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NOD2/CARD15 基因型作为急性淋巴细胞白血病和急性髓系白血病患者骨髓移植结局预后指标的潜在作用:一项系统综述

英文原题:The Potential Role of NOD2/CARD15 Genotype as a Prognostic Indicator for Bone Marrow Transplantation Outcomes in Patients With Acute Lymphoblastic Leukemia and Acute Myeloid Leukemia: A Systematic Review.

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The Potential Role of NOD2/CARD15 Genotype as a Prognostic Indicator for Bone Marrow Transplantation Outcomes in Patients With Acute Lymphoblastic Leukemia and Acute Myeloid Leukemia: A Systematic Review.

PubMed 2024/01/15(内容时间) Cureus

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中文摘要

造血干细胞移植(HSCT)已成为急性髓系白血病(AML)和特定亚型急性淋巴细胞白血病(ALL)的一种突破性治疗选择。NOD2/CARD15 基因的预后意义已在多种因素中进行了探索,涵盖了不同的患者队列和基因变异。用于干细胞移植的同胞供者和无关供者,其遗传变异与移植物抗宿主病的发生率之间存在显著关联。白血病患者的干细胞移植涉及众多考量因素,包括患者生存率、复发率、疾病分期、供受者年龄以及相容性。

本研究深入探讨了 NOD2/CARD15 基因及其突变,以评估其作为筛查工具的适用性。一项涵盖 PubMed、ScienceDirect 和 Google Scholar 的综合文献检索共获得 4,840 篇文章。在去除重复文献并应用纳入和排除标准后,我们将检索结果缩小至 876 篇文章。随后对摘要和标题进行筛选,最终选定 230 篇相关文章。

进一步排除 198 篇与研究问题无关的文章后,对 32 篇全文文章进行了仔细审查,并依据纳入和排除标准进行评估。研究重点放在专门探讨 NOD2/CARD15 作为 HSCT 结局预测因素的文章上,最终纳入 19 篇文章。NOD2 和 CARD15 等单核苷酸多态性(SNPs)已证明其作为预测移植后复发和疾病结局的可靠遗传标记的潜力。携带这些遗传标记阳性的患者表现出总生存期和无事件生存期缩短,以及移植相关死亡率升高。已考虑采用干扰素-γ和胞壁酰三肽磷脂酰乙醇胺进行干预,以减轻这些SNP的炎症效应,从而增强NK 细胞对异常细胞的作用,并可能延长患者生存期。NOD2/CARD15分型可能有助于识别复发风险较高的患者,并改善其异基因干细胞移植后的临床结局,尤其是在ALL患者中。

然而,在AML患者中未观察到显著变化。此外,本研究强调了适应性免疫应答和固有免疫应答及其相互作用在干细胞移植免疫学中的关键作用。

展开英文摘要原文

Hematopoietic stem-cell transplantation (HSCT) has emerged as a groundbreaking therapeutic option for acute myeloid leukemia (AML) and specific subtypes of acute lymphoblastic leukemia (ALL). The prognostic significance of the NOD2/CARD15 gene has been explored alongside various factors, encompassing diverse patient cohorts and gene variants.

Siblings and unrelated donors used for stem cell transplantation exhibit significant associations between their genetic variations and graft-versus-host disease incidence. The transplantation of stem cells for leukemia patients involves numerous considerations, including patient survival, relapse rates, disease stage, donor and recipient ages, and compatibility.

This study delved into research on the NOD2/CARD15 gene and its mutations to assess its suitability as a screening tool. A comprehensive literature search encompassing PubMed, ScienceDirect, and Google Scholar articles yielded 4,840 articles. After removing duplicates and applying inclusion and exclusion criteria, we narrowed the search results to 876 articles. Subsequent screening of abstracts and titles resulted in the selection of 230 relevant articles.

Further exclusion of 198 articles unrelated to the research question led to the scrutinizing of 32 full-text articles, which were assessed against inclusion and exclusion criteria. Emphasis was placed on articles that specifically investigated the role of NOD2/CARD15 as a predictive factor for HSCT outcomes, ultimately resulting in the inclusion of 19 articles in this study. Single nucleotide polymorphisms (SNPs) such as NOD2 and CARD15 have demonstrated their potential as reliable genetic markers for predicting post-transplantation relapse and disease outcomes.

Patients positive for these genetic markers have exhibited reduced overall survival and event-free survival and increased transplant-related mortality. Interventions with interferon-gamma and muramyl tripeptide phosphatidylethanolamine have been considered to mitigate the inflammatory effects of these SNPs, thus enhancing the influence of natural killer cells on abnormal cells and potentially extending patient survival.

NOD2/CARD15 typing may aid in identifying patients at higher risk for relapse and improving their clinical outcomes after allogeneic stem cell transplant, particularly in ALL patients.

However, no remarkable change was observed in AML patients.

Additionally, this study underscores the pivotal roles of adaptive and innate immune responses and their interplay in stem cell transplant immunology.

论文信息

作者
Ahmadinia L、Rangrej SB、Miranda M、Shailer C、Ahmed W、Carvalho V、Rathore R
第一作者单位
Basic Sciences, Saint James School of Medicine, Arnos Vale, VCT.
通讯作者单位
Pharmacology and Therapeutics, Saint James School of Medicine, Arnos Vale, VCT.
文献类型
综述
期刊
Cureus2024 Jan
原文标识
PubMed 38361685 · DOI 10.7759/cureus.52329