MYASTHENIA-GRAVIS - T-EPITOPES ON THE DELTA-SUBUNIT OF HUMAN MUSCLE ACETYLCHOLINE-RECEPTOR

被引:0
作者
PROTTI, MP
MANFREDI, AA
WU, XD
MOIOLA, L
HOWARD, JF
CONTITRONCONI, BM
机构
[1] UNIV MINNESOTA,COLL BIOL SCI,DEPT BIOCHEM,1479 GORTNER AVE,ST PAUL,MN 55108
[2] UNIV N CAROLINA,DEPT NEUROL,CHAPEL HILL,NC 27599
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D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune T cell lines specific for muscle nicotinic acetylcholine receptor (AChR) were propagated from the blood of three myasthenia gravis patients by the use of a pool of synthetic peptides (delta-pool) corresponding to the complete sequence of the delta-subunit of human muscle AChR. Propagation of AChR-specific T cell lines was attempted unsuccessfully from four other myasthenia gravis patients and from four healthy controls. The lines had CD3+, CD4+, CD8- phenotype, strongly recognized the delta-pool, and cross-reacted vigorously with nondenatured AChR purified from mammalian muscle. They did not cross-react detectably with pools of similar overlapping synthetic peptides corresponding to the complete sequences of the alpha- and gamma-subunits of human muscle AChR. The sequence segments of the delta-subunit that contain T epitopes were identified by investigating the response of the three CD4+ T cell lines to the individual synthetic peptides forming the delta-pool. Each line had an individual pattern of peptide recognition. Although no immuno-dominant region, recognized in association with different DR haplotypes, could be identified, the sequence segments most strongly recognized by the CD4+ T cell lines were clustered within residues 121-290. One of the peptides more strongly recognized by the T cells corresponded to a sequence segment with high predicted propensity to form an amphipathic alpha-helix, a structural motif proposed to be typical of T epitopes.
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页码:2253 / 2261
页数:9
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共 48 条
[1]  
BELLONE M, 1988, J IMMUNOL, V143, P256
[2]   IMMUNOGENICITY AND TOLEROGENICITY OF SELF-MAJOR HISTOCOMPATIBILITY COMPLEX PEPTIDES [J].
BENICHOU, G ;
TAKIZAWA, PA ;
HO, PT ;
KILLION, CC ;
OLSON, CA ;
MCMILLAN, M ;
SERCARZ, EE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1341-1346
[3]   CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX-RESTRICTED CYTOLYTIC LYMPHOCYTES-T RECOGNIZE A LIMITED NUMBER OF SITES ON THE INFLUENZA HEMAGGLUTININ [J].
BRACIALE, TJ ;
SWEETSER, MT ;
MORRISON, LA ;
KITTLESEN, DJ ;
BRACIALE, VL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (01) :277-281
[4]   INFLUENCES OF ANTIGEN PROCESSING ON THE EXPRESSION OF THE T-CELL REPERTOIRE - EVIDENCE FOR MHC-SPECIFIC HINDERING STRUCTURES ON THE PRODUCTS OF PROCESSING [J].
BRETT, SJ ;
CEASE, KB ;
BERZOFSKY, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (01) :357-373
[5]  
CELIS E, 1988, J IMMUNOL, V140, P1808
[6]  
CHRISTADOSS P, 1986, J IMMUNOL, V136, P2437
[7]   INTERLEUKIN-2 PRODUCTION USED TO DETECT ANTIGENIC PEPTIDE RECOGNITION BY T-HELPER LYMPHOCYTES FROM ASYMPTOMATIC HIV-SEROPOSITIVE INDIVIDUALS [J].
CLERICI, M ;
STOCKS, NI ;
ZAJAC, RA ;
BOSWELL, RN ;
BERNSTEIN, DC ;
MANN, DL ;
SHEARER, GM ;
BERZOFSKY, JA .
NATURE, 1989, 339 (6223) :383-385
[8]   T-CELL VACCINATION [J].
COHEN, IR ;
WEINER, HL .
IMMUNOLOGY TODAY, 1988, 9 (11) :332-335
[9]   CELLULAR IMMUNE-RESPONSE AGAINST ACETYLCHOLINE-RECEPTOR IN MYASTHENIA-GRAVIS .1. RELEVANCE TO CLINICAL COURSE AND PATHOGENESIS [J].
CONTITRONCONI, BM ;
MORGUTTI, M ;
SGHIRLANZONI, A ;
CLEMENTI, F .
NEUROLOGY, 1979, 29 (04) :496-501
[10]   MAMMALIAN MUSCLE ACETYLCHOLINE-RECEPTOR - A SUPRAMOLECULAR STRUCTURE FORMED BY 4 RELATED PROTEINS [J].
CONTITRONCONI, BM ;
GOTTI, CM ;
HUNKAPILLER, MW ;
RAFTERY, MA .
SCIENCE, 1982, 218 (4578) :1227-1229