Laboratory of Molecular Immunology, National Institute of Allergy and Infectious Diseases.
Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases.
J Clin Invest. 2023 Oct 2;133(19):e164918. doi: 10.1172/JCI164918.
BACKGROUNDWarts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome is a primary immunodeficiency disorder caused by heterozygous gain-of-function CXCR4 mutations. Myelokathexis is a kind of neutropenia caused by neutrophil retention in bone marrow and in WHIM syndrome is associated with lymphopenia and monocytopenia. The CXCR4 antagonist plerixafor mobilizes leukocytes to the blood; however, its safety and efficacy in WHIM syndrome are undefined.METHODSIn this investigator-initiated, single-center, quadruple-masked phase III crossover trial, we compared the total infection severity score (TISS) as the primary endpoint in an intent-to-treat manner in 19 patients with WHIM who each received 12 months treatment with plerixafor and 12 months treatment with granulocyte CSF (G-CSF, the standard of care for severe congenital neutropenia). The treatment order was randomized for each patient.RESULTSPlerixafor was nonsuperior to G-CSF for TISS (P = 0.54). In exploratory endpoints, plerixafor was noninferior to G-CSF for maintaining neutrophil counts of more than 500 cells/μL (P = 0.023) and was superior to G-CSF for maintaining lymphocyte counts above 1,000 cells/μL (P < 0.0001). Complete regression of a subset of large wart areas occurred on plerixafor in 5 of 7 patients with major wart burdens at baseline. Transient rash occurred on plerixafor, and bone pain was more common on G-CSF. There were no significant differences in drug preference or quality of life or the incidence of drug failure or serious adverse events.CONCLUSIONPlerixafor was not superior to G-CSF in patients with WHIM for TISS, the primary endpoint. Together with wart regression and hematologic improvement, the infection severity results support continued study of plerixafor as a potential treatment for WHIM syndrome.TRIAL REGISTRATIONClinicaltrials.gov NCT02231879.FUNDINGThis study was funded by the Division of Intramural Research, National Institute of Allergy and Infectious Diseases.
疣、低丙种球蛋白血症、感染和骨髓嗜中性粒细胞滞留(WHIM)综合征是一种由 CXCR4 杂合获得性功能突变引起的原发性免疫缺陷病。骨髓嗜中性粒细胞滞留是一种中性粒细胞在骨髓中滞留引起的中性粒细胞减少症,而 WHIM 综合征与淋巴细胞减少症和单核细胞减少症有关。CXCR4 拮抗剂培利昔单抗将白细胞动员到血液中;然而,其在 WHIM 综合征中的安全性和疗效尚未确定。
在这项由研究人员发起的、单中心、四重盲、三期交叉试验中,我们以意向治疗的方式比较了 19 名 WHIM 患者的总感染严重程度评分(TISS)作为主要终点,每位患者分别接受 12 个月的培利昔单抗治疗和 12 个月的粒细胞集落刺激因子(G-CSF,严重先天性中性粒细胞减少症的标准治疗)治疗。每位患者的治疗顺序是随机的。
培利昔单抗在 TISS 方面不比 G-CSF 优越(P=0.54)。在探索性终点方面,培利昔单抗在维持中性粒细胞计数高于 500 个/μL(P=0.023)方面与 G-CSF 相当,在维持淋巴细胞计数高于 1000 个/μL(P<0.0001)方面优于 G-CSF。在基线时大疣负担较大的 7 名患者中,有 5 名患者的一部分大疣区出现完全消退。培利昔单抗治疗后出现短暂皮疹,G-CSF 治疗后骨痛更常见。药物偏好、生活质量或药物失败或严重不良事件的发生率无显著差异。
在 WHIM 患者中,培利昔单抗在 TISS 方面并不优于 G-CSF,这是主要终点。与疣消退和血液学改善一起,感染严重程度的结果支持继续研究培利昔单抗作为 WHIM 综合征的潜在治疗方法。
Clinicaltrials.gov NCT02231879。
本研究由国家过敏和传染病研究所内部研究司资助。