BK Virus-Specific T Cell Response Associated with HLA Genotypes, RhD Status, and CMV or EBV Serostatus in Healthy Donors for Optimized Cell Therapy

Altres autors/es

Institut Català de la Salut

[Mora Buch R, Tomás Marín M] Advanced & Cell Therapy Services, Blood and Tissue Bank (BST), Barcelona, Spain. Advanced & Cell Therapy Services, Blood and Tissue Bank (BST), Barcelona, Spain. [Pasamar H] Advanced & Cell Therapy Services, Blood and Tissue Bank (BST), Barcelona, Spain. [Enrich E, Rudilla F] Grup de Recerca de Medicina Transfusional, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona (VHIR-UAB), Barcelona, Spain. Immunogenetics and Histocompatibility Laboratory, Blood and Tissue Bank (BST), Barcelona, Spain. [Peña Gómez C] Barcelona Supercomputing Center, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Data de publicació

2025-10-14T08:35:02Z

2025-10-14T08:35:02Z

2025-06-19



Resum

BK virus; HLA genotype; T cell donors


Virus BK; Genotipo HLA; Donantes de células T


Virus BK; Genotip HLA; Donants de cèl·lules T


Purpose: The increasing application of virus-specific T cell therapy for treating BK virus infections in immunocompromised patients highlights the necessity for rapid identification of compatible cell donors with optimal BK-specific T cell response. This study aims to characterize the BK virus-specific T cell response in relation to demographic factors, blood group, serological status, and HLA genotypes using samples from a cell donor registry. Methods: Peripheral blood mononuclear cells from cell donors were stimulated with peptide pools derived from VP1 and LTA proteins, and the IFN-γ production was analyzed using ELISpot and validated by flow cytometry. Results: Our findings provide an overview of the T cell response to BK virus proteins in healthy donors, revealing associations with demographic characteristics, RhD status, CMV or EBV serological status, and HLA alleles. Remarkably, RhD-negative, CMV-seronegative, and EBV-seronegative donors showed a major T cell response against BK virus proteins. Notably, certain HLA alleles were associated with either enhanced or diminished T cell response. Furthermore, our results suggest that HLA-B leader dimorphism, specifically the presence of threonine at position 2, influences the VP1-specific immune response, resulting in enhanced T cell activation. Conclusion: This study, beyond advancing our understanding of the relationship between donor characteristics and BK virus-specific T cell response, has significant implications for improving the selection of optimal cell donors for patient-specific adoptive therapy.

Tipus de document

Article


Versió publicada

Llengua

Anglès

Publicat per

Springer

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Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

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