Evidence map›Paper›PMID 28504668›Full record

ArticleNature biotechnology2017

HLA-E-expressing pluripotent stem cells escape allogeneic responses and lysis by NK cells.

Germán G Gornalusse, Roli K Hirata, Sarah E Funk, Laura Riolobos, Vanda S Lopes, Gabriel Manske, Donna Prunkard, Aric G Colunga, Laïla-Aïcha Hanafi, Dennis O Clegg and 2 more

Abstract read
In one paragraph

Article in Nature biotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 361 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
361citing papers in PubMed, 2 pooled it
22.3field-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

361 citing papers in PubMed, 2 syntheses or guidelines pooled it, 611 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Allogeneic CD70-Targeted Chimeric Antigen Receptor T-Cell Therapy for Advanced Renal Cell Carcinoma: Results From the Phase I TRAVERSE Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
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  8. CD8MedComm · 2026
    Review
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  19. Article
  20. CAR-macrophages: a new chapter in cancer immunotherapy.Acta biochimica et biophysica Sinica · 2026
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Germán G GornalusseDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Roli K HirataDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Sarah E FunkDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Laura RiolobosDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Vanda S LopesCenter for Stem Cell Biology and Engineering, Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, USA.
Gabriel ManskeDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Donna PrunkardDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Aric G ColungaDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Laïla-Aïcha HanafiClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Dennis O CleggCenter for Stem Cell Biology and Engineering, Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, USA.
Cameron TurtleClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
David W RussellDepartment of Medicine, University of Washington, Seattle, Washington, USA.
University of Washington · USFred Hutch Cancer Center · USUniversity of California, Santa Barbara · US

Funding

RESEARCH TRAINING IN HEMATOLOGYT32HL007093 · NHLBI · UNIVERSITY OF WASHINGTON · PI Janis L Abkowitz · 1985 to 2026
$13.9M
Stem Cell and Transplantation BiologyU54DK106829 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DEREK L STIREWALT · 2015 to 2026
$9.1M
GENE TARGETING BY VIRAL VECTORSR01DK055759 · NIDDK · UNIVERSITY OF WASHINGTON · PI RUSSELL, DAVID W · 1999 to 2017
$5.8M
Universal Donor MegakaryocytesR01HL130770 · NHLBI · UNIVERSITY OF WASHINGTON · PI STAMATOYANNOPOULOS, THALIA · 2015 to 2018
$1.6M
NHLBI NIH HHS R01 HL130770NHLBI NIH HHS T32 HL007093NIDDK NIH HHS R01 DK055759NIDDK NIH HHS U54 DK106829
6 · The paper itself

Abstract

Polymorphisms in the human leukocyte antigen (HLA) class I genes can cause the rejection of pluripotent stem cell (PSC)-derived products in allogeneic recipients. Disruption of the Beta-2 Microglobulin (B2M) gene eliminates surface expression of all class I molecules, but leaves the cells vulnerable to lysis by natural killer (NK) cells. Here we show that this 'missing-self' response can be prevented by forced expression of minimally polymorphic HLA-E molecules. We use adeno-associated virus (AAV)-mediated gene editing to knock in HLA-E genes at the B2M locus in human PSCs in a manner that confers inducible, regulated, surface expression of HLA-E single-chain dimers (fused to B2M) or trimers (fused to B2M and a peptide antigen), without surface expression of HLA-A, B or C. These HLA-engineered PSCs and their differentiated derivatives are not recognized as allogeneic by CD8

Indexed as

AnimalsFemaleGraft RejectionHLA AntigensHumansKiller Cells, NaturalMicePluripotent Stem CellsTransplantsHLA Antigens

Identifiers

PMID28504668
PMCPMC5548598
OpenAlexW2616215756

What OpenQuestion holds

Textmetadata
LicenceTDM
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.