# Can Double-Negative B Cells and Marginal Zone B Cells Have a Potential Impact on the Outcome of Kidney Transplantation?

**Authors:** Ariadni Fouza, Asimina Fylaktou, Maria Daoudaki, Persefoni Talimtzi, Anneta Tagkouta, Lampros Vagiotas, Georgios Katsanos, Georgios Tsoulfas, Nikolaos Antoniadis

PMC · DOI: 10.3390/jcm14103312 · Journal of Clinical Medicine · 2025-05-09

## TL;DR

This study explores how specific B cell populations may influence kidney transplant outcomes over a year.

## Contribution

The study identifies a potential link between marginal zone B cell frequency and rejection risk after kidney transplantation.

## Key findings

- MZB and DN cell frequencies and numbers increased 12 months after transplantation.
- Lower MZB cell frequency (<20.6%) predicted rejection risk with 72.7% sensitivity and 69.6% specificity.
- No correlation was found between cell populations and graft function at any time point.

## Abstract

Objectives/Background: B lymphocytes are involved in both graft function and rejection. The role of double-negative (DN) and marginal zone B (MZB) lymphocytes in transplantation remains unclear. This study aims to investigate their role one year after transplant. Methods: The frequency and absolute numbers of DN and MZB cells were determined by flow cytometry before transplantation and at 3, 6 and 12 months after transplant. They were correlated with graft function and rejection. Results: Both the frequency and absolute number of MZB and DN cells increased 12 months after transplantation. Variations were observed in the populations studied at different time points. The observed decrease in the frequency of MZB lymphocytes in kidney recipients with rejection at 12 months, the end of follow-up, was associated with rejection episodes. On ROC curve analysis, a cut-off value of <20.6% could be a predictor of rejection risk in the first 12 months after transplantation (sensitivity 72.7%, specificity 69.6%). No relationship was found between the frequencies and absolute numbers of cell populations and graft function at any time point. Conclusions: The kinetics of B cells (DN and MZB) were determined over the course of 12 months after kidney transplantation. The frequency of MZ B cells was associated with rejection episodes.

## Full-text entities

- **Genes:** Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, PCSK7 (proprotein convertase subtilisin/kexin type 7) [NCBI Gene 9159] {aka LPC, PC7, PC8, SPC7}, TNFRSF1A (TNF receptor superfamily member 1A) [NCBI Gene 7132] {aka CD120a, FPF, TBP1, TNF-R, TNF-R-I, TNF-R55}, Cd40 (CD40 antigen) [NCBI Gene 21939] {aka Bp50, GP39, HIGM1, IGM, IMD3, T-BAM}, ITGAX (integrin subunit alpha X) [NCBI Gene 3687] {aka CD11C, SLEB6}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CD27 (CD27 molecule) [NCBI Gene 939] {aka S152, S152. LPFS2, T14, TNFRSF7, Tp55}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IGHD6-13 (immunoglobulin heavy diversity 6-13) [NCBI Gene 28487] {aka DN1, IGHD613}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, Cd40lg (CD40 ligand) [NCBI Gene 21947] {aka CD154, CD40-L, Cd40l, HIGM1, IGM, IMD3}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, CR2 (complement C3d receptor 2) [NCBI Gene 1380] {aka C3DR, CD21, CR, CVID7, SLEB9}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, BCR (BCR activator of RhoGEF and GTPase) [NCBI Gene 613] {aka ALL, BCR1, CML, D22S11, D22S662, PHL}
- **Diseases:** infection (MESH:D007239), hematological disorders (MESH:D006402), arthritis (MESH:D001168), malaria (MESH:D008288), DN (MESH:D005671), Chronic Kidney Disease (MESH:D051436), cardiac arrest (MESH:D006323), malignancy (MESH:D009369), inflammatory (MESH:D007249), injury to (MESH:D014947), SLE (MESH:D008180), ischemia (MESH:D007511), AMR (MESH:C565965), deterioration of renal function (MESH:D058186), autoimmune diseases (MESH:D001327)
- **Chemicals:** basiliximab (MESH:D000077552), tacrolimus (MESH:D016559), mycophenolate mofetil (MESH:D009173)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721], Mus musculus (house mouse, species) [taxon 10090], hepatitis C virus [taxon 11103], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12112073/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12112073/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12112073/full.md

---
Source: https://tomesphere.com/paper/PMC12112073