# The viability of ABO-incompatible kidney transplants: a single-center cohort in China

**Authors:** Yiding Chen, Jiashan Pan, Dongsheng Li, Kun Wang, Handong Ding, Fei Zhang, Wenbo Wang, Pengfei Li, Jinbiao Zhong, Guiyi Liao

PMC · DOI: 10.3389/fimmu.2026.1747411 · Frontiers in Immunology · 2026-02-17

## TL;DR

This study shows that ABO-incompatible kidney transplants in China have similar short- to mid-term outcomes as compatible transplants, despite higher initial costs.

## Contribution

The study provides new evidence on the safety and feasibility of ABOi-LDKT in a Chinese population.

## Key findings

- ABOi-LDKT showed comparable 1- and 3-year patient and graft survival to ABOc-LDKT in the single-center cohort.
- Hospitalization costs were higher for ABOi-LDKT due to desensitization procedures.
- No significant differences were found in complications, infections, or acute rejection between the groups.

## Abstract

ABO-incompatible living donor kidney transplantation (ABOi-LDKT) offers a potential solution to organ shortages, but its safety and economic impact in China remain uncertain. This study evaluated short- to mid-term outcomes of ABOi-LDKT in a Chinese population by integrating evidence from a meta-analysis and a single-center cohort.

We performed a meta-analysis of 18 studies including 15,611 kidney transplant recipients to compare graft and patient survival between ABOi-LDKT and ABO-compatible LDKT (ABOc-LDKT). In parallel, we conducted a retrospective single-center cohort study of 41 ABOi-LDKT and 132 ABOc-LDKT recipients transplanted between 2021 and 2022. Outcomes included patient and graft survival, renal function, postoperative complications, infections, delayed graft function (DGF), acute rejection, and hospitalization costs.

The meta-analysis showed lower 1-year graft survival and 3-year patient survival in ABOi-LDKT than in ABOc-LDKT. In contrast, our single-center cohort demonstrated comparable 1- and 3-year patient and graft survival between groups. No significant differences were observed in surgical complications, infections, DGF, or acute rejection. ABOi-LDKT recipients showed better renal function at two weeks post-transplant, with no sustained differences thereafter. Hospitalization costs were higher in the ABOi-LDKT group, reflecting additional desensitization procedures.

In this Chinese single-center cohort, ABOi-LDKT achieved short- to mid-term clinical outcomes comparable to ABOc-LDKT despite higher upfront costs. When combined with contemporary desensitization protocols, ABOi-LDKT appears to be a safe and feasible strategy to expand access to living donor kidney transplantation in settings with severe organ shortages.

## Full-text entities

- **Genes:** ABO (ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) [NCBI Gene 28] {aka A3GALNT, A3GALT1, GTA, GTB, NAGAT}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** CMV (MESH:D003586), bleeding (MESH:D006470), ischemia (MESH:D007511), dehiscence (MESH:D013529), AMR (MESH:D020274), Pneumocystis jirovecii pneumonia (MESH:D011020), fibrosis (MESH:D005355), inflammatory (MESH:D007249), pulmonary infection (MESH:D012141), ureteral stenosis (MESH:D014515), oliguria (MESH:D009846), CDC (MESH:D019966), kidney transplantation (MESH:D007674), infectious (MESH:D003141), BK virus infection (MESH:D014777), death (MESH:D003643), reperfusion injury (MESH:D015427), DGF (MESH:D051799), UTI (MESH:D014552), wound infection (MESH:D014946), postoperative complication (MESH:D011183), ESRD (MESH:D007676), COVID-19 (MESH:D000086382), Infection (MESH:D007239), effusion (MESH:D000080324)
- **Chemicals:** methylprednisolone (MESH:D008775), Mezlocillin sodium (MESH:D008802), MMF (MESH:D009173), methylprednisolone sodium succinate (MESH:D008776), Ganciclovir (MESH:D015774), SMZ-TMP (MESH:D015662), steroids (MESH:D013256), Prednisone (MESH:D011241), creatinine (MESH:D003404), DTPA (MESH:D004369), Sulbactam sodium (MESH:D013407), Tacrolimus (MESH:D016559), 99mTc-DTPA (-), Rituximab (MESH:D000069283)
- **Species:** Fungi (kingdom) [taxon 4751], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Betapolyomavirus hominis (species) [taxon 1891762]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12953097/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953097/full.md

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Source: https://tomesphere.com/paper/PMC12953097