Evidence map›Paper›PMID 33484967›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2021

BMI1 enables extensive expansion of functional erythroblasts from human peripheral blood mononuclear cells.

Senquan Liu, Mengyao Wu, Moira Lancelot, Jiusheng Deng, Yongxing Gao, John D Roback, Tong Chen, Linzhao Cheng

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  11. Analyses of erythropoiesis from embryonic stem cell-CD34Journal of cellular and molecular medicine · 2022
    Article
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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

8 authors at 5 institutions in 2 countries.

Senquan LiuBlood and Cell Therapy Institute, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, China; Division of Hematology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Mengyao WuDivision of Hematology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Division of Hematology, Huashan Hospital of Fudan University, Shanghai 200040, China.
Moira LancelotCenter for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
Jiusheng DengCenter for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
Yongxing GaoDivision of Hematology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
John D RobackCenter for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA. Electronic address: jroback@emory.edu.
Tong ChenDivision of Hematology, Huashan Hospital of Fudan University, Shanghai 200040, China. Electronic address: chentong@fudan.edu.cn.
Linzhao ChengBlood and Cell Therapy Institute, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, China; Division of Hematology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. Electronic address: lcheng2@jh.edu.
Emory University · USJohns Hopkins Medicine · USFudan University · CNHuashan Hospital · CNJohns Hopkins University · US

Funding

Engineering iPSC-RBCs for TransfusionR01HL138656 · NHLBI · EMORY UNIVERSITY · PI ROBACK, JOHN D, STOWELL, SEAN R · 2017 to 2020
$2.9M
Genetically enhanced human erythrocytes generated from expandable stem cellsR01HL130676 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CHENG, LINZHAO · 2015 to 2018
$2.0M
NHLBI NIH HHS R01 HL130676NHLBI NIH HHS R01 HL138656
6 · The paper itself

Abstract

Transfusion of red blood cells (RBCs) from ABO-matched but genetically unrelated donors is commonly used for treating anemia and acute blood loss. Increasing demand and insufficient supply for donor RBCs, especially those of universal blood types or free of known and unknown pathogens, has called for ex vivo generation of functional RBCs by large-scale cell culture. However, generating physiological numbers of transfusable cultured RBCs (cRBCs) ex vivo remains challenging, due to our inability to either extensively expand primary RBC precursors (erythroblasts) or achieve efficient enucleation once erythroblasts have been expanded and induced to differentiation and maturation. Here, we report that ectopic expression of the human BMI1 gene confers extensive expansion of human erythroblasts, which can be derived readily from adult peripheral blood mononuclear cells of either healthy donors or sickle cell patients. These extensively expanded erythroblasts (E3s) are able to proliferate exponentially (>1 trillion-fold in 2 months) in a defined culture medium. Expanded E3 cells are karyotypically normal and capable of terminal maturation with approximately 50% enucleation. Additionally, E3-derived cRBCs can circulate in a mouse model following transfusion similar to primary human RBCs. Therefore, we provide a facile approach of generating physiological numbers of human functional erythroblasts ex vivo.

Indexed as

AdultAnimalsCell Culture TechniquesCell DifferentiationCell ProliferationCells, CulturedErythroblastsErythrocytesErythrocyte TransfusionFetal BloodHumansLeukocytes, MononuclearMiceModels, AnimalPolycomb Repressive Complex 1BMI1 protein, humanPolycomb Repressive Complex 1BMI1enucleationerythroblastsgene editingRBCsickle cell diseasetransfusion

Identifiers

PMID33484967
PMCPMC8116606
OpenAlexW3125088247

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.