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25例携带RMRP 70 A→G软骨毛发发育不全的阿米什患者的免疫和临床特征

Immunologic and clinical features of 25 Amish patients with RMRP 70 A-->G cartilage hair hypoplasia.

作者信息

Rider Nicholas L, Morton D Holmes, Puffenberger Erik, Hendrickson Christine L, Robinson Donna L, Strauss Kevin A

机构信息

Penn State Hershey Medical Center, Division of Allergy and Immunology, Hershey, PA 17033, USA.

出版信息

Clin Immunol. 2009 Apr;131(1):119-28. doi: 10.1016/j.clim.2008.11.001. Epub 2009 Jan 16.

Abstract

Cartilage-hair hypoplasia is a short limbed skeletal dysplasia associated with impairments in host-defense. To better understand the clinical heterogeneity of this disorder, we studied 25 Amish patients with homozygous mutations in RMRP (RMRP 70 A>G). Despite mutation homogeneity, eight (32%) patients had severe or recurrent infections, two (8%) of these children underwent bone-marrow transplantation for combined immunodeficiency, and the remainder were healthy. Features distinguishing patients who underwent bone marrow transplantation from others were shorter birth length, and lower serum IgG, undetectable serum IgA, and elevated circulating NK cells before 2 years of age. Irrespective of clinical phenotype, most patients had lymphopenia and reduced lymphocyte proliferation to mitogens in vitro. Our cohort analysis suggests that many patients with cartilage-hair hypoplasia are at risk for infection susceptibility particularly during the first 2 years of life. Gauging this risk is difficult, and thus careful monitoring of all patients with cartilage-hair hypoplasia is warranted.

摘要

软骨毛发发育不全是一种短肢型骨骼发育不良疾病,与宿主防御功能受损有关。为了更好地理解这种疾病的临床异质性,我们研究了25名患有RMRP纯合突变(RMRP 70 A>G)的阿米什患者。尽管突变具有同质性,但8名(32%)患者有严重或反复感染,其中2名(8%)儿童因联合免疫缺陷接受了骨髓移植,其余患者健康。接受骨髓移植的患者与其他患者的区别特征包括出生时身长较短,2岁前血清IgG较低、血清IgA检测不到以及循环NK细胞升高。无论临床表型如何,大多数患者都有淋巴细胞减少症,并且体外对有丝分裂原的淋巴细胞增殖反应降低。我们的队列分析表明,许多软骨毛发发育不全患者有感染易感性风险,尤其是在生命的头2年。评估这种风险很困难,因此有必要对所有软骨毛发发育不全患者进行仔细监测。

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