Novel bispecific nanobody mitigates experimental intestinal inflammation in mice by targeting TNF‐α and IL‐23p19 bioactivities

Author:

Wang Jiewen1,Kang Guangbo1,Lu Huiying2ORCID,de Marco Ario3,Yuan Haibin1,Feng Zelin4,Gao Mengxue1,Wang Xiaoli4,Wang Huahong5,Zhang Xiaolan6,Wang Yuli178,Zhang Miao19,Wang Ping10,Feng Yuanhang1,Liu Zhanju2ORCID,Cao Xiaocang4,Huang He1ORCID

Affiliation:

1. Frontiers Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology Tianjin University Tianjin China

2. Center for Inflammatory Bowel Disease Research and Department of Gastroenterology, The Shanghai Tenth People's Hospital Tongji University School of Medicine Shanghai China

3. Laboratory for Environmental and Life Sciences University of Nova Gorica Nova Gorica Slovenia

4. Department of Gastroenterology and Hepatology, Tianjin Medical University General Hospital Tianjin Medical University Tianjin China

5. Department of Gastroenterology Peking University First Hospital Beijing China

6. Department of Gastroenterology The Second Hospital of Hebei Medical University Shijiazhuang China

7. Tianjin Pharmaceutical Da Ren Tang Group Corporation Limited, Traditional Chinese Pharmacy Research Institute Tianjin Key Laboratory of Quality Control in Chinese Medicine Tianjin China

8. State Key Laboratory of Drug Delivery Technology and Pharmacokinetics Tianjin Institute of Pharmaceutical Research Tianjin China

9. China Resources Biopharmaceutical Company Limited Beijing China

10. New Technology R&D Department Tianjin Modern Innovative TCM Technology Company Limited Tianjin China

Abstract

AbstractBackgroundInflammatory bowel diseases (IBDs) pose significant challenges in terms of treatment non‐response, necessitating the development of novel therapeutic approaches. Although biological medicines that target TNF‐α (tumour necrosis factor‐α) have shown clinical success in some IBD patients, a substantial proportion still fails to respond.MethodsWe designed bispecific nanobodies (BsNbs) with the ability to simultaneously target human macrophage‐expressed membrane TNF‐α (hmTNF‐α) and IL‐23. Additionally, we fused the constant region of human IgG1 Fc (hIgG1 Fc) to BsNb to create BsNb‐Fc.  Our study encompassed in vitro and in vivo characterization of BsNb and BsNb‐Fc.ResultsBsNb‐Fc exhibited an improved serum half‐life, targeting capability and effector function than BsNb. It's demonstrated that BsNb‐Fc exhibited superior anti‐inflammatory effects compared to the anti‐TNF‐α mAb (infliximab, IFX) combined with anti‐IL‐12/IL‐23p40 mAb (ustekinumab, UST) by Transwell co‐culture assays. Notably, in murine models of acute colitis brought on by 2,4,6‐trinitrobenzene sulfonic acid(TNBS) and dextran sulphate sodium (DSS), BsNb‐Fc effectively alleviated colitis severity. Additionally, BsNb‐Fc outperformed the IFX&UST combination in TNBS‐induced colitis, significantly reducing colon inflammation in mice with colitis produced by TNBS and DSS.ConclusionThese findings highlight an enhanced efficacy and improved biostability of BsNb‐Fc, suggesting its potential as a promising therapeutic option for IBD patients with insufficient response to TNF‐α inhibition.Key points A bispecific nanobody (BsNb) was created to target TNF‐α and IL‐23p19, exhibiting high affinity and remarkable stability. BsNb‐Fc inhibited the release of cytokines in CD4+T cells during co‐culture experiments. BsNb‐Fc effectively alleviated colitis severity in mouse model with acute colitis induced by DSS or TNBS, outperforming the IFX&UST combination.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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