Anti-inflammatory therapy with nebulized dornase alfa for severe COVID-19 pneumonia: a randomized unblinded trial

Author:

Porter Joanna C12,Inshaw Jamie3,Solis Vincente Joel2,Denneny Emma12,Evans Rebecca2,Temkin Mia I4,De Vasconcelos Nathalia4,Aramburu Iker Valle4,Hoving Dennis4,Basire Donna1,Crissell Tracey2,Guinto Jesusa2,Webb Alison2,Esmail Hanif25,Johnston Victoria25ORCID,Last Anna26,Rampling Thomas25,Lippert Lena7,Helbig Elisa Theresa7,Kurth Florian7,Williams Bryan25,Flynn Aiden3,Lukey Pauline T8,Birault Veronique9,Papayannopoulos Venizelos4ORCID

Affiliation:

1. UCL Respiratory, University College London

2. University College London Hospitals NHS Trust

3. Exploristics

4. Antimicrobial Defence Lab, The Francis Crick Institute

5. National Institute for Health Research, University College London Hospital Biomedical Research Centre

6. Clinical Research Department, London School of Hygiene and Tropical Medicine

7. Charité – Universitätsmedizin Berlin, Department of Infectious Diseases and Respiratory Medicine

8. Target to Treatment Consulting Ltd

9. Translation, The Francis Crick Institute

Abstract

Background:Prinflammatory extracellular chromatin from neutrophil extracellular traps (NETs) and other cellular sources is found in COVID-19 patients and may promote pathology. We determined whether pulmonary administration of the endonuclease dornase alfa reduced systemic inflammation by clearing extracellular chromatin.Methods:Eligible patients were randomized (3:1) to the best available care including dexamethasone (R-BAC) or to BAC with twice-daily nebulized dornase alfa (R-BAC + DA) for seven days or until discharge. A 2:1 ratio of matched contemporary controls (CC-BAC) provided additional comparators. The primary endpoint was the improvement in C-reactive protein (CRP) over time, analyzed using a repeated-measures mixed model, adjusted for baseline factors.Results:We recruited 39 evaluable participants: 30 randomized to dornase alfa (R-BAC +DA), 9 randomized to BAC (R-BAC), and included 60 CC-BAC participants. Dornase alfa was well tolerated and reduced CRP by 33% compared to the combined BAC groups (T-BAC). Least squares (LS) mean post-dexamethasone CRP fell from 101.9 mg/L to 23.23 mg/L in R-BAC +DA participants versus a 99.5 mg/L to 34.82 mg/L reduction in the T-BAC group at 7 days; p=0.01. The anti-inflammatory effect of dornase alfa was further confirmed with subgroup and sensitivity analyses on randomised participants only, mitigating potential biases associated with the use of CC-BAC participants. Dornase alfa increased live discharge rates by 63% (HR 1.63, 95% CI 1.01–2.61, p=0.03), increased lymphocyte counts (LS mean: 1.08 vs 0.87, p=0.02) and reduced circulating cf-DNA and the coagulopathy marker D-dimer (LS mean: 570.78 vs 1656.96 μg/mL, p=0.004).Conclusions:Dornase alfa reduces pathogenic inflammation in COVID-19 pneumonia, demonstrating the benefit of cost-effective therapies that target extracellular chromatin.Funding:LifeArc, Breathing Matters, The Francis Crick Institute (CRUK, Medical Research Council, Wellcome Trust).Clinical trial number:NCT04359654.

Funder

LifeArc

Francis Crick Institute

University College London

NIHR University College London Hospitals Biomedical Research Centre

European Molecular Biology Organization

Publisher

eLife Sciences Publications, Ltd

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