Blocking GPR15 counteracts integrin-dependent T cell gut homing in vivo
© The Author(s) 2024. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For permissions, please email: journals.permissionsoup.com..
BACKGROUND AND AIMS: The G protein coupled receptor GPR15 is expressed on and functionally important for T cells homing to the large intestine. However, the precise mechanisms by which GPR15 controls gut homing have been unclear. Thus, we aimed to elucidate these mechanisms as well as to explore the potential of targeting GPR15 for interfering with T cell recruitment to the colon in IBD.
METHODS: We used dynamic adhesion and transmigration assays as well as a humanized in vivo model of intestinal cell trafficking to study GPR15-dependent effects on gut homing. Moreover, we analysed GPR15 and integrin expression in patients with and without IBD cross-sectionally and longitudinally.
RESULTS: GPR15 controlled T cell adhesion to MAdCAM-1 and VCAM-1 upstream of α4β7 and α4β1 integrin, respectively. Consistently, high co-expression of these integrins with GPR15 was found on T cells from patients with IBD and GPR15 also promoted T cell recruitment to the colon in humanized mice. Anti-GPR15 antibodies effectively blocked T cell gut homing in vitro and in vivo. In vitro data as well as observations in a cohort of patients treated with vedolizumab suggest that this might be more effective than inhibiting α4β7.
CONCLUSIONS: GPR15 seems to have a broad, but organ-selective impact on T cell trafficking and is therefore a promising target for future therapy of IBD. Further studies are needed.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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Enthalten in: |
Journal of Crohn's & colitis - (2024) vom: 18. Jan. |
Sprache: |
Englisch |
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Beteiligte Personen: |
Schramm, Sebastian [VerfasserIn] |
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Date Revised 20.01.2024 published: Print-Electronic Citation Status Publisher |
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doi: |
10.1093/ecco-jcc/jjae012 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM367340615 |
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520 | |a © The Author(s) 2024. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For permissions, please email: journals.permissionsoup.com. | ||
520 | |a BACKGROUND AND AIMS: The G protein coupled receptor GPR15 is expressed on and functionally important for T cells homing to the large intestine. However, the precise mechanisms by which GPR15 controls gut homing have been unclear. Thus, we aimed to elucidate these mechanisms as well as to explore the potential of targeting GPR15 for interfering with T cell recruitment to the colon in IBD | ||
520 | |a METHODS: We used dynamic adhesion and transmigration assays as well as a humanized in vivo model of intestinal cell trafficking to study GPR15-dependent effects on gut homing. Moreover, we analysed GPR15 and integrin expression in patients with and without IBD cross-sectionally and longitudinally | ||
520 | |a RESULTS: GPR15 controlled T cell adhesion to MAdCAM-1 and VCAM-1 upstream of α4β7 and α4β1 integrin, respectively. Consistently, high co-expression of these integrins with GPR15 was found on T cells from patients with IBD and GPR15 also promoted T cell recruitment to the colon in humanized mice. Anti-GPR15 antibodies effectively blocked T cell gut homing in vitro and in vivo. In vitro data as well as observations in a cohort of patients treated with vedolizumab suggest that this might be more effective than inhibiting α4β7 | ||
520 | |a CONCLUSIONS: GPR15 seems to have a broad, but organ-selective impact on T cell trafficking and is therefore a promising target for future therapy of IBD. Further studies are needed | ||
650 | 4 | |a Journal Article | |
700 | 1 | |a Liu, Li-Juan |e verfasserin |4 aut | |
700 | 1 | |a Saad, Marek |e verfasserin |4 aut | |
700 | 1 | |a Dietz, Lisa |e verfasserin |4 aut | |
700 | 1 | |a Dedden, Mark |e verfasserin |4 aut | |
700 | 1 | |a Müller, Tanja M |e verfasserin |4 aut | |
700 | 1 | |a Atreya, Imke |e verfasserin |4 aut | |
700 | 1 | |a Voskens, Caroline J |e verfasserin |4 aut | |
700 | 1 | |a Atreya, Raja |e verfasserin |4 aut | |
700 | 1 | |a Neurath, Markus F |e verfasserin |4 aut | |
700 | 1 | |a Zundler, Sebastian |e verfasserin |4 aut | |
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