Clinical Use of ZSCAN4 for Telomere Elongation in Hematopoietic Stem Cells.

NEJM evidence Pub Date : 2025-03-01 Epub Date: 2025-02-25 DOI:10.1056/EVIDoa2400252
Kasiani C Myers, Stella M Davies, Carolyn Lutzko, Robin Wahle, David D Grier, Geraldine Aubert, Kevin Norris, Duncan M Baird, Minako Koga, Akihiro C Ko, Tomokazu Amano, Misa Amano, Hong Yu, Minoru S H Ko
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Abstract

Background: Extremely short telomeres in patients with dyskeratosis congenita and related telomere biology disorders (TBDs) lead to premature cellular senescence and bone marrow failure. Zinc finger and SCAN domain-containing 4 (ZSCAN4) elongates telomeres by recombination.

Methods: We report a clinical study in which EXG34217, the term given for autologous CD34+ hematopoietic stem cells from patients with TBD exposed to a temperature-sensitive Sendai virus vector encoding human ZSCAN4 at 33°C for 24 hours, was infused into patients without preconditioning.

Results: Four patients were enrolled; two experienced successful CD34+ mobilization during the second mobilization attempt and underwent apheresis and EXG34217 infusion, with follow-up of 5 and 24 months (both ongoing). We observed telomere elongation (1.06- to 1.34-fold) in CD34+ cells ex vivo. In one patient, the treatment was associated with a change in the mean absolute neutrophil count (ANC) from 1.78×103 to 3.18×103 cells/μl; the lymphocyte subpopulation telomere length changed from 3.6 to 6.7 kb (50th percentile for age). In the other patient, the treatment was associated with a change in the lowest ANC from 0.6×103/μl to 1.2×103/μl; this has occurred in 5 months without the patient receiving prior intermittent low-dose granulocyte-colony-stimulating factor injections. During mobilization, all patients experienced mild to moderate bone pain or pain after line replacement, and one patient had a blood infection associated with fever and hypoxemia. After EXG34217 infusion, no acute safety issues were noted; in one patient mild to moderate long-term cardiac and pulmonary adverse events were noted; these were similar to symptoms of the patient's underlying conditions.

Conclusions: Although definitive conclusions cannot be drawn from the two EXG34217-treated patients, these results warrant further investigation of CD34+ cells exposed to ZSCAN4 for treating TBDs. (Funded by Elixirgen Therapeutics; ClinicalTrials.gov number, NCT04211714.).

ZSCAN4检测造血干细胞端粒伸长的临床应用
背景:先天性角化不良患者的端粒极短及相关的端粒生物学障碍(tbd)导致细胞过早衰老和骨髓衰竭。锌指和含扫描结构域4 (ZSCAN4)通过重组延长端粒。方法:我们报告了一项临床研究,将EXG34217 (TBD患者的自体CD34+造血干细胞的术语)在33°C下暴露于编码人类ZSCAN4的温度敏感的仙台病毒载体24小时,在没有预处理的情况下输注到患者体内。结果:入组4例患者;2例在第二次动员尝试中成功动员CD34+,并进行了分离和EXG34217输注,随访5个月和24个月(均在进行中)。我们在体外观察到CD34+细胞的端粒伸长(1.06- 1.34倍)。在一名患者中,治疗与平均绝对中性粒细胞计数(ANC)从1.78×103到3.18×103细胞/μl的变化有关;淋巴细胞亚群端粒长度从3.6 KB变化到6.7 KB(年龄的第50百分位数)。在另一名患者中,治疗与最低ANC从0.6×103/μl变化到1.2×103/μl相关;这是在5个月内发生的,患者之前没有接受间歇性低剂量粒细胞集落刺激因子注射。在活动期间,所有患者均出现轻度至中度骨痛或换线后疼痛,1例患者出现与发热和低氧血症相关的血液感染。EXG34217输注后,未发现急性安全性问题;1例患者出现轻度至中度长期心脏和肺部不良事件;这些症状与患者的潜在疾病相似。结论:虽然不能从两例exg34217治疗的患者中得出明确的结论,但这些结果值得进一步研究暴露于ZSCAN4的CD34+细胞治疗TBDs。(由Elixirgen Therapeutics资助;ClinicalTrials.gov号码:NCT04211714)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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