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Cellular adhesion molecules changes in myocardium during first year post heart transplant
M Zembala1, R Wojnicz, M Zakliczyński
1Silesian Centre of Heart Disease, Zabrze, Poland.
Annals of Transplantation
|January 1, 1997
Summary
Intercellular adhesion molecule-1 (ICAM-1) and vascular adhesion molecule-1 (VCAM-1) were not initially present after heart transplant but increased significantly at one year. This suggests ICAM-1 and VCAM-1 monitoring may help detect chronic rejection.
Area of Science:
- Immunology
- Cardiology
- Transplantation Medicine
Background:
- Increased intercellular adhesion molecule-1 (ICAM-1) and vascular adhesion molecule-1 (VCAM-1) in the myocardium post-orthotopic heart transplantation (OHT) are linked to organ rejection.
- Understanding the temporal expression of these adhesion molecules is crucial for managing post-transplant complications.
Purpose of the Study:
- To investigate the dynamic changes in ICAM-1 and VCM-1 expression in the myocardium during the first year following OHT.
- To evaluate the potential of these adhesion molecules as biomarkers for chronic rejection.
Main Methods:
- Endomyocardial biopsy specimens from 11 OHT patients were collected at 7, 30, 90, and 360 days post-transplant.
- Immunohistochemistry using monoclonal antibodies was performed to assess ICAM-1 and VCAM-1 expression.
- Immunoreactivity scores were semiquantitatively assessed and compared over time.
Main Results:
- Histological signs of rejection were observed at various time points, with varying frequencies.
- ICAM-1 and VCAM-1 expression was largely absent at 7, 30, and 90 days post-OHT.
- A significant increase in ICAM-1 and VCAM-1 expression was observed at 360 days (p < 0.05).
Conclusions:
- The early absence of ICAM-1 and VCAM-1 may indicate the effectiveness of triple immunosuppressive therapy.
- The emergence of ICAM-1 and VCAM-1 expression at one year post-OHT suggests a role in chronic rejection.
- Immunohistological monitoring of adhesion molecules during routine biopsies may aid in the early detection of chronic cardiac allograft rejection.