CIRCULATING IMMUNOGLOBULIN G1 ANTIBODY IN PATIENTS WITH ULCERATIVE-COLITIS AGAINST THE COLONIC EPITHELIAL PROTEIN DETECTED BY A NOVEL MONOCLONAL-ANTIBODY

被引:10
作者
DASGUPTA, A [1 ]
MANDAL, A [1 ]
DAS, KM [1 ]
机构
[1] UNIV MED & DENT NEW JERSEY,ROBERT WOOD JOHNSON MED SCH,DEPT MED,DIV GASTROENTEROL & HEPATOL,NEW BRUNSWICK,NJ 08903
关键词
D O I
10.1136/gut.35.12.1712
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Autoimmunity has been implicated in the pathogenesis of ulcerative colitis (UC). Several studies have shown amplified immunoglobulin G1 (IgG1) antibody response in UC; however the immunoreactive antigen(s) is unknown. To study this antigen(s), mucosal colonic extract was prepared by sonication, ultracentrifugation followed by ion exchange chromatography in fast protein liquid chromatography. The fraction (enriched colonic peptide), that was most reactive to a novel monoclonal antibody, 7E(12)H(12) (IgM isotype), was isolated and used to examine the immunoreactivity against the patients' serum samples. Two hundred and thirteen coded samples from 111 patients with UC (symptomatic and untreated (63), symptomatic and treated (26), remission (22)); 47 with Crohn's disease (CD) (40 were symptomatic and untreated, and 30 had colonic disease); 29 with acute diarrhoea caused by specific pathogen(s); 10 with systemic lupus erythematosus, and 16 normal subjects were examined against the enriched colonic peptide by IgG subtype specific enzyme linked immunosorbent assays (ELISAs). Total IgG antibody reactivity was significantly (p<0.01) higher only in symptomatic and untreated UC patients compared with each of the non-UC group, but the sensitivity was only 50%. IgG2 and IgG3 reactivities were not different among various groups. The IgG1 antibody reactivity against the enriched colonic peptide, however, differentiated UC patients from CD and each of the other non-UC groups. Seventy nine per cent of the patients with UC, treated or untreated, symptomatic or in remission, had significantly (p<0.0001) higher IgG1 antibody against the enriched colonic peptide when compared with each of the other non-UC groups. Only 12% of CD serum samples and none of the other control serum samples reacted. Using purified serum IgG1 and 7E(12)H(12)-IgM, by sandwich ELISA, we confirmed that 7E(12)H(12) reactive peptide indeed reacts with UC-IgG1 antibody but not with control IgG1.
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页码:1712 / 1717
页数:6
相关论文
共 25 条
[1]  
ARONSON RA, 1983, J IMMUNOL, V131, P2796
[2]   ULCERATIVE-COLITIS SPECIFIC CYTO-TOXIC IGG-AUTOANTIBODIES AGAINST COLONIC EPITHELIAL CANCER-CELLS [J].
AUER, IO ;
GROSCH, L ;
HARDORFER, C ;
RODER, A .
GUT, 1988, 29 (12) :1639-1647
[3]   ULCERATIVE-COLITIS SERUM RECOGNIZES THE M(R) 40K PROTEIN ON COLONIC ADENOCARCINOMA CELLS FOR ANTIBODY-DEPENDENT CELLULAR CYTOTOXICITY [J].
BIANCONE, L ;
DAS, KM ;
ROBERTS, AI ;
EBERT, EC .
DIGESTION, 1993, 54 (04) :237-242
[4]  
BIANCONE L, 1992, Gastroenterology, V102, pA595
[5]   AUTOANTIBODIES IN HUMAN ULCERATIVE COLITIS [J].
BROBERGER, O ;
PERLMANN, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1959, 110 (05) :657-674
[6]  
DAS KM, 1987, J IMMUNOL, V139, P77
[7]   A SHARED AND UNIQUE EPITOPE(S) ON HUMAN-COLON, SKIN, AND BILIARY EPITHELIUM DETECTED BY A MONOCLONAL-ANTIBODY [J].
DAS, KM ;
VECCHI, M ;
SAKAMAKI, S .
GASTROENTEROLOGY, 1990, 98 (02) :464-469
[8]   ANTIBODY-DEPENDENT CELL-MEDIATED CYTO-TOXICITY IN SERUM SAMPLES FROM PATIENTS WITH ULCERATIVE-COLITIS - RELATIONSHIP TO DISEASE-ACTIVITY AND RESPONSE TO TOTAL COLECTOMY [J].
DAS, KM ;
KADONO, Y ;
FLEISCHNER, GM .
AMERICAN JOURNAL OF MEDICINE, 1984, 77 (05) :791-796
[9]   MR-40 000 HUMAN COLONIC EPITHELIAL PROTEIN EXPRESSION IN COLONIC MUCOSA AND PRESENCE OF CIRCULATING ANTI-MR-40 000 ANTIBODIES IN COTTON TOP TAMARINS WITH SPONTANEOUS COLITIS [J].
DAS, KM ;
VECCHI, M ;
SQUILLANTE, L ;
DASGUPTA, A ;
HENKE, M ;
CLAPP, N .
GUT, 1992, 33 (01) :48-54
[10]   AUTOIMMUNITY IN INFLAMMATORY BOWEL-DISEASE [J].
DAS, KM .
CANADIAN JOURNAL OF GASTROENTEROLOGY, 1993, 7 (02) :102-109