Youssef Jihad Georges, Bitar Mohammad Z, Zahiruddin Faisal, Al-Saadi Mukhtar, Elshawwaf Mahmoud, Yau Simon, Goodarzi Ahmad, Javitt Jonathan C
Houston Methodist Research Institute, Houston Methodist Hospital, Houston, TX.
Department of Academic Pulmonology, Houston Methodist Hospital, Houston, TX.
Crit Care Explor. 2022 Jan 5;4(1):e0607. doi: 10.1097/CCE.0000000000000607. eCollection 2022 Jan.
Aviptadil, a synthetic form of human vasoactive intestinal peptide, has entered clinical trials to treat critical coronavirus disease 2019 pneumonia with respiratory failure. Vasoactive intestinal peptide protects the lung against a broad array of injuries by binding to the vasoactive intestinal peptide receptor 1 receptor of alveolar type II cells, the cells that severe acute respiratory syndrome coronavirus 2 binds to. As the role of Aviptadil in treating pregnant patients with critical coronavirus disease 2019 pneumonia is unknown, the authors report successful treatment in such a patient who is ineligible for phase 3 trials of Aviptadil.
Under an open-label Food and Drug Administration-approved Expanded Access Protocol NCT04453839, a 32-year-old female patient Gravida 6 Para 4 at 27-week gestation, body mass index 42.5 kg/m, admitted to the ICU of a quaternary care hospital with critical coronavirus disease 2019 was treated in January 2021 and followed for 4 months post-ICU admission. Standard of care included remdesivir, methylprednisolone, enoxaparin, and inhaled epoprostenol. In addition, the patient received three successive 12-hour IV infusions of Aviptadil at 50/100/150 pmol/kg/hr escalating doses, per randomized clinical trial NCT04311697. Human subjects' protection was overseen by the Institutional Review Board of the Houston Methodist Hospital. The patient was enrolled in the treatment and was given informed consent approved by the Food and Drug Administration and the Institutional Review Board. Data on the patient was incorporated based on her consent for de-identified data to be used in research given at the time of hospital admission in a manner approved by the Institutional Review Board (PRO00025607). Baseline inflammatory markers, arterial blood gases, radiologic imaging, oxygen requirements, Pao/Fio, continuous fetal monitoring at baseline, throughout the patient's treatment with the investigational drug, and throughout the patient's hospital course.
The rapid clinical improvement seen in this patient treated with IV vasoactive intestinal peptide is consistent with the theory that vasoactive intestinal peptide protects the alveolar type II cell, ameliorates cytokine storm, and improves oxygenation in acute lung injury. This specific role of vasoactive intestinal peptide in the lung may be vital to combating the lethal effects of severe acute respiratory syndrome coronavirus 2 infection. In addition, the role of vasoactive intestinal peptide in the human maternal-fetal interface suggests that vasoactive intestinal peptide is a safe treatment of severe coronavirus disease 2019 respiratory failure during pregnancy.
血管活性肠肽的合成形式阿维普坦已进入临床试验,用于治疗伴有呼吸衰竭的重症2019冠状病毒病肺炎。血管活性肠肽通过与肺泡II型细胞的血管活性肠肽受体1结合来保护肺部免受多种损伤,而严重急性呼吸综合征冠状病毒2正是与这些细胞结合。由于阿维普坦在治疗患有重症2019冠状病毒病肺炎的孕妇中的作用尚不清楚,作者报告了对一名不符合阿维普坦3期试验条件的此类患者进行成功治疗的情况。
根据美国食品药品监督管理局批准的开放标签扩大准入方案NCT04453839,一名32岁、孕6产4、妊娠27周、体重指数42.5kg/m²的女性患者于2021年1月入住一家四级护理医院的重症监护病房,患有重症2019冠状病毒病,并在重症监护病房入院后随访4个月。标准治疗包括瑞德西韦、甲泼尼龙、依诺肝素和吸入性依前列醇。此外,根据随机临床试验NCT04311697,患者接受了三次连续12小时的阿维普坦静脉输注,剂量分别为50/100/150pmol/kg/hr递增。休斯顿卫理公会医院的机构审查委员会对人体受试者保护进行监督。该患者被纳入治疗,并获得了美国食品药品监督管理局和机构审查委员会批准的知情同意书。基于患者同意在入院时以机构审查委员会批准的方式使用去识别化数据用于研究,纳入了该患者的数据(PRO00025607)。记录了基线炎症标志物、动脉血气、影像学检查、氧气需求、Pao/Fio、在基线时、在患者接受研究药物治疗期间以及在患者整个住院过程中的连续胎儿监测情况。
该接受静脉注射血管活性肠肽治疗的患者出现的快速临床改善与血管活性肠肽保护肺泡II型细胞、减轻细胞因子风暴并改善急性肺损伤中的氧合作用的理论一致。血管活性肠肽在肺部的这一特定作用可能对于对抗严重急性呼吸综合征冠状病毒2感染的致命影响至关重要。此外,血管活性肠肽在人母胎界面中的作用表明,血管活性肠肽是治疗孕期重症2019冠状病毒病呼吸衰竭的一种安全疗法。