Although T-cell-defined tumor antigens have recently been identified in several tumors, human neoplastic cells are considered to be poorly immunogenic. The development of clinical approaches to the immunotherapy of human tumors thus requires the identification of effective adjuvants. Dendritic cells (DC) are a specialized system of antigen-presenting cells (APC) that could be utilized as natural adjuvants to elicit antitumor immune responses. In an attempt to overcome the problem of the low frequency of mature DC in peripheral blood, several methods have been applied for the ex vivo generation of human DC by culturing mobilized CD34+ cells or monocytes with combinations of cytokines. As shown in murine models as well as in the human system, after loading with peptides or tumor lysates or infection with recombinant viral vectors, DC expressing tumor antigens are able to elicit specific antitumor T cells and to mediate tumor regression. These initial results suggest that this new approach may lead to effective antitumor responses even in heavily pretreated patients bearing advanced cancers, but further clinical trials are required to validate the efficacy of vaccination with tumor-antigen-loaded DC.

Human dendritic cells: natural adjuvants in antitumor immunotherapy / M. Di Nicola, A. Anichini, R. Mortarini, M. Bregni, G. Parmiani, A. M. Gianni. - In: CYTOKINES CELLULAR & MOLECULAR THERAPY. - ISSN 1368-4736. - 4:4(1998 Dec), pp. 265-73-273.

Human dendritic cells: natural adjuvants in antitumor immunotherapy

A.M. Gianni
Ultimo
1998

Abstract

Although T-cell-defined tumor antigens have recently been identified in several tumors, human neoplastic cells are considered to be poorly immunogenic. The development of clinical approaches to the immunotherapy of human tumors thus requires the identification of effective adjuvants. Dendritic cells (DC) are a specialized system of antigen-presenting cells (APC) that could be utilized as natural adjuvants to elicit antitumor immune responses. In an attempt to overcome the problem of the low frequency of mature DC in peripheral blood, several methods have been applied for the ex vivo generation of human DC by culturing mobilized CD34+ cells or monocytes with combinations of cytokines. As shown in murine models as well as in the human system, after loading with peptides or tumor lysates or infection with recombinant viral vectors, DC expressing tumor antigens are able to elicit specific antitumor T cells and to mediate tumor regression. These initial results suggest that this new approach may lead to effective antitumor responses even in heavily pretreated patients bearing advanced cancers, but further clinical trials are required to validate the efficacy of vaccination with tumor-antigen-loaded DC.
Cell Movement; Dendritic Cells; Gene Transfer Techniques; Humans; Clinical Trials as Topic; Antigens, Neoplasm; Cell Differentiation; Vaccination; Neoplasms; Cells, Cultured; Antigen-Presenting Cells; Cell Division; T-Lymphocytes
Settore MED/06 - Oncologia Medica
dic-1998
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/184560
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