Clinical evaluation of allogeneic eye drops from cord blood platelet lysate

dc.contributor.authorSamarkanova, Dinara
dc.contributor.authorMartín, Sara
dc.contributor.authorBisbe, Laia
dc.contributor.authorPuig, Javier
dc.contributor.authorCalatayud Pinuaga, Marta
dc.contributor.authorRodriguez Gómez, Luciano
dc.contributor.authorAzqueta, Carmen
dc.contributor.authorColl, Ruth
dc.contributor.authorCasaroli Marano, Ricardo Pedro
dc.contributor.authorMadrigal, Alejandro
dc.contributor.authorRebulla, Paolo
dc.contributor.authorQuerol Giner, Sergi
dc.contributor.authorBarcelona CBED Study Group.
dc.date.accessioned2022-03-03T16:16:00Z
dc.date.available2022-03-03T16:16:00Z
dc.date.issued2020-07-31
dc.date.updated2022-03-03T16:16:00Z
dc.description.abstractBackground - Current treatments for several corneal lesions show limited efficacy. Here we report the clinical evaluation of the efficacy of a novel eye drop preparation produced in a public cord blood (CB) bank. Material and methods - In a multicentre, retrospective, consecutive case study we evaluated 33 patients (46 eyes) unresponsive to conventional treatments who required urgent intervention. The patients were given allogeneic eye drops obtained from cord blood platelet lysate (CBED) to treat severe ocular surface lesions under a compassionate use protocol. The CBED were prepared from CB units donated for haematopoietic stem cell transplantation that did not contain the minimum stem cell dose required for this use. Patients were grouped by acute conditions (neurotrophic ulcers: group I; other corneal ulcers: group II; corneal burns: group III), and chronic conditions (ocular graft-versus-host disease: group IV; severe dry eye syndrome: group V). The patients received one or two drops of the product to the affected eye four to six times per day for 19 days. A further 19-day cycle of treatment could be repeated according to the initial clinical response. Results - Patients received a median of 19 CBED vials (interquartile range 19-57, range 19-442) to complete the therapy. Group I-II-III patients showed full and partial ulcer recovery in 25 (78%) and six (19%) eyes respectively. One eye (3%) did not respond to treatment. For groups IV-V improvement was reported for 12 (85%) eyes and lesions worsened on treatment in both eyes (15%) of one patient. No severe adverse events were directly attributed to CBED. Discussion - Promptly available CBED resulted in a well-tolerated allogeneic treatment that showed evidence of efficacy in this cohort of patients. These positive results support further studies on CBED from platelet lysate as a novel product of CB banks. A prospective clinical trial in neurotrophic keratitis (NCT03084861) is ongoing to confirm these preliminary data. Keywords: cord blood, eye drops, corneal ulcers, neurotrophic keratitis, dry eye.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec710221
dc.identifier.issn1723-2007
dc.identifier.urihttps://hdl.handle.net/2445/183733
dc.language.isoeng
dc.publisherEdizioni SIMTI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2450/2020.0130-20
dc.relation.ispartofBlood Transfusion, 2020, vol. 19, num. 4, p. 347-356
dc.relation.urihttps://doi.org/10.2450/2020.0130-20
dc.rights(c) Edizioni SIMTI, 2020
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)
dc.subject.classificationMalalties de la còrnia
dc.subject.otherCornea diseases
dc.titleClinical evaluation of allogeneic eye drops from cord blood platelet lysate
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Carregant...
Miniatura
Nom:
710221.pdf
Mida:
1.58 MB
Format:
Adobe Portable Document Format