Evidence map›Paper›PMID 35328655›Full record

ArticleInternational journal of molecular sciences2022

A New Human Platelet Lysate for Mesenchymal Stem Cell Production Compliant with Good Manufacturing Practice Conditions.

Katia Mareschi, Elena Marini, Alessia Giovanna Santa Banche Niclot, Marta Barone, Giuseppe Pinnetta, Aloe Adamini, Manuela Spadea, Luciana Labanca, Graziella Lucania, Ivana Ferrero and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Katia MareschiDepartment of Public Health and Paediatrics, The University of Turin, Piazza Polonia 94, 10126 Torino, Italy.ORCID 0000-0003-2889-0394
Elena MariniDepartment of Public Health and Paediatrics, The University of Turin, Piazza Polonia 94, 10126 Torino, Italy.
Alessia Giovanna Santa Banche NiclotDepartment of Public Health and Paediatrics, The University of Turin, Piazza Polonia 94, 10126 Torino, Italy.
Marta BaroneDepartment of Public Health and Paediatrics, The University of Turin, Piazza Polonia 94, 10126 Torino, Italy.ORCID 0000-0002-1865-7938
Giuseppe PinnettaStem Cell Transplantation and Cellular Therapy Laboratory, Paediatric Onco-Haematology Division, Regina Margherita Children's Hospital, City of Health and Science of Turin, 10126 Torino, Italy.
Aloe AdaminiStem Cell Transplantation and Cellular Therapy Laboratory, Paediatric Onco-Haematology Division, Regina Margherita Children's Hospital, City of Health and Science of Turin, 10126 Torino, Italy.
Manuela SpadeaDepartment of Public Health and Paediatrics, The University of Turin, Piazza Polonia 94, 10126 Torino, Italy.ORCID 0000-0001-7728-904X
Luciana LabancaBlood Component Production and Validation Center, City of Health and Science of Turin, S. Anna Hospital, 10126 Turin, Italy.
Graziella LucaniaBlood Component Production and Validation Center, City of Health and Science of Turin, S. Anna Hospital, 10126 Turin, Italy.
Ivana FerreroStem Cell Transplantation and Cellular Therapy Laboratory, Paediatric Onco-Haematology Division, Regina Margherita Children's Hospital, City of Health and Science of Turin, 10126 Torino, Italy.
Franca FagioliDepartment of Public Health and Paediatrics, The University of Turin, Piazza Polonia 94, 10126 Torino, Italy.ORCID 0000-0002-9257-900X
Piedmont Reference Center for Epidemiology and Cancer Prevention · ITUniversity of Turin · IT

Funding

Ministry of Education, Universities and Research MARK_RILO_19
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are classified as advanced therapy medicinal products, a new category of GMP (good manufacturing practice)-compliant medicines for clinical use. We isolated MSCs from 5 bone marrow (BM) samples using human platelet lysate (HPL) instead of foetal bovine serum (FBS). We used a new method of HPL production consisting of treating platelet (PLTs) pools with Ca-Gluconate to form a gel clot, then mechanically squeezing to release growth factors. We compared the new HPL (HPL-S) with the standard (HPL-E) obtained by freezing/thawing cycles and by adding heparin. HPL-S had not PLTs and fibrinogen but the quantity of proteins and growth factors was comparable to HPL-E. Therefore, HPL-S needed fewer production steps to be in compliance with GMP conditions. The number of colonies forming unit-fibroblasts (CFU-F) and the maintenance of stem markers showed no significant differences between MSCs with HPL-E and HPL-S. The cumulative population doubling was higher in MSCs with HPL-E in the earlier passages, but we observed an inverted trend of cell growth at the fourth passage. Immunophenotypic analysis showed a significant lower expression of HLA-DR in the MSCs with HPL-S (1.30%) than HPL-E (14.10%). In conclusion, we demonstrated that HPL-S is an effective alternative for MSC production under GMP conditions.

Indexed as

Mesenchymal Stem CellsBlood PlateletsCell DifferentiationCell ProliferationCells, CulturedCulture MediaHumansImmunophenotypingIntercellular Signaling Peptides and ProteinsCulture MediaIntercellular Signaling Peptides and ProteinsGMPhuman platelet lysatemesenchymal stem cells

Identifiers

PMID35328655
PMCPMC8953582
OpenAlexW4220856198

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.