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To overcome the limited efficacy of immune checkpoint blockade, there is a need to find novel cancer immunotherapeutic strategies for the optimal treatment of cancer. The novel anti-4-1BB×PDL1 bispecific antibody-ABL503 (also known as TJ-L14B)-was designed to simultaneously target PDL1 and 4-1BB and demonstrated strong antitumor T-cell responses without considerable toxicity. In this study, we investigated the mechanisms by which the combination of ABL503 and anti-PD1 blockade affected the reinvigoration of exhausted tumor-infiltrating CD8+ T cells (CD8+ TIL) and antitumor efficacy.
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Jeon et al. (Tue,) studied this question.
synapsesocial.com/papers/68e6a28cb6db64358762610a — DOI: https://doi.org/10.1158/1078-0432.ccr-23-2864
Seung Hyuck Jeon
Seoul National University Bundang Hospital
Gihoon You
ABL Bio (South Korea)
Junsik Park
Yonsei University
Clinical Cancer Research
Yonsei University
Korea Advanced Institute of Science and Technology
University of Ulsan
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