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   <dc:title>Chimeric HLA antibody receptor T cells for targeted therapy of antibody-mediated rejection in transplantation</dc:title>
   <dc:creator>Betriu Méndez, Sergi</dc:creator>
   <dc:creator>Rovira Juárez, Jordi</dc:creator>
   <dc:creator>Arana Aliaga, Carolt</dc:creator>
   <dc:creator>García Busquets, Ainhoa</dc:creator>
   <dc:creator>Martinez Florensa, Mario</dc:creator>
   <dc:creator>Ramírez Bajo, María José</dc:creator>
   <dc:creator>Bañón Maneus, Elisenda</dc:creator>
   <dc:creator>Lazo Rodríguez, Marta</dc:creator>
   <dc:creator>Bartoló Ibars, Ariadna</dc:creator>
   <dc:creator>Claas, Francis H.J.</dc:creator>
   <dc:creator>Mulder, Arend</dc:creator>
   <dc:creator>Heidt, Sebastiaan</dc:creator>
   <dc:creator>Juan Otero, Manel</dc:creator>
   <dc:creator>Bayés Genís, Beatriz Enriqueta</dc:creator>
   <dc:creator>Campistol Plana, Josep M.</dc:creator>
   <dc:creator>Palou Ribera, Eduard</dc:creator>
   <dc:creator>Diekmann, Fritz</dc:creator>
   <dcterms:abstract>The presence of donor-specific antibodies (DSA), mainly against HLA, increases the risk of allograft rejection. Moreover, antibody-mediated rejection (ABMR) remains an important barrier to optimal long-term outcomes after solid organ transplantation. The development of chimeric autoantibody receptor T lymphocytes has been postulated for targeted therapy of autoimmune diseases. We aimed to develop a targeted therapy for DSA desensitization and ABMR, generating T cells with a chimeric HLA antibody receptor (CHAR) that specifically eliminates DSA-producing B cells. We have genetically engineered an HLA-A2-specific CHAR (A2-CHAR) and transduced it into human T cells. Then, we have performed in vitro experiments such as cytokine measurement, effector cell activation, and cytotoxicity against anti-HLA-A2 antibody-expressing target cells. In addition, we have performed A2-CHAR-Tc cytotoxic assays in an immunodeficient mouse model. A2-CHAR expressing T cells could selectively eliminate HLA-A2 antibody-producing B cells in vitro. The cytotoxic capacity of A2-CHAR expressing T cells mainly depended on Granzyme B release. In the NSG mouse model, A2-CHAR-T cells could identify and eradicate HLA-A2 antibody-producing B cells even when those cells are localized in the bone marrow. This ability is effector:target ratio dependent. CHAR technology generates potent and functional human cytotoxic T cells to target alloreactive HLA class I antibody-producing B cells. Thus, we consider that CHAR technology may be used as a selective desensitization protocol or an ABMR therapy in transplantation.© 2023 The Authors. HLA: Immune Response Genetics published by John Wiley &amp;amp; Sons Ltd.</dcterms:abstract>
   <dcterms:issued>2025-11-14T06:45:00Z</dcterms:issued>
   <dcterms:issued>2025-11-14T06:45:00Z</dcterms:issued>
   <dcterms:issued>2023-10-01</dcterms:issued>
   <dcterms:issued>2025-10-30T14:59:46Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1111/tan.15156</dc:relation>
   <dc:relation>HLA, 2023, vol.102, 449-463</dc:relation>
   <dc:relation>https://doi.org/10.1111/tan.15156</dc:relation>
   <dc:rights>cc-by-nc (c) Betriu Méndez, Sergi et al., 2025</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:source>Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)</dc:source>
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