# Kidney transplant outcomes in HLA desensitized patients with pretransplant CDC and/or FCM positive crossmatches

**Authors:** Johan Noble, Céline Dard, Diane Giovannini, Hamza Naciri Bennani, Pierre Fournier, Béatrice Bardy, Anne Bourdin, Farida Imerzoukene, Lionel Motte, Florian Terrec, Paolo Malvezzi, Thomas Jouve, Lionel Rostaing

PMC · DOI: 10.3389/fimmu.2025.1612462 · 2025-06-23

## TL;DR

This study shows that desensitization therapy allows HLA-incompatible kidney transplants to have similar long-term success as compatible transplants, though rejection rates are higher.

## Contribution

The study demonstrates that immunoadsorption-based desensitization enables successful kidney transplants in HLA-incompatible patients with high cPRA and positive crossmatches.

## Key findings

- HLA-incompatible patients had similar graft survival rates as HLA-compatible patients at 1 year and last follow-up.
- HLA-incompatible patients experienced significantly more biopsy-proven antibody-mediated rejections.
- Infectious complication rates were similar between HLA-compatible and HLA-incompatible groups.

## Abstract

Kidney transplant (KT) candidates with very high calculated panel reactive alloantibody (cPRA >95%) have limited chances to receive an HLA-matched transplant unless they undergo pretransplant desensitization.

To assess the efficacy of immunoadsorption (IA) in desensitizing pretransplant KT candidates with high cPRA and positive crossmatch.

This was a single-center retrospective cohort study involving highly HLA-sensitized patients (cPRA >85%). Forty-nine patients underwent HLA-incompatible (HLAi) KT, of whom 25 (51%) received kidneys from deceased donors. Of these 49 patients, 23 had either a positive complement-dependent cytotoxic cross-match (CDC) and/or a positive flow cytometry cross-match (FCM). The remaining 26 patients had donor-specific anti-HLA (DSAs) detectable only by Luminex (CDC and FCM cross-matches were negative). Only CDC-positive and FCM-positive patients were desensitized. These 49 patients were compared with 160 patients who had cPRA >85% but underwent HLA-compatible (HLAc) KT, i.e., without pretransplant DSAs.

Pretransplant desensitization included IA sessions, rituximab, tacrolimus, steroids, and mycophenolate mofetil. Induction therapy consisted of antithymocyte globulins.

The mean follow-up duration was 7.4 ± 4 years. At 1-year and at last follow-up, 43 patient and death-censored graft survival rates were similar between HLAc and HLAi patients. However, HLAi patients experienced significantly more biopsy-proven rejections compared to HLAc patients. These rejections were predominantly antibody-mediated. Finally, the rate of infectious complications was similar between HLAc and HLAi patients.

IA in addition to immunosuppression is an effective option for desensitizing HLAi patients, yielding favorable long-term outcomes.

## Full-text entities

- **Genes:** HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}
- **Diseases:** CDC (MESH:C537866), infectious complications (MESH:D003141)
- **Chemicals:** rituximab (MESH:D000069283), mycophenolate mofetil (MESH:D009173), tacrolimus (MESH:D016559), CDC (-), steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12229852/full.md

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Source: https://tomesphere.com/paper/PMC12229852