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Variable mannose-binding lectin expression during postoperative acute-phase response
J W Olivier Van Till1, Marja A Boermeester, Piet W Modderman
1Department of Surgery, Academic Medical Center Amsterdam, University of Amsterdam, The Netherlands.
Background:
Low plasma concentrations and genetic polymorphisms of mannan-binding lectin (MBL) have been associated with infectious disease complications during various conditions. The present study examined the nature and expression of MBL deficiency during a surgery-induced acute-phase response.
Methods:
Blood was sampled from 20 consecutive patients before and 1, 3, 5, 7, and 10 days and 6 weeks after a uniform abdominal operation (transhiatal esophagectomy). Plasma concentrations of MBL, C-reactive protein (CRP), and secretory phospholipase A2 (sPLA2) were measured. Patients were classified as low- or high-level MBL producers by their preoperative concentration (<0.5 or > or = 0.5 micrograms/mL), and were cross-verified for actual MBL deficiency by nucleotide sequencing of both the MBL promoter and exon-1 alleles.
Results:
Baseline plasma MBL concentrations correlated with maximal postoperative plasma concentrations (r = 0.88; p < 0.0001). This was not found for CRP and sPLA2 (r = 0.19 and r = 0.08, respectively). Alleles responsible for structural MBL variants were detected in 40% of patients and were associated with significantly reduced MBL concentrations (p = 0.005). The baseline cut-off value in plasma of 0.5 micrograms/mL clearly identified individuals with variant exon-1 alleles (sensitivity 100%, specificity 83%).
Conclusions:
Baseline MBL plasma concentrations are predictive of MBL expression during the acute-phase response. A baseline cut-off value of 0.5 micrograms/mL can be used to identify patients with variants in the exon-1 region of the MBL gene without the need for nucleotide sequencing. Clinical studies may use this easy and quick method to identify MBL deficient patients preoperatively, as they are conditionally at risk for infectious complications.
Insights
Low mannose-binding lectin (MBL) levels predict MBL expression during acute-phase responses. A baseline plasma MBL concentration of 0.5 µg/mL effectively identifies MBL gene variants, aiding in preoperative risk assessment for infections.
Area of Science:
- Immunology
- Genetics
- Surgical Medicine
Background:
- Low mannose-binding lectin (MBL) concentrations and genetic variations are linked to infectious complications.
- MBL deficiency's role during surgery-induced acute-phase responses requires further investigation.
Purpose of the Study:
- To investigate MBL expression and deficiency during an acute-phase response following surgery.
- To determine if baseline MBL levels predict MBL expression post-surgery.
- To assess the utility of a specific MBL plasma concentration cutoff for identifying MBL gene variants.
Main Methods:
- Collected blood samples from 20 patients undergoing abdominal surgery (transhiatal esophagectomy) at multiple time points.
- Measured plasma concentrations of MBL, C-reactive protein (CRP), and secretory phospholipase A2 (sPLA2).
- Classified patients based on preoperative MBL levels (<0.5 or ≥0.5 µg/mL) and confirmed MBL deficiency via genetic sequencing.
Main Results:
- Baseline MBL concentrations strongly correlated with maximal postoperative MBL levels (r = 0.88, p < 0.0001).
- No significant correlation was observed between baseline and maximal concentrations for CRP or sPLA2.
- Genetic variants in MBL alleles were found in 40% of patients, associated with lower MBL levels (p = 0.005).
- A baseline MBL cutoff of 0.5 µg/mL demonstrated 100% sensitivity and 83% specificity in identifying exon-1 MBL variants.
Conclusions:
- Preoperative plasma MBL concentration is a reliable predictor of MBL expression during the acute-phase response.
- A baseline MBL cutoff of 0.5 µg/mL can identify patients with MBL exon-1 variants without genetic sequencing.
- This simple method allows for preoperative identification of MBL-deficient patients at risk for infectious complications.
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