Evidence map›Paper›PMID 34068404›Full record

ReviewInternational journal of molecular sciences2021

Human Platelet Lysate for Good Manufacturing Practice-Compliant Cell Production.

Michaela Oeller, Sandra Laner-Plamberger, Linda Krisch, Eva Rohde, Dirk Strunk, Katharina Schallmoser

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
7.0field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 80 citations in OpenAlex.

  1. Pooled it
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  3. From Donation to Innovation: New Blood-Derived Products.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
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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

6 authors at 1 institution in 1 country.

Michaela OellerDepartment of Transfusion Medicine, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.
Sandra Laner-PlambergerDepartment of Transfusion Medicine, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.ORCID 0000-0002-1416-6023
Linda KrischDepartment of Transfusion Medicine, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.
Eva RohdeDepartment of Transfusion Medicine, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.
Dirk StrunkSpinal Cord Injury and Tissue Regeneration Center Salzburg, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.ORCID 0000-0003-1810-867X
Katharina SchallmoserDepartment of Transfusion Medicine, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.ORCID 0000-0002-7204-0058
University of Salzburg · AT

Funding

Horizon 2020 Framework Programme 731377Horizon 2020 Framework Programme 733006Paracelsus Medizinische Privatuniversität "Rise Project" R-20/04/137-PLSSalzburger Landesregierung Land Salzburg 20102-F2001080-FPR "Cancer Cluster II"Salzburger Landesregierung Land Salzburg/IWB/EFRE 2014 - 2020 P1812596 "EV-TT"Salzburger Landesregierung Land Salzburg/WISS 2025 20102-F1900731-KZP "EV-TT - Bpro"
6 · The paper itself

Abstract

Numerous cell-based therapeutics are currently being tested in clinical trials. Human platelet lysate (HPL) is a valuable alternative to fetal bovine serum as a cell culture medium supplement for a variety of different cell types. HPL as a raw material permits animal serum-free cell propagation with highly efficient stimulation of cell proliferation, enabling humanized manufacturing of cell therapeutics within a reasonable timeframe. Providers of HPL have to consider dedicated quality issues regarding identity, purity, potency, traceability and safety. Release criteria have to be defined, characterizing the suitability of HPL batches for the support of a specific cell culture. Fresh or expired platelet concentrates from healthy blood donors are the starting material for HPL preparation, according to regulatory requirements. Pooling of individual platelet lysate units into one HPL batch can balance donor variation with regard to essential platelet-derived growth factors and cytokines. The increasingly applied pathogen reduction technologies will further increase HPL safety. In this review article, aspects and regulatory requirements of whole blood donation and details of human platelet lysate manufacturing are presented. International guidelines for raw materials are discussed, and defined quality controls, as well as release criteria for safe and GMP-compliant HPL production, are summarized.

Indexed as

Cell DifferentiationAnimalsBlood PlateletsCell Culture TechniquesCell ProliferationCulture MediaHumansCulture Mediacell therapygood manufacturing practice (GMP)human platelet lysate (HPL)platelet concentratesregenerationregenerative medicine

Identifiers

PMID34068404
PMCPMC8153614
OpenAlexW3160510297

What OpenQuestion holds

Textmetadata
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.