Authors
Sandra Laner-Plamberger, Michaela Oeller, Thierry Burnouf, Reinhard Henschler, Katharina Schallmoser
Published in
Vox sanguinis. Oct 14, 2026. Epub Oct 14, 2026.
Abstract
Global demand is rising for human platelet lysate (HPL) in the manufacture of cell-based medicinal products, but platelet resources are scarce. As protocols for the production process and quality testing are heterogeneous, the Working Party on Cellular Therapies of the International Society of Blood Transfusion (ISBT) has recently conducted a survey to obtain information from blood establishments worldwide.
The survey was created at limesurvey.net and consisted of 29 questions on the use of platelet concentrates (PCs) for HPL production to determine the status, conditions, standardization efforts, area of application, and potential difficulties. The link was sent to all ISBT members, and data were analyzed descriptively.
Of 78 participating centers, 12 routinely produce HPL according to in-house protocols, mainly by pooling expired PCs, whereas quality control testing is established in 10 institutions. HPL is used for basic research (n = 7) and for the manufacture of cell-based medicinal products (n = 7).
HPL manufacture is still heterogeneous and limited to a few blood centers worldwide. Prospective collaborations between these institutions may contribute to the efforts for international harmonization and consistent regulation of HPL applications.
PMID:
42875042
Bibliographic data and abstract were imported from PubMed on 15 Oct 2026.
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