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Soluble HLA-G levels in heart transplant recipients: Dynamics and correlation with clinical outcomes
Zulaika Grille-Cancela1, Eduardo Barge-Caballero1, Natalia Suárez-Fuentetaja2
1Servicio de Cardiología, Complejo Hospitalario Universitario A Coruña (CHUAC), Instituto de Investigación Biomédica de A Coruña (INIBIC), A Coruña, Spain; Grupo de Investigación Cardiovascular (GRINCAR), Universidad de A Coruña (UDC), A Coruña, Spain; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares, Instituto de Salud Carlos III, Madrid, Spain.
Insights
Serum levels of soluble human leukocyte antigen-G (s-HLA-G) decreased in the first year after heart transplantation (HT). Higher s-HLA-G levels correlated with increased infection risk but not rejection or long-term survival.
Area of Science:
- Immunology
- Transplantation Medicine
- Biomarker Research
Background:
- Heart transplantation (HT) is a life-saving procedure but faces challenges like rejection and infection.
- Soluble human leukocyte antigen-G (s-HLA-G) is an immune tolerance marker with potential prognostic value in transplantation.
- Understanding s-HLA-G dynamics post-HT is crucial for monitoring outcomes.
Purpose of the Study:
- To track the serum levels of s-HLA-G during the first 12 months after HT.
- To investigate the association between s-HLA-G levels and clinical outcomes, including rejection, infection, and survival.
Main Methods:
- An observational study of 59 heart transplant recipients.
- Serum s-HLA-G levels were measured pre-HT and at 1, 3, 6, and 12 months post-HT.
- Area Under the Curve (AUC) of s-HLA-G levels was calculated and correlated with rejection scores, coronary allograft vasculopathy (CAV), infections, and long-term survival.
Main Results:
- s-HLA-G levels showed a significant decrease within the first year post-HT (p=0.020).
- A higher AUC for s-HLA-G was associated with increased infection rates (p=0.006).
- No significant correlation was found between s-HLA-G AUC and acute rejection burden, CAV development, or long-term patient/graft survival.
Conclusions:
- s-HLA-G levels naturally decline in the first year after heart transplantation.
- Elevated s-HLA-G during this period may indicate a higher susceptibility to infections.
- s-HLA-G does not appear to be a reliable predictor of acute rejection, CAV, or long-term survival in HT patients.
Purpose:
To describe the evolution of the serum levels of soluble HLA-G (s-HLA-G) during the first 12 months after heart transplantation (HT) and to correlate it with clinical outcomes.
Methods:
Observational study based in a single-center cohort of 59 patients who underwent HT between December-2003 and March-2010. Soluble HLA-G levels were measured from serum samples extracted before HT, and 1, 3, 6 and 12 months after HT. The cumulative burden of s-HLA-G expression during the first post-transplant year was assessed by means of the area under the curve (AUC) of s-HLA-G levels over time and correlated with the acute rejection burden -as assessed by a rejection score-, the presence of coronary allograft vasculopathy (CAV) grade ≥ 1 and infections during the first post-transplant year; as well as with long-term patient and graft survival. Mean follow-up was 12.4 years.
Results:
Soluble HLA-G levels decreased over the first post-transplant year (p = 0.020). The AUC of s-HLA-G levels during the first post-transplant year was higher among patients with infections vs. those without infections (p = 0.006). No association was found between the AUC of s-HLA-G levels and the burden of acute rejection or the development of CAV. Overall long-term survival, long-term survival free of late graft failure and cancer-free survival were not significantly different in patients with an AUC of s-HLA-G levels higher or lower than the median of the study population.
Conclusions:
Soluble HLA-G levels decreased over the first year after HT. Higher HLA-G expression was associated with a higher frequency of infections, but not with the burden of acute rejection or the development of CAV, neither with long-term patient or graft survival.
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