在成人单单位脐带血移植后,携带CTLA-4 AA基因型rs231775的受者复发率更高,总生存期更差。

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2024-12-02 DOI:10.1080/10428194.2024.2434925
Takaaki Konuma, Megumi Hamatani-Asakura, Maki Monna-Oiwa, Seiko Kato, Masamichi Isobe, Kazuaki Yokoyama, Yasuhito Nannya, Satoshi Takahashi
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引用次数: 0

摘要

我们回顾性研究了CTLA-4多态性对在我院接受单单位脐带血移植(CBT)的成年患者预后的影响。CTLA-4基因分型采用实时聚合酶链反应与TaqMan®SNP基因分型检测rs231775。这项研究包括143对受体-供体配对。多因素分析显示,受体rs231775 AA与较差的总生存期(OS)相关(风险比[HR], 2.92;p = 0.008),复发率较高(HR, 4.79;P = 0.002),但供体rs231775没有。受体和供体的rs231775多态性不影响非复发死亡率、造血恢复或急性和慢性移植物抗宿主病。rs231775 GG+GA受体对OS和复发的有益作用在高危疾病状态和髓系疾病患者亚组中显著。CTLA-4 rs231775在受体中的多态性可能与单单位CBT的临床结果有关。
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Higher relapse and worse overall survival in recipients with CTLA-4 AA genotype of rs231775 following single-unit cord blood transplantation in adults.

We retrospectively investigated the impact of CTLA-4 polymorphism on outcomes for adult patients who received single-unit cord blood transplantation (CBT) at our institution. CTLA-4 genotyping was performed using real-time polymerase chain reaction with the TaqMan® SNP genotyping assay for rs231775. This study included 143 recipient-donor pairs. The multivariate analysis showed that recipient rs231775 AA was associated with worse overall survival (OS) (hazard ratio [HR], 2.92; p = 0.008) and a higher relapse rate (HR, 4.79; p = 0.002), but donor rs231775 was not. The rs231775 polymorphism in recipients and donors did not affect non-relapse mortality, hematopoietic recovery, or acute and chronic graft-versus-host disease. The beneficial effects of rs231775 GG+GA recipients on OS and relapse were notable in subgroups of patients with high-risk disease status and those with myeloid diseases. The polymorphism of CTLA-4 rs231775in recipients might be associated with the clinical outcomes of single-unit CBT.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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