Differential Expression of Leukocyte Functions Associated Antigen-1 (LFA-1) on Peripheral Blood Mononuclear Cells in Patients with Crohn's Disease

被引:0
作者
Yada, Shinichiro [1 ]
Matsumoto, Takayuki [1 ]
Esaki, Motohiro [1 ]
Jo, Yukihiko [1 ]
Koga, Hideki [1 ]
Nakamura, Shotaro [1 ]
Iida, Mitsuo [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Higashi Ku, Fukuoka 8130031, Japan
基金
日本学术振兴会;
关键词
Crohn's disease; LFA-1; infliximab; total parenteral nutrition; Crohn's Disease Activity Index; NECROSIS-FACTOR-ALPHA; T-CELLS; MONOCLONAL-ANTIBODY; ADHESION MOLECULES; ULCERATIVE-COLITIS; LAMINA PROPRIA; TNF-ALPHA; ACTIVATION; INFLIXIMAB; ICAM-1;
D O I
10.1002/ibd.20935
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: The leukocyte Function associated antigen-1 (LFA-1) intracellular adhesion molecule-1 pathway is presumed to play a pivotal role in the perpetuation of inflammatory bowel disease. We aimed to elucidate the effect of 2 different therapies on LFA-1 expression in patients with Crohn's disease (CD) and correlate LFA-1 expression with disease activity. Methods: fit all, 30 patients with active CD were recruited for the present investigation. Eleven patients were treated with infliximab and 19 patients with total parenteral nutrition. The clinical activity and the expression of LFA-1 in peripheral blood mononuclear cells were assessed prior to and 4 weeks after treatment. Clinical activity was determined by measuring the Crohn's Disease Activity Index and LFA-1 expression was measured by mean fluorescence intensity (MFI) under fluorescence-activated cell sorter analysis. Results: In each treatment group the clinical disease activity index decreased significantly 4 weeks after treatment. In patients treated with infliximab, LFA-1 expression decreased significantly (mean MFI decreased from 1983 to 1487, P < 0.05). However, LFA-1 expression remained unchanged in the total parenteral nutrition group (mean MFI elevated from 1684 to 1902, P > 0.05), Conclusions: The mechanism of therapeutic action on CD is different between infliximab and total parenteral nutrition.
引用
收藏
页码:1379 / 1384
页数:6
相关论文
共 35 条
[1]  
Abraham C, 1999, J IMMUNOL, V162, P4399
[2]   Clinical relevance of advances in genetics and pharmacogenetics of IBD [J].
Ahmad, T ;
Tamboli, CP ;
Jewell, D ;
Colombel, JF .
GASTROENTEROLOGY, 2004, 126 (06) :1533-1549
[3]   Identical T cell clones are located within the mouse gut epithelium and lamina propria and circulate in the thoracic duct lymph [J].
Arstila, T ;
Arstila, TP ;
Calbo, S ;
Selz, F ;
Malassis-Seris, M ;
Vassalli, P ;
Kourilsky, P ;
Guy-Grand, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (05) :823-834
[4]   Alteration in expression of β2 integrins on lamina propria lymphocytes in ulcerative colitis and Crohn's disease [J].
Bernstein, CN ;
Sargent, M ;
Rector, E .
CLINICAL IMMUNOLOGY, 2002, 104 (01) :67-72
[5]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[6]  
Boismenu R, 1996, J IMMUNOL, V157, P985
[7]   REGIONAL SPECIALIZATION OF INTRAEPITHELIAL T-CELLS IN THE MURINE SMALL AND LARGE-INTESTINE [J].
BOLL, G ;
RUDOLPHI, A ;
SPIESS, S ;
REIMANN, J .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1995, 41 (02) :103-113
[8]  
Chen T, 1999, EUR J IMMUNOL, V29, P809, DOI 10.1002/(SICI)1521-4141(199903)29:03<809::AID-IMMU809>3.0.CO
[9]  
2-X
[10]   The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease [J].
Cuthbert, AP ;
Fisher, SA ;
Mirza, MM ;
King, K ;
Hampe, J ;
Croucher, PJP ;
Mascheretti, S ;
Sanderson, J ;
Forbes, A ;
Mansfield, J ;
Schreiber, S ;
Lewis, CM ;
Mathew, CG .
GASTROENTEROLOGY, 2002, 122 (04) :867-874