Cargando…

Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients

To obtain a qualitative as well as quantitative view immune reconstitution following umbilical cord blood (UCB) transplantation of paediatric patients, we utilised a broad panel of flow cytometry markers to monitor the phenotypes of lymphoid and myeloid cells at 1‐12 months post‐transplant. Samples...

Descripción completa

Detalles Bibliográficos
Autores principales: Girdlestone, John, Raymond, Meera, Shaw, Bronwen, Tulpule, Sameer, Devlia, Vikesh R., Danby, Robert, Ahyee, Trudy, Saudemont, Aurore, Hough, Rachael, Veys, Paul, Ruggeri, Annalisa, Vora, Ajay, Marks, David I., Gibson, Brenda, Wynn, Robert, Madrigal, Alejandro, Navarrete, Cristina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176140/
https://www.ncbi.nlm.nih.gov/pubmed/35847689
http://dx.doi.org/10.1002/jha2.12
Descripción
Sumario:To obtain a qualitative as well as quantitative view immune reconstitution following umbilical cord blood (UCB) transplantation of paediatric patients, we utilised a broad panel of flow cytometry markers to monitor the phenotypes of lymphoid and myeloid cells at 1‐12 months post‐transplant. Samples were received from 46 patients with a median age of 3.3 years and survival was 76% at 1 year. Monocytes were at similar or higher median levels than in adult controls at all times tested, with a high CD16+ proportion in the first 3 months. NK cells were also within adult ranges, with a CD56++ high proportion in the first 6 months. B cell recovery was seen from 2 months in most patients and T cells from 3 months, both were delayed with anti‐thymocyte globulin (ATG) treatment. CD4:CD8 ratios were high in the first 6 months, and the proportion of T cells with recent thymic emigrant and naïve phenotypes rose from 3 months. NK and plasmacytoid dendritic cell numbers remained at reduced levels in patients not surviving to 1 year. Our results can serve as a useful reference for detailed monitoring of immune reconstitution in paediatric recipients of UCB.