Longitudinal dynamics of Epstein-Barr virus-specific cytotoxic T lymphocytes during posttransplant lymphoproliferative disorder

被引:27
|
作者
Kuzushima, K
Kimura, H
Hoshino, Y
Yoshimi, A
Tsuge, I
Horibe, K
Morishima, T
Tsurumi, T
Kojima, S
机构
[1] Aichi Canc Ctr, Res Inst, Div Virol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Nagoya Univ, Sch Med, Dept Pediat Dev Pediat, Nagoya, Aichi 466, Japan
[3] Nagoya Univ, Sch Med, Dept Hlth Sci, Nagoya, Aichi 466, Japan
来源
JOURNAL OF INFECTIOUS DISEASES | 2000年 / 182卷 / 03期
基金
日本学术振兴会;
关键词
D O I
10.1086/315791
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epstein-Barr virus (EBV)-associated lymphoproliferative disorder (LPD) is a serious complication after allogeneic bone marrow transplantation (BMT). Dynamics of EBV-specific cytotoxic T lymphocytes (CTL), which are important in controlling EBV during the LPD, have not been fully elucidated A patient with Wiskot-Aldrich's syndrome was diagnosed as suffering from LPD on day 47 after BMT. Fluorescence-activated cell sorter (FACS) analysis for interferon-gamma production revealed that >70% of the patient's CD8(+) T cells were EBV specific. The patient's lymphocytes were directly cytotoxic to donor-derived EBV-positive lymphoblastoid cells, which was blocked by an anti-class I antibody. EBV-specific CD8(+) T cell counts declined in parallel with EBV genome load, and full recovery of LPD was obtained with relaxation of immunosuppressive drags. The results illustrate longitudinal dynamics of EBV-specific CTL during the posttransplant LPD; they also illustrate the advantages of using FAGS analysis for EBV-specific CTL to make decisions about treatment.
引用
收藏
页码:937 / 940
页数:4
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