Microscopic Colitis Evolved Into Inflammatory Bowel Diseases Is Characterized by Increased Th1/Tc1 Cells in Colonic Mucosal Lamina Propria

Abstract

Background

An association between microscopic colitis (MC), i.e., lymphocytic colitis (LC) and collagenous colitis (CC), and inflammatory bowel diseases (IBD) has been noticed. A subset of MC cases may evolve into IBD, and IBD in remission may present as MC in a histologic pattern. Moreover, MC and IBD may coexist in different regions of the bowel. A link between MC and IBD in their pathogenesis is, therefore, suggested. Abnormal mucosal immunity is likely the key.

Methods

We reviewed 2324 MC cases in Calgary over 14 years and identified 20 cases evolved into IBD (IBD transformers). 13 of them were further investigated for colonic mucosal lamina propria mononuclear cells (LPMNCs), as opposed to 22 cases whose MC resolved. On their index colonic biopsy immunohistochemistry was performed to detect major T cell subsets characterized by key cytokines and master transcription factors (IFNγ and T-bet for Th1/Tc1, GATA-3 for Th2/Tc2, IL-17 and RORc for Th17/Tc17, FoxP3 for Treg/Tcreg) as well as TNFα⁺ cells (partly representing Th1). LPMNCs positive for each marker were counted (average number per high-power field).

Results

IBD transformers had increased IFNγ⁺, T-bet⁺, TNF-α⁺, and GATA-3⁺ LPMNCs compared to the MC-resolved cases. The LC-to-IBD subgroup had increased IFNγ⁺ and GATA-3⁺ cells compared to the LC-resolved subgroup. The CC-to-IBD subgroup had increased T-bet⁺, TNF-α⁺, and GATA-3⁺ cells compared to the CC-resolved subgroup. Among MC-resolved patients, more TNF-α⁺ and RORc⁺ cells were seen in LC than in CC.

Conclusion

Th1/Tc1- and TNFα-producing cells, and likely a subset of Th2/Tc2 cells as well, may be involved in the MC-to-IBD transformation.

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