Evidence map›Paper›PMID 37761990›Full record

ArticleInternational journal of molecular sciences2023

Mesenchymal Stromal Cell-Derived Small Extracellular Vesicles Modulate Apoptosis, TNF Alpha and Interferon Gamma Response Gene mRNA Expression in T Lymphocytes.

Andrea Fracchia, Drirh Khare, Samar Da'na, Reuven Or, Amnon Buxboim, Boaz Nachmias, Claudine Barkatz, Regina Golan-Gerstl, Swasti Tiwari, Polina Stepensky and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

15 authors at 3 institutions in 2 countries.

Andrea FracchiaDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.
Drirh KhareDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.
Samar Da'naDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.
Reuven OrDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.
Amnon BuxboimDepartment of Cell and Developmental Biology, Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Boaz NachmiasFaculty of Medicine, Hebrew University of Jerusalem, Jerusalem 9112001, Israel.ORCID 0000-0002-7341-2167
Claudine BarkatzDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.
Regina Golan-GerstlDepartment of Pediatrics, Hadassah-Hebrew University Medical Center, Jerusalem 9112001, Israel.ORCID 0000-0003-3224-9495
Swasti TiwariDepartment of Molecular Medicine & Biotechnology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow 226014, India.ORCID 0000-0002-1701-2636
Polina StepenskyDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.
Yuval NevoInfo-CORE, Bioinformatics Unit of the I-CORE at the Hebrew University of Jerusalem, Jerusalem 9112001, Israel.
Hadar BenyaminiInfo-CORE, Bioinformatics Unit of the I-CORE at the Hebrew University of Jerusalem, Jerusalem 9112001, Israel.
Sharona ElgavishInfo-CORE, Bioinformatics Unit of the I-CORE at the Hebrew University of Jerusalem, Jerusalem 9112001, Israel.
Osnat Almogi-HazanDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.ORCID 0000-0002-2961-612X
Batia AvniDepartment of Bone Marrow Transplantation & Cancer Immunotherapy, Hadassah Medical Center, Jerusalem 9112001, Israel.ORCID 0000-0001-8516-2751
Hebrew University of Jerusalem · ILHadassah Medical Center · ILSanjay Gandhi Post Graduate Institute of Medical Sciences · IN

Funding

Department of Science and Technology, Government of India 0000-0000Ministry of Science & Technology, Israel 0000-0000
6 · The paper itself

Abstract

Recent studies have highlighted the therapeutic potential of small extracellular bodies derived from mesenchymal stem cells (MSC-sEVs) for various diseases, notably through their ability to alter T-cell differentiation and function. The current study aimed to explore immunomodulatory pathway alterations within T cells through mRNA sequencing of activated T cells cocultured with bone marrow-derived MSC-sEVs. mRNA profiling of activated human T cells cocultured with MSC-sEVs or vehicle control was performed using the QIAGEN Illumina sequencing platform. Pathway networks and biological functions of the differentially expressed genes were analyzed using Ingenuity pathway analysis (IPA)

Indexed as

Extracellular VesiclesTumor Necrosis Factor-alphaApoptosisHumansInterferon-gammaT-LymphocytesInterferon-gammaTumor Necrosis Factor-alphagene set enrichment analysisIngenuity Pathway Analysismesenchymal stem cellsnext-generation sequencingsmall extracellular vesiclesT lymphocytes

Identifiers

PMID37761990
PMCPMC10530670
OpenAlexW4386443923

What Socratic 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 Socratic graph.