Evidence map›Paper›PMID 33198819›Full record

ReviewStem cell research & therapy2020

Differentiation of human induced pluripotent stem cells into erythroid cells.

Mohsen Ebrahimi, Mehdi Forouzesh, Setareh Raoufi, Mohammad Ramazii, Farhoodeh Ghaedrahmati, Maryam Farzaneh

Open access · goldAbstract readReview
In one paragraph

Review in Stem cell research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Blood Pharming of Red Cells.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 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

6 authors at 6 institutions in 1 country.

Mohsen EbrahimiNeonatal and Children's Health Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Mehdi ForouzeshLegal Medicine Organization of Iran, Legal Medicine Research Center, Legal Medicine organization, Tehran, Iran.
Setareh RaoufiFaculty of Medical Sciences and Technologies, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Mohammad RamaziiKerman University of Medical Sciences, University of Kerman, Kerman, Iran.
Farhoodeh GhaedrahmatiDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Maryam FarzanehPhysiology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. Maryamfarzaneh2013@yahoo.com.ORCID 0000-0001-6239-8745
Ahvaz Jundishapur University of Medical Sciences · IRGolestan University of Medical Sciences · IRIranian Legal Medicine Organization · IRIsfahan University of Medical Sciences · IRIslamic Azad University, Science and Research Branch · IRKerman University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the last years, several strategies have been made to obtain mature erythrocytes or red blood cells (RBC) from the bone marrow or umbilical cord blood (UCB). However, UCB-derived hematopoietic stem cells (HSC) are a limited source and in vitro large-scale expansion of RBC from HSC remains problematic. One promising alternative can be human pluripotent stem cells (PSCs) that provide an unlimited source of cells. Human PSCs, including embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), are self-renewing progenitors that can be differentiated to lineages of ectoderm, mesoderm, and endoderm. Several previous studies have revealed that human ESCs can differentiate into functional oxygen-carrying erythrocytes; however, the ex vivo expansion of human ESC-derived RBC is subjected to ethical concerns. Human iPSCs can be a suitable therapeutic choice for the in vitro/ex vivo manufacture of RBCs. Reprogramming of human somatic cells through the ectopic expression of the transcription factors (OCT4, SOX2, KLF4, c-MYC, LIN28, and NANOG) has provided a new avenue for disease modeling and regenerative medicine. Various techniques have been developed to generate enucleated RBCs from human iPSCs. The in vitro production of human iPSC-derived RBCs can be an alternative treatment option for patients with blood disorders. In this review, we focused on the generation of human iPSC-derived erythrocytes to present an overview of the current status and applications of this field.

Indexed as

Human Embryonic Stem CellsInduced Pluripotent Stem CellsCell DifferentiationEmbryonic Stem CellsErythroid CellsHumansKruppel-Like Factor 4Kruppel-Like Factor 4Blood disordersDifferentiationErythrocytesInduced pluripotent stem cellsLarge-scaleReprogramming

Identifiers

PMID33198819
PMCPMC7667818
OpenAlexW3102679996

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.