Evidence map›Paper›PMID 23687092›Full record

ArticleBlood2013

Human iPS cell-derived hematopoietic progenitor cells induce T-cell anergy in in vitro-generated alloreactive CD8(+) T cells.

Eun-Mi Kim, Gohar Manzar, Nicholas Zavazava

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Human iPSC banking: barriers and opportunities.Journal of biomedical science · 2019
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Stem cell therapy for inflammatory bowel disease.Journal of gastroenterology · 2015
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. 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

3 authors at 2 institutions in 1 country.

Eun-Mi KimDivision of Immunology, Department of Internal Medicine, University of Iowa Hospitals and Clinics & Iowa City Veterans Affairs Medical Center, Iowa City, IA 52242, USA.
Gohar Manzar
Nicholas Zavazava
University of Iowa Hospitals and Clinics · USUniversity of Iowa · US

Funding

EMBRYONIC STEM CELLS INDUCE SPECIFIC GRAFT TOLERANCER01HL073015 · NHLBI · UNIVERSITY OF IOWA · PI ZAVAZAVA, NICHOLAS · 2004 to 2012
$2.5M
STEM CELL-DERIVED INSUIN PRODUCING CELLS CORRECT HYPERGLYCEMIA IN DIABETIC MICEI01BX001125 · VA · IOWA CITY VA MEDICAL CENTER · PI ZAVAZAVA, NICHOLAS · 2012 to 2015
–
BLRD VA I01 BX001125NHLBI NIH HHS 3R01HL073015-04A1S1NHLBI NIH HHS 5R01HL073015-08NHLBI NIH HHS R01 HL073015
6 · The paper itself

Abstract

Human induced pluripotent stem cells (iPSCs) have emerged as an alternative source of pluripotent stem cells that can be used for tissue regeneration in place of the controversial human embryonic stem cells. However, immunologic knowledge about iPSC derivatives remains enigmatic. Here, we characterized human iPS-derived CD34(+) hematopoietic progenitor cells (HPCs). These HPCs poorly express major histocompatibility complex (MHC) I antigens and are MHC-II negative. Interestingly, they moderately express nonclassical HLA-G and HLA-E molecules. Consequently, alloreactive HLA-A2-specific cytotoxic T cells failed to recognize HLA-A2-expressing HPCs but became anergic. Subsequent upregulation of MHC-I using interferon-γ stimulation and provision of CD28 cosignaling led to T-cell activation, confirming that poor delivery of signals 1 and 2 by the HPCs mediated T-cell anergy. These data indicate for the first time that HPCs induce T-cell anergy, a unique characteristic of iPSC-derived cells that confers immunologic advantage for allogenic transplantation. Although iPSCs are ideal for patient-tailored treatments with the anticipation that no immunosuppression will be required, in cases of gene defects, their derivatives could be used to treat diseases in nonhistocompatible recipients.

Indexed as

CD8-Positive T-LymphocytesCells, CulturedClonal AnergyEmbryonic Stem CellsFibroblastsHematopoietic Stem CellsHLA AntigensHumansInduced Pluripotent Stem CellsInterferon-gammaLymphocyte ActivationT-Lymphocytes, CytotoxicHLA AntigensInterferon-gamma

Identifiers

PMID23687092
PMCPMC3695361
OpenAlexW2041178941

What OpenQuestion holds

Textmetadata
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.