生物
干扰素
免疫学
病毒学
α-干扰素
Ⅰ型干扰素
干扰素γ
免疫
遗传学
计算生物学
免疫系统
α-干扰素
细胞因子
疾病
γ干扰素
作者
Joel Babdor,Ravi K. Patel,Brittany Davidson,Kelvin Koser,Cecilia Noecker,Maha K. Rahim,Jordan E. Bisanz,Iliana Tenvooren,Diana M. Marquez,M. L. Calvo,Vrinda Johri,Elizabeth McCarthy,Avneet Shaheed,Christina Ekstrand,Allison M. Weakley,Feiqiao Brian Yu,Kristen Krip,Kashif A. Shaikh,Hajera Amatullah,Oliver Fiehn
出处
期刊:Cell
[Cell Press]
日期:2026-03-09
卷期号:189 (10): 3144-3163.e20
被引量:1
标识
DOI:10.1016/j.cell.2026.02.003
摘要
Human immune systems are highly variable, with most variation attributable to non-genetic sources. The gut microbiome crucially shapes the immune system; however, its relationship with the baseline immune states of healthy humans remains incompletely understood. Therefore, we performed multi-omic profiling of 110 healthy participants through the ImmunoMicrobiome study. A factor-based integrative approach identified coordinated variation, revealing that the interferon response was amongst the most variable immune features in healthy participants. Microbiome composition, pathways, and stool metabolites varied concomitantly with interferon response pathways. Longitudinal data spanning more than a year indicated the significant stability of these parameters within individuals over time. Our study provides extensive data to examine the relationship between the immune states and microbiomes of healthy individuals at steady state, which paves the way for delineating inter-individual differences relevant for disease susceptibility and responses to therapy.
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