Targeting TL1A and DR3: the new frontier of anti-cytokine therapy in IBD
TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated...
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| Vydáno v: | Gut Ročník 74; číslo 4; s. 652 - 668 |
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| Jazyk: | angličtina |
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BMJ Publishing Group Ltd and British Society of Gastroenterology
01.04.2025
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| ISSN: | 0017-5749, 1468-3288, 1468-3288 |
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| Abstract | TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated cytokine system. The significance of TL1A:DR3 signalling in the pathogenesis of inflammatory bowel disease (IBD) is supported by several converging lines of evidence.To provide a comprehensive understanding of what is currently known regarding the TL1A/DR3 system in the context of IBD.TL1A and DR3 are expressed by cellular subsets with important roles for the initiation and maintenance of intestinal inflammation, serving as potent universal costimulators of effector immune responses, indicating their participation in the pathogenesis of IBD. Recent evidence also supports a homoeostatic role for TL1A:DR3 via regulation of Tregs and innate lymphoid cells. TL1A and DR3 are also expressed by stromal cells and may contribute to inflammation-induced or inflammation-independent intestinal fibrogenesis. Finally, discovery of genetic polymorphisms with functional consequences may allow for patient stratification, including differential responses to TL1A-targeted therapeutics.TL1A:DR3 signalling plays a central and multifaceted role in the immunological pathways that underlie intestinal inflammation, such as that observed in IBD. Such evidence provides the foundation for developing pharmaceutical approaches targeting this ligand-receptor pair in IBD. |
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| AbstractList | TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated cytokine system. The significance of TL1A:DR3 signalling in the pathogenesis of inflammatory bowel disease (IBD) is supported by several converging lines of evidence. Herein, we aim to provide a comprehensive understanding of what is currently known regarding the TL1A/DR3 system in the context of IBD. TL1A and DR3 are expressed by cellular subsets with important roles for the initiation and maintenance of intestinal inflammation, serving as potent universal costimulators of effector immune responses, indicating their participation in the pathogenesis of IBD. Recent evidence also supports a homoeostatic role for TL1A:DR3 via regulation of Tregs and innate lymphoid cells. TL1A and DR3 are also expressed by stromal cells and may contribute to inflammation-induced or inflammation-independent intestinal fibrogenesis. Finally, discovery of genetic polymorphisms with functional consequences may allow for patient stratification, including differential responses to TL1A-targeted therapeutics. In conclusion, TL1A:DR3 signalling plays a central and multifaceted role in the immunological pathways that underlie intestinal inflammation, such as that observed in IBD. Such evidence provides the foundation for developing pharmaceutical approaches targeting this ligand-receptor pair in IBD. TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated cytokine system. The significance of TL1A:DR3 signalling in the pathogenesis of inflammatory bowel disease (IBD) is supported by several converging lines of evidence.To provide a comprehensive understanding of what is currently known regarding the TL1A/DR3 system in the context of IBD.TL1A and DR3 are expressed by cellular subsets with important roles for the initiation and maintenance of intestinal inflammation, serving as potent universal costimulators of effector immune responses, indicating their participation in the pathogenesis of IBD. Recent evidence also supports a homoeostatic role for TL1A:DR3 via regulation of Tregs and innate lymphoid cells. TL1A and DR3 are also expressed by stromal cells and may contribute to inflammation-induced or inflammation-independent intestinal fibrogenesis. Finally, discovery of genetic polymorphisms with functional consequences may allow for patient stratification, including differential responses to TL1A-targeted therapeutics.TL1A:DR3 signalling plays a central and multifaceted role in the immunological pathways that underlie intestinal inflammation, such as that observed in IBD. Such evidence provides the foundation for developing pharmaceutical approaches targeting this ligand-receptor pair in IBD. TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated cytokine system. The significance of TL1A:DR3 signalling in the pathogenesis of inflammatory bowel disease (IBD) is supported by several converging lines of evidence. Herein, we aim to provide a comprehensive understanding of what is currently known regarding the TL1A/DR3 system in the context of IBD. TL1A and DR3 are expressed by cellular subsets with important roles for the initiation and maintenance of intestinal inflammation, serving as potent universal costimulators of effector immune responses, indicating their participation in the pathogenesis of IBD. Recent evidence also supports a homoeostatic role for TL1A:DR3 via regulation of Tregs and innate lymphoid cells. TL1A and DR3 are also expressed by stromal cells and may contribute to inflammation-induced or inflammation-independent intestinal fibrogenesis. Finally, discovery of genetic polymorphisms with functional consequences may allow for patient stratification, including differential responses to TL1A-targeted therapeutics. In conclusion, TL1A:DR3 signalling plays a central and multifaceted role in the immunological pathways that underlie intestinal inflammation, such as that observed in IBD. Such evidence provides the foundation for developing pharmaceutical approaches targeting this ligand-receptor pair in IBD.TNF-like cytokine 1A (TL1A) and its functional receptor, death-domain receptor 3 (DR3), are members of the TNF and TNFR superfamilies, respectively, with recognised roles in regulating innate and adaptive immune responses; additional existence of a decoy receptor, DcR3, indicates a tightly regulated cytokine system. The significance of TL1A:DR3 signalling in the pathogenesis of inflammatory bowel disease (IBD) is supported by several converging lines of evidence. Herein, we aim to provide a comprehensive understanding of what is currently known regarding the TL1A/DR3 system in the context of IBD. TL1A and DR3 are expressed by cellular subsets with important roles for the initiation and maintenance of intestinal inflammation, serving as potent universal costimulators of effector immune responses, indicating their participation in the pathogenesis of IBD. Recent evidence also supports a homoeostatic role for TL1A:DR3 via regulation of Tregs and innate lymphoid cells. TL1A and DR3 are also expressed by stromal cells and may contribute to inflammation-induced or inflammation-independent intestinal fibrogenesis. Finally, discovery of genetic polymorphisms with functional consequences may allow for patient stratification, including differential responses to TL1A-targeted therapeutics. In conclusion, TL1A:DR3 signalling plays a central and multifaceted role in the immunological pathways that underlie intestinal inflammation, such as that observed in IBD. Such evidence provides the foundation for developing pharmaceutical approaches targeting this ligand-receptor pair in IBD. |
| Author | Pizarro, Theresa T Cominelli, Fabio Menghini, Paola Bamias, Giorgos |
| Author_xml | – sequence: 1 givenname: Giorgos surname: Bamias fullname: Bamias, Giorgos organization: GI Unit, 3rd Academic Department of Internal Medicine, National and Kapodistrian University of Athens, Sotiria Hospital, Athens, Greece – sequence: 2 givenname: Paola surname: Menghini fullname: Menghini, Paola organization: Digestive Health Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA – sequence: 3 givenname: Theresa T orcidid: 0000-0003-3163-915X surname: Pizarro fullname: Pizarro, Theresa T organization: Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA – sequence: 4 givenname: Fabio orcidid: 0000-0002-1571-1548 surname: Cominelli fullname: Cominelli, Fabio email: fabio.cominelli@uhhospitals.org organization: Digestive Health Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39266053$$D View this record in MEDLINE/PubMed |
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120 Michelsen (2025041509001196000_74.4.652.58) 2009; 4 Lawrance (2025041509001196000_74.4.652.105) 2017; 11 2025041509001196000_74.4.652.119 2025041509001196000_74.4.652.118 Sheikh (2025041509001196000_74.4.652.23) 2003; 2 2025041509001196000_74.4.652.126 Valatas (2025041509001196000_74.4.652.50) 2019; 10 2025041509001196000_74.4.652.125 2025041509001196000_74.4.652.69 2025041509001196000_74.4.652.122 2025041509001196000_74.4.652.121 2025041509001196000_74.4.652.67 2025041509001196000_74.4.652.124 Wang (2025041509001196000_74.4.652.18) 2014; 15 2025041509001196000_74.4.652.66 2025041509001196000_74.4.652.123 2025041509001196000_74.4.652.65 Pham (2025041509001196000_74.4.652.88) 2017; 13 2025041509001196000_74.4.652.64 2025041509001196000_74.4.652.120 2025041509001196000_74.4.652.62 2025041509001196000_74.4.652.61 2025041509001196000_74.4.652.60 Latiano (2025041509001196000_74.4.652.48) 2011; 6 Pai (2025041509001196000_74.4.652.29) 2020; 15 2025041509001196000_74.4.652.17 2025041509001196000_74.4.652.15 2025041509001196000_74.4.652.14 2025041509001196000_74.4.652.13 2025041509001196000_74.4.652.12 2025041509001196000_74.4.652.11 2025041509001196000_74.4.652.99 2025041509001196000_74.4.652.10 2025041509001196000_74.4.652.98 2025041509001196000_74.4.652.97 2025041509001196000_74.4.652.96 2025041509001196000_74.4.652.95 2025041509001196000_74.4.652.93 2025041509001196000_74.4.652.92 2025041509001196000_74.4.652.91 Cavallini (2025041509001196000_74.4.652.16) 2013; 8 2025041509001196000_74.4.652.19 Liu (2025041509001196000_74.4.652.116) 2014; 9 2025041509001196000_74.4.652.104 2025041509001196000_74.4.652.103 2025041509001196000_74.4.652.106 2025041509001196000_74.4.652.100 2025041509001196000_74.4.652.89 2025041509001196000_74.4.652.102 2025041509001196000_74.4.652.101 2025041509001196000_74.4.652.87 2025041509001196000_74.4.652.86 2025041509001196000_74.4.652.85 2025041509001196000_74.4.652.84 2025041509001196000_74.4.652.82 2025041509001196000_74.4.652.80 2025041509001196000_74.4.652.90 Jacobs (2025041509001196000_74.4.652.107) 2024; 15 2025041509001196000_74.4.652.39 2025041509001196000_74.4.652.37 2025041509001196000_74.4.652.36 2025041509001196000_74.4.652.35 2025041509001196000_74.4.652.34 2025041509001196000_74.4.652.33 Steele (2025041509001196000_74.4.652.109) 2021; 12 2025041509001196000_74.4.652.32 2025041509001196000_74.4.652.31 2025041509001196000_74.4.652.30 Li (2025041509001196000_74.4.652.78) 2018; 9 Sands (2025041509001196000_74.4.652.2) 2023; 164 2025041509001196000_74.4.652.28 2025041509001196000_74.4.652.27 2025041509001196000_74.4.652.26 2025041509001196000_74.4.652.25 2025041509001196000_74.4.652.24 2025041509001196000_74.4.652.22 2025041509001196000_74.4.652.21 2025041509001196000_74.4.652.20 2025041509001196000_74.4.652.8 2025041509001196000_74.4.652.9 2025041509001196000_74.4.652.4 2025041509001196000_74.4.652.5 2025041509001196000_74.4.652.6 Masterson (2025041509001196000_74.4.652.108) 2015; 21 2025041509001196000_74.4.652.7 Richard (2025041509001196000_74.4.652.63) 2018; 14 Reinisch (2025041509001196000_74.4.652.113) 2024; 18 Zhao (2025041509001196000_74.4.652.83) 2020; 48 2025041509001196000_74.4.652.1 2025041509001196000_74.4.652.3 Shih (2025041509001196000_74.4.652.81) 2011; 6 2025041509001196000_74.4.652.59 2025041509001196000_74.4.652.57 2025041509001196000_74.4.652.55 2025041509001196000_74.4.652.54 2025041509001196000_74.4.652.53 2025041509001196000_74.4.652.52 2025041509001196000_74.4.652.51 Schmitt (2025041509001196000_74.4.652.94) 2024; 221 Ditrich (2025041509001196000_74.4.652.56) 2020; 13 2025041509001196000_74.4.652.49 2025041509001196000_74.4.652.47 2025041509001196000_74.4.652.46 2025041509001196000_74.4.652.45 2025041509001196000_74.4.652.44 2025041509001196000_74.4.652.43 2025041509001196000_74.4.652.42 2025041509001196000_74.4.652.41 2025041509001196000_74.4.652.40 |
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| Title | Targeting TL1A and DR3: the new frontier of anti-cytokine therapy in IBD |
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