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人类垂体生长激素接受者中蛋白质错误折叠引发阿尔茨海默病的发展历程

The Unfolding Story of Protein Misfolding Causing Alzheimer Disease in Recipients of Human Pituitary Growth Hormone.

作者信息

Graber Evan G, Hosseini Sayed M Hadi, Wilson Darrell M, Rogol Alan D

机构信息

Division of Endocrinology, Department of Pediatrics Nemours Children's Health, Wilmington, DL 19803, USA, and Sidney Kimmel Medical College, Philadelphia, PA 19107, USA.

Computational Brain Research and Intervention (C-Brain) Laboratory, Department of Psychiatry and Behavioral Science, Stanford University, Palo Alto, CA 94304, USA.

出版信息

J Endocr Soc. 2025 Feb 17;9(3):bvaf029. doi: 10.1210/jendso/bvaf029. eCollection 2025 Feb 4.

Abstract

Human growth hormone (hGH) has been in clinical use for children with GH deficiency (GHD) since the late 1950s. The original formulations were considered very safe with few adverse events reported. That changed remarkably in 1985 when the first patients with GHD, who had been treated with cadaveric hGH, were diagnosed with Creutzfeldt-Jakob disease (CJD). Fortunately, that same year a robust supply of recombinant hGH was released to the market whose adverse event profile did not include CJD. Patients who had received National Hormone and Pituitary Program hGH have been continuously followed since 1985. It is clear that prions are causative for CJD. Within the last 10 years there have been reports that similar preparations of cadaveric hGH may have been contaminated with amyloid β (Aβ) protein, a material that is related to Alzheimer disease. Eight patients in the United Kingdom, who had received cadaveric hGH extracted in an analogous manner to that in the United States, had conditions compatible with Alzheimer disease, although they did not fulfill all of the requirements for that diagnosis. In this report we discuss the findings of both CJD and Alzheimer disease, especially as they relate to a possible transmission of the diseases by prions and Aβ protein.

摘要

自20世纪50年代末以来,人生长激素(hGH)一直用于治疗生长激素缺乏症(GHD)患儿。最初的制剂被认为非常安全,报告的不良事件很少。1985年情况发生了显著变化,当时首批接受尸体来源hGH治疗的GHD患者被诊断出患有克雅氏病(CJD)。幸运的是,同年一种大量供应的重组hGH投放市场,其不良事件不包括CJD。自1985年以来,接受国家激素和垂体项目hGH治疗的患者一直在接受持续随访。很明显,朊病毒是CJD的病因。在过去10年里,有报告称类似的尸体来源hGH制剂可能被淀粉样β(Aβ)蛋白污染,Aβ蛋白是一种与阿尔茨海默病相关的物质。在英国,8名接受了与美国类似方式提取的尸体来源hGH治疗的患者,其病情符合阿尔茨海默病,尽管他们并未满足该诊断的所有要求。在本报告中,我们讨论了CJD和阿尔茨海默病的研究结果,尤其是它们与朊病毒和Aβ蛋白可能传播疾病的关系。

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