LYTIC MONOCLONAL-ANTIBODY TO TRYPANOSOMA-CRUZI BLOOD-STREAM TRYPOMASTIGOTES WHICH RECOGNIZES AN EPITOPE EXPRESSED IN TISSUES AFFECTED IN CHAGAS-DISEASE

被引:15
作者
ZWIRNER, NW [1 ]
MALCHIODI, EL [1 ]
CHIARAMONTE, MG [1 ]
FOSSATI, CA [1 ]
机构
[1] UNIV BUENOS AIRES,FAC FARM & BIOQUIM,CONICET,INST ESTUDIOS IMMUNIDAD HUMORAL,CATEDRA INMUNOL,F,RA-1113 BUENOS AIRES,ARGENTINA
关键词
D O I
10.1128/IAI.62.6.2483-2489.1994
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been suggested that molecular mimicry between the antigens of Trypanosoma cruzi and the host could have a role in the onset of the chronic stage of Chagas' disease. In this article, we report on a monoclonal antibody (MAb), CAK20.12 (immunoglobulin G2b), which reacts with a polypeptidic epitope of a 150-kDa antigen expressed on the surface of several strains of T. cruzi. This MAb also causes lysis of bloodstream trypomastigotes. Serum samples from 30 of 30 patients with chronic and 11 of 13 patients with acute Chagas' disease present specific antibodies to this antigen. MAb CAK20.12 reacts, by indirect immunofluorescence, with human and syngeneic murine striated muscle tissue, with the smooth muscle layer of cardiac arteries, with the lamina muscularis mucosae and the external striated muscle layer of the esophagus, and with the smooth muscle cells of the colon from normal syngeneic mice. Reactivity with the small intestine was very weak, and no reactivity with ventricle or atrium tissue was detected. Adsorption with an antigenic fraction from normal murine striated muscle or from T. cruzi epimastigotes confirmed that MAb CAK20.12 recognizes a common epitope present in parasites and host tissues. MAb CAK20.12, lytic for the infective form of T. cruzi, recognizes an epitope expressed in striated and smooth muscle cells of the host tissues affected in the chronic stage of Chagas' disease.
引用
收藏
页码:2483 / 2489
页数:7
相关论文
共 45 条
[1]   A TUBULIN-RELATED 55 KILODALTON SURFACE-ANTIGEN RECOGNIZED BY DIFFERENT TRYPANOSOMA-CRUZI STAGE-SPECIFIC MONOCLONAL-ANTIBODIES FROM INFECTED MICE [J].
ALCINA, A ;
FRESNO, M .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1988, 29 (2-3) :181-190
[2]  
ALVAREZ M, 1968, Boletin Chileno de Parasitologia, V23, P4
[3]   MURINE ASCITIC FLUIDS CONTAIN VARYING AMOUNTS OF AN INHIBITOR THAT INTERFERES WITH COMPLEMENT-MEDIATED EFFECTOR FUNCTIONS OF MONOCLONAL-ANTIBODIES [J].
APPELMELK, BJ ;
VERWEIJVANVUGHT, AMJJ ;
MAASKANT, JJ ;
THIJS, LG ;
MACLAREN, DM .
IMMUNOLOGY LETTERS, 1992, 33 (02) :135-138
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]  
Brener Z., 1980, Advances in Parasitology, V18, P247, DOI 10.1016/S0065-308X(08)60401-7
[6]  
CARBONETTO CH, 1990, CLIN EXP IMMUNOL, V82, P93, DOI 10.1111/j.1365-2249.1990.tb05409.x
[7]   INDUCTION OF MACROPHAGE ACTIVATION AND OPSONIZING ANTIBODIES BY TRYPANOSOMA-CRUZI SUBPOPULATIONS [J].
CELENTANO, AM ;
CAPPA, SMG .
PARASITE IMMUNOLOGY, 1992, 14 (02) :155-167
[8]  
CICARELLI RMB, 1989, J IMMUNOL, V142, P1685
[9]  
FISCHER E, 1988, IMMUNOLOGY, V65, P299
[10]   CHARACTERIZATION OF AN 18-KILODALTON BRUCELLA CYTOPLASMIC PROTEIN WHICH APPEARS TO BE A SEROLOGICAL MARKER OF ACTIVE INFECTION OF BOTH HUMAN AND BOVINE BRUCELLOSIS [J].
GOLDBAUM, FA ;
LEONI, J ;
WALLACH, JC ;
FOSSATI, CA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (08) :2141-2145