ArticleFrontiers in immunology2026
Innate-immune crosstalk orchestrates T cell-mediated rejection in kidney transplants.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: T cell-mediated rejection (TCMR) remains a major barrier to long-term kidney allograft survival, driven by recipient immune responses against donor antigens. A comprehensive understanding of the cellular and molecular mechanisms underlying TCMR is essential for developing novel diagnostic and therapeutic strategies. Methods: We integrated two public single-cell RNA sequencing datasets (GSE145927 and E-MTAB-12051) to construct a comprehensive single-cell atlas of kidney allograft biopsies. Unsupervised clustering, functional scoring, trajectory inference, gene regulatory network analysis, and cell-cell communication analysis were performed. Key findings were validated in a murine TCMR model. Results: In the single TCMR sample analyzed, we observed several cell populations that were enriched and may be associated with TCMR. An NQO1 Conclusion: This hypothesis-generating study, based on a single TCMR case, provides a single-cell atlas of the TCMR immune microenvironment and suggests several subsets and pathways that may be involved. Our findings suggest that innate immune cells may initiate and amplify adaptive responses through chemokine and inflammatory networks, providing new insights into the potential role of innate immunity in allograft injury. The DUSP1
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.