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Updated: Jan 26, 2026

Robot-Assisted Kidney Transplantation
Published on: July 19, 2021
Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
Joanna M Schaenman1, Maura Rossetti2, Erik Lum3
1Division of Infectious Diseases, Department of Medicine, UCLA Immunogenetics Center, Los Angeles, CA.
Older kidney transplant recipients show increased proinflammatory gene expression and decreased immune cell function genes compared to younger patients. This immune dysfunction may explain higher infection and mortality risks in older adults post-transplant.
Area of Science:
- Immunology
- Transplantation Science
- Gerontology
Background:
- Older transplant recipients face higher infection and mortality rates than younger counterparts.
- Age-associated immune dysfunction in older transplant patients remains poorly understood.
Purpose of the Study:
- To investigate age-related differences in gene expression in kidney transplant recipients.
- To identify molecular mechanisms underlying increased vulnerability in older transplant patients.
Main Methods:
- Gene expression analysis of peripheral blood mononuclear cells from 60 kidney transplant recipients (23 older, 37 younger).
- Patients were matched for antithymocyte induction and donor type.
- Comparison of gene expression profiles between older (≥ 60 years) and younger (30-59 years) groups 3 months post-transplant.
Main Results:
- Older patients exhibited upregulated proinflammatory genes (e.g., IL1-β, IL-6).
- Genes associated with B-cell and T-cell function (e.g., CCR7, CD27) were downregulated in older recipients.
- Increased binding sites for proinflammatory transcription factors (e.g., C/EBP-β) and decreased sites for IRF2 were observed in older patients.
Conclusions:
- Significant gene expression differences exist between older and younger kidney transplant recipients.
- Upregulation of inflammatory genes and downregulation of adaptive immunity genes in older recipients.
- These molecular changes may underlie the increased susceptibility to infection and malignancy in older transplant patients.
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