Evidence map›Paper›PMID 42533592›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2026

Rag1-based time-stamp tracing of T-cell developmental origins.

Menglin Jiang, Yichao Li, Xinying Zong, Xiaolei Hao, Clifford Guy, Wojciech Rosikiewicz, Minghong He, Lu Bai, Wenjun Huang, Vivek Choudhary and 2 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Menglin JiangDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Yichao LiDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Xinying ZongDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Xiaolei HaoDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Clifford GuyDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Wojciech RosikiewiczCenter for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN, United States.
Minghong HeDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Lu BaiDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Wenjun HuangDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Vivek ChoudharyDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Yong ChengDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, United States.
Yongqiang FengDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN, United States.ORCID 0000-0002-2320-5063

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Shondra Michelle Miller · 1985 to 2026
$166.9M
Robust immune tolerance conferred by Foxp3 transcriptional regulationR01AI153138 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI FENG, YONGQIANG · 2021 to 2025
$2.2M
A novel genetic tool to investigate T cell development and functionR21AI146614 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI FENG, YONGQIANG · 2019 to 2020
$494k
American Lebanese Syrian Associated CharitiesNCI NIH HHS P30 CA021765NIAID NIH HHS R01 AI153138NIAID NIH HHS R21 AI146614NIH HHS R01 AI153138NIH HHS R21 AI146614Special Postdoctoral Fellowships of the Academic Programs Office of St. Jude Children's Research HospitalSt. Jude Children's Research Hospital
6 · The paper itself

Abstract

The postnatal T‑cell pool comprises cells at diverse developmental stages, complicating efforts to resolve T‑cell differentiation, maturation, and long‑term adaptation. To address this challenge, we developed Rag1‑mediated time-stamp tracing, a genetic strategy that enables time‑resolved tracking of T‑cell developmental origins. We validate the specificity and temporal resolution of this approach across multiple analytical platforms, including flow cytometry, imaging, and single‑cell multiomics. Applying this strategy to thymic regulatory T (Treg) cell development, we show that time-stamp tracing resolves distinct phases of Treg cell induction, maturation, and long‑term adaptation within heterogeneous populations. This analysis identifies precursor populations for thymic Treg cell induction, uncovers a maturation program in nascent Treg cells marked by CD73 upregulation and progressive DNA hypomethylation at Treg cell-specific loci, and distinguishes long‑lived mature Treg cells characterized by activation and clonal expansion. Together, these findings establish Rag1‑based time-stamp tracing as a versatile and unbiased approach for resolving T‑cell developmental origins across immunological contexts.

Indexed as

Homeodomain ProteinsT-Lymphocytes, RegulatoryAnimalsCell DifferentiationDNA MethylationFlow CytometryMiceMice, TransgenicThymus GlandHomeodomain ProteinsRAG-1 proteinregulatory T cellsT-cell ontogenytime-stamp tracing

Identifiers

PMID42533592
PMCPMC13423983

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.