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Accumulation of Activated Invariant Natural Killer T Cells in the Tumor Microenvironment after α-Galactosylceramide-Pulsed Antigen Presenting Cells
- Source :
- Journal of Clinical Immunology. 32:1071-1081
- Publication Year :
- 2012
- Publisher :
- Springer Science and Business Media LLC, 2012.
-
Abstract
- The intravenous administration of α-Galactosylceramide (α-GalCer)-pulsed antigen presenting cells (APCs) is well tolerated and the increased IFN-γ producing cells in the peripheral blood after the treatment appeared to be associated with prolonged survival. An exploratory study protocol was designed with the preoperative administration of α-GalCer-pulsed APCs to clarify the mechanisms of these findings, while especially focusing on the precise tumor site.Patients with operable advanced lung cancer received an intravenous injection of α-GalCer-pulsed APCs before surgery. The resected lung and tumor infiltrating lymphocytes (TILs) as well as peripheral blood mononuclear cells were collected and the invariant NKT (iNKT) cell-specific immune responses were analyzed.Four patients completed the study protocol. We observed a significant increase in iNKT cell numbers in the TILs and augmented IFN-γ production by the α-GalCer-stimulated TILs.The administration of α-GalCer-pulsed APCs successfully induced the dramatic infiltration and activation of iNKT cells in the tumor microenvironment.
- Subjects :
- Male
Lung Neoplasms
medicine.medical_treatment
Immunology
Receptors, Antigen, T-Cell
Antigen-Presenting Cells
Galactosylceramides
Adenocarcinoma
Antigen
Carcinoma, Non-Small-Cell Lung
Tumor Microenvironment
Humans
Immunology and Allergy
Medicine
Receptor
Antigen-presenting cell
Aged
Tumor microenvironment
CD40
biology
business.industry
Tumor-infiltrating lymphocytes
Immunotherapy
Natural killer T cell
Carcinoma, Squamous Cell
biology.protein
Natural Killer T-Cells
Lymph Nodes
business
Subjects
Details
- ISSN :
- 15732592 and 02719142
- Volume :
- 32
- Database :
- OpenAIRE
- Journal :
- Journal of Clinical Immunology
- Accession number :
- edsair.doi.dedup.....6ccdff43c1fd16e3a0dbd4f0b24f092c
- Full Text :
- https://doi.org/10.1007/s10875-012-9697-9