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(Journal of Leukocyte Biology. 2002;72:312-320.)
© 2002 by Society for Leukocyte Biology

Human dendritic cell mediated cytotoxicity against breast carcinoma cells in vitro

Department of Surgery, Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri

Correspondence: T. Mohanakumar, Ph.D., Washington University School of Medicine, Department of Surgery and Pathology, Box-8109, 3328 CSRB, 660 S. Euclid Avenue, St. Louis, MO 63110. E-mail: kumart{at}msnotes.wustl.edu

Dendritic cells (DC) are an important subset of antigen-presenting cells characterized by their potent capacity to activate immunologically naïve T cells. However, their role in effector function in tumor resistance is less well characterized. We report here that activated human peripheral blood DC acquire a potent antitumor effect against breast cancer cell lines in vitro, leading to growth inhibition and apoptosis of the tumor cell. The antitumor effect of DC was augmented by proinflammatory stimuli induced by lipopolysaccharide (LPS) treatment. Tumor necrosis factor (TNF-) produced after DC activation was responsible for the antitumor activity of DC. Interferon-, interleukin-15, or LPS treatment of DC markedly augmented the effector function of DC against most of the breast cells, indicating heterogeneity of the tumor and its susceptibility to cytokine-mediated damage. Treatment of LPS-activated DC or cell-free supernatant with anti-human TNF- significantly reduces the antitumor effect against the tumor cells tested. These results suggest that in addition to their predominant role as immune regulatory cells, DC could serve as innate effector cells in tumor immunity.

Key Words: apoptosis • TNF- • IFN- • LPS

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