Case Report: Regulatory T Cell-Independent Induction of Remission in a Patient With Collagenous Colitis

Frontiers in Medicine

卷:8

Masatomo Kimura¹  Yasuhiro Masuta²  Ryutaro Takada²  Akane Hara²  Kosuke Minaga²  Shigenaga Matsui²  Hajime Honjo²  Mizuki Tomooka²  Tomoe Yoshikawa²  Keisuke Yoshikawa²  Masayuki Kurimoto²  Ken Kamata²  Ikue Sekai²  Takuya Matsubara²  Tomohiro Watanabe²  Masashi Kono²  Yasuo Otsuka²  Masatoshi Kudo² 

[1] Department of Diagnostic Pathology, Kindai University Hospital, Osaka, Japan;

[2] Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka, Japan;

关键词: collagenous colitis;    CD8+ T cells;    regulatory T cells;    Foxp3;    immunohistochemistry;   

DOI  :  10.3389/fmed.2021.678268

来源: DOAJ

【 摘 要 】

Collagenous colitis (CC), a prototypical microscopic colitis, is a chronic inflammatory disorder of the colon. The diagnosis of CC depends on the pathological examination. The colonic mucosa of patients with CC is characterized by the presence of a substantially thickened collagen band (>10μm) under the surface epithelium. In addition, intraepithelial and lamina propria lymphocytes are markedly increased in patients with CC. However, the roles played by the lymphocytes accumulating in the colonic mucosa of patients with CC are poorly defined. Recent studies indicate that T cells infiltrating the colonic mucosa of patients with CC are mainly represented by CD4+ T cells, CD8+ T cells, and forkhead box P3 (FOXP3)+ regulatory T cells (Tregs). Given that activation of CD4+/CD8+ T cells and FOXP3+ Tregs usually mediates pro-inflammatory and anti-inflammatory responses, respectively, alterations in the colonic numbers of these adaptive T cells might be related to the resolution of colitis in patients with CC. We determined alterations in the composition of colonic T cells by extensive immunohistochemical (IHC) analyses in a case of CC successfully treated with budesonide and metronidazole. Colonic lamina propria immune cells mainly comprised CD3+ T cells, CD4+ T cells, CD8+ T cells, CD68+ macrophages, and FOXP3+ Tregs, but not CD20+ B cells or myeloperoxidase (MPO)+ granulocytes in the active phase. During remission, the numbers of CD3+ T cells, CD4+ T cells, CD8+ T cells, and CD68+ macrophages did not change significantly in the colonic lamina propria, whereas FOXP3+ Tregs were markedly decreased, suggesting that induction of remission was achieved in a Treg-independent manner. Thus, our study indicates that accumulation of FOXP3+ Tregs in the colonic mucosa of patients with CC might be a counter-regulatory mechanism reflecting persistent inflammation and that induction of remission might be achieved without activation of Tregs.

【 授权许可】

Unknown