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Originally published online as doi:10.1189/jlb.1104654 on April 27, 2005

Published online before print April 27, 2005
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(Journal of Leukocyte Biology. 2005;78:383-392.)
© 2005 by Society for Leukocyte Biology

Lipopolysaccharide stimulation converts vigorously washed dendritic cells (DCs) to nonexhausted DCs expressing CD70 and evoking long-lasting type 1 T cell responses

Sanju Iwamoto*,1, Makoto Ishida*, Keiko Takahashi*, Ken Takeda{dagger} and Akira Miyazaki*

* Department of Biochemistry, School of Medicine, Showa University, Tokyo, Japan; and
{dagger} Department of Hygiene Chemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Japan

1 Correspondence: Department of Biochemistry, School of Medicine, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan. E-mail: iwasanju{at}med.showa-u.ac.jp

A great variety of in vitro culture protocols for human monocyte-derived dendritic cells (mo-DCs) has been used to generate DCs suitable for use in immunotherapy. It is thought that activated DCs undergo one-way differentiation into "exhausted" DCs. In the present study, we contrived an in vitro method for facilitating expression of CD70 by mature DCs. This was achieved by vigorous washing of mo-DCs before exposure to lipopolysaccharide (LPS). Unexpectedly, these mature DCs retain expression of some interleukin (IL)-12 family members after extended periods and maintain their ability to stimulate type 1 T cell responses. In contrast, DCs exposed to IL-4 before LPS stimulation or LPS-stimulated DCs not exposed to washing stress before activation failed to express CD70 and did differentiate into exhausted DCs. It is interesting that DCs expressing CD70 (CD70+ DCs) induced interferon-{gamma} production from purified, allogeneic CD8+ T cells through a direct CD27-CD70 interaction. This is evidence for a pathway resulting in generation of CD8 T effectors by B7-independent mechanisms. These data suggest that exposure of immature DCs to LPS stimulation contributes to their terminal differentiation into CD70+ DCs, which have potent ability to prolong type 1 T cell responses through alternative pathways.

Key Words: CD27 • CD88 • CTLA-4 • IFN-{gamma} • IL-4




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