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病例报告:粒细胞-巨噬细胞集落刺激因子沙格司亭未能挽救两名 JAGN1 突变严重先天性中性粒细胞减少症患者的中性粒细胞表型。

Case report: Granulocyte-macrophage colony-stimulating factor sargramostim did not rescue the neutrophil phenotype in two patients with JAGN1-mutant severe congenital neutropenia.

机构信息

Division of Pediatric Stem Cell Transplantation and Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Department of Pediatrics, University Medical Center Ulm, Ulm, Germany.

出版信息

Front Immunol. 2024 Sep 2;15:1373495. doi: 10.3389/fimmu.2024.1373495. eCollection 2024.

Abstract

BACKGROUND

Homozygous or compound heterozygous mutations in JAGN1 cause severe congenital neutropenia. JAGN1-mutant patients present with severe early-onset bacterial infections and most have been described as low-responders to recombinant granulocyte colony-stimulating factor (G-CSF) therapy. In a murine, hematopoietic JAGN1 knockout model, which displays susceptibility to Candida albicans infection in the absence of neutropenia, treatment with granulocyte-macrophage-CSF (GM-CSF) was able to restore the functional defect of neutrophils.

PATIENTS

We present two unrelated patients with biallelic JAGN1 mutations, who were both treated with subcutaneous GM-CSF (sargramostim) after treatment failure to G-CSF. The first patient was an 18-year-old pregnant woman who received GM-CSF at 12 weeks of gestation up to a dose of 10 µg/kg/d for 7 days. The second patient was a 5-month-old girl who received GM-CSF for a total of 9 days at a dose of up to 20 µg/kg/d. GM-CSF did not increase neutrophil counts in our patients. Treatment was stopped when neutrophil numbers declined further, no beneficial effect was noticed, and patients presented with infections. No adverse effects were observed in either patient and the fetus. Both patients ultimately underwent successful hematopoietic stem cell transplantation.

DISCUSSION

Both patients showed a high recurrence rate of severe infections on G-CSF treatment. GM-CSF therapy did not ameliorate the clinical phenotype, in contrast to the improvement of neutrophil function observed in the JAGN1 mouse model. No major additional extra-hematopoietic manifestations were evident in our patients.

CONCLUSION

In two unrelated patients, GM-CSF did not have any beneficial effect on neutrophil counts. Patients with JAGN1-mutant SCN with reduced G-CSF responsiveness and elevated infection rate should be evaluated early for stem cell transplantation.

摘要

背景

JAGN1 纯合或复合杂合突变可导致严重先天性中性粒细胞减少症。JAGN1 突变患者表现为严重的早发性细菌感染,大多数患者被描述为对重组粒细胞集落刺激因子(G-CSF)治疗反应不佳。在缺乏中性粒细胞减少症的情况下易感染白色念珠菌的造血 JAGN1 敲除小鼠模型中,粒细胞-巨噬细胞集落刺激因子(GM-CSF)治疗能够恢复中性粒细胞的功能缺陷。

患者

我们介绍了两例具有双等位基因 JAGN1 突变的无关患者,他们在 G-CSF 治疗失败后均接受了皮下 GM-CSF(沙格司亭)治疗。第一例患者是一名 18 岁的孕妇,在妊娠 12 周时接受 GM-CSF 治疗,剂量为 10µg/kg/d,持续 7 天。第二例患者是一名 5 个月大的女孩,共接受 GM-CSF 治疗 9 天,剂量高达 20µg/kg/d。GM-CSF 并未增加我们患者的中性粒细胞计数。当中性粒细胞数量进一步下降且未观察到有益效果且患者出现感染时,停止了治疗。两名患者均未出现不良反应,且胎儿正常。两名患者最终均成功进行了造血干细胞移植。

讨论

两名患者在 G-CSF 治疗时均表现出严重感染的高复发率。GM-CSF 治疗并未改善临床表型,与 JAGN1 小鼠模型中观察到的中性粒细胞功能改善相反。我们的患者没有明显的额外造血系统表现。

结论

在两名无关患者中,GM-CSF 对中性粒细胞计数没有任何有益作用。具有 JAGN1 突变的 SCN 且对 G-CSF 反应性降低和感染率升高的患者应尽早进行干细胞移植评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d02/11404322/d7c764ae968f/fimmu-15-1373495-g001.jpg

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