Detection and activation of human Vα24+ natural killer T cells using α-galactosyl ceramide-pulsed dendritic cells Journal Article


Authors: Fujii, S. I.; Shimizu, K.; Steinman, R. M.; Dhodapkar, M. V.
Article Title: Detection and activation of human Vα24+ natural killer T cells using α-galactosyl ceramide-pulsed dendritic cells
Abstract: Human CD1d-restricted natural killer T (NKT) cells, which are postulated to regulate the immune response in several clinical settings, can be activated by α-galactosylceramide (α-GalCer) presented by CD1d molecules on antigen presenting cells (APCs). Simple methods to quantify NKT function in fresh blood will greatly benefit studies targeting NKT cells in humans. Here we show that freshly isolated human NKT cells can be readily quantified by an enzyme-linked immunospot (ELISPOT) assay and have a Th1 profile (secreting interferon-γ, but not IL-4), after stimulation using α-GalCer loaded APCs. Using this assay, we also evaluated APC requirements for human NKT cell activation in fresh blood. Monocyte-derived dendritic cells (DCs) are more effective than monocytes/macrophages for detecting and activating NKT cells in fresh blood, with mature α-GalCer pulsed DCs being optimal. DCs are also efficient APCs for expanding NKT cells in culture and generating NKT cell lines. NKT cells expanded with DCs were functional, secreting both IFN-γ and IL-4, and killing NKT-sensitive targets. Optimal activation of these lines was seen using mature DCs loaded with 10-100 ng/ml of α-GalCer. DCs matured with several different stimuli were effective. These data help to establish the conditions for loading DCs with α-GalCer for immune therapeutic targeting of NKT cells, and provide a new simple assay to monitor NKT function in humans. © 2002 Elsevier Science B.V. All rights reserved.
Keywords: controlled study; unclassified drug; human cell; t lymphocyte; cell function; cell maturation; dendritic cell; interleukin 4; cell line; cell differentiation; assay; cell type; blood; lymphocyte activation; dendritic cells; immunotherapy; gamma interferon; cell culture; evaluation; cell isolation; natural killer cell; killer cells, natural; t-lymphocyte subsets; th1 cell; enzyme-linked immunosorbent assay; monocyte; monocytes; macrophage; macrophages; cytokine release; enzyme linked immunospot assay; histocompatibility antigens class ii; cell activation; antigen presenting cell; normal human; alpha galactosylceramide; cd1d antigen; galactosylceramide; il-4; interleukin-4; nkt cells; immunologic techniques; interferon type ii; galactosylceramides; antigens, differentiation, b-lymphocyte; α-galactosylceramide; interferon-γ; enzyme-linked immunospot; humans; human; priority journal; article
Journal Title: Journal of Immunological Methods
Volume: 272
Issue: 1-2
ISSN: 0022-1759
Publisher: Elsevier Science, Inc.  
Date Published: 2003-01-15
Start Page: 147
End Page: 159
Language: English
DOI: 10.1016/s0022-1759(02)00497-0
PUBMED: 12505720
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 12 September 2014 -- Source: Scopus
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