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FOXP3+T Cells and TGF-?1 in Colonic Mucosa of Children with Crohn¡¯s Disease
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±æÁÖÇö ( Gil Joo-Hyun )
ÀÌÈ¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
¿ÀÁ¤Àº ( Oh Jung-Eun )
ÀÌÈ¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
¼Á¤¿Ï ( Seo Jeong-Wan )
ÀÌÈ¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
Á¶¹Î¼± ( Cho Min-Sun )
ÀÌÈ¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø º´¸®Çб³½Ç
Á¶±â¿µ ( Cho Ky-Young )
ÀÌÈ¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
À¯Àº¼± ( Yoo Eun-Sun )
ÀÌÈ¿©ÀÚ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
KMID : 0816120110140030258
Abstract
Purpose: Forkhead box protein 3 (FOXP3)+T cells are the major regulatory T cells controlling all aspects of the immune response. Transforming growth factor-? (TGF-?) is a suppressive cytokine which mediates the suppressive action of FOXP3+T cells. The aim of this study was to investigate the role of FOXP3+T cells, TGF-? in colonic mucosa of children with Crohn¡¯s disease (CD).
Methods: Colonic mucosal biopsies were obtained from 10 children with CD (12¡15 years of age) and 11 control (8¡15 years of age). Frequencies of FOXP3+T, CD4+T cells and TGF-?1 expression were examined in the lamina propria (LP) and lymphoid aggregates or follicles (LA/F) by immunohistochemistry, and later evaluated by association with disease activity.
Results: In the LP of CD group, frequencies of FOXP3+T, CD4+T cells, proportion of FOXP3/CD4+T cells and TGF-?1 expression significantly increased compared to the control. In the LA/F of CD group, frequency of FOXP3+T cells, proportion of FOXP3/CD4+T cells and TGF-?1 expression significantly increased compared to the control (p£¼0.05). CD4+T cells also increased compared to the control, but this finding was not significant. In the LP and LA/F of CD group, frequency of FOXP3+T cells exhibited positive correlation with CD4+T cells (p£¼0.05). In the LP and LA/F of CD group, TGF-?1 expression had positive correlation with CRP, Pediatric Crohn¡¯s Disease Activity Index, and negative correlation with hematocrit and albumin (p£¼0.05).
Conclusion: Increased frequency of FOXP3+T cells and TGF-?1 expression in colonic mucosa of CD can be interpreted as a compensatory increase towards achieving down-regulation of immune responses.
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T-lymphocytes;Regulatory;Crohn¡¯s disease;FOXP3;CD4;Transforming growth factor beta;Child;Disease activity
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