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Updated: Jan 28, 2026

Cardiopulmonary Bypass in a Mouse Model: A Novel Approach
Published on: September 22, 2017
Immune Unresponsiveness to Cardiopulmonary Bypass Is Associated With Unfavorable Outcome in Infants Requiring Cardiac
Alexis Chenouard1, Mélanie Petrier2, Constance Bridonneau2
1CHU Nantes, Réanimation Pédiatrique, Nantes, France; Nantes Université, CHU Nantes, INSERM, Center for Research in Transplantation and Translational Immunology UMR 1064, Nantes, France.
Insights
Analyzing the whole blood immune response in infants undergoing cardiac surgery with cardiopulmonary bypass (CPB) revealed distinct transcriptomic signatures. Preoperative TNFSF12 levels predict CPB-related complications in pediatric cardiac surgery patients.
Area of Science:
- Pediatric cardiac surgery
- Immunology
- Transcriptomics
Background:
- Cardiopulmonary bypass (CPB) triggers complex immune responses, potentially causing complications in pediatric cardiac surgery.
- Infants under 3 months are particularly vulnerable to CPB-related postoperative complications.
Purpose of the Study:
- To investigate the whole blood transcriptomic response to CPB in infants undergoing cardiac surgery.
- To identify immune signatures associated with CPB-induced postoperative complications.
- To evaluate the predictive potential of these signatures for identifying at-risk patients.
Main Methods:
- Whole blood transcriptomic analysis was performed on infants (≤3 months) undergoing cardiac surgery with CPB.
- Immune transcriptomic signatures related to CPB were defined.
- Gene expression differences were compared between patients with complicated and uncomplicated outcomes.
- Preoperative plasma TNFSF12 abundance was assessed for predictive value.
Main Results:
- A distinct immune transcriptomic signature related to CPB was identified.
- Fewer genes (18) were differentially expressed in patients with complicated outcomes compared to the uncomplicated group (>2,000 genes).
- Preoperative plasma TNFSF12 abundance effectively predicted CPB-induced complications, validated in an external cohort.
Conclusions:
- The study defined an immune transcriptomic signature associated with CPB in infants undergoing cardiac surgery.
- Preoperative TNFSF12 levels serve as a promising biomarker for predicting CPB-related complications.
- These findings offer insights into the pathophysiology of CPB-induced complications and potential risk stratification strategies.
Abstract:
Cardiopulmonary bypass (CPB) induces a complex immune response which can lead to complications after pediatric cardiac surgery. We hypothesized that analyzing the whole blood transcriptomic response after cardiac surgery with or without CPB in children would provide new insights into the pathophysiological mechanisms of CPB-related postoperative complications. In this study focusing on infants ≤3 months of age requiring CPB who are more likely to develop postoperative complications, we defined an immune transcriptomic signature related to CPB. Among the genes included in the CPB signature, we identified only 18 genes that were differentially expressed after surgery in patients with a complicated outcome. In contrast, more than 2,000 genes were differentially expressed before and after the surgery in the uncomplicated group. We demonstrated the predictive potential of the preoperative plasma TNFSF12 abundance to identify patients at risk of CPB-induced complications, which was confirmed in an external cohort.
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