WT1-specific CD8+cytotoxic T cells with the capacity for antigen-specific expansion accumulate in the bone marrow in MDS

被引:2
|
作者
Suwabe, Tatsuya [1 ]
Shibasaki, Yasuhiko [2 ]
Sato, Hiroyuki [3 ]
Tamura, Suguru [1 ]
Katagiri, Takayuki [1 ]
Nemoto, Hiroki [1 ,4 ]
Kasami, Takuya [4 ]
Kozakai, Takashi [4 ]
Nanba, Ayako [5 ]
Kitajima, Toshiki [5 ]
Fuse, Kyoko [1 ]
Ushiki, Takashi [1 ]
Sone, Hirohito [1 ]
Narita, Miwako [3 ]
Masuko, Masayoshi [2 ]
机构
[1] Niigata Univ, Dept Hematol Endocrinol & Metab, Fac Med, Niigata, Japan
[2] Niigata Univ Med & Dent Hosp, Dept Hematopoiet Cell Transplantat, Niigata, Japan
[3] Niigata Univ, Grad Sch Hlth Sci, Lab Hematol & Oncol, Niigata, Japan
[4] Niigata Minami Hosp, Dept Hematol, Niigata, Japan
[5] Saiseikai Niigata Hosp, Dept Hematol, Niigata, Japan
关键词
Myelodysplastic syndrome; Wilms' tumor 1; CD8-positive T-lymphocytes; Bone marrow; Immunoassay;
D O I
10.1007/s12185-021-03083-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Wilms' tumor 1 (WT1) is a tumor-associated antigen and immunotherapy target in myelodysplastic syndrome (MDS). Further information is needed on the characteristics of WT1-specific CD8 + T cells to develop immunotherapeutic strategies for MDS. To clarify the frequency, distribution, and phenotype of WT1-specific CD8 + T cells, which occur innately in MDS patients, we analyzed paired peripheral blood (PB) and bone marrow (BM) samples from 39 patients with MDS or acute myeloid leukemia with myelodysplasia-related changes. The median frequency of WT1 tetramer-binding CD8 + T cells in the CD8 + T cell population was 0.11% in PB and 0.18% in BM. A further tetramer assay combined with mixed lymphocyte peptide culture (MLPC assay) was used to detect functional WT1-specific CD8 + T cells that could respond to the WT1 peptide. Functional WT1-specific CD8 + T cells were detected in BM in 61% of patients, which was significantly higher than in PB (23%, p = 0.001). The frequency of these cells estimated by the MLPC assay was tenfold higher in BM than in PB. The majority of WT1 tetramer-binding CD8 + T cells in BM had a unique phenotype with co-expression of CD39 and CXCR4. These findings will facilitate the development of novel immunotherapeutic strategies for MDS.
引用
收藏
页码:723 / 734
页数:12
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