Di Mascio Michele
AIDS Imaging Research Section (Integrated Research Facility)/ Mathematical Biology Section (Biostatistics Research Branch), Division of Clinical Research, National Institute of Allergy and Infectious Diseases, The National Institutes of Health, Rockville, MD, 20852, USA.
Cancer Stud Ther. 2020 Jul;5(2). Epub 2020 Jul 19.
The success of an antiviral drug depends on its potency to neutralize the virus in vitro and its ability after administration in vivo to reach the anatomic compartments that fuel viral dissemination in the body. For instance, remdesivir, a potent SARS-CoV-2 antiviral drug based on studies in vitro, if administered orally would be poorly effective because low drug levels would reach the lungs due to its high first pass destruction in the liver. This is the reason remdesivir can only be administered intravenously, a requirement that clearly limits its use as a prophylactic agent for COVID-19, although novel formulations for its easier administration are under development. Whether an antiviral prophylaxis could further control or even stop the COVID-19 epidemic in synergy with other non-pharmacological based mitigation strategies is today unknown. Since the mid-1960s, pharmacologists have investigated the use of lipid-based nanoparticles for efficient delivery of antivirals to tissues, for example by transforming the route of administration from intravenous to oral, subcutaneous or aerosol administrations. These novel encapsulation strategies have also the potential to maintain high levels of the antiviral drugs in tissues, with reduced dose frequency compared to the non-encapsulated drug. Several lipid-based nanoparticles are today approved by the US Food and Drug Administration or being tested in clinical studies with favorable toxicity profiles. Nonhuman primate models of coronavirus infection offer unique platforms to accelerate the search for SARS-CoV-2 antiviral prophylaxis. Paradigms, to corroborate this claim, are borrowed from nonhuman primate research studies, some of which had a profound impact on global public health in the specific setting of the AIDS pandemic. Sharing information from nonhuman primate research programs, invoking principles of scientific transparency and bioethics similar to those universally agreed for human studies, would also likely significantly help our collective fight (as the human species) against this public health emergency.
抗病毒药物的成功取决于其在体外中和病毒的效力,以及给药后在体内到达为病毒在体内传播提供“燃料”的解剖学部位的能力。例如,瑞德西韦是一种基于体外研究的强效抗SARS-CoV-2病毒药物,如果口服,效果会很差,因为由于其在肝脏中的首过效应很高,到达肺部的药物水平会很低。这就是瑞德西韦只能静脉给药的原因,这一要求显然限制了它作为COVID-19预防药物的使用,尽管正在开发更易于给药的新剂型。抗病毒预防措施能否与其他基于非药物的缓解策略协同作用,进一步控制甚至阻止COVID-19疫情,目前尚不清楚。自20世纪60年代中期以来,药理学家一直在研究使用脂质纳米颗粒将抗病毒药物高效递送至组织,例如通过将给药途径从静脉给药转变为口服、皮下或气溶胶给药。这些新型封装策略还具有在组织中维持高浓度抗病毒药物的潜力,与未封装的药物相比,给药频率降低。如今,几种脂质纳米颗粒已获得美国食品药品监督管理局批准,或正在进行毒性特征良好的临床研究测试。冠状病毒感染的非人灵长类动物模型为加速寻找抗SARS-CoV-2病毒预防措施提供了独特的平台。为证实这一说法,可借鉴非人灵长类动物研究中的范例,其中一些在艾滋病大流行的特定背景下对全球公共卫生产生了深远影响。分享非人灵长类动物研究项目的信息,援引与人类研究普遍认可的科学透明度和生物伦理原则相似的原则,也可能会极大地帮助我们(作为人类)共同抗击这一公共卫生紧急事件。