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基于微生物组对异基因造血干细胞移植结果的预测

Microbiome-based prediction of allogeneic hematopoietic stem cell transplantation outcome.

作者信息

Shtossel Oshrit, Eshel Adi, Fried Shalev, Geva Mika, Danylesko Ivetta, Yerushalmi Ronit, Shem-Tov Noga, Fein Joshua A, Fabbrini Marco, Shimoni Avichai, Turjeman Sondra, Louzoun Yoram, Nagler Arnon, Koren Omry, Shouval Roni

机构信息

Department of Mathematics, Bar-Ilan University, Ramat Gan 52900, Israel.

The Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel.

出版信息

Genome Med. 2025 Jul 17;17(1):80. doi: 10.1186/s13073-025-01507-8.

Abstract

BACKGROUND

Allogeneic hematopoietic stem cell transplantation (HSCT) is potentially curative for hematologic malignancies but is frequently complicated by relapse and immune-mediated complications, such as graft-versus-host disease (GVHD). Emerging evidence suggests a role for the intestinal and oral microbiome in modulating HSCT outcomes, yet predictive models incorporating microbiome data remain limited.

METHODS

We applied the RATIO (suRvival Analysis lefT barrIer lOss) model to longitudinal stool and saliva microbiome data from 204 adult HSCT recipients to predict the timing of seven outcomes: overall survival (OS), non-relapse mortality (NRM), relapse, acute GVHD (grades II-IV and III-IV), chronic GVHD, and oral chronic GVHD. A total of 514 stool and 1291 saliva samples were collected over 70 weeks post-HSCT. Model performance was evaluated using the concordance index (CI) and Spearman correlation coefficient (SCC), with SHAP (SHapley Additive exPlanations) analysis used for model interpretability.

RESULTS

Oral and stool microbial dysbiosis peaked within the first 2 weeks post-HSCT, followed by partial recovery. Using the RATIO model, we found that microbiome features from early time points (weeks 1-2) were most predictive of short-term complications such as acute GVHD, while later samples (weeks 36-70) were more informative for long-term outcomes, including overall survival. RATIO outperformed traditional survival models (Cox and Random Survival Forest) across most outcomes (median CI > 0.65), with stool microbiota showing greater predictive power than saliva. SHAP analysis identified specific stool genera, including Collinsella and Eggerthella, associated with shorter time to various complications. External validation using a pediatric GVHD cohort confirmed the model's generalizability and reproducibility. External validation using a pediatric HSCT cohort (n = 90) confirmed the reproducibility and generalizability of these microbiome-based predictions.

CONCLUSIONS

Microbiome profiling of stool and saliva samples offers robust, time-sensitive prediction of post-HSCT complications. The RATIO model enables interpretable, time-to-event prediction across multiple outcomes and may inform microbiome-guided interventions to improve transplant success.

摘要

背景

异基因造血干细胞移植(HSCT)对血液系统恶性肿瘤具有潜在的治愈作用,但常伴有复发和免疫介导的并发症,如移植物抗宿主病(GVHD)。新出现的证据表明肠道和口腔微生物群在调节HSCT结果中发挥作用,但纳入微生物群数据的预测模型仍然有限。

方法

我们将RATIO(生存分析左屏障损失)模型应用于204名成年HSCT受者的纵向粪便和唾液微生物群数据,以预测七个结果的发生时间:总生存期(OS)、非复发死亡率(NRM)、复发、急性GVHD(II-IV级和III-IV级)、慢性GVHD和口腔慢性GVHD。在HSCT后的70周内共收集了514份粪便样本和1291份唾液样本。使用一致性指数(CI)和Spearman相关系数(SCC)评估模型性能,使用SHAP(Shapley加性解释)分析进行模型解释。

结果

口腔和粪便微生物失调在HSCT后的前2周内达到峰值,随后部分恢复。使用RATIO模型,我们发现早期时间点(第1-2周)的微生物群特征最能预测急性GVHD等短期并发症,而后期样本(第36-70周)对包括总生存期在内的长期结果更具信息量。在大多数结果中(中位数CI>0.65),RATIO优于传统生存模型(Cox模型和随机生存森林模型),粪便微生物群显示出比唾液更强的预测能力。SHAP分析确定了特定的粪便属,包括柯林斯菌属和埃格特菌属,它们与各种并发症发生时间较短相关。使用儿科GVHD队列进行的外部验证证实了该模型的普遍性和可重复性。使用儿科HSCT队列(n = 90)进行的外部验证证实了这些基于微生物群的预测的可重复性和普遍性。

结论

粪便和唾液样本的微生物群分析为HSCT后并发症提供了强大的、对时间敏感的预测。RATIO模型能够对多个结果进行可解释的、事件发生时间的预测,并可能为微生物群指导的干预措施提供信息,以提高移植成功率。

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