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Updated: May 16, 2026

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Large decrease of anti-tetanus anatoxin and anti-pneumococcal antibodies at one year after renal transplantation
Emine Nilufer Broeders1, Karl M Wissing, Lidia Ghisdal
1Universite Libre de Bruxelles, Brussels, Belgium. ebroeder@ulb.ac.be
Kidney transplant recipients on MMF and CNI show reduced antibody levels post-transplant. Pre-transplant immunization is recommended to maintain protective antibody titers.
Area of Science:
- Immunology
- Nephrology
- Transplantation
Background:
- Kidney transplant recipients (KTR) often have impaired antibody synthesis due to immunosuppressive drugs like azathioprine (AZA) and cyclosporine (CsA).
- Mycophenolate mofetil (MMF) is commonly used with calcineurin inhibitors (CNI) for immunosuppression in KTR.
Purpose of the Study:
- To prospectively evaluate the impact of MMF combined with a CNI on plasma antibody levels in kidney transplant recipients.
- To assess changes in anti-tetanus (TAnAb) and anti-pneumococcal (PnPsAb) antibody titers in KTR post-transplantation.
Main Methods:
- A prospective cohort study involving 94 KTR and 49 healthy controls.
- Measurement of serum titers for TAnAb and PnPsAb (against serotypes 14, 19F, 23F) at baseline (T0) and 12 months post-transplant (T12).
Main Results:
- KTR had significantly lower TAnAb detection rates (71% vs. 98%) and titers (1.46 UI/ml vs. 2.74) compared to controls at baseline.
- TAnAb titers in KTR decreased significantly from T0 to T12 (1.46 to 0.31 UI/ml) with a short half-life (7.7 months).
- PnPsAb titers also significantly decreased in KTR between T0 and T12, with half-lives ranging from 9.2 to 11.9 months.
Conclusions:
- MMF and CNI treatment in KTR leads to a profound and significant reduction in TAnAb and PnPsAb titers within the first year post-transplant.
- Pre-transplant immunization is crucial for KTR to establish and maintain adequate antibody levels after transplantation.
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