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通过对慢性肉芽肿病患者的粒细胞进行 mRNA 转染来纠正 NADPH 氧化酶。

NADPH oxidase correction by mRNA transfection of apheresis granulocytes in chronic granulomatous disease.

机构信息

Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.

CELLSCRIPT, LLC, Madison, WI.

出版信息

Blood Adv. 2020 Dec 8;4(23):5976-5987. doi: 10.1182/bloodadvances.2020003224.

Abstract

Granulocytes from patients with chronic granulomatous disease (CGD) have dysfunctional phagocyte reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase that fails to generate sufficient antimicrobial reactive oxidative species. CGD patients with severe persistent fungal or bacterial infection who do not respond to antibiotic therapy may be given apheresis-derived allogeneic granulocyte transfusions from healthy volunteers to improve clearance of intractable infections. Allogeneic granulocyte donors are not HLA matched, so patients who receive the donor granulocyte products may develop anti-HLA alloimmunity. This not only precludes future use of allogeneic granulocytes in an alloimmunized CGD recipient, but increases the risk of graft failure of those recipients who go on to need an allogeneic bone marrow transplant. Here, we provide the first demonstration of efficient functional restoration of CGD patient apheresis granulocytes by messenger RNA (mRNA) electroporation using a scalable, Good Manufacturing Practice-compliant system to restore protein expression and NADPH oxidase function. Dose-escalating clinical-scale in vivo studies in a nonhuman primate model verify the feasibility, safety, and persistence in peripheral blood of infusions of mRNA-transfected autologous granulocyte-enriched apheresis cells, supporting this novel therapeutic approach as a potential nonalloimmunizing adjunct treatment of intractable infections in CGD patients.

摘要

慢性肉芽肿病 (CGD) 患者的粒细胞吞噬细胞还原型烟酰胺腺嘌呤二核苷酸磷酸 (NADPH) 氧化酶功能失调,无法产生足够的抗菌反应性氧化物质。对严重持续性真菌感染或细菌感染且对抗生素治疗无反应的 CGD 患者,可给予来自健康志愿者的异体粒细胞单采输注,以改善难治性感染的清除。异体粒细胞供者与 HLA 不匹配,因此接受供者粒细胞产品的患者可能会产生抗 HLA 同种异体免疫。这不仅排除了在同种免疫 CGD 受者中再次使用异体粒细胞的可能性,而且增加了那些需要同种异体骨髓移植的受者发生移植物衰竭的风险。在这里,我们首次通过使用可扩展的符合良好生产规范的系统进行信使 RNA(mRNA)电穿孔,展示了对 CGD 患者单采粒细胞进行有效功能恢复的方法,该系统可恢复蛋白质表达和 NADPH 氧化酶功能。在非人类灵长类动物模型中进行的剂量递增临床规模体内研究验证了输注经 mRNA 转染的自体富含粒细胞的单采细胞的可行性、安全性和外周血持久性,支持这种新的治疗方法作为 CGD 患者难治性感染的潜在非同种免疫辅助治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f4d/7724899/7ec5766ecc27/advancesADV2020003224absf1.jpg

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