Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, Washington.
Clin Cancer Res. 2024 Sep 13;30(18):4240-4250. doi: 10.1158/1078-0432.CCR-24-0875.
Whether and how the oral microbiome and its changes in allogeneic hematopoietic cell transplantation (alloHCT) recipients may contribute to oral chronic GVHD (cGVHD) pathogenesis is unknown. In addition, although the oral and colonic microbiota are distinct in healthy adults, whether oral microbes may ectopically colonize the gut in alloHCT patients is unknown.
To address these knowledge gaps, longitudinal oral and fecal samples were collected prospectively in the multicenter Close Assessment and Testing for Chronic GVHD study (NCT04188912). Through shotgun metagenomic sequencing of the samples collected at baseline, oral cGVHD onset, first post-cGVHD onset visit, and 1-year post-HCT time points in patients with oral cGVHD (cases; N = 29) or without any cGVHD (controls; N = 51), we examined whether (i) oral and/or gut microbiomes and their longitudinal trajectories differ between cases and controls and (ii) oral and gut microbiomes overlap in alloHCT recipients, especially those developing cGVHD.
A total of 195 samples were analyzed. The onset of oral cGVHD was characterized by an expansion of Streptococcus salivarius and Veillonella parvula in the oral microbiome. High levels of oral/gut microbiota overlap were observed, particularly in patients with oral cGVHD, suggesting ectopic colonization of the gut by oral bacteria.
The unusual coalescence of two distant niches in these patients may result in short- or long-term consequences for the host, a novel avenue for future research. In addition, this study suggests a contribution of the oral microbiome to oral cGVHD pathogenesis.
异体造血细胞移植(alloHCT)受者的口腔微生物组及其变化是否以及如何有助于口腔慢性移植物抗宿主病(cGVHD)的发病机制尚不清楚。此外,尽管健康成年人的口腔和结肠微生物群不同,但口腔微生物是否可能在 alloHCT 患者中异位定植于肠道尚不清楚。
为了解决这些知识空白,我们前瞻性地在多中心密切评估和慢性移植物抗宿主病检测研究(NCT04188912)中连续收集口腔和粪便样本。通过对基线、口腔 cGVHD 发病、首次 cGVHD 发病后就诊和 alloHCT 后 1 年时间点采集的样本进行 shotgun 宏基因组测序,我们研究了口腔 cGVHD 患者(病例;N=29)或无任何 cGVHD 患者(对照组;N=51)的口腔和/或肠道微生物组及其纵向轨迹是否存在差异,以及口腔和肠道微生物组是否存在重叠,特别是在发生 cGVHD 的 alloHCT 受者中。
共分析了 195 个样本。口腔 cGVHD 的发病特征是口腔微生物组中链球菌唾液亚种和小韦荣球菌的扩张。观察到口腔/肠道微生物组的高度重叠,特别是在发生口腔 cGVHD 的患者中,这表明口腔细菌异位定植于肠道。
这些患者两个遥远生态位的异常融合可能导致宿主的短期或长期后果,这是未来研究的一个新途径。此外,本研究提示口腔微生物组可能参与口腔 cGVHD 的发病机制。