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International Immunology Advance Access originally published online on July 18, 2005
International Immunology 2005 17(9):1143-1155; doi:10.1093/intimm/dxh292
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© The Japanese Society for Immunology. 2005. All rights reserved. For permissions, please e-mail: journals.permissions@oupjournals.org

Ex vivo expanded human CD4+ regulatory NKT cells suppress expansion of tumor antigen-specific CTLs

Takuya Osada1,2, Michael A. Morse1,3, H. Kim Lyerly1,2,4 and Timothy M. Clay1,2

1 Program in Molecular Therapeutics, Departments of 2 Surgery, 3 Medicine, 4 Immunology and Pathology, Duke University Medical Center, 401 MSRB, Research Drive, Durham, NC 27710, USA

Correspondence to: T. M. Clay; E-mail: tim.clay{at}duke.edu

NKT cells can produce large amounts of both Th1- and Th2-type cytokines and are an important regulatory cell type. To elucidate their role in acquired immunity, we examined the effect of human V{alpha}24+Vß11+ NKT cells or CD1d-specific ligand {alpha}-galactosylceramide ({alpha}GalCer) on the in vitro generation of antigen-specific CTLs from PBMCs using autologous MART-1(26–35) peptide-pulsed dendritic cells as stimulators. Flow cytometry using tetramer for MART-1(26–35) peptide revealed that NKT cells have inhibitory effects on CTL generation. Cytokine analysis using cytometric bead array assay and ELISA showed higher IL-4 and IL-10 secretion in the {alpha}GalCer(+) and/or NKT cell(+) culture setting, whereas IL-13 secretion in the culture was not affected by the presence of {alpha}GalCer. The CD4+ NKT cell subset seemed to play a major role in this inhibitory effect by secreting large amounts of Th2-type cytokines. Interestingly however, unlike recent reports utilizing mouse models, IL-13 was not a main effector molecule in our human system. Culture with {alpha}GalCer in the presence of cytokine-neutralizing antibodies for the Th2 cytokines, IL-4, IL-5 and IL-10, resulted in enhanced CTL generation, suggesting the dominant role of Th2 cytokines over Th1 cytokines. Thus, CD4+ NKT cells can work as immunoregulatory T cells that suppress anti-tumor immune response and, therefore, NKT cells or {alpha}GalCer could be used as therapeutic modalities to modulate systemic immune responses, such as autoimmune diseases. Conversely, the use of NKT cells along with anti-Th2 cytokine-neutralizing antibodies or CD4-negative NKT cell subset could enhance the generation of antigen-specific CTLs for adoptive immunotherapy.

Keywords: CTL, cytokines, dendritic cell, tumor immunity, T lymphocytes

Transmitting editor: T. Tedder


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