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Kaeuferle, T.* ; Eiz-Vesper, B.* ; Moosmann, A.* ; Behrends, U.* ; Decker, M.* ; Gutjahr, L.* ; Mautner, J. ; Klein, F.* ; Kreer, C.* ; Reger, M.* ; Busch, D.H.* ; D'Ippolito, E.* ; Kohlmayer, F.* ; Menzel, A.* ; Willier, S.* ; Maecker-Kolhoff, B.* ; Feuchtinger, T.*

Guiding antiviral cell therapy approaches with an online resource of clinically scored epitopes, T-cell receptors, and B-cell receptors.

Transfus. Med. Hemother. 52, 350–359 (2025)
Verlagsversion DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Introduction: The clinical application of cell-based immunotherapies is a rapidly emerging field, and recent advances in gene therapy have opened up a new era of innovative treatment approaches. Introducing a specific T-cell receptor (TCR) against viral epitopes or chimeric antigen receptor (CAR) into T cells and effector cells allows reprogramming of their specificity and utilization for advanced therapeutic applications in infectious diseases and virus-induced malignancies. Many technologies have been developed to genetically engineer T cells, and existing databases in silico predict or describe identified viral epitopes, TCRs, or B-cell receptors (BCRs). However, their therapeutic application is still hampered by limited knowledge on their clinical impact. Methods: An open-access online resource was developed, integrating a data-mining algorithm scoring the epitopes, TCRs, and BCRs (ETB database) according to clinical evidence. Results: We hereby present a new level of clinical evidence-based knowledge transfer for selecting individual protective TCRs or BCRs for therapeutic application. The database is publicly available at https://app.bitcare.de/epitopeFrontend/. Conclusion: Redirecting T-cell specificity by genetic engineering using clinically protective TCR or CAR sequences will not only bring significant progress to the field of adoptive T-cell therapies but also lay the groundwork for broader applications such as off-the-shelf approaches.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Adoptive T-cell transfer; Antibodies; Antigens; B-cell receptor; Epitope; Immune response; Infections; MHC; T cells; T-cell receptor; Virus; Cytomegalovirus; Infections
ISSN (print) / ISBN 1660-3796
e-ISSN 1424-5493
Quellenangaben Band: 52, Heft: 6, Seiten: 350–359 Artikelnummer: , Supplement: ,
Verlag Karger
Verlagsort Allschwilerstrasse 10, Ch-4009 Basel, Switzerland
Begutachtungsstatus Peer reviewed
Förderungen DZIF Group Host Control of Viral Latency and Reactivation, Department of Medicine III, LMU Klinikum, Munich, Germany
German Center for Infection Research (DZIF)