T cell receptor δ repertoire in inflamed and noninflamed colon of patients with IBD analyzed by CDR3 spectratyping

被引:20
作者
Holtmeier, W
Hennemann, A
May, E
Duchmann, R
Caspary, WF
机构
[1] Goethe Univ Frankfurt, Med Klin 2, Div Gastroenterol, D-60590 Frankfurt, Germany
[2] Univ Munich, Dept Biol 2, D-80539 Munich, Germany
[3] Free Univ Berlin, Klinikum Benjamin Franklin, Med Klin 1, D-12200 Berlin, Germany
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2002年 / 282卷 / 06期
关键词
gamma/delta mucosal immunology; Crohn's disease; ulcerative colitis;
D O I
10.1152/ajpgi.00224.2001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
gamma/delta T cells might play an important role in autoimmune conditions like inflammatory bowel disease (IBD). In the present study, we characterized the T cell receptor (TCR)-delta repertoire by complementarity determining region 3 (CDR3) spectratyping in the inflamed and noninflamed mucosa and in the peripheral blood of subjects with Crohn's disease and ulcerative colitis. In contrast to previously published data about alpha/beta T cells, we rarely found oligoclonal expansions of gamma/delta T cells specific only for the inflamed mucosa. The same dominant gamma/delta T cell expansions were also present in the noninflamed colon. Furthermore, the peripheral gamma/delta TCR repertoire was oligoclonal but clearly distinct from that in the inflamed intestine. Thus our results do not support a role for antigen-specific gamma/delta T cells in IBD, and dominant gamma/delta T cells of the peripheral blood are not likely to be derived from the inflamed gut. However, in several patients, the TCR-delta-repertoire was highly diversified, whereas in others we observed a loss of dominant gamma/delta T cell clones when inflamed and noninflamed mucosa were compared. In conclusion, those changes indicate that gamma/delta T cells might play an important role in a subset of patients with IBD.
引用
收藏
页码:G1024 / G1034
页数:11
相关论文
共 53 条
[1]   LOCALIZATION OF GAMMA-DELTA-T-CELLS TO THE INTESTINAL EPITHELIUM IS INDEPENDENT OF NORMAL MICROBIAL COLONIZATION [J].
BANDEIRA, A ;
MOTASANTOS, T ;
ITOHARA, S ;
DEGERMANN, S ;
HEUSSER, C ;
TONEGAWA, S ;
COUTINHO, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (01) :239-244
[2]   TOLERANCE OF T-CELL RECEPTOR GAMMA-DELTA-CELLS IN THE INTESTINE [J].
BARRETT, TA ;
TATSUMI, Y ;
BLUESTONE, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (06) :1755-1762
[3]   MODULATION OF EPITHELIAL-CELL GROWTH BY INTRAEPITHELIAL GAMMA-DELTA T-CELLS [J].
BOISMENU, R ;
HAVRAN, WL .
SCIENCE, 1994, 266 (5188) :1253-1255
[4]   NON-RANDOM EXPRESSION OF T-CELL RECEPTOR-GAMMA AND RECEPTOR-DELTA VARIABLE GENE SEGMENTS IN FUNCTIONAL LYMPHOCYTE-T CLONES FROM HUMAN PERIPHERAL-BLOOD [J].
BORST, J ;
WICHERINK, A ;
VANDONGEN, JJM ;
DEVRIES, E ;
COMANSBITTER, WM ;
WASSENAAR, F ;
VANDENELSEN, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (09) :1559-1568
[5]  
BRAEGGER CP, 1994, ANN ALLERGY, V72, P135
[6]  
BUCHT A, 1995, CLIN EXP IMMUNOL, V99, P57
[7]  
BURGIO VL, 1995, GASTROENTEROLOGY, V109, P1029
[8]   Recognition by gamma/delta T cells [J].
Chien, YH ;
Jores, R ;
Crowley, MP .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :511-532
[9]  
Chott A, 1996, J IMMUNOL, V156, P3024
[10]   THE V-DELTA-1 T-CELL RECEPTOR REPERTOIRE IN HUMAN SMALL-INTESTINE AND COLON [J].
CHOWERS, Y ;
HOLTMEIER, W ;
HARWOOD, J ;
MORZYCKAWROBLEWSKA, E ;
KAGNOFF, MF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :183-190