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ObjectiveInjection of dendritic cells (DC) engineered with recombinant adenoviral vectors to produce interleukin-12 (IL-12) inside experimental murine tumors frequently achieves complete regressions. In such a system the function of CD8(+) T cells has been shown to be an absolute requirement, in contrast to observations made upon depletion of CD4(+) T cells, which minimally affected the outcome. The aim of this work was to study the possible involvement of natural killer (NK) cells in this setting.Materials, methods, and resultsDepletions with anti-AsialoGM1 antiserum showed only a small decrease in the proportion of complete regressions obtained that correlated with induction of NK activities in lymphatic tissues into which DC migrate, whereas combined depletions of CD4(+) and NK cells completely eliminated the antitumor effects. Likewise in vivo neutralization of interferon-gamma (IFN-gamma) also eliminated those therapeutic effects. Trying to define the cellular role played by NK cells in vivo, it was observed that injection of cultured DC inside the spleen of T- and B-cell-deficient (Rag1(-/-)) mice induced upregulation of NK activity only if DC had been adenovirally engineered to produce IL-12. In addition, identically transfected fibroblasts also activated NK cells, indicating that IL-12 transfection was the unique requirement. Equivalent human DC only activated in vitro the cytolytic and cytokine-secreting functions of autologous NK cells if transfected to express human IL-12.ConclusionsOverall, these results point out an important role played by NK cell activation in the potent immunotherapeutic effects elicited by intratumoral injection of IL-12--secreting DC and that NK activation under these conditions is mainly, if not only, dependent on IL-12.

Original publication

DOI

10.1016/s0301-472x(01)00792-5

Type

Journal article

Journal

Experimental hematology

Publication Date

03/2002

Volume

30

Pages

195 - 204

Addresses

Gene Therapy Unit, Department of Internal Medicine, University of Navarra, Pamplona, Spain.

Keywords

Dendritic Cells, Killer Cells, Natural, Cells, Cultured, Animals, Mice, Inbred BALB C, Mice, Inbred C57BL, Humans, Mice, Colonic Neoplasms, Neoplasms, Experimental, Fluorescein-5-isothiocyanate, Glycosphingolipids, G(M1) Ganglioside, Granulocyte-Macrophage Colony-Stimulating Factor, Interleukin-4, Interleukin-12, Antibodies, Monoclonal, Fluorescent Dyes, Immunotherapy, Cell Separation, Transfection, Genetic Engineering, Neoplasm Transplantation, Magnetics, CD4 Antigens