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Published on: January 28, 2020
Prognostic values of soluble CD30 and CD30 gene polymorphisms in heart transplantation
Elisa Frisaldi1, Raffaele Conca, Paola Magistroni
1Department of Genetics, Biology and Biochemistry, University of Turin, Turin, Italy.
Insights
Pretransplant soluble CD30 (sCD30) levels predict heart transplant (HT) patient survival. Lower pretransplant sCD30 levels are associated with significantly better outcomes in heart transplant recipients.
Area of Science:
- Immunology
- Transplantation Medicine
- Genetics
Background:
- Pretransplant soluble CD30 (sCD30) is a known predictor of kidney graft outcomes.
- The predictive value of sCD30 for heart transplant (HT) outcomes remains unestablished.
- The CD30 promoter microsatellite ((CCAT)n repeats) can influence gene transcription.
Purpose of the Study:
- To investigate the role of pretransplant soluble CD30 (sCD30) levels as a predictor of heart transplant (HT) outcomes.
- To explore the association between CD30 microsatellite (CCAT)n repeats and sCD30 levels in HT patients and donors.
Main Methods:
- Assessed serum sCD30 levels in 83 HT patients and 77 donors.
- Analyzed the number of (CCAT)n repeats in the CD30 promoter region.
- Correlated sCD30 levels and microsatellite variations with patient survival post-transplantation.
Main Results:
- Soluble CD30 (sCD30) levels were non-significantly increased in HT patients compared to controls.
- No significant differences were observed in CD30 microsatellite allele frequencies between patients and donors.
- A negative correlation was found between (CCAT)n repeat number and sCD30 levels in donors.
- Patients with pretransplant sCD30 levels ≤30 U/ml demonstrated significantly improved survival rates.
Conclusions:
- Pretransplant soluble CD30 (sCD30) levels are a significant predictor of heart transplant (HT) patient survival.
- sCD30 serves as a valuable biomarker for assessing prognosis after heart transplantation.
Abstract:
Pretransplant soluble CD30 (sCD30) is a predictor of kidney graft outcome. Its status as a predictor of heart transplant (HT) outcome has not been established. We have studied this question by assessing sCD30 levels and the number of (CCAT)n repeats of the microsatellite in the CD30 promoter region, which is able alone to repress gene transcription, in the sera of 83 HT patients and 77 of their donors. sCD30 was non-significantly increased in the patients, whereas there were no differences in the CD30 microsatellite allele frequencies. A negative correlation between the number of (CCAT)n and sCD30 levels was evident in the donors. Patients with pretransplant sCD30
