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Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
Minimum mycophenolic acid levels are associated with donor-specific antibody formation
Guido Filler1,2,3, Ekaterina Kirilova Todorova1, Kevin Bax1
1Department of Pediatrics, Schulich School of Medicine & Dentistry, London, ON, Canada.
Abstract:
Although de novo DSA are associated with inferior graft survival, there are no effective strategies to prevent their formation. Underexposure to MPA (prodrug: MMF) also contributes to rejection rates early after transplantation, but the effect of this phenomenon on the formation of DSA long-term post-transplantation is unknown. Data are expressed as mean (standard deviation). All available data from 32 renal transplant recipients (age at transplantation 7.5 [4.5] yr) on tacrolimus and MPA immunosuppression with an average follow-up of 9.4 (s.d. 4.6) yr were analyzed. DSA were measured using the Luminex assay (>500 MFI was considered DSA-positive). Tacrolimus and MPA levels were measured with the Abbot Tacro II and EMIT assay, respectively. Among 1964 MPA and 3462 tacrolimus trough levels, the average MPA trough level was 3.2 (1.5) mg/L and the average tacrolimus level was 6.7 (2.8) ng/mL. At last follow-up, only 5/32 patients had undetectable DSA, with 5/32 having no class I antibodies and 6/32 having no class II antibodies. DSA formation was associated with a lower minimum MPA trough level (0.27 [0.23] vs. 0.47 [0.18] mg) and cystatin C eGFR (48 [21] vs. 70 [23] mL/min/1.73 m(2)) for class I DSA formers. The average eGFR of patients without class I DSA was 70 (23) mL/min/1.73 m(2), whereas the average eGFR of patients with class I DSA was 48 (21) mL/min/1.73 m(2) (p = 0.0071). MPA trough levels <1.3 mg/L long-term post-transplantation are associated with the formation of DSA. The association between the formation of DSA and minimum MPA exposure may support a strategy for preventing the formation of DSA.
Insights
Low mycophenolic acid (MPA) levels in renal transplant patients are linked to the development of de novo donor-specific antibodies (DSA). Maintaining adequate MPA exposure may help prevent DSA formation and improve long-term graft survival.
Area of Science:
- Nephrology
- Immunology
- Transplantation Medicine
Background:
- De novo donor-specific antibodies (DSA) are a major cause of graft loss after transplantation.
- Effective strategies to prevent DSA formation remain limited.
- The long-term impact of suboptimal mycophenolic acid (MPA) exposure on DSA development is not well understood.
Purpose of the Study:
- To investigate the association between MPA exposure and the long-term formation of DSA in renal transplant recipients.
- To determine if MPA trough levels correlate with the presence of class I and class II DSA.
Main Methods:
- Retrospective analysis of data from 32 renal transplant recipients.
- Long-term follow-up averaging 9.4 years.
- Measurement of de novo DSA using Luminex assay.
- Monitoring of tacrolimus and MPA trough levels.
Main Results:
- Most patients (27/32) developed detectable DSA.
- Lower minimum MPA trough levels were associated with class I DSA formation.
- Lower estimated glomerular filtration rate (eGFR) was also linked to class I DSA.
- MPA trough levels below 1.3 mg/L were associated with DSA development.
Conclusions:
- Suboptimal MPA exposure, indicated by trough levels <1.3 mg/L, is associated with DSA formation in renal transplant recipients.
- Monitoring and potentially optimizing MPA levels could be a strategy to prevent DSA.
- Further research is needed to confirm these findings and establish clinical guidelines.
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