Karnaukhova E, Ophir Y, Golding B
Division of Hematology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892, USA.
Amino Acids. 2006 Jun;30(4):317-32. doi: 10.1007/s00726-005-0324-4. Epub 2006 May 26.
Human alpha-1-proteinase inhibitor is a well-characterized protease inhibitor with a wide spectrum of anti-protease activity. Its major physiological role is inhibition of neutrophil elastase in the lungs, and its deficiency is associated with progressive ultimately fatal emphysema. Currently in the US, only plasma-derived human alpha-1-proteinase inhibitor is available for augmentation therapy, which appears to be insufficient to meet the anticipated clinical demand. Moreover, despite effective viral clearance steps in the manufacturing process, the potential risk of contamination with new and unknown pathogens still exists. In response, multiple efforts to develop recombinant versions of human alpha-1-proteinase inhibitor, as an alternative to the plasma-derived protein, have been reported. Over the last two decades, various systems have been used to express the human gene for alpha-1-proteinase inhibitor. This paper reviews the recombinant versions of human alpha-1-proteinase inhibitor produced in various hosts, considers current major safety and efficacy issues regarding recombinant glycoproteins as potential therapeutics, and the factors that are impeding progress in this area(1).
人α1-抗胰蛋白酶是一种特性明确的蛋白酶抑制剂,具有广泛的抗蛋白酶活性。其主要生理作用是抑制肺部的中性粒细胞弹性蛋白酶,其缺乏与进行性最终致命的肺气肿有关。目前在美国,仅血浆源性人α1-抗胰蛋白酶可用于补充治疗,但这似乎不足以满足预期的临床需求。此外,尽管在制造过程中有有效的病毒清除步骤,但仍存在被新的和未知病原体污染的潜在风险。作为回应,已有多项开发重组人α1-抗胰蛋白酶版本的努力被报道,以替代血浆源性蛋白。在过去二十年中,已使用各种系统来表达人α1-抗胰蛋白酶基因。本文综述了在各种宿主中产生的重组人α1-抗胰蛋白酶版本,考虑了关于重组糖蛋白作为潜在治疗药物的当前主要安全性和有效性问题,以及阻碍该领域进展的因素(1)。