Evidence map›Paper›PMID 37552988›Full record

ArticleCell reports. Medicine2023

High-dimensional profiling of pediatric immune responses to solid organ transplantation.

Mahil Rao, Meelad Amouzgar, James T Harden, M Gay Lapasaran, Amber Trickey, Brian Armstrong, Jonah Odim, Tracia Debnam, Carlos O Esquivel, Sean C Bendall and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Single-cell transcriptional landscape of liver transplant rejection reveals tissue persistence of clonally expanded, treatment-resistant T cells.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  5. Graft-derived extracellular vesicles transport miRNAs to modulate macrophage polarization after heart transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  6. Article
  7. Article
  8. Article
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 at 3 institutions in 1 country.

Mahil RaoDepartment of Pediatrics, Division of Pediatric Critical Care Medicine, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Transplant Immunology Lab, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Meelad AmouzgarImmunology Graduate Program, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
James T HardenTransplant Immunology Lab, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Immunology Graduate Program, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
M Gay LapasaranTransplant Immunology Lab, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Amber TrickeyDepartment of Surgery, Division of Abdominal Transplant Surgery, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Brian ArmstrongRho, Inc., Durham, NC, USA.
Jonah OdimNational Institutes of Health, Bethesda, MD, USA.
Tracia DebnamNational Institutes of Health, Bethesda, MD, USA.
Carlos O EsquivelTransplant Immunology Lab, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Department of Surgery, Division of Abdominal Transplant Surgery, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Sean C BendallProgram in Immunology, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Department of Pathology, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Olivia M MartinezTransplant Immunology Lab, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Department of Surgery, Division of Abdominal Transplant Surgery, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Program in Immunology, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Sheri M KramsTransplant Immunology Lab, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Department of Surgery, Division of Abdominal Transplant Surgery, Stanford University School of Medicine, Palo Alto, CA 94304, USA; Program in Immunology, Stanford University School of Medicine, Palo Alto, CA 94304, USA. Electronic address: smkrams@stanford.edu.
Palo Alto University · USStanford University · USNational Institutes of Health · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Biomarkers for Post-Transplant Lymphoproliferative Disorders in ChildrenU01AI104342 · NIAID · STANFORD UNIVERSITY · PI ESQUIVEL, CARLOS O · 2013 to 2018
$7.7M
Exosomes and the Immune Response in Allograft Outcomes in Pediatric Transplant RecipientsU01AI135950 · NIAID · STANFORD UNIVERSITY · PI KRAMS, SHERI M. · 2018 to 2022
$6.1M
RhoFED T-SCCCU01AI178768 · NIAID · RHO FEDERAL SYSTEMS DIVISION, INC. · PI ARMSTRONG, BRIAN · 2023 to 2023
$1.5M
NIAID NIH HHS U01 AI104342NIAID NIH HHS U01 AI135950NIAID NIH HHS U01 AI178768
6 · The paper itself

Abstract

Solid organ transplant remains a life-saving therapy for children with end-stage heart, lung, liver, or kidney disease; however, ∼33% of allograft recipients experience acute rejection within the first year after transplant. Our ability to detect early rejection is hampered by an incomplete understanding of the immune changes associated with allograft health, particularly in the pediatric population. We performed detailed, multilineage, single-cell analysis of the peripheral blood immune composition in pediatric solid organ transplant recipients, with high-dimensional mass cytometry. Supervised and unsupervised analysis methods to study cell-type proportions indicate that the allograft type strongly influences the post-transplant immune profile. Further, when organ-specific differences are considered, graft health is associated with changes in the proportion of distinct T cell subpopulations. Together, these data form the basis for mechanistic studies into the pathobiology of rejection and allow for the development of new immunosuppressive agents with greater specificity.

Indexed as

Kidney DiseasesKidney TransplantationOrgan TransplantationChildHumansImmunityTransplantation, HomologousallograftCyTOFpediatricrejectiontransplantation

Identifiers

PMID37552988
PMCPMC10439249
OpenAlexW4385638030

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.