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Respir Care. 2020 Oct;65(10):1427-1432. doi: 10.4187/respcare.07938. Epub 2020 Jun 9.
2
SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor.严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)进入细胞依赖于 ACE2 和 TMPRSS2,可被一种临床验证的蛋白酶抑制剂所阻断。
Cell. 2020 Apr 16;181(2):271-280.e8. doi: 10.1016/j.cell.2020.02.052. Epub 2020 Mar 5.
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Emergence of a novel human coronavirus threatening human health.新型人类冠状病毒的出现威胁人类健康。
Nat Med. 2020 Mar;26(3):317-319. doi: 10.1038/s41591-020-0796-5.
4
Safety, Tolerability, and Effects of Sodium Bicarbonate Inhalation in Cystic Fibrosis.碳酸氢钠吸入治疗囊性纤维化的安全性、耐受性和效果。
Clin Drug Investig. 2020 Feb;40(2):105-117. doi: 10.1007/s40261-019-00861-x.
5
Dual Inhibition of the Lactate Transporters MCT1 and MCT4 Is Synthetic Lethal with Metformin due to NAD+ Depletion in Cancer Cells.乳酸转运蛋白 MCT1 和 MCT4 的双重抑制与二甲双胍联合使用具有合成致死性,这是由于癌细胞中 NAD+ 的耗竭。
Cell Rep. 2018 Dec 11;25(11):3047-3058.e4. doi: 10.1016/j.celrep.2018.11.043.
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Tissue Factor Facilitates Wound Healing in Human Airway Epithelial Cells.组织因子促进人呼吸道上皮细胞的伤口愈合。
Chest. 2019 Mar;155(3):534-539. doi: 10.1016/j.chest.2018.10.007. Epub 2018 Oct 22.
7
Coupling between an electrostatic network and the Zn binding site modulates Hv1 activation.静电网络与 Zn 结合位点的偶联调节 Hv1 的激活。
J Gen Physiol. 2018 Jun 4;150(6):863-881. doi: 10.1085/jgp.201711822. Epub 2018 May 9.
8
Administration of Inhaled Pulmonary Vasodilators to the Mechanically Ventilated Neonatal Patient.对机械通气新生儿患者使用吸入性肺血管扩张剂
Paediatr Drugs. 2017 Jun;19(3):183-192. doi: 10.1007/s40272-017-0221-9.
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The effects of lung recruitment maneuvers on exhaled breath condensate pH.肺复张手法对呼出气冷凝液pH值的影响。
J Breath Res. 2015 Sep 3;9(3):036009. doi: 10.1088/1752-7155/9/3/036009.
10
pH modulates the activity and synergism of the airway surface liquid antimicrobials β-defensin-3 and LL-37.pH调节气道表面液体抗菌剂β-防御素-3和LL-37的活性及协同作用。
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一种消除人类气道上皮细胞中 SARS-CoV-2 复制的治疗方法,作为气溶胶吸入对健康人体是安全的。

A Treatment to Eliminate SARS-CoV-2 Replication in Human Airway Epithelial Cells Is Safe for Inhalation as an Aerosol in Healthy Human Subjects.

机构信息

Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine.

Division of Pulmonology, Allergy and Sleep Medicine, Riley Hospital for Children, Indianapolis, Indiana.

出版信息

Respir Care. 2021 Jan;66(1):113-119. doi: 10.4187/respcare.08425. Epub 2020 Sep 22.

DOI:10.4187/respcare.08425
PMID:32962996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7856523/
Abstract

BACKGROUND

Low airway surface pH is associated with many airway diseases, impairs antimicrobial host defense, and worsens airway inflammation. Inhaled Optate is designed to safely raise airway surface pH and is well tolerated in humans. Raising intracellular pH partially prevents activation of SARS-CoV-2 in primary normal human airway epithelial (NHAE) cells, decreasing viral replication by several mechanisms.

METHODS

We grew primary NHAE cells from healthy subjects, infected them with SARS-CoV-2 (isolate USA-WA1/2020), and used clinical Optate at concentrations used in humans in vivo to determine whether Optate would prevent viral infection and replication. Cells were pretreated with Optate or placebo prior to infection (multiplicity of infection = 1), and viral replication was determined with plaque assay and nucleocapsid (N) protein levels. Healthy human subjects also inhaled Optate as part of a Phase 2a safety trial.

RESULTS

Optate almost completely prevented viral replication at each time point between 24 h and 120 h, relative to placebo, on both plaque assay and N protein expression ( < .001). Mechanistically, Optate inhibited expression of major endosomal trafficking genes and raised NHAE intracellular pH. Optate had no effect on NHAE cell viability at any time point. Inhaled Optate was well tolerated in 10 normal subjects, with no change in lung function, vital signs, or oxygenation.

CONCLUSIONS

Inhaled Optate may be well suited for a clinical trial in patients with pulmonary SARS-CoV-2 infection. However, it is vitally important for patient safety that formulations designed for inhalation with regard to pH, isotonicity, and osmolality be used. An inhalational treatment that safely prevents SARS-CoV-2 viral replication could be helpful for treating patients with pulmonary SARS-CoV-2 infection.

摘要

背景

低气道表面 pH 值与许多气道疾病有关,会损害抗菌宿主防御功能,并加重气道炎症。吸入性 Optate 的设计目的是安全地提高气道表面 pH 值,并且在人体中具有良好的耐受性。提高细胞内 pH 值可部分预防 SARS-CoV-2 在原代正常人呼吸道上皮 (NHAE) 细胞中的激活,通过多种机制降低病毒复制。

方法

我们从健康受试者中培养原代 NHAE 细胞,用 SARS-CoV-2(分离株 USA-WA1/2020)感染这些细胞,并使用临床 Optate 的浓度在体内感染人类,以确定 Optate 是否可以预防病毒感染和复制。细胞在用 Optate 或安慰剂预处理后感染(感染复数=1),并用噬斑测定法和核衣壳(N)蛋白水平测定病毒复制。健康的人类受试者还参与了一项 2a 期安全性试验,吸入 Optate。

结果

与安慰剂相比,Optate 在 24 小时至 120 小时之间的每个时间点几乎完全阻止了病毒复制,无论是在噬斑测定法还是 N 蛋白表达方面(<0.001)。从机制上讲,Optate 抑制了主要内体运输基因的表达并提高了 NHAE 细胞内 pH 值。Optate 在任何时间点对 NHAE 细胞活力均无影响。在 10 名正常受试者中,吸入 Optate 具有良好的耐受性,肺功能、生命体征或氧合均无变化。

结论

吸入性 Optate 可能非常适合患有肺部 SARS-CoV-2 感染的患者的临床试验。但是,出于患者安全的考虑,设计用于吸入的制剂必须注意 pH 值、等渗性和渗透压。一种安全地预防 SARS-CoV-2 病毒复制的吸入性治疗方法可能有助于治疗患有肺部 SARS-CoV-2 感染的患者。