Details

Autor(en) / Beteiligte

• McElvaney, Oliver J.
• McEvoy, Natalie L.
• Boland, Fiona
• McElvaney, Oisín F.
• Hogan, Grace
• Donnelly, Karen
• Friel, Oisín
• Browne, Emmet
• Fraughen, Daniel D.
• Murphy, Mark P.
• Clarke, Jennifer
• Choileáin, Orna Ní
• O’Connor, Eoin
• McGuinness, Rory
• Boylan, Maria
• Kelly, Alan
• Hayden, John C.
• Collins, Ann M.
• Cullen, Ailbhe
• Hyland, Deirdre
• Carroll, Tomás P.
• Geoghegan, Pierce
• Laffey, John G.
• Hennessy, Martina
• Martin-Loeches, Ignacio
• McElvaney, Noel G.
• Curley, Gerard F.

Titel

A randomized, double-blind, placebo-controlled trial of intravenous alpha-1 antitrypsin for ARDS secondary to COVID-19

Ist Teil von

• Med (New York, N.Y. : Online), 2022-04, Vol.3 (4), p.233-248.e6

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2022

Quelle

MEDLINE

Beschreibungen/Notizen

• Patients with severe coronavirus disease 2019 (COVID-19) develop a febrile pro-inflammatory cytokinemia with accelerated progression to acute respiratory distress syndrome (ARDS). Here we report the results of a phase 2, multicenter, randomized, double-blind, placebo-controlled trial of intravenous (IV) plasma-purified alpha-1 antitrypsin (AAT) for moderate to severe ARDS secondary to COVID-19 (EudraCT 2020-001391-15). Patients (n = 36) were randomized to receive weekly placebo, weekly AAT (Prolastin, Grifols, S.A.; 120 mg/kg), or AAT once followed by weekly placebo. The primary endpoint was the change in plasma interleukin (IL)-6 concentration at 1 week. In addition to assessing safety and tolerability, changes in plasma levels of IL-1β, IL-8, IL-10, and soluble tumor necrosis factor receptor 1 (sTNFR1) and clinical outcomes were assessed as secondary endpoints. Treatment with IV AAT resulted in decreased inflammation and was safe and well tolerated. The study met its primary endpoint, with decreased circulating IL-6 concentrations at 1 week in the treatment group. This was in contrast to the placebo group, where IL-6 was increased. Similarly, plasma sTNFR1 was substantially decreased in the treatment group while remaining unchanged in patients receiving placebo. IV AAT did not definitively reduce levels of IL-1β, IL-8, and IL-10. No difference in mortality or ventilator-free days was observed between groups, although a trend toward decreased time on ventilator was observed in AAT-treated patients. In patients with COVID-19 and moderate to severe ARDS, treatment with IV AAT was safe, feasible, and biochemically efficacious. The data support progression to a phase 3 trial and prompt further investigation of AAT as an anti-inflammatory therapeutic. ECSA-2020-009; Elaine Galwey Research Bursary. [Display omitted] •Patients with COVID-19-associated ARDS were randomized to receive IV AAT or placebo•Patients receiving IV AAT had decreased IL-6, sTNFR1, and CRP at 1 week•Differential glycosylation of endogenous AAT was preserved in the treatment group•Treatment with IV AAT was safe and well tolerated Treatment options for patients with severe coronavirus disease 2019 (COVID-19), particularly those who progress to acute respiratory distress syndrome (ARDS), are limited. ARDS is a highly inflammatory state hallmarked by airway damage, respiratory failure, and increased mortality. Alpha-1 antitrypsin (AAT) is an anti-inflammatory protein produced by the liver and present the bloodstream. We investigated the use of AAT purified from the blood of healthy donors as a therapeutic option for patients with COVID-19-associated ARDS. Treatment with AAT resulted in decreased inflammation at 1 week, was safe and well tolerated, and did not interfere with patients’ ability to generate their own protective response to COVID-19. The results suggest a potential role for AAT in treating COVID-19-associated ARDS and other inflammatory diseases. McElvaney and colleagues present the results of a randomized placebo-controlled trial of alpha-1 antitrypsin (AAT) for patients with acute respiratory distress syndrome secondary to COVID-19. Circulating levels of interleukin-6 and other pro-inflammatory mediators were decreased at 1 week in the treatment group, identifying a potential anti-inflammatory therapeutic for critical illness.