Evidence map›Paper›PMID 37511568›Full record

ArticleInternational journal of molecular sciences2023

Hypoimmunogenic Human Pluripotent Stem Cells as a Powerful Tool for Liver Regenerative Medicine.

Piera Trionfini, Elena Romano, Marco Varinelli, Lorena Longaretti, Paola Rizzo, Roberta Giampietro, Annalina Caroli, Sistiana Aiello, Marta Todeschini, Federica Casiraghi and 3 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  10. Special Issue "Stem Cell Biology & Regenerative Medicine".International journal of molecular sciences · 2023
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  11. 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

13 authors at 1 institution in 1 country.

Piera TrionfiniIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0002-6599-0709
Elena RomanoIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.
Marco VarinelliIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0001-9046-9555
Lorena LongarettiIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0002-4366-4152
Paola RizzoIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.
Roberta GiampietroIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0002-2349-5224
Annalina CaroliIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.
Sistiana AielloIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.
Marta TodeschiniIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0003-3422-8815
Federica CasiraghiIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.
Giuseppe RemuzziIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0002-6194-3446
Ariela BenigniIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0002-4721-5485
Susanna TomasoniIstituto di Ricerche Farmacologiche Mario Negri IRCCS, 24126 Bergamo, Italy.ORCID 0000-0002-7212-2512
Mario Negri Institute for Pharmacological Research · IT

Funding

Roche (Italy) NATelethon Foundation GGP20073
6 · The paper itself

Abstract

Induced pluripotent stem cells (iPSC) have huge potential as cell therapy for various diseases, given their potential for unlimited self-renewal and capability to differentiate into a wide range of cell types. Although autologous iPSCs represents the ideal source for patient-tailored regenerative medicine, the high costs of the extensive and time-consuming production process and the impracticability for treating acute conditions hinder their use for broad applications. An allogeneic iPSC-based strategy may overcome these issues, but it carries the risk of triggering an immune response. So far, several approaches based on genome-editing techniques to silence human leukocyte antigen class I (HLA-I) or II (HLA-II) expression have been explored to overcome the immune rejection of allogeneic iPSCs. In this study, we employed the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/CRISPR associated protein 9) system to delete the β2-Microglobulin (

Indexed as

Induced Pluripotent Stem CellsPluripotent Stem CellsGene EditingHistocompatibility Antigens Class IHumansLiverRegenerative MedicineHistocompatibility Antigens Class Icell therapyendothelial cellshepatic stellate cellshepatocyteshypoimmunogenic iPSCregenerative medicine

Identifiers

PMID37511568
PMCPMC10380710
OpenAlexW4385225114

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.