| Literature DB >> 33643315 |
Xianzhang Luo1,2, Ji Zhang1, Sijuan Zou3, Xinqiang Wang1, Gen Chen4, Zhen Li4, Kaiyan Li5, Mengqing Wang1, Zhishui Chen1, Changshen Ming1, Xiaohua Zhu3, Nianqiao Gong1.
Abstract
Integration of non-vascularized bone grafting and bone marrow aspirate infusion in transplantation may provide clinical benefit. Here we have incorporated bone fragment co-transplantation and bone marrow aspirate infusion (BF-BM) into living kidney transplantation (LKT). Twenty LKT recipients receiving bone fragments and bone marrow aspirates donated from their corresponding donors were enrolled into a retrospective study. A contemporaneous control group was formed of 38 out of 128 conventional LKT recipients, selected using propensity score matching by a 1:2 Greedy algorithm. Ultrasonography, contrast-enhanced ultrasonography (US/CEUS) and SPECT/CT showed that the co-transplanted bone fragments remained viable for 6 months, subsequently shrank, and finally degenerated 10 months post-transplantation. BF-BM resulted in earlier kidney recovery and more robust long-term kidney function. Throughout 5 years of follow-up, BF-BM had regulatory effects on dendritic cells (DCs), T helper (Th1/Th2) cells and regulatory T cells (Tregs). Both alloantigen-specific lymphocyte proliferation and panel reactive antibody levels were negative in all recipients with or without BF-BM. In addition, the BF-BM group experienced few complications during the 5-year follow-up (as did the donors)-this was not different from the controls. In conclusion, BF-BM is safe and benefits recipients by protecting the kidney and regulating the immune response.Entities:
Keywords: bone fragment co-transplantation; bone marrow aspirate infusion; immune regulation; kidney protection; living kidney transplantation (LKT)
Year: 2021 PMID: 33643315 PMCID: PMC7904687 DOI: 10.3389/fimmu.2021.630710
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561