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Immune Heterogeneity Before and After Cardiopulmonary Bypass in Children

A Study of Immune Heterogeneity Before and After Cardiopulmonary Bypass in Children Undergoing Cardiac Surgery Based on ScRNA-seq

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06214182
Enrollment
3
Registered
2024-01-19
Start date
2024-01-01
Completion date
2025-01-31
Last updated
2025-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventricular Septal Defect

Brief summary

The goal of this observational study is to learn about functional heterogeneity of immune cells before and after cardiopulmonary bypass (CPB) in children with congenital heart disease (CHD). The main question\[s\] it aims to answer are: * Does CPB cause immune paralysis after CHD surgery? * How does the functional heterogeneity of immune cells change before and after CPB in children undergoing CHD surgery? Participants will receive 3ml of peripheral blood before CPB, 2 hours after CPB, and 3 days after CPB, and the peripheral blood samples will be sequenced by single cell to explore the immune heterogeneity before and after CPB.

Detailed description

CPB-induced immune paralysis is the main cause of postoperative infection in CHD, which seriously affects the prognosis of children. The underlying mechanism of CPB-induced immune paralysis has not been fully determined. This study intends to use scRNA-seq to describe gene transcription profiles of immune cells in peripheral blood of children undergoing CHD surgery before and after CPB, and explore the differences within and between different immune cell populations including T cells and the changes of immune cells in different sequences. To fill the gap in the study of immune mechanism in CPB-induced immune paralysis microenvironment at single-cell resolution.

Interventions

None listed

Sponsors

The Children's Hospital of Zhejiang University School of Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
31 Days to 1 Years
Healthy volunteers
No

Inclusion criteria

1. Birth weight range: 2500-6000g; 2. Operation duration \>90min;

Exclusion criteria

1. preterm infants or preoperative infections; 2. systemic immune diseases and serious complications: such as rheumatoid arthritis, systemic lupus erythematosus, severe liver and kidney function damage, leukemia, etc.; 3. Patients who have received an organ transplant; 4. Patients who have received immunomodulatory drugs: patients who have received immunomodulatory drugs before surgery; 5. Parents refused to participate or were unable to provide sufficient samples: Parents or legal guardians refused to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Expression of genesFrom enrollment to the end of CPB at 3 daysThe gene expression in single cells of peripheral blood samples was detected

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026