Evidence map›Paper›PMID 42493242›Full record

ArticleHLA2026

Integrated Immunological Engineering Platform for Scalable Production of iPSC-Derived Megakaryocytes.

Rabea Dettmer, Alice Rovai, Linus Schröder, Thea Reinkens, Willem Wolkers, Rainer Blasczyk, Constanca Figueiredo

Abstract read
In one paragraph

Article in HLA, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Rabea DettmerInstitute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0001-8017-098X
Alice RovaiInstitute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0002-4301-5742
Linus SchröderInstitute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0009-0000-4683-2249
Thea ReinkensInstitute of Human Genetics, Hannover Medical School, Hannover, Germany.
Willem WolkersBiostabilization Laboratory-Lower Saxony Centre for Biomedical Engineering, Implant Research and Development, University of Veterinary Medicine Hannover, Hannover, Germany.
Rainer BlasczykInstitute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0003-3875-3190
Constanca FigueiredoInstitute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.

Funding

Bundesamt für Ausrüstung, Informationstechnik und Nutzung der Bundeswehr BAAINBw MHH-HF-ZB3-2024Stiftung des DRK-Blutspendienst NSTOB StiBSD/2023/D3745
6 · The paper itself

Abstract

Severe thrombocytopenia and impaired platelet function remain major clinical challenges in hematologic diseases, chemotherapy, bone marrow failure, surgery and obstetric haemorrhage. Conventional platelet transfusions are limited by donor dependency, short shelf life, storage constraints, and immune-mediated platelet refractoriness caused primarily by HLA incompatibility. Here, we present a scalable, donor-independent platform to generate universally compatible, low-immunogenic megakaryocytes (MKs) from induced pluripotent stem cells (iPSCs). Human iPSCs were genetically engineered by shRNA-mediated silencing of β2-microglobulin (β2M) and/or class II transactivator (CIITA). Differentiation of HLA-silenced iPSCs resulted in MKs with reduced HLA class I and II expression, capable to release functional platelets in vitro and sustain platelet production in humanised mice with physiological distribution. To enhance product safety, gamma irradiation effectively eliminated proliferative contaminants while preserving MK function. This platform integrates immune engineering with scalable iPSC-based manufacturing and safety optimization, addressing key limitations of conventional donor-derived platelet products. Together, these findings demonstrate that HLA-silenced iPSC-derived MKs represent a promising off-the-shelf source of functional platelets with reduced immunogenicity. By combining donor-independent production, targeted immune engineering, and scalable manufacturing, this promising approach has the potential to improve transfusion support, overcome platelet refractoriness associated with HLA incompatibility, and expand access to readily available platelet therapies across diverse clinical settings.

Indexed as

Blood PlateletsInduced Pluripotent Stem CellsMegakaryocytesAnimalsbeta 2-MicroglobulinCell DifferentiationCells, CulturedGene SilencingHumansMiceNuclear ProteinsPlatelet TransfusionRNA, Small InterferingTrans-Activatorsbeta 2-MicroglobulinMHC class II transactivator proteinNuclear ProteinsRNA, Small InterferingTrans-ActivatorsHLA silencingiPSC‐derived megakaryocytesmegakaryocyte transfusiontransfusion medicineuniversal cell therapy

Identifiers

PMID42493242
PMCPMC13395570

What OpenQuestion holds

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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.