Department of Pathology Johns Hopkins University School of Medicine.
Department of Molecular Microbiology, Johns Hopkins Bloomberg School of Public Health.
mBio. 2022 Dec 20;13(6):e0286222. doi: 10.1128/mbio.02862-22. Epub 2022 Oct 31.
Monkeypox, a zoonosis caused by the orthopox monkeypox virus (MPXV) that is endemic to Central and West Africa, was previously linked to sporadic outbreaks and rare, travel-associated cases. An outbreak of monkeypox in 2022 has spurred a public health emergency of international concern, and this outbreak is unprecedented in terms of its scale and epidemiology. The outbreak has been focused overwhelmingly in men who have sex with men; however, the trajectory of the outbreak remains uncertain, with spread now being reported in women and children. The mortality has been low (<1%), yet the morbidity is high. Vaccines and oral antiviral agents that have been developed to protect against smallpox are available for use against monkeypox. However, the supply has been unable to match the demand during the outbreak. Passive antibody-based therapies, such as hyperimmune globulin (HIG), monoclonal antibodies, and convalescent plasma (CP), have been used against a diverse array of infectious diseases, culminating in their extensive use during the COVID-19 pandemic. Passive antibody-based therapies could play a role in the treatment of monkeypox, either as a temporizing role amid a shortfall in vaccines and antivirals or a complementary role to direct-acting antivirals. Drawing on the collective experience to date, there are regulatory, administrative, and logistical challenges to the implementation of antibody-based therapies. Their efficacy is contingent upon early administration and the presence of high-titer antibodies against the targeted pathogen. Research is needed to address questions pertaining to how to qualify HIG and CP and to determine their relative efficacy against MPXV, compared to antecedent therapies and preventative strategies. Monkeypox is an infection caused by the monkeypox virus (MPXV). The clinical findings in monkeypox include fever and rash. Historically, most cases of human monkeypox were reported in Africa. This changed in 2022, with a massive escalation in the number of cases across multiple countries, mainly affecting men who have sex with men. Although vaccines and oral antiviral medications are available for the treatment of monkeypox, their supply has been overwhelmed by the unprecedented number of cases. Antibody-based therapies (ABTs) have long been used to treat infectious diseases. They are produced in a laboratory or from plasma that has been collected from individuals who have recovered from an infection or have been vaccinated against that infection (in this case, monkeypox). ABTs could play a role in the treatment of monkeypox, either while awaiting oral medications or as a complementary treatment for patients that are at risk of severe disease.
猴痘是一种由正痘猴痘病毒(MPXV)引起的人畜共患病,流行于中非和西非。此前,它与零星暴发和罕见的、与旅行相关的病例有关。2022 年的一次猴痘暴发引发了国际关注的公共卫生紧急事件,这次暴发在规模和流行病学方面都是前所未有的。暴发主要集中在与男性发生性关系的男性中;然而,疫情的轨迹仍不确定,现在已报告女性和儿童中出现病例。死亡率较低(<1%),但发病率较高。已开发出用于预防天花的疫苗和口服抗病毒药物可用于预防猴痘。然而,在疫情期间,供应无法满足需求。被动抗体疗法,如特免球蛋白(HIG)、单克隆抗体和恢复期血浆(CP),已被用于治疗多种传染病,最终在 COVID-19 大流行期间广泛使用。被动抗体疗法可能在猴痘的治疗中发挥作用,无论是在疫苗和抗病毒药物短缺时作为临时治疗,还是作为直接作用抗病毒药物的补充治疗。根据迄今为止的集体经验,实施抗体疗法存在监管、行政和后勤方面的挑战。它们的疗效取决于早期给药以及针对目标病原体的高滴度抗体的存在。需要研究如何确定 HIG 和 CP 的资格以及确定它们相对于先前的治疗方法和预防策略对 MPXV 的相对疗效。
猴痘是由猴痘病毒(MPXV)引起的感染。猴痘的临床发现包括发热和皮疹。历史上,大多数人类猴痘病例报告发生在非洲。这种情况在 2022 年发生了变化,多个国家的病例数量急剧增加,主要影响与男性发生性关系的男性。虽然有疫苗和口服抗病毒药物可用于治疗猴痘,但由于前所未有的病例数量,供应已经不堪重负。抗体疗法(ABT)长期以来一直用于治疗传染病。它们是在实验室中生产的,或者是从已从感染中康复或已接种该感染疫苗的个体(在这种情况下,是猴痘)中收集的血浆中生产的。ABT 可以在治疗猴痘中发挥作用,无论是在等待口服药物期间,还是作为对有患严重疾病风险的患者的补充治疗。