Child Neurology and Psychiatry Unit, ASST Spedali Civili Hospital, Brescia, Italy.
Clinical and Experimental Sciences Department, University of Brescia, c/o ASST Spedali Civili, 25123, Brescia, Italy.
Orphanet J Rare Dis. 2019 Feb 28;14(1):61. doi: 10.1186/s13023-019-1030-8.
Warts Hypogammaglobulinemia Immunodeficiency Myelokathexis (WHIM) syndrome is a primary immunodeficiency characterized by recurrent bacterial infections, severe chronic neutropenia, with lymphopenia, monocytopenia and myelokathexis which is caused by heterozygous gain of functions mutations of the CXC chemokine receptor 4 (CXCR4). WHIM patients display an increased incidence of non-hematopoietic conditions, such as congenital heart disease suggesting that abnormal CXCR4 may put these patients at increased risk of congenital anomalies. Studies conducted on CXCR4 and SDF-1-deficient mice have demonstrated the role of CXCR4 signaling in neuronal cell migration and brain development. In particular, CXCR4 conditional knockout mice display abnormal cerebellar morphology and poor coordination and balance on motor testing.
In order to evaluate a possible neurological involvement in WHIM syndrome subjects, we performed neurological examination, including International Cooperative Ataxia Rating Scale, cognitive and psychopathological assessment and brain Magnetic Resonance Imaging (MRI) in 6 WHIM patients (age range 8-51 years) with typical gain of functions mutations of CXCR4 (R334X or G336X). In three cases (P3, P5, P6) neurological evaluation revealed fine and global motor coordination disorders, balance disturbances, mild limb ataxia and excessive talkativeness. Brain MRI showed an abnormal orientation of the cerebellar folia involving bilaterally the gracilis and biventer lobules together with the tonsils in four subjects (P3, P4, P5, P6). The neuropsychiatric evaluation showed increased risk of internalizing and/or externalizing problems in four patients (P2, P3, P4, P6).
Taken together, these observations suggest CXCR4 gain of function mutations can be associated with cerebellar malformation, mild neuromotor and psychopathological dysfunction in WHIM patients.
疣、低丙种球蛋白血症、免疫缺陷、骨髓嗜中性粒细胞减少症(WHIM)综合征是一种以复发性细菌感染、严重慢性中性粒细胞减少症为特征的原发性免疫缺陷病,伴有淋巴细胞减少、单核细胞减少和骨髓嗜中性粒细胞减少,这是由 CXC 趋化因子受体 4(CXCR4)的杂合获得性功能突变引起的。WHIM 患者表现出非造血疾病的发生率增加,如先天性心脏病,这表明异常的 CXCR4 可能使这些患者患先天性异常的风险增加。对 CXCR4 和 SDF-1 缺陷型小鼠的研究表明,CXCR4 信号在神经元细胞迁移和大脑发育中起作用。特别是,CXCR4 条件性敲除小鼠显示小脑形态异常和运动测试中协调和平衡不良。
为了评估 WHIM 综合征患者中可能存在的神经病变,我们对 6 名具有典型 CXCR4 获得性功能突变(R334X 或 G336X)的 WHIM 患者(年龄范围 8-51 岁)进行了神经学检查,包括国际合作共济失调评分、认知和心理病理评估以及大脑磁共振成像(MRI)。在 3 例(P3、P5、P6)中,神经学评估显示精细和全身运动协调障碍、平衡障碍、轻度肢体共济失调和过度健谈。MRI 显示 4 名患者(P3、P4、P5、P6)双侧小脑叶片方向异常,涉及 gracilis 和 biventer 叶以及扁桃体。神经心理学评估显示 4 名患者(P2、P3、P4、P6)存在内化和/或外化问题的风险增加。
综上所述,这些观察结果表明,CXCR4 获得性功能突变可与 WHIM 患者的小脑畸形、轻度神经运动和心理病理功能障碍相关。