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范可尼贫血患儿免疫功能受损。

Impaired immune function in children with Fanconi anaemia.

机构信息

Divisions of Bone Marrow Transplant and Immune Deficiency, Department of Pediatrics, Cincinnati Children's Hospital and Medical Center, Cincinnati, OH 45229, USA.

出版信息

Br J Haematol. 2011 Jul;154(2):234-40. doi: 10.1111/j.1365-2141.2011.08721.x. Epub 2011 May 4.

DOI:10.1111/j.1365-2141.2011.08721.x
PMID:21542827
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5922775/
Abstract

Fanconi anaemia is an autosomal recessive or X-linked disease characterized by progressive bone marrow failure, variable congenital abnormalities and a predisposition to malignancy. Reports of immune function in this population are limited, and include only specific areas of immune performance, showing variable defects. We report a cross-sectional immunological assessment in 10 children with FA. Absolute numbers of B cells and natural killer (NK) cells were reduced compared to controls (P = 0·048 and P = 0·0002, respectively), while absolute number of T cells were within normal range. Perforin and granzyme content of NK cells was reduced (P < 0·00001 and P = 0·0057, respectively) along with the NK cell cytotoxicity (P < 0·001). Antigen proliferation in response to tetanus was decreased (P = 0·008) while responses to candida and phytohaemagglutinin were not. Cytotoxic T cell function was also reduced (P < 0·0001). Immunoglobulin G levels were normal in those evaluated. Our series represents the first attempt at a comprehensive quantitative and functional evaluation of immune function in this rare group of patients and demonstrates a significant deficit in the NK cell compartment, a novel quantitative B cell defect, along with abnormal cytotoxic function. These findings may be especially relevant in this patient population with known predisposition to DNA damage and malignancy.

摘要

范可尼贫血是一种常染色体隐性或 X 连锁疾病,其特征为进行性骨髓衰竭、多种先天性异常以及恶性肿瘤易感性。该人群的免疫功能报告有限,仅包括免疫功能的特定领域,显示出不同的缺陷。我们报告了 10 例 FA 患儿的横断面免疫学评估。与对照组相比,B 细胞和自然杀伤 (NK) 细胞的绝对数量减少(P = 0.048 和 P = 0.0002),而 T 细胞的绝对数量在正常范围内。NK 细胞的穿孔素和颗粒酶含量减少(P < 0.00001 和 P = 0.0057),同时 NK 细胞的细胞毒性降低(P < 0.001)。破伤风抗原增殖反应降低(P = 0.008),而对白念珠菌和植物血凝素的反应不受影响。细胞毒性 T 细胞功能也降低(P < 0.0001)。评估的 IgG 水平正常。我们的系列代表了首次对这组罕见患者的免疫功能进行全面定量和功能评估,表明 NK 细胞区室存在显著缺陷,存在新型定量 B 细胞缺陷以及异常的细胞毒性功能。这些发现对于已知具有 DNA 损伤和恶性肿瘤易感性的患者群体可能特别重要。

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本文引用的文献

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Dyskeratosis congenita: a combined immunodeficiency with broad clinical spectrum--a single-center pediatric experience.先天性角化不良症:一种具有广泛临床表型的联合免疫缺陷病——单中心儿科经验。
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Head and neck squamous cell carcinoma in 13 patients with Fanconi anemia after hematopoietic stem cell transplantation.13例范可尼贫血患者造血干细胞移植后发生的头颈部鳞状细胞癌
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Nat Rev Genet. 2007 Oct;8(10):735-48. doi: 10.1038/nrg2159. Epub 2007 Sep 4.
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Molecular pathogenesis of Fanconi anemia: recent progress.范可尼贫血的分子发病机制:最新进展
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Phase 1 study of HPV16-specific immunotherapy with E6E7 fusion protein and ISCOMATRIX adjuvant in women with cervical intraepithelial neoplasia.E6E7融合蛋白联合免疫刺激复合物(ISCOMATRIX)佐剂用于宫颈上皮内瘤变女性的HPV16特异性免疫疗法的1期研究。
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