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In Vivo Spatial Transcriptomics for Bleeding-free Profiling Human Internal Organs

Sun, H.; Guo, F.; Zhao, X.; Wan, Y.; Zhang, X.; Sun, J.; He, X.; Gai, B.; Xiong, C.; Ma, Y.; Qu, J.; Li, P.; Gao, F.; Zhao, X.; Ji, X.; Yang, Z.; Mak, L.-Y.; Yap, Y. H.; Ke, J.; Shi, P.

2026-07-09 genetic and genomic medicine
10.64898/2026.07.06.26357355 medRxiv
Show abstract

Despite the significant technical advancement in spatial transcriptomics, its clinical usage is largely untapped. Here, we develop an integrated system, ENDO-Genome, for minimally invasive in-body transcript sampling to facilitate live spatial transcriptomic analysis of human internal organs. This is achieved by integrating a nanoarrayed biochip with existing endoscope to perform pressure-sensor-calibrated "Touch & Go" RNA extraction directly from human internal organs, including the highly vascularized liver or kidney, without the need for tissue biopsy, voiding any bleeding risks. By a demonstration using gastrointestinal endoscopy, multiplexed landscape of 55 mRNA transcripts was obtained from multiple locations of human intestinal tract via a 5-minute operation in routine examinations. Benefiting from a sequencing-free approach, each assay costs less than 10 US dollars. For the clinical study involving 15 Crohn' s disease (CD) patients, no complication case was reported out of 47 ENDO-Genome operations, showcasing the gentle deposition and excellent safety of the technique. The live spatial transcriptomics provides direct in vivo pictures of the heterogenous spatial transcriptional programs underlying CD pathological response at different intestinal locations, revealing distinct ileal phenotypes. This is manifested by unique microscale scattering of inflammation gene clusters, along with the discovery of a tissue-specific cooperative mechanisms between inflammation and RNA methylation regulations at single- or multi-cell scales.

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