Publication:
Alloreactive Immune Response Associated to Human Mesenchymal Stromal Cells Treatment: A Systematic Review.

dc.contributor.authorSanabria-de la Torre, Raquel
dc.contributor.authorQuiñones-Vico, María I
dc.contributor.authorFernández-González, Ana
dc.contributor.authorSánchez-Díaz, Manuel
dc.contributor.authorMontero-Vílchez, Trinidad
dc.contributor.authorSierra-Sánchez, Álvaro
dc.contributor.authorArias-Santiago, Salvador
dc.date.accessioned2023-02-09T11:43:43Z
dc.date.available2023-02-09T11:43:43Z
dc.date.issued2021-07-05
dc.description.abstractThe well-known immunomodulatory and regenerative properties of mesenchymal stromal cells (MSCs) are the reason why they are being used for the treatment of many diseases. Because they are considered hypoimmunogenic, MSCs treatments are performed without considering histocompatibility barriers and without anticipating possible immune rejections. However, recent preclinical studies describe the generation of alloantibodies and the immune rejection of MSCs. This has led to an increasing number of clinical trials evaluating the immunological profile of patients after treatment with MSCs. The objective of this systematic review was to evaluate the generation of donor specific antibodies (DSA) after allogeneic MSC (allo-MSC) therapy and the impact on safety or tolerability. Data from 555 patients were included in the systematic review, 356 were treated with allo-MSC and the rest were treated with placebo or control drugs. A mean of 11.51% of allo-MSC-treated patients developed DSA. Specifically, 14.95% of these patients developed DSA and 6.33% of them developed cPRA. Neither the production of DSA after treatment nor the presence of DSA at baseline (presensitization) were correlated with safety and/or tolerability of the treatment. The number of doses administrated and human leucocyte antigen (HLA) mismatches between donor and recipient did not affect the production of DSA. The safety of allo-MSC therapy has been proved in all the studies and the generation of alloantibodies might not have clinical relevance. However, there are very few studies in the area. More studies with adequate designs are needed to confirm these results.
dc.identifier.doi10.3390/jcm10132991
dc.identifier.issn2077-0383
dc.identifier.pmcPMC8269175
dc.identifier.pmid34279481
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269175/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2077-0383/10/13/2991/pdf?version=1625481290
dc.identifier.urihttp://hdl.handle.net/10668/18221
dc.issue.number13
dc.journal.titleJournal of clinical medicine
dc.journal.titleabbreviationJ Clin Med
dc.language.isoen
dc.organizationHospital Universitario Virgen de las Nieves
dc.organizationHospital Universitario Virgen de las Nieves
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectadverse events
dc.subjectalloantibodies
dc.subjectclinical trials
dc.subjectdonor specific antibodies
dc.subjectimmunogenicity
dc.subjectmesenchymal stromal cells
dc.subjectsafety
dc.titleAlloreactive Immune Response Associated to Human Mesenchymal Stromal Cells Treatment: A Systematic Review.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number10
dspace.entity.typePublication

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