TY - JOUR
T1 - TRBC2-targeting antibody–drug conjugates for the treatment of T cell cancers
AU - Ge, Jiaxin
AU - Urban, Joshua
AU - DiNapoli, Sarah R.
AU - Lee, Bum Seok
AU - Ahmedna, Taha
AU - Nichakawade, Tushar D.
AU - Mog, Brian J.
AU - Lu, Steve
AU - Li, Xuyang
AU - Marcou, Nikita
AU - Glavaris, Stephanie
AU - Douglass, Jacqueline
AU - Liu, Jin
AU - Konig, Maximilian F.
AU - Watson, Evangeline
AU - Popoli, Maria
AU - Peske, J. David
AU - Rozati, Sima
AU - Sterling, Cole H.
AU - Wagner-Johnston, Nina
AU - Ambinder, Richard F.
AU - Gabrielson, Kathy
AU - Mullighan, Charles G.
AU - Papadopoulos, Nickolas
AU - Bettegowda, Chetan
AU - Pardoll, Drew M.
AU - Zhou, Shibin
AU - Sur, Surojit
AU - Kinzler, Kenneth W.
AU - Vogelstein, Bert
AU - Paul, Suman
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Antibody–drug conjugates (ADCs) have been remarkably successful in treating solid and hematological malignancies. Generation of ADCs for T cell cancers is challenging because the ADCs must selectively target cancerous T cells while sparing some normal T cells necessary for immune function. T cells express one of two TRBC alleles: TRBC1 or TRBC2. Normal T cells are composed of about 40% TRBC1-expressing and 60% TRBC2-expressing cells. In contrast, T cell malignancies are characterized by the clonal expression of either TRBC1 or TRBC2. Selective targeting of TRBC1 or TRBC2 enables the killing of cancer cells but preserves about 60–40% of the normal T cells. To enable such a therapy for cancers expressing TRBC2, here we developed a high-affinity anti-TRBC2 antibody. An ADC generated with this antibody and a pyrrolobenzodiazepine dimer payload showed specific killing of TRBC2+ cancers in vitro and in mouse models. The anti-TRBC2 ADC provides a promising, off-the-shelf therapy for patients with T cell cancers.
AB - Antibody–drug conjugates (ADCs) have been remarkably successful in treating solid and hematological malignancies. Generation of ADCs for T cell cancers is challenging because the ADCs must selectively target cancerous T cells while sparing some normal T cells necessary for immune function. T cells express one of two TRBC alleles: TRBC1 or TRBC2. Normal T cells are composed of about 40% TRBC1-expressing and 60% TRBC2-expressing cells. In contrast, T cell malignancies are characterized by the clonal expression of either TRBC1 or TRBC2. Selective targeting of TRBC1 or TRBC2 enables the killing of cancer cells but preserves about 60–40% of the normal T cells. To enable such a therapy for cancers expressing TRBC2, here we developed a high-affinity anti-TRBC2 antibody. An ADC generated with this antibody and a pyrrolobenzodiazepine dimer payload showed specific killing of TRBC2+ cancers in vitro and in mouse models. The anti-TRBC2 ADC provides a promising, off-the-shelf therapy for patients with T cell cancers.
UR - https://www.scopus.com/pages/publications/105025668397
UR - https://www.scopus.com/pages/publications/105025668397#tab=citedBy
U2 - 10.1038/s43018-025-01069-z
DO - 10.1038/s43018-025-01069-z
M3 - Article
C2 - 41429932
AN - SCOPUS:105025668397
SN - 2662-1347
VL - 6
SP - 2011
EP - 2024
JO - Nature Cancer
JF - Nature Cancer
IS - 12
ER -