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Monitoring Neutrophil Elastase and Cathepsin G Activity in Human Sputum Samples
Published on: May 21, 2021
Elastase and granzymes during meningococcal disease in children: correlation to disease severity
Job B M van Woensel1, Maarten H Biezeveld, C Erik Hack
1Paediatric Intensive Care Unit, Emma Children's Hospital, Academic Medical Center, P.O. Box 22660, 1100DD Amsterdam, The Netherlands. j.b.vanwoensel@amc.uva.nl
Insights
Human neutrophil elastase and granzyme B levels correlate with meningococcal disease severity in children. Prolonged neutrophil activation indicates greater organ dysfunction, impacting patient outcomes.
Area of Science:
- Pediatric critical care medicine
- Infectious diseases
- Immunology
Background:
- Meningococcal disease is a severe infection in children.
- Understanding the inflammatory response is crucial for predicting outcomes.
Purpose of the Study:
- To investigate human neutrophil elastase (HNE) and granzymes A/B in pediatric meningococcal disease.
- To correlate enzyme levels with disease severity and organ dysfunction.
Main Methods:
- Clinical observational cohort study in a pediatric intensive care unit.
- Measured HNE and granzymes A/B using ELISA on admission, day 3, and day 7.
- Included 61 children with distinct meningitis, meningitis and shock, or fulminant septicemia.
Main Results:
- Elevated HNE on admission, highest in fulminant septicemia.
- Granzyme B (and marginally Granzyme A) increased in patients with shock.
- Slower decrease in HNE levels correlated with increased need for respiratory and circulatory support.
Conclusions:
- HNE and granzyme B are linked to initial meningococcal disease severity.
- Sustained neutrophil activation is associated with more extensive organ dysfunction.
Objective:
To investigate the levels of human neutrophil elastase and lymphocyte-derived granzymes A and B in relation to disease severity in children with meningococcal disease.
Design:
Clinical observational cohort study.
Setting:
Paediatric intensive care unit.
Patients:
All patients with meningococcal disease during the study period were included.
Measurements And Results:
Blood sampling was done on the day of admission and on days 3 and 7. Assays for elastase and granzymes were done with ELISA. Sixty-one patients were included: 19 having distinct meningitis; 17 meningitis and shock; and 25 fulminant septicaemia. On admission levels of elastase were increased in all patients, being highest in those with fulminant septicaemia and lowest in those with distinct meningitis. Granzyme A (although marginally) and granzyme B levels were only increased in patients with shock. In 20 of the 28 patients admitted for > or = 3 days elastase decreased from admission ("rapid-decrease" group). In the remaining 8 patients, elastase started to decrease after 2 days ("slow-decrease" group). Patients of the "slow-decrease" group had a higher temperature up to day 4, needed more respiratory support (mean airway pressure in cm H2O on days 3 and 4: p=0.02 and p<0.01, respectively), and more circulatory support (>2 inotropic agents on day 3; p=0.04) compared with the "rapid-decrease" group.
Conclusions:
Human neutrophil elastase and granzyme B are related with disease severity during the initial phase of meningococcal disease and prolonged neutrophil activation is associated with the extent of organ dysfunction during the period thereafter.
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