Activated HLA-DR+CD38+ Effector Th1/17 Cells Distinguish Crohn’s Disease-associated Perianal Fistulas from Cryptoglandular Fistulas

Author:

Ouboter Laura F12ORCID,Lindelauf Ciska2,Jiang Qinyue2,Schreurs Mette2,Abdelaal Tamim R345,Luk Sietse J6,Barnhoorn Marieke C1,Hueting Willem E7,Han-Geurts Ingrid J8,Peeters Koen C M J9,Holman Fabian A9,Koning Frits2,van der Meulen-de Jong Andrea E1,Pascutti Maria Fernanda2

Affiliation:

1. Department of Gastroenterology and Hepatology, Leiden University Medical Center , Leiden , the Netherlands

2. Department of Immunology, Leiden University Medical Center , Leiden , the Netherlands

3. Department of Radiology, Leiden University Medical Center , Leiden , the Netherlands

4. Bioinformatics Lab, Delft University of Technology , Delft , the Netherlands

5. Systems and Biomedical Engineering Department, Faculty of Engineering Cairo University , Giza , Egypt

6. Department of Hematology, Leiden University Medical Center , Leiden , the Netherlands

7. Department of Surgery, Alrijne hospital , Leiderdorp , the Netherlands

8. Department of Surgery, Proctos Clinic , Bilthoven , the Netherlands

9. Department of Surgery, Leiden University Medical Center , Leiden , the Netherlands

Abstract

Abstract Background Perianal fistulas are a debilitating complication of Crohn’s disease (CD). Due to unknown reasons, CD-associated fistulas are in general more difficult to treat than cryptoglandular fistulas (non-CD-associated). Understanding the immune cell landscape is a first step towards the development of more effective therapies for CD-associated fistulas. In this work, we characterized the composition and spatial localization of disease-associated immune cells in both types of perianal fistulas by high-dimensional analyses. Methods We applied single-cell mass cytometry (scMC), spectral flow cytometry (SFC), and imaging mass cytometry (IMC) to profile the immune compartment in CD-associated perianal fistulas and cryptoglandular fistulas. An exploratory cohort (CD fistula, n = 10; non-CD fistula, n = 5) was analyzed by scMC to unravel disease-associated immune cell types. SFC was performed on a second fistula cohort (CD, n = 10; non-CD, n = 11) to comprehensively phenotype disease-associated T helper (Th) cells. IMC was used on a third cohort (CD, n = 5) to investigate the spatial distribution/interaction of relevant immune cell subsets. Results Our analyses revealed that activated HLA-DR+CD38+ effector CD4+ T cells with a Th1/17 phenotype were significantly enriched in CD-associated compared with cryptoglandular fistulas. These cells, displaying features of proliferation, regulation, and differentiation, were also present in blood, and colocalized with other CD4+ T cells, CCR6+ B cells, and macrophages in the fistula tracts. Conclusions Overall, proliferating activated HLA-DR+CD38+ effector Th1/17 cells distinguish CD-associated from cryptoglandular perianal fistulas and are a promising biomarker in blood to discriminate between these 2 fistula types. Targeting HLA-DR and CD38-expressing CD4+ T cells may offer a potential new therapeutic strategy for CD-related fistulas.

Publisher

Oxford University Press (OUP)

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