补充丙酸可促进终末期肾病患者调节性 T 细胞的扩增,但对肾移植患者没有促进作用。

Frontiers in transplantation Pub Date : 2024-09-09 eCollection Date: 2024-01-01 DOI:10.3389/frtra.2024.1404740
Moritz Anft, Fabian Meyer, Sirin Czygan, Felix S Seibert, Benjamin J Rohn, Fotios Tsimas, Richard Viebahn, Timm H Westhoff, Ulrik Stervbo, Nina Babel, Panagiota Zgoura
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引用次数: 0

摘要

在之前的一项研究中,我们发现透析患者补充丙酸具有抗炎作用。本研究旨在分析与透析患者相比,丙酸对肾移植患者慢性炎症状态和 T 细胞组成的影响。共有 10 名透析患者和 16 名接受标准三联免疫抑制疗法的肾移植患者在 30 天内每天接受 2 × 500 毫克丙酸。我们对补充丙酸前后的细胞免疫系统进行了分析,并在此后的 30-90 天进行了随访。我们测量了主要的免疫细胞类型,并对包括调节性 T 细胞(Tregs)、B 细胞和树突状细胞在内的 T 细胞进行了深入分析。此外,我们还通过分析第三方抗原特异性 T 细胞对 recall(破伤风白喉疫苗)抗原刺激后的功能活性和抗原反应性进行了评估。在透析患者中,我们观察到摄入丙酸后 CD25highCD127- Tregs 的扩增。与此相反,在接受免疫抑制治疗的移植患者中,补充同样的丙酸并不会导致Tregs扩增。我们也没有观察到主要免疫细胞亚群的频率有任何变化,除了 CD4+/CD8+ 的分布,移植人群中 CD4+ T 细胞增加,CD8+ T 细胞减少。我们的数据表明,含有丙酸盐的膳食补充剂可能会通过Treg扩增,对减轻透析患者的全身炎症有好处。但是,在移植患者中却没有观察到这种效果,这可能是由于免疫抑制剂阻碍了 Treg 的扩增。
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Propionic acid supplementation promotes the expansion of regulatory T cells in patients with end-stage renal disease but not in renal transplant patients.

In a previous study, we showed an anti-inflammatory effect of propionic acid supplementation in dialysis patients. The present study intends to analyze the effect of propionic acid on the chronic inflammatory state and T-cell composition in kidney transplant patients compared to dialysis patients. A total of 10 dialysis patients and 16 kidney transplant patients under immunosuppressive standard triple immunosuppressive therapy received 2 × 500 mg propionic acid per day for 30 days. The cellular immune system was analyzed before and after the propionic acid supplementation and 30-90 days thereafter as a follow-up. We measured the main immune cell types and performed an in-depth characterization of T cells including regulatory T cells (Tregs), B cells, and dendritic cells. In addition, we assessed the functional activity and antigenic responsiveness by analysis of third-party antigen-specific T cells after their stimulation by recall (tetanus diphtheria vaccine) antigen. In dialysis patients, we observed an expansion of CD25highCD127- Tregs after propionic acid intake. In contrast, the same supplementation did not result in any expansion of Tregs in transplant patients under immunosuppressive therapy. We also did not observe any changes in the frequencies of the main immune cell subsets except for CD4+/CD8+ distribution with an increase of CD4+ T cells and decrease of CD8+ T cells in the transplant population. Our data suggest that dietary supplements containing propionate might have a beneficial effect decreasing systemic inflammation in dialysis patients through Treg expansion. However, this effect was not observed in transplant patients, which could be explained by counteracting effect of immunosuppressive drugs preventing Treg expansion.

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