Preclinical Safety.

IF 2 4区 医学 Q3 RESPIRATORY SYSTEM
Ronald K Wolff, James D Blanchard
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引用次数: 0

Abstract

Several inhaled proteins and peptides have been developed to treat indications in the respiratory tract or systemically with varying degrees of success. This section will summarize the preclinical and clinical studies for inhaled Pulmozyme® (recombinant human deoxyribonuclease, rhDNase), insulin, human growth hormone (hGH), cyclosporine, alpha-1 antitrypsin, measles vaccine, and anti-immunoglobulin E (IgE). For Pulmozyme® (rhDNase), monkeys had positive serum antibody titers to rhDNase and allergic/hypersensitivity (type I) lung lesions in response to foreign protein likely due to differences in homology between monkey and human DNases. However, in patients, the levels of rhDNase antibodies were low and of no consequence. For inhaled insulin in rats, dogs and monkeys, there were no adverse effects related to insulin or excipients. In clinical trials, over 13,000 patients were safely treated with inhaled insulin for an average of 1 year. Some patients had higher antibody levels than comparators, but these antibodies did not decrease the effectiveness, safety or tolerability of inhaled insulin over time and/or affect clinical outcomes. Inhaled hGH had no adverse effects in monkeys, healthy volunteers or pediatric patients, but its absorption from the lungs was too low (<5%) in pediatric patients to be successful as a medical product. Inhaled cyclosporine had no unexpected systemic toxicity or clinically limiting findings in the respiratory tract in rat and dogs; it also had promising Phase 2 clinical data but failed in Phase 3. Inhaled alpha-1 antitrypsin also failed in a recent Phase 2/3 trial. A liquid inhaled measles vaccine was safe, well tolerated and produced an appropriate immune response in Phase 2/3 studies for children ages 10-35 months, but not younger. A dry powder inhaled vaccine in monkeys had no adverse effects and produced an immune response; Phase 1 trials are underway. Inhaled anti-IgE was well tolerated in monkeys and asthma patients, but systemic delivery had superior results in patients.

临床前安全性。
已经开发了几种吸入蛋白和多肽来治疗呼吸道或全身适应症,并取得了不同程度的成功。本节将总结吸入型Pulmozyme®(重组人脱氧核糖核酸酶,rhDNase)、胰岛素、人生长激素(hGH)、环孢素、α -1抗胰蛋白酶、麻疹疫苗和抗免疫球蛋白E (IgE)的临床前和临床研究。对于Pulmozyme®(rhDNase),猴子对rhDNase的血清抗体滴度呈阳性,并对外源蛋白产生过敏/超敏反应(I型)肺部病变,这可能是由于猴子和人类dna酶的同源性差异。然而,在患者中,rhDNase抗体水平很低,没有任何后果。对于吸入胰岛素的大鼠、狗和猴子,没有与胰岛素或辅料相关的不良反应。在临床试验中,超过13000名患者安全地接受了平均1年的吸入胰岛素治疗。一些患者的抗体水平高于对照组,但这些抗体不会随着时间的推移降低吸入胰岛素的有效性、安全性或耐受性和/或影响临床结果。吸入生长激素对猴子、健康志愿者或儿科患者没有不良影响,但其从肺部的吸收量太低(
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来源期刊
CiteScore
6.70
自引率
2.90%
发文量
34
审稿时长
>12 weeks
期刊介绍: Journal of Aerosol Medicine and Pulmonary Drug Delivery is the only peer-reviewed journal delivering innovative, authoritative coverage of the health effects of inhaled aerosols and delivery of drugs through the pulmonary system. The Journal is a forum for leading experts, addressing novel topics such as aerosolized chemotherapy, aerosolized vaccines, methods to determine toxicities, and delivery of aerosolized drugs in the intubated patient. Journal of Aerosol Medicine and Pulmonary Drug Delivery coverage includes: Pulmonary drug delivery Airway reactivity and asthma treatment Inhalation of particles and gases in the respiratory tract Toxic effects of inhaled agents Aerosols as tools for studying basic physiologic phenomena.
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