先天性巨核细胞性血小板减少症(CAMT)小儿患者异体造血干细胞移植后的 T 细胞重建。

IF 2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI:10.2174/1871530323666230801100113
Shideh Namazi Bayegi, Amir Ali Hamidieh, Maryam Behfar, Amene Saghazadeh, Mahmood Bozorgmehr, Nader Tajik, Ali-Akbar Delbandi, Samaneh Delavari, Mehdi Shekarabi, Nima Rezaei
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引用次数: 0

摘要

背景:先天性巨核细胞血小板减少症(CAMT)是一种常染色体隐性遗传的骨髓衰竭综合征,以缺乏巨核细胞和血小板减少为特征。该病的病因是编码血小板生成素(TPO)受体的 c-Mpl 基因发生突变。这种遗传性疾病的主要治疗方法是异体造血干细胞移植(allo-HSCT)。然而,移植相关死亡率、急性和慢性移植物抗宿主疾病(GvHD)的发生以及对机会性感染的易感性是移植的主要障碍。T细胞重建的延迟和不同功能的CD4和CD8 T细胞亚群再生的不平衡主要影响移植后的并发症。我们报告了一例CAMT病例,该患者在allo-HSCT后出现急性GvHD,但没有慢性GvHD的症状和体征:四岁时,她出现瘀斑和紫癜。在实验室检查中,观察到全血细胞减少,无器官肿大,骨髓活检细胞数低于 5%。初步诊断为特发性再生障碍性贫血,她接受了泼尼松龙、环孢素和抗胸腺细胞球蛋白(ATG)治疗,但效果不佳。基因分析显示,c-Mpl 基因第 10 外显子发生了 c.1481T>G(p. L494W)突变,确诊为 CAMT。患者接受了来自健康同胞供体的异体造血干细胞移植。由于长期接受免疫抑制药物治疗以及反复输血和血小板,患者出现了异体免疫反应和免疫紊乱。因此,我们对异基因造血干细胞移植后的 T 淋巴细胞再生情况进行了评估:结论:急性GvHD的成功治疗可防止病情恶化为慢性GvHD,同时通过增加Treg:Tcons比率实现延迟T细胞重建。
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The Reconstitution of T-cells after Allogeneic Hematopoietic Stem Cell Transplant in a Pediatric Patient with Congenital Amegakaryocytic Thrombocytopenia (CAMT).

Background: Congenital amegakaryocytic thrombocytopenia (CAMT) is a bone marrow failure syndrome with autosomal recessive inheritance characterized by the lack of megakaryocytes and thrombocytopenia. The cause of the disease is a mutation in the c-Mpl gene, which encodes the thrombopoietin (TPO) receptor. The main treatment for this genetic disorder is an allogeneic hematopoietic stem cell transplant (allo-HSCT). However, transplant-related mortality, development of acute and chronic graft-versushost disease (GvHD), and susceptibility to opportunistic infections are major barriers to transplantation. Delay in the reconstitution of T cells and imbalance in the regeneration of distinct functional CD4 and CD8 T-cell subsets mainly affect post-transplant complications. We report a case of CAMT, who developed acute GvHD but had no signs and symptoms of chronic GvHD following allo-HSCT.

Case presentation: At the age of four, she presented with petechiae and purpura. In laboratory investigations, pancytopenia without organomegaly, and cellularity less than 5% in bone marrow biopsy, were observed. A primary diagnosis of idiopathic aplastic anemia was made, and she was treated with prednisolone, cyclosporine, and anti-thymocyte globulin (ATG), which did not respond. Genetic analysis revealed the mutation c.1481T>G (p. L494W) in exon 10 of the c-Mpl gene, and the diagnosis of CAMT was confirmed. The patient underwent allo-HSCT from a healthy sibling donor. Alloimmunization reactions and immune disorders were present due to long-term treatment with immunosuppressive medications and repeated blood and platelet transfusions. Hence, the regeneration of T-lymphocytes after allo-HSCT was evaluated.

Conclusion: Successful treatment of acute GvHD prevented advancing the condition to chronic GvHD, and this was accompanied by delayed T-cell reconstitution through an increase in Treg:Tcons ratio.

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来源期刊
Endocrine, metabolic & immune disorders drug targets
Endocrine, metabolic & immune disorders drug targets ENDOCRINOLOGY & METABOLISMIMMUNOLOGY-IMMUNOLOGY
CiteScore
4.60
自引率
5.30%
发文量
217
期刊介绍: Aims & Scope This journal is devoted to timely reviews and original articles of experimental and clinical studies in the field of endocrine, metabolic, and immune disorders. Specific emphasis is placed on humoral and cellular targets for natural, synthetic, and genetically engineered drugs that enhance or impair endocrine, metabolic, and immune parameters and functions. Moreover, the topics related to effects of food components and/or nutraceuticals on the endocrine-metabolic-immune axis and on microbioma composition are welcome.
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