Evidence map›Paper›PMID 31116895›Full record

ArticleStem cells (Dayton, Ohio)2019

In Utero Transplantation of Expanded Autologous Amniotic Fluid Stem Cells Results in Long-Term Hematopoietic Engraftment.

Stavros P Loukogeorgakis, Panicos Shangaris, Enrica Bertin, Chiara Franzin, Martina Piccoli, Michela Pozzobon, Sindhu Subramaniam, Alfonso Tedeschi, Aimee G Kim, Haiying Li and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Regenerative medicine: prenatal approaches.The Lancet. Child & adolescent health · 2022
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. The Future of In Utero Gene Therapy.Molecular diagnosis & therapy · 2020
    Review
  8. 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

20 authors at 5 institutions in 4 countries.

Stavros P LoukogeorgakisStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Panicos ShangarisStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.ORCID 0000-0003-2750-8405
Enrica BertinStem Cell and Regenerative Medicine Laboratory, Fondazione Instituto di Ricerca Pediatrica Città della Speranza, University of Padova, Padova, Italy.
Chiara FranzinStem Cell and Regenerative Medicine Laboratory, Fondazione Instituto di Ricerca Pediatrica Città della Speranza, University of Padova, Padova, Italy.
Martina PiccoliStem Cell and Regenerative Medicine Laboratory, Fondazione Instituto di Ricerca Pediatrica Città della Speranza, University of Padova, Padova, Italy.
Michela PozzobonStem Cell and Regenerative Medicine Laboratory, Fondazione Instituto di Ricerca Pediatrica Città della Speranza, University of Padova, Padova, Italy.
Sindhu SubramaniamStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Alfonso TedeschiStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Aimee G KimCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Haiying LiCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Camila G FachinCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Andre I B S DiasStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
John D StratigisCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Nicholas J AhnCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Adrian J ThrasherMolecular and Cellular Immunology Section, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Paola BonfantiStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
William H PeranteauCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Anna L DavidResearch Department of Maternal and Fetal Medicine, Institute for Women's Health, University College London, London, United Kingdom.
Alan W FlakeCenter for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Paolo De CoppiStem Cells and Regenerative Medicine, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Children's Hospital of Philadelphia · USGreat Ormond Street Hospital · GBCittà della Speranza Foundation · ITInstitute for Reproductive Health · USUniversity of Padua · IT

Funding

Wellcome TrustWellcome Trust 098539/Z/12/Z
6 · The paper itself

Abstract

In utero transplantation (IUT) of hematopoietic stem cells (HSCs) has been proposed as a strategy for the prenatal treatment of congenital hematological diseases. However, levels of long-term hematopoietic engraftment achieved in experimental IUT to date are subtherapeutic, likely due to host fetal HSCs outcompeting their bone marrow (BM)-derived donor equivalents for space in the hematopoietic compartment. In the present study, we demonstrate that amniotic fluid stem cells (AFSCs; c-Kit+/Lin-) have hematopoietic characteristics and, thanks to their fetal origin, favorable proliferation kinetics in vitro and in vivo, which are maintained when the cells are expanded. IUT of autologous/congenic freshly isolated or cultured AFSCs resulted in stable multilineage hematopoietic engraftment, far higher to that achieved with BM-HSCs. Intravascular IUT of allogenic AFSCs was not successful as recently reported after intraperitoneal IUT. Herein, we demonstrated that this likely due to a failure of timely homing of donor cells to the host fetal thymus resulted in lack of tolerance induction and rejection. This study reveals that intravascular IUT leads to a remarkable hematopoietic engraftment of AFSCs in the setting of autologous/congenic IUT, and confirms the requirement for induction of central tolerance for allogenic IUT to be successful. Autologous, gene-engineered, and in vitro expanded AFSCs could be used as a stem cell/gene therapy platform for the in utero treatment of inherited disorders of hematopoiesis. Stem Cells 2019;37:1176-1188.

Indexed as

Amniotic FluidAnimalsCells, CulturedFemaleFetal DiseasesFetal Stem CellsGraft SurvivalHematologic DiseasesHematopoietic Stem CellsHematopoietic Stem Cell TransplantationMice, Inbred BALB CMice, Inbred C57BLPregnancyStem Cell TransplantationTransplantation, AutologousAutologous stem cell transplantationCell cultureFetal stem cellsHematopoiesisTransplantation tolerance

Identifiers

PMID31116895
PMCPMC6773206
OpenAlexW2944896219

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.