Evidence map›Paper›PMID 29871694›Full record

ArticleStem cell research & therapy2018

Safety and efficacy of human embryonic stem cell-derived astrocytes following intrathecal transplantation in SOD1

Michal Izrael, Shalom Guy Slutsky, Tamar Admoni, Louisa Cohen, Avital Granit, Arik Hasson, Joseph Itskovitz-Eldor, Lena Krush Paker, Graciela Kuperstein, Neta Lavon and 7 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 72 citations in OpenAlex.

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  5. Pleiotrophin/Midkine Pathway Is Dysregulated in a TDP-43Neuropathology : official journal of the Japanese Society of Neuropathology · 2026
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  9. Characterization of Isolated Human Astrocytes from Aging Brain.International journal of molecular sciences · 2025
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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

17 authors at 1 institution in 1 country.

Michal IzraelNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel. m.izrael@kadimastem.com.
Shalom Guy SlutskyNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Tamar AdmoniNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Louisa CohenNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Avital GranitNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Arik HassonNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Joseph Itskovitz-EldorNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Lena Krush PakerNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Graciela KupersteinNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Neta LavonNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Shiran Yehezkel IonescuNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Leonardo Javier SolmeskyNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Rachel ZaguriNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Alina ZhuravlevNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Ella VolmanNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Judith ChebathNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Michel RevelNeurodegenerative Diseases Department at Kadimastem Ltd, Pinchas Sapir 7, Weizmann Science Park, Nes-Ziona, Israel.
Weizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmyotrophic lateral sclerosis (ALS) is a motor neuron (MN) disease characterized by the loss of MNs in the central nervous system. As MNs die, patients progressively lose their ability to control voluntary movements, become paralyzed and eventually die from respiratory/deglutition failure. Despite the selective MN death in ALS, there is growing evidence that malfunctional astrocytes play a crucial role in disease progression. Thus, transplantation of healthy astrocytes may compensate for the diseased astrocytes.

methodsWe developed a good manufacturing practice-grade protocol for generation of astrocytes from human embryonic stem cells (hESCs). The first stage of our protocol is derivation of astrocyte progenitor cells (APCs) from hESCs. These APCs can be expanded in large quantities and stored frozen as cell banks. Further differentiation of the APCs yields an enriched population of astrocytes with more than 90% GFAP expression (hES-AS). hES-AS were injected intrathecally into hSOD1

resultsIn vitro, hES-AS possess the activities of functional healthy astrocytes, including glutamate uptake, promotion of axon outgrowth and protection of MNs from oxidative stress. A secretome analysis shows that these hES-AS also secrete several inhibitors of metalloproteases as well as a variety of neuroprotective factors (e.g. TIMP-1, TIMP-2, OPN, MIF and Midkine). Intrathecal injections of the hES-AS into transgenic hSOD1

conclusionOur findings demonstrate the safety and potential therapeutic benefits of intrathecal injection of hES-AS for the treatment of ALS.

Indexed as

Amyotrophic Lateral SclerosisAnimalsAstrocytesDisease Models, AnimalHuman Embryonic Stem CellsHumansInjections, SpinalMiceRatsSuperoxide Dismutase-1Superoxide Dismutase-1Amyotrophic lateral sclerosisAstrocytesHuman embryonic stem cellsSuperoxide dismutase 1

Identifiers

PMID29871694
PMCPMC5989413
OpenAlexW2807380934

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.