Mucosal T cells bearing TCRγδ play a protective role in intestinal inflammation

被引:134
作者
Inagaki-Ohara, K [1 ]
Chinen, T
Matsuzaki, G
Sasaki, A
Sakamoto, Y
Hiromatsu, K
Nakamura-Uchiyama, F
Nawa, Y
Yoshimura, A
机构
[1] Miyazaki Univ, Miyazaki Med Coll, Dept Infect Dis, Div Parasit Dis, Kiyotake, Miyazaki 8891692, Japan
[2] Univ Ryukyus, Ctr Mol Biosci, Div Mol Microbiol, Nishihara, Okinawa 90301, Japan
[3] Kyushu Univ, Med Inst Bioregulat, Dept Immunol, Higashi Ku, Fukuoka 812, Japan
关键词
D O I
10.4049/jimmunol.173.2.1390
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intestinal intraepithelial lymphocytes (IEL) bearing TCRgammadelta represent a major T cell population in the murine intestine. However, the role of gammadelta IEL in inflammatory bowel diseases (IBD) remains controversial. In this study, we show that gammadelta IEL is an important protective T cell population against IBD. gammadelta T cell-deficient (CS-/-) mice developed spontaneous colitis with age and showed high susceptibility to Th1-type 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis at a young age. Transfer of gammadelta IEL to Cdelta(-/-) mice ameliorated TNBS-induced colitis, which correlated with decrease of IFN-gamma and TNF-alpha production and an increase of TGF-beta production by IEL. Furthermore, a high level of IL-15, which inhibits activation-induced cell death to terminate inflammation, was expressed more in intestinal epithelial cells (EC) from TNBS-treated Cdelta(-/-) mice than in those from wild-type mice. EC from wild-type mice significantly suppressed the IFN-gamma production of IEL from TNBS-treated Cdelta(-/-) mice, whereas EC from TNBS-treated Cdelta(-/-) mice did not. These data indicate that gammadelta IEL play important roles in controlling IBD by regulating mucosal T cell activation cooperated with EC function. Our study suggests that enhancement of regulatory gammadelta T cell activity is a possible new cell therapy for colitis.
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页码:1390 / 1398
页数:9
相关论文
共 44 条
[31]  
O'Neil DA, 1999, J IMMUNOL, V163, P6718
[32]   IL-15-dependent activation-induced cell death-resistant Th1 type CD8αβ+NK1.1+ T cells for the development of small intestinal inflammation [J].
Ohta, N ;
Hiroi, T ;
Kweon, MN ;
Kinoshita, N ;
Jang, MH ;
Mashimo, T ;
Miyazaki, JI ;
Kiyono, H .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :460-468
[33]   CD1D IS INVOLVED IN T-CELL INTESTINAL EPITHELIAL-CELL INTERACTIONS [J].
PANJA, A ;
BLUMBERG, RS ;
BALK, SP ;
MAYER, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (03) :1115-1119
[34]  
Peng SL, 1997, J IMMUNOL, V158, P2464
[35]   A unique subset of self-specific intraintestinal T cells maintains gut integrity [J].
Poussier, P ;
Ning, T ;
Banerjee, D ;
Julius, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (11) :1491-1497
[36]   REGULATORY INTERACTIONS BETWEEN CD45RB(HIGH) AND CD45RB(LOW) CD4(+) T-CELLS ARE IMPORTANT FOR THE BALANCE BETWEEN PROTECTIVE AND PATHOGENIC CELL-MEDIATED-IMMUNITY [J].
POWRIE, F ;
CORREAOLIVEIRA, R ;
MAUZE, S ;
COFFMAN, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (02) :589-600
[37]   Cytotoxic T lymphocyte-associated antigen 4 plays an essential role in the function of CD25+CD4+ regulatory cells that control intestinal inflammation [J].
Read, S ;
Malmström, V ;
Powrie, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :295-302
[38]   Intestinal epithelial cells both express and respond to interleukin 15 [J].
Reinecker, HC ;
MacDermott, RP ;
Mirau, S ;
Dignass, A ;
Podolsky, DK .
GASTROENTEROLOGY, 1996, 111 (06) :1706-1713
[39]   Cytokine-inducible SH2 protein-3 (CIS3/SOCS3) inhibits Janus tyrosine kinase by binding through the N-terminal kinase inhibitory region as well as SH2 domain [J].
Sasaki, A ;
Yasukawa, H ;
Suzuki, A ;
Kamizono, S ;
Syoda, T ;
Kinjyo, I ;
Sasaki, M ;
Johnston, JA ;
Yoshimura, A .
GENES TO CELLS, 1999, 4 (06) :339-351
[40]   Activation of natural killer T cells by α-galactosylceramide in the presence of CD1d provides protection against colitis in mice [J].
Saubermann, LJ ;
Beck, P ;
De Jong, YP ;
Pitman, RS ;
Ryan, MS ;
Kim, HS ;
Exley, M ;
Snapper, S ;
Balk, SP ;
Hagen, SJ ;
Kanauchi, O ;
Motoki, K ;
Sakai, T ;
Terhorst, C ;
Koezuka, Y ;
Podolsky, DK ;
Blumberg, RS .
GASTROENTEROLOGY, 2000, 119 (01) :119-+