Dixit Rashmi, Herz Jenny, Dalton Richard, Booy Robert
The Children's Hospital, Westmead, Sydney, Australia.
Biointelect, Sydney, Australia.
Vaccine. 2016 Feb 24;34(9):1152-61. doi: 10.1016/j.vaccine.2016.01.016. Epub 2016 Jan 20.
Passive immunotherapy using polyclonal antibodies (immunoglobulins) has been used for over a century in the treatment and post-exposure prophylaxis of various infections and toxins. Heterologous polyclonal antibodies are obtained from animals hyperimmunised with a pathogen or toxin.
The aims of this review are to examine the history of animal polyclonal antibody therapy use, their development into safe and effective products and the potential application to humans for emerging and neglected infectious diseases.
A literature search of OVID Medline and OVID Embase databases was undertaken to identify articles on the safety, efficacy and ongoing development of polyclonal antibodies. The search contained database-specific MeSH and EMTREE terms in combination with pertinent text-words: polyclonal antibodies and rare/neglected diseases, antivenins, immunoglobulins, serum sickness, anaphylaxis, drug safety, post marketing surveillance, rabies, human influenza, Dengue, West Nile, Nipah, Hendra, Marburg, MERS, Hemorrhagic Fever Virus, and Crimean-Congo. No language limits were applied. The final search was completed on 20.06.2015. Of 1960 articles, title searches excluded many irrelevant articles, yielding 303 articles read in full. Of these, 179 are referenced in this study.
Serum therapy was first used in the 1890s against diphtheria. Early preparation techniques yielded products contaminated with reactogenic animal proteins. The introduction of enzymatic digestion, and purification techniques substantially improved their safety profile. The removal of the Fc fragment of antibodies further reduces hypersensitivity reactions. Clinical studies have demonstrated the efficacy of polyclonal antibodies against various infections, toxins and venoms. Products are being developed against infections for which prophylactic and therapeutic options are currently limited, such as avian influenza, Ebola and other zoonotic viruses.
Polyclonal antibodies have been successfully applied to rabies, envenomation and intoxication. Polyclonal production provides an exciting opportunity to revolutionise the prognosis of both longstanding neglected tropical diseases as well as emerging infectious threats to humans.
使用多克隆抗体(免疫球蛋白)的被动免疫疗法已用于各种感染和毒素的治疗及暴露后预防达一个多世纪。异源多克隆抗体是从用病原体或毒素进行超免疫的动物获得的。
本综述旨在研究动物多克隆抗体治疗的使用历史、其发展为安全有效的产品以及在新兴和被忽视的传染病人类应用方面的潜在应用。
对OVID Medline和OVID Embase数据库进行文献检索,以识别关于多克隆抗体安全性、有效性和持续发展的文章。检索包含特定于数据库的医学主题词(MeSH)和EMTREE术语以及相关文本词:多克隆抗体和罕见/被忽视疾病、抗蛇毒血清、免疫球蛋白、血清病、过敏反应、药物安全性、上市后监测、狂犬病、人类流感、登革热、西尼罗河病毒、尼帕病毒、亨德拉病毒、马尔堡病毒、中东呼吸综合征、出血热病毒和克里米亚-刚果出血热病毒。未设语言限制。最终检索于2015年6月20日完成。在1960篇文章中,通过标题检索排除了许多不相关的文章,得到303篇全文阅读文章。其中,本研究引用了179篇。
血清疗法于19世纪90年代首次用于治疗白喉。早期制备技术产生的产品被具有反应原性的动物蛋白污染。酶消化和纯化技术的引入显著改善了其安全性。去除抗体的Fc片段进一步降低了超敏反应。临床研究已证明多克隆抗体对各种感染、毒素和毒液有效。正在开发针对目前预防和治疗选择有限的感染(如禽流感、埃博拉病毒和其他人畜共患病毒)的产品。
多克隆抗体已成功应用于狂犬病、蛇咬伤中毒和其他中毒情况。多克隆生产为彻底改变长期被忽视的热带疾病以及对人类新出现感染威胁的预后提供了一个令人兴奋的机会。