Evidence map›Paper›PMID 32425928›Full record

ArticleFrontiers in immunology2020

Myeloid-Derived Suppressor Cells in Kidney Transplant Recipients and the Effect of Maintenance Immunotherapy.

María Iglesias-Escudero, David Sansegundo-Arribas, Paloma Riquelme, David Merino-Fernández, Sandra Guiral-Foz, Carmen Pérez, Rosalia Valero, Juan Carlos Ruiz, Emilio Rodrigo, Patricia Lamadrid-Perojo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. LDLRJournal of clinical and translational hepatology · 2026
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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

13 authors at 4 institutions in 3 countries.

María Iglesias-EscuderoTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
David Sansegundo-ArribasTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Paloma RiquelmeSection of Experimental Surgery, Department of Surgery, University Hospital of Regensburg, Regensburg, Germany.
David Merino-FernándezTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Sandra Guiral-FozTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Carmen PérezTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Rosalia ValeroTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Juan Carlos RuizTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Emilio RodrigoTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Patricia Lamadrid-PerojoTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
James A HutchinsonSection of Experimental Surgery, Department of Surgery, University Hospital of Regensburg, Regensburg, Germany.
Jordi OchandoDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Marcos López-HoyosTransplantation and Autoimmunity Group, Marqués de Valdecilla Health Research Institute (IDIVAL) Santander, Spain.
Instituto de Investigación Marqués de Valdecilla · ESMarqués de Valdecilla University Hospital · ESUniversity Hospital Regensburg · DEInstituto de Salud Carlos III · ES

Funding

Myeloid Specific Targeted Nanoimunotherapy for Organ Transplant AcceptanceR01AI139623 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI OCHANDO, JORDI · 2018 to 2022
$2.3M
NIAID NIH HHS R01 AI139623
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSC) represent a heterogeneous group of myeloid regulatory cells that were originally described in cancer. Several studies in animal models point to MDSC as important players in the induction of allograft tolerance due to their immune modulatory function. Most of the published studies have been performed in animal models, and the data addressing MDSCs in human organ transplantation are scarce. We evaluated the phenotype and function of different MDSCs subsets in 38 kidney transplant recipients (KTRs) at different time points. Our data indicate that monocytic MDSCs (Mo-MDSC) increase in KTR at 6 and 12 months posttransplantation. On the contrary, the percentages of polymorphonuclear MDSC (PMN-MDSC) and early-stage MDSC (e-MDSC) are not significantly increased. We evaluated the immunosuppressive activity of Mo-MDSC in KTR and confirmed their ability to increase regulatory T cells (Treg)

Indexed as

Kidney TransplantationAdultAgedFemaleHumansImmunosuppressive AgentsLymphocyte ActivationMaleMiddle AgedMyeloid-Derived Suppressor CellsSirolimusT-LymphocytesTOR Serine-Threonine KinasesTransplantation ToleranceImmunosuppressive AgentsMTOR protein, humanSirolimusTOR Serine-Threonine Kinasesimmunosuppressionkidney transplantationmTOR inhibitionmyeloid-derived suppressor cellstacrolimus

Identifiers

PMID32425928
PMCPMC7203496
OpenAlexW3022976756

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.