Lung transplantation: Current insights and outcomes
View abstract on PubMed
Summary
This summary is machine-generated.Predicting lung transplant rejection remains challenging due to limited biomarkers. Donor-derived cell-free DNA and transcriptomics show promise for early diagnosis of acute rejection and chronic lung allograft dysfunction (CLAD).
Area Of Science
- Immunology
- Transplantation Medicine
- Biomarker Discovery
Background
- Immune-mediated rejection complicates lung transplantation outcomes.
- Chronic lung allograft dysfunction (CLAD) is a leading cause of mortality, necessitating early diagnostic tools.
Purpose Of The Study
- To review novel and existing technologies for identifying immune-mediated rejection mechanisms in lung transplantation.
- To highlight emerging biomarkers for improved precision medicine in lung allograft recipients.
Main Methods
- Review of omics technologies (genomics, epigenomics, transcriptomics) and bioinformatic platforms.
- Analysis of clinical trial data for biomarker performance.
- Discussion of emerging biomarkers like exosomes, telomere length, DNA methylation, and neutrophil extracellular traps (NETs).
Main Results
- Genomic biomarkers, particularly donor-derived cell-free DNA in plasma and bronchoalveolar lavage fluid, show diagnostic potential for acute rejection and CLAD phenotypes.
- Transcriptomic analysis led to the Molecular Microscope® Diagnostic System (MMDx) for interpreting molecular signatures in lung biopsies.
- Several other potential biomarkers are under investigation but have not yet entered clinical trials.
Conclusions
- Omics technologies are crucial for understanding lung allograft rejection pathways and discovering specific biomarkers.
- Donor-derived cell-free DNA and transcriptomic signatures represent promising avenues for early detection and management of lung transplant rejection.
- Further research into novel biomarkers is essential for advancing precision medicine in lung transplantation.

