Quantitation of antigen-reactive T cells in peripheral blood by IFNgamma-ELISPOT assay and chromium-release assay: a four-centre comparative trial

Details

Serval ID
serval:BIB_6E7AEA6CB188
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Quantitation of antigen-reactive T cells in peripheral blood by IFNgamma-ELISPOT assay and chromium-release assay: a four-centre comparative trial
Journal
Journal of Immunological Methods
Author(s)
Scheibenbogen  C., Romero  P., Rivoltini  L., Herr  W., Schmittel  A., Cerottini  J. C., Woelfel  T., Eggermont  A. M., Keilholz  U.
ISSN
0022-1759 (Print)
Publication state
Published
Issued date
10/2000
Volume
244
Number
1-2
Pages
81-9
Notes
Comparative Study
Evaluation Studies
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't --- Old month value: Oct 20
Abstract
The ELISPOT assay is increasingly being used for the monitoring of the induction of antigen-reactive T cells in cancer vaccination trials. In order to evaluate the reliability of T cell frequency analysis with the ELISPOT assay, a comparative study was performed in four European laboratories. Six samples from healthy subjects were analyzed for the frequency of influenza-reactive CD8+ T cells in peripheral blood mononuclear cells (PBMC) by IFNgamma-ELISPOT assay. In addition, one laboratory determined cytotoxic T cell precursor (CTL) frequencies in these samples by limiting dilution chromium-release assay (LDA), and three laboratories performed a variant of the LDA, the multiple microculture assay (MMA). Consistent frequencies of influenza peptide-reactive T cells were obtained with the ELISPOT assay in all four laboratories. The numbers detected by ELISPOT assay correlated closely with those determined by LDA. In contrast, the frequencies obtained with the MMA differed considerably and showed little correlation with the other two assays. This study shows that it is possible to use the ELISPOT assay to determine with reliability antigen-reactive T cells in a multicenter setting. We suggest that this assay may be suitable for monitoring cancer vaccine trials.
Keywords
Antigens, Viral/*immunology CD8-Positive T-Lymphocytes/*immunology/secretion Chromium Radioisotopes Enzyme-Linked Immunosorbent Assay/*methods Epitopes, T-Lymphocyte/immunology HIV-1 Reverse Transcriptase/immunology HLA-A2 Antigen/immunology Humans Immunodominant Epitopes/immunology Indicator Dilution Techniques Interferon Type II/secretion Leukocytes, Mononuclear/immunology Lymphocyte Activation/immunology Peptide Fragments/immunology T-Lymphocytes, Cytotoxic/immunology Viral Matrix Proteins/immunology
Pubmed
Web of science
Create date
28/01/2008 11:13
Last modification date
20/08/2019 14:27
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