Giri Neelam, Alter Blanche P, Penrose Keri, Falk Roni T, Pan Yuanji, Savage Sharon A, Williams Marcus, Kemp Troy J, Pinto Ligia A
Division of Cancer Epidemiology and Genetics, Clinical Genetics Branch, National Cancer Institute, National Institutes of Health, Rockville, Maryland.
Division of Infectious Diseases, Department of Medicine, Human Papillomavirus Immunology Laboratory, Leidos Biomedical Research, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Am J Hematol. 2015 Aug;90(8):702-8. doi: 10.1002/ajh.24046. Epub 2015 May 28.
Immune function abnormalities have been reported in patients with Fanconi anemia (FA), dyskeratosis congenita (DC) and, rarely, in Shwachman-Diamond syndrome (SDS), and Diamond-Blackfan anemia (DBA), but large systematic studies are lacking. We assessed immunological parameters in 118 patients with these syndromes and 202 unaffected relatives. We compared the results in patients with reference values, and with values in relatives after adjusting for age, sex, corticosteroid treatment, and severe bone marrow failure (BMF). Adult patients (≥18 years) with FA had significantly lower immunoglobulins (IgG, IgA and IgM), total lymphocytes, and CD4 T cells than reference values or adult relatives (P < 0.001); children with FA had normal values. Both children and adults with FA had lower B- and NK cells (P < 0.01) than relatives or reference values. Patients with DC had essentially normal immunoglobulins but lower total lymphocytes than reference values or relatives, and lower T-, B-, and NK-cells; these changes were more marked in children than adults (P < 0.01). Most patients with DBA and SDS had normal immunoglobulins and lymphocytes. Lymphoproliferative responses, serum cytokine levels, including tumor necrosis factor-α and interferon-γ, and cytokine levels in supernatants from phytohemagglutinin-stimulated cultures were similar across patient groups and relatives. Only patients with severe BMF, particularly those with FA and DC, had higher serum G-CSF and Flt3-ligand and lower RANTES levels compared with all other groups or relatives (P < 0.05). Overall, immune function abnormalities were seen mainly in adult patients with FA, which likely reflects their disease-related progression, and in children with DC, which may be a feature of early-onset severe disease phenotype.
范可尼贫血(FA)、先天性角化不良(DC)患者中曾有免疫功能异常的报道,而施-戴二氏综合征(SDS)和先天性纯红细胞再生障碍性贫血(DBA)患者中则鲜有此类报道,但目前尚缺乏大型系统性研究。我们评估了118例患有这些综合征的患者以及202名未受影响亲属的免疫学参数。我们将患者的结果与参考值进行了比较,并在对年龄、性别、皮质类固醇治疗和严重骨髓衰竭(BMF)进行校正后,与亲属的值进行了比较。成年(≥18岁)FA患者的免疫球蛋白(IgG、IgA和IgM)、总淋巴细胞和CD4 T细胞显著低于参考值或成年亲属(P < 0.001);FA儿童的值正常。FA儿童和成人的B细胞和NK细胞均低于亲属或参考值(P < 0.01)。DC患者的免疫球蛋白基本正常,但总淋巴细胞低于参考值或亲属,T细胞、B细胞和NK细胞也较低;这些变化在儿童中比在成人中更明显(P < 0.01)。大多数DBA和SDS患者的免疫球蛋白和淋巴细胞正常。各患者组和亲属的淋巴细胞增殖反应、血清细胞因子水平(包括肿瘤坏死因子-α和干扰素-γ)以及植物血凝素刺激培养上清液中的细胞因子水平相似。与所有其他组或亲属相比,只有严重BMF患者,特别是FA和DC患者,血清G-CSF和Flt3配体水平较高,RANTES水平较低(P < 0.05)。总体而言,免疫功能异常主要见于成年FA患者,这可能反映了其疾病相关进展,以及DC儿童患者,这可能是早发性严重疾病表型的一个特征。