Evidence map›Paper›PMID 30503142›Full record

ArticleCell stem cell2019

Human Intestinal Allografts Contain Functional Hematopoietic Stem and Progenitor Cells that Are Maintained by a Circulating Pool.

Jianing Fu, Julien Zuber, Mercedes Martinez, Brittany Shonts, Aleksandar Obradovic, Hui Wang, Sai-Ping Lau, Amy Xia, Elizabeth E Waffarn, Kristjana Frangaj and 14 more

Abstract read
In one paragraph

Article in Cell stem cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
–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

42 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Immunogenomic landscape of the T cell repertoire after human lung transplantation and its clinical relevance.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Tolerance Induction Strategies in Organ Transplantation: Current Status and Future Perspectives.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Review
  12. Article
  13. Chimerism-Mediated Tolerance in Intestinal Transplantation.Gastroenterology clinics of North America · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Jianing FuColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Julien ZuberColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Mercedes MartinezDepartment of Pediatrics, Columbia University, New York, NY 10032, USA.
Brittany ShontsColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Aleksandar ObradovicColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Hui WangColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Sai-Ping LauColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Amy XiaColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Elizabeth E WaffarnColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Kristjana FrangajColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Thomas M SavageColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Michael T SimpsonColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Suxiao YangColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Xinzheng V GuoHuman Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Michelle MironColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Microbiology & Immunology, Columbia University, New York, NY 10032, USA.
Takashi SendaColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Surgery, Columbia University, New York, NY 10032, USA.
Kortney RogersColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Adeeb RahmanHuman Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Siu-Hong HoColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA.
Yufeng ShenCenter for Computational Biology and Bioinformatics, Department of Systems Biology, Columbia University, New York, NY 10032, USA.
Adam GriesemerColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Surgery, Columbia University, New York, NY 10032, USA.
Donna L FarberColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Microbiology & Immunology, Columbia University, New York, NY 10032, USA; Department of Surgery, Columbia University, New York, NY 10032, USA.
Tomoaki KatoDepartment of Surgery, Columbia University, New York, NY 10032, USA.
Megan SykesColumbia Center for Translational Immunology, Department of Medicine, Columbia University, New York, NY 10032, USA; Department of Microbiology & Immunology, Columbia University, New York, NY 10032, USA; Department of Surgery, Columbia University, New York, NY 10032, USA. Electronic address: megan.sykes@columbia.edu.

Funding

Transcriptomics and Repertoire ProfilingP01AI106697 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Donna L. Farber · 2013 to 2026
$31.3M
Viral Assays CoreU19AI128949 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Donna L. Farber, Peter Alan Sims · 2017 to 2026
$26.4M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007367 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI REINER, STEVEN L · 1985 to 2021
$25.1M
Columbia University Graduate Training Program in Microbiology and ImmunologyT32AI106711 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Nicholas Arpaia, Uttiya Basu · 2014 to 2026
$2.1M
Helios Mass CytometerS10OD023547 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI RAHMAN, ADEEB HABIBUR · 2017 to 2017
$667k
BD Biosciences InfluxS10OD020056 · OD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SNOECK, HANS-WILLEM E · 2015 to 2015
$600k
Becton Dickinson LSR II Analytical Flow CytometerS10RR027050 · NCRR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CLYNES, RAPHAEL A. · 2011 to 2011
$413k
NCRR NIH HHS S10 RR027050NIAID NIH HHS P01 AI106697NIAID NIH HHS T32 AI106711NIAID NIH HHS U19 AI128949NIGMS NIH HHS T32 GM007367NIH HHS S10 OD020056NIH HHS S10 OD023547
6 · The paper itself

Abstract

Human intestinal transplantation often results in long-term mixed chimerism of donor and recipient blood in transplant patients. We followed the phenotypes of chimeric peripheral blood cells in 21 patients receiving intestinal allografts over 5 years. Donor lymphocyte phenotypes suggested a contribution of hematopoietic stem and progenitor cells (HSPCs) from the graft. Surprisingly, we detected donor-derived HSPCs in intestinal mucosa, Peyer's patches, mesenteric lymph nodes, and liver. Human gut HSPCs are phenotypically similar to bone marrow HSPCs and have multilineage differentiation potential in vitro and in vivo. Analysis of circulating post-transplant donor T cells suggests that they undergo selection in recipient lymphoid organs to acquire immune tolerance. Our longitudinal study of human HSPCs carried in intestinal allografts demonstrates their turnover kinetics and gradual replacement of donor-derived HSPCs from a circulating pool. Thus, we have demonstrated the existence of functioning HSPCs in human intestines with implications for promoting tolerance in transplant recipients.

Indexed as

Cell MovementAnimalsCell DifferentiationCell LineCell LineageChimerismGraft vs Host DiseaseHematopoietic Stem CellsHumansImmune ToleranceIntestinal MucosaIntestinesLiverLymph NodesMicePeyer's Patchescirculating poolhematopoietic progenitor cellhematopoietic stem cellimmune toleranceintestinal allograftintestinal transplantationmixed chimerismrecent thymic immigrantsrecipient repopulationT cell receptor

Identifiers

PMID30503142
PMCPMC6398344

What OpenQuestion holds

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LicenceTDM
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.