.7 months for RCC patients; no significant untoward effects were noted. Furthermore, immune function, as evaluated by cutaneous delayed-type hypersensitivity reactions to recall antigens and by peripheral blood proliferative responses to tumor-specific and nonspecific stimuli, presented a clear tendency to recover in vaccinated patients. These data indicate that dendritic cell-tumor cell hybrid vaccination affects the natural history of advanced cancer and provide support for its study in less advanced patients, who should, more likely, benefit even more from this approach.

Citing Articles

Complete response to fifth-line anti-PD-1 rechallenge in fumarate hydratase-mutated papillary renal cell carcinoma.

Portugal I, Clavijo-Salomon M NPJ Precis Oncol. 2024; 8(1):251.

PMID: 39496729 PMC: 11535469. DOI: 10.1038/s41698-024-00750-3.


Feasibility Study for the Use of Gene Electrotransfer and Cell Electrofusion as a Single-Step Technique for the Generation of Activated Cancer Cell Vaccines.

Usaj M, Pavlin M, Kanduser M J Membr Biol. 2024; 257(5-6):377-389.

PMID: 39133276 PMC: 11584437. DOI: 10.1007/s00232-024-00320-5.


Profiling of Tumor-Infiltrating Immune Cells and Their Impact on Survival in Glioblastoma Patients Undergoing Immunotherapy with Dendritic Cells.

Peres N, Lepski G, Fogolin C, Evangelista G, Flatow E, de Oliveira J Int J Mol Sci. 2024; 25(10).

PMID: 38791312 PMC: 11121326. DOI: 10.3390/ijms25105275.


Adjuvant Vaccination with Allogenic Dendritic Cells Significantly Prolongs Overall Survival in High-Grade Gliomas: Results of a Phase II Trial.

Lepski G, Bergami-Santos P, Pinho M, Chauca-Torres N, Evangelista G, Teixeira S Cancers (Basel). 2023; 15(4).

PMID: 36831580 PMC: 9953909. DOI: 10.3390/cancers15041239.


Nanomaterial-Based Drug Delivery System Targeting Lymph Nodes.

Cheng Z, Que H, Chen L, Sun Q, Wei X Pharmaceutics. 2022; 14(7).

PMID: 35890268 PMC: 9325242. DOI: 10.3390/pharmaceutics14071372.


References
1.
Nair S, Snyder D, Rouse B, Gilboa E . Regression of tumors in mice vaccinated with professional antigen-presenting cells pulsed with tumor extracts. Int J Cancer. 1997; 70(6):706-15. DOI: 10.1002/(sici)1097-0215(19970317)70:6<706::aid-ijc13>3.0.co;2-7. View

2.
Della Bella S, Gennaro M, Vaccari M, Ferraris C, Nicola S, Riva A . Altered maturation of peripheral blood dendritic cells in patients with breast cancer. Br J Cancer. 2003; 89(8):1463-72. PMC: 2394334. DOI: 10.1038/sj.bjc.6601243. View

3.
Avigan D . Fusions of breast cancer and dendritic cells as a novel cancer vaccine. Clin Breast Cancer. 2003; 3 Suppl 4:S158-63. DOI: 10.3816/cbc.2003.s.006. View

4.
Okada H, Tahara H, Shurin M, Attanucci J, Fellows W, Lotze M . Bone marrow-derived dendritic cells pulsed with a tumor-specific peptide elicit effective anti-tumor immunity against intracranial neoplasms. Int J Cancer. 1998; 78(2):196-201. DOI: 10.1002/(sici)1097-0215(19981005)78:2<196::aid-ijc13>3.0.co;2-9. View

5.
Trefzer U, Weingart G, Chen Y, Herberth G, Adrian K, Winter H . Hybrid cell vaccination for cancer immune therapy: first clinical trial with metastatic melanoma. Int J Cancer. 2000; 85(5):618-26. DOI: 10.1002/(sici)1097-0215(20000301)85:5<618::aid-ijc4>3.0.co;2-z. View