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Biased usage of BV gene families of T-cell receptors of WT1 (Wilms' tumor gene)-specific CD8+ T cells in patients with myeloid malignancies.

Authors :
Tanaka-Harada Y
Kawakami M
Oka Y
Tsuboi A
Katagiri T
Elisseeva OA
Nishida S
Shirakata T
Hosen N
Fujiki F
Murao A
Nakajima H
Oji Y
Kanda Y
Kawase I
Sugiyama H
Source :
Cancer science [Cancer Sci] 2010 Mar; Vol. 101 (3), pp. 594-600. Date of Electronic Publication: 2009 Dec 04.
Publication Year :
2010

Abstract

WT1 (Wilms' tumor gene 1) protein is a potent pan-tumor-associated antigen (TAA) and WT1-specific cytotoxic T lymphocytes (WT1 tetramer(+) CD8(+) T cells) are spontaneously induced in patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). We conducted a single-cell level comparative analysis of T-cell receptor beta-chain variable region (TCR-BV) gene families of a total of 1242 spontaneously induced WT1 tetramer(+) CD8(+) T cells in HLA-A*2402(+) patients with AML or MDS and those in healthy donors (HDs). This is the first report of direct usage analysis of TCR-BV gene families of individual TAA-specific CD8(+) T cells at single-cell level. Usage analysis using single-cell RT-PCR of TCR-BV gene families of individual FACS-sorted WT1 tetramer(+) CD8(+) T cells showed for the first time (i) that BVs 5, 6, 20, and 27 were commonly biased in both HDs and patients; (ii) that BV4 was commonly biased in HDs and MDS patients; (iii) that BV19 was commonly biased in the patients; and (iv) that BVs 7 and 28, BVs 9 and 15, and BVs 12 and 29 were specifically biased in HDs, AML, and MDS patients, respectively. However, statistical analysis of similarity among HD, AML, and MDS of individual usage frequencies of 24 kinds of TCR-BV gene families indicated that the usage frequencies of TCR-BV gene families in AML and MDS patients reflect those in HDs. These findings represent a novel insight for a better understanding of WT1-specific immune response.

Details

Language :
English
ISSN :
1349-7006
Volume :
101
Issue :
3
Database :
MEDLINE
Journal :
Cancer science
Publication Type :
Academic Journal
Accession number :
20132220
Full Text :
https://doi.org/10.1111/j.1349-7006.2009.01453.x