Plasma and airway levels of surfactant protein D degradation reflect progression of ARDS in entilated patients with SARS-CoV-2
Plasma and airway levels of surfactant protein D degradation reflect progression of ARDS in entilated patients with SARS-CoV-2
Background: Patients with COVID-19 present severe respiratory symptoms progressing to acute respiratory distress syndrome (ARDS). Upon infection, SARS-CoV-2 destroys cells expressing the ACE2 receptor including alveolar type II cells (AT2). These cells are found in the alveolar-capillary barrier which normally secrete pulmonary surfactant, a complex of lipid and surfactant proteins (SPA, SP-B, SP-C, SP-D). Exogenous surfactant therapy (mainly composed of phospholipids, SP-B, and SP-C) has been successful in treating neonatal respiratory distress syndrome (nRDS) caused by surfactant deficiency in preterm babies.Plasma SP-D has been proposed as a marker of lung injury in COVID-19 but so far, no reports have evaluated sequential SP-D levels in both airway and plasma. As part of a clinical trial repurposing surfactant therapy to treat adult ventilated COVID-19 patients, we hypothesized that plasma SP-D levels may reflect decreased lung integrity and that SP-D degradation in plasma and airway samples from COVID-19 patients may reflect disease progression and severity. Method(s): Enzyme-linked immunosorbent assay (ELISA) was used to quantify SP-D concentration in patient plasma and tracheal aspirate samples. Western Blotting was used to identify any protein degradation. Sequential daily plasma and airway samples were analysed. Result(s): SP-D concentration in serum was 10-20 times higher in patients ventilated for COVID-19 than in healthy volunteers. Additionally, the concentration of SP-D in plasma has shown to be 10-100-fold higher than in tracheal aspirates. Furthermore, degraded fragments of SP-D were detected at a higher ratio than intact SP-D in plasma of ventilated patients. This ratio decreased with administration of surfactant therapy (containing phospholipids and SP-B and SP-C but no SPA or SP-D). Conclusion(s): Increased serum SP-D and decreased tracheal aspirate SP-D from ventilated COVID-19 patients suggested leakage of pulmonary surfactant into the bloodstream caused by damage to the alveolar-capillary barrier in diseased lungs. The ratio of degraded vs. intact SP-D found in the plasma was compared before and after therapeutic surfactant administration. The results indicated that levels of SP-D in plasma and tracheal aspirates together with the ratio of degraded and intact SP-D in the plasma may be useful indicators of the severity of COVID-19 lung disease progression.
Castillo, T.
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Madsen, J.
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Postle, A.
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Brealey, D.
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Fink, J.B.
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Grocott, M.
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Dushianthan, A.
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Clark, H.W.
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17 May 2022
Castillo, T.
79d343d2-8612-4524-9a14-3c5ce27f89a0
Madsen, J.
498618b2-038a-4cc0-9fd8-db166610f2de
Postle, A.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Brealey, D.
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Fink, J.B.
56085c50-313c-4eb1-9cd7-6fd1f269ffba
Grocott, M.
1e87b741-513e-4a22-be13-0f7bb344e8c2
Dushianthan, A.
013692a2-cf26-4278-80bd-9d8fcdb17751
Clark, H.W.
580ed7d2-5812-4d40-822d-51de09cce603
Castillo, T., Madsen, J., Postle, A., Brealey, D., Fink, J.B., Grocott, M., Dushianthan, A. and Clark, H.W.
(2022)
Plasma and airway levels of surfactant protein D degradation reflect progression of ARDS in entilated patients with SARS-CoV-2.
American Journal of Respiratory and Critical Care Medicine, 205.
(doi:10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a5713).
Record type:
Meeting abstract
Abstract
Background: Patients with COVID-19 present severe respiratory symptoms progressing to acute respiratory distress syndrome (ARDS). Upon infection, SARS-CoV-2 destroys cells expressing the ACE2 receptor including alveolar type II cells (AT2). These cells are found in the alveolar-capillary barrier which normally secrete pulmonary surfactant, a complex of lipid and surfactant proteins (SPA, SP-B, SP-C, SP-D). Exogenous surfactant therapy (mainly composed of phospholipids, SP-B, and SP-C) has been successful in treating neonatal respiratory distress syndrome (nRDS) caused by surfactant deficiency in preterm babies.Plasma SP-D has been proposed as a marker of lung injury in COVID-19 but so far, no reports have evaluated sequential SP-D levels in both airway and plasma. As part of a clinical trial repurposing surfactant therapy to treat adult ventilated COVID-19 patients, we hypothesized that plasma SP-D levels may reflect decreased lung integrity and that SP-D degradation in plasma and airway samples from COVID-19 patients may reflect disease progression and severity. Method(s): Enzyme-linked immunosorbent assay (ELISA) was used to quantify SP-D concentration in patient plasma and tracheal aspirate samples. Western Blotting was used to identify any protein degradation. Sequential daily plasma and airway samples were analysed. Result(s): SP-D concentration in serum was 10-20 times higher in patients ventilated for COVID-19 than in healthy volunteers. Additionally, the concentration of SP-D in plasma has shown to be 10-100-fold higher than in tracheal aspirates. Furthermore, degraded fragments of SP-D were detected at a higher ratio than intact SP-D in plasma of ventilated patients. This ratio decreased with administration of surfactant therapy (containing phospholipids and SP-B and SP-C but no SPA or SP-D). Conclusion(s): Increased serum SP-D and decreased tracheal aspirate SP-D from ventilated COVID-19 patients suggested leakage of pulmonary surfactant into the bloodstream caused by damage to the alveolar-capillary barrier in diseased lungs. The ratio of degraded vs. intact SP-D found in the plasma was compared before and after therapeutic surfactant administration. The results indicated that levels of SP-D in plasma and tracheal aspirates together with the ratio of degraded and intact SP-D in the plasma may be useful indicators of the severity of COVID-19 lung disease progression.
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Published date: 17 May 2022
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Local EPrints ID: 495395
URI: http://eprints.soton.ac.uk/id/eprint/495395
ISSN: 1073-449X
PURE UUID: 0f5ea5ec-b941-429d-8a85-7bf265e7389b
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Date deposited: 12 Nov 2024 17:56
Last modified: 13 Nov 2024 02:56
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Author:
T. Castillo
Author:
J. Madsen
Author:
D. Brealey
Author:
J.B. Fink
Author:
A. Dushianthan
Author:
H.W. Clark
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