Evidence map›Paper›PMID 28855509›Full record

ArticleNature communications2017

MHC matching improves engraftment of iPSC-derived neurons in non-human primates.

Asuka Morizane, Tetsuhiro Kikuchi, Takuya Hayashi, Hiroshi Mizuma, Sayuki Takara, Hisashi Doi, Aya Mawatari, Matthew F Glasser, Takashi Shiina, Hirohito Ishigaki and 8 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 135 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed, 2 pooled it
10.4field-weighted citation impact, top 1% 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

135 citing papers in PubMed, 2 syntheses or guidelines pooled it, 239 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
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  8. Article
  9. Investigating the efficacy, methods, and challenges of induced pluripotent stem cells (iPSC) therapy in Parkinson's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  10. Review
  11. Review
  12. Article
  13. Stem Cell-Based Approaches in Parkinson's Disease Research.International journal of stem cells · 2025
    Review
  14. Article
  15. Article
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  17. Article
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  20. Review

75 more citing papers are in PubMed but not listed here.

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

18 authors at 5 institutions in 2 countries.

Asuka MorizaneDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Tetsuhiro KikuchiDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.ORCID http://orcid.org/0000-0003-2332-4967
Takuya HayashiRIKEN Center for Life Science Technologies (CLST), Hyogo, 650-0047, Japan.
Hiroshi MizumaRIKEN Center for Life Science Technologies (CLST), Hyogo, 650-0047, Japan.ORCID http://orcid.org/0000-0001-8970-9486
Sayuki TakaraRIKEN Center for Life Science Technologies (CLST), Hyogo, 650-0047, Japan.
Hisashi DoiRIKEN Center for Life Science Technologies (CLST), Hyogo, 650-0047, Japan.
Aya MawatariRIKEN Center for Life Science Technologies (CLST), Hyogo, 650-0047, Japan.
Matthew F GlasserDepartment of Neuroscience, Washington University School of Medicine, St. Louis, M0, 63110, USA.
Takashi ShiinaDepartment of Molecular Life Science, Tokai University, School of Medicine, Kanagawa, 259-1143, Japan.
Hirohito IshigakiDepartment of Pathology, Shiga University of Medical Science, Shiga, 520-2192, Japan.
Yasushi ItohDepartment of Pathology, Shiga University of Medical Science, Shiga, 520-2192, Japan.
Keisuke OkitaDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.ORCID http://orcid.org/0000-0001-5806-1090
Emi YamasakiDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Daisuke DoiDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Hirotaka OnoeRIKEN Center for Life Science Technologies (CLST), Hyogo, 650-0047, Japan.
Kazumasa OgasawaraDepartment of Pathology, Shiga University of Medical Science, Shiga, 520-2192, Japan.
Shinya YamanakaDepartment of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Jun TakahashiDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan. jbtaka@cira.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0003-3642-9186
Kyoto University · JPShiga University of Medical Science · JPGladstone Institutes · USTokai University · JPWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The banking of human leukocyte antigen (HLA)-homozygous-induced pluripotent stem cells (iPSCs) is considered a future clinical strategy for HLA-matched cell transplantation to reduce immunological graft rejection. Here we show the efficacy of major histocompatibility complex (MHC)-matched allogeneic neural cell grafting in the brain, which is considered a less immune-responsive tissue, using iPSCs derived from an MHC homozygous cynomolgus macaque. Positron emission tomography imaging reveals neuroinflammation associated with an immune response against MHC-mismatched grafted cells. Immunohistological analyses reveal that MHC-matching reduces the immune response by suppressing the accumulation of microglia (Iba-1+) and lymphocytes (CD45+) into the grafts. Consequently, MHC-matching increases the survival of grafted dopamine neurons (tyrosine hydroxylase: TH+). The effect of an immunosuppressant, Tacrolimus, is also confirmed in the same experimental setting. Our results demonstrate the rationale for MHC-matching in neural cell grafting to the brain and its feasibility in a clinical setting.Major histocompatibility complex (MHC) matching improves graft survival rates after organ transplantation. Here the authors show that in macaques, MHC-matched iPSC-derived neurons provide better engraftment in the brain, with a lower immune response and higher survival of the transplanted neurons.

Indexed as

AnimalsDopaminergic NeuronsFemaleGraft RejectionHaplotypesHLA AntigensImmunohistochemistryInduced Pluripotent Stem CellsLymphocytesMacacaMajor Histocompatibility ComplexMaleMicrogliaPositron-Emission TomographyHLA Antigens

Identifiers

PMID28855509
PMCPMC5577234
OpenAlexW2745770472

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.