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Updated: Feb 20, 2026

Induction of Intestinal Inflammation by Adoptive Transfer of CBir1 TCR Transgenic CD4+ T Cells to Immunodeficient Mice
Published on: December 16, 2021
GB20-5A8-31, an anti-TL1A antibody for treating inflammatory bowel disease
Yu Huang1, Qiongying You1, Tianqi Yao1
1Drug Discovery, Center for Research and Development, Kexing Biopharm Co., Ltd., Shenzhen, Guangdong, China.
Abstract:
Inflammatory bowel disease (IBD) remains a critical unmet medical challenge, with a substantial number of patients experiencing ineffective treatment or therapeutic failure over time. Here, GB20-5A8-31, a novel anti-TNF-like ligand 1A (TL1A) antibody, was engineered for high potency and superior developability. GB20-5A8-31 exhibited ultra-high affinity (KD = 5.11×10-11 M) for human TL1A, potent inhibition of TL1A signaling in vitro. Meanwhile, GB20-5A8-31 demonstrated potent anti-inflammatory effects and anti-fibrotic tendencies in both the 2,4,6-trinitro-benzenesulfonic acid-induced rat and dextran sulfate-induced hTLIA-transgenic mouse acute IBD models. Its favorable pharmacokinetic profile, including an extended half-life (T1/2 = 248.54 h) in hFcRn-transgenic Sprague-Dawley rats, supports sustained target engagement. Crucially, GB20-5A8-31 exhibits advantageous biophysical properties-including high stability, solubility, and low aggregation-which facilitate the development of high-concentration formulations aimed at improving patient compliance. In summary, these findings indicate that GB20-5A8-31 is a therapeutic candidate for IBD with promising preclinical efficacy and the potential to advance to the Chemistry, Manufacturing and Controls research.
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