T-CELL EPITOPES ON THE HUMAN ACETYLCHOLINE-RECEPTOR ALPHA-SUBUNIT RESIDUES-10-84 IN MYASTHENIA-GRAVIS

被引:6
作者
AHLBERG, R
YI, Q
ENG, H
PIRSKANEN, R
LEFVERT, AK
机构
[1] KAROLINSKA HOSP, DEPT MED, S-10401 STOCKHOLM 60, SWEDEN
[2] KAROLINSKA HOSP, IMMUNOL RES LAB, S-10401 STOCKHOLM 60, SWEDEN
[3] SODER SJUKHUSET, DEPT NEUROL, STOCKHOLM, SWEDEN
关键词
D O I
10.1111/j.1365-3083.1992.tb02958.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In myasthenia gravis the production of anti-acetylcholine receptor antibodies is modulated by acetylcholine receptor-specific T cells. Most B- and T-cell epitopes are located on the alpha-subunit of the receptor. In order to map the fine specificity of the antigen-specific T cells in myasthenia gravis, T-cell stimulation in response to 70 hexapeptides was studied in 24 patients and 24 healthy individuals. The hexapeptides overlapped with one amino acid and represented residues 10-84 of the NH2-terminal part of the alpha-subunit of the receptor. The IFN-gamma secretion from single T cells was used to detect T-cell stimulation. A significant difference in the T-cell response to several of the peptides was found between patients and healthy controls. The majority of the hexapeptides induced T-cell stimulation in at least one of the patients. Peptide-induced T-cell stimulation was evident in all but one of the patients. The results indicate that different epitopes and multiple T-cell clones are involved in the T-cell recognition of the acetylcholine receptor.
引用
收藏
页码:435 / 442
页数:8
相关论文
共 24 条
[1]  
ALLEN PM, 1985, J IMMUNOL, V135, P368
[2]   INVITRO PROLIFERATIVE RESPONSES AND ANTIBODY-TITERS SPECIFIC TO HUMAN ACETYLCHOLINE-RECEPTOR SYNTHETIC PEPTIDES IN PATIENTS WITH MYASTHENIA-GRAVIS AND RELATION TO HLA CLASS-II GENES [J].
BROCKE, S ;
BRAUTBAR, C ;
STEINMAN, L ;
ABRAMSKY, O ;
ROTHBARD, J ;
NEUMANN, D ;
FUCHS, S ;
MOZES, E .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (06) :1894-1900
[3]   DIFFERENT HLA DR-DQ ASSOCIATIONS IN SUBGROUPS OF IDIOPATHIC MYASTHENIA-GRAVIS [J].
CARLSSON, B ;
WALLIN, J ;
PIRSKANEN, R ;
MATELL, G ;
SMITH, CIE .
IMMUNOGENETICS, 1990, 31 (5-6) :285-290
[4]   REVERSE ELISPOT ASSAY FOR CLONAL ANALYSIS OF CYTOKINE PRODUCTION .1. ENUMERATION OF GAMMA-INTERFERON-SECRETING CELLS [J].
CZERKINSKY, C ;
ANDERSSON, G ;
EKRE, HP ;
NILSSON, LA ;
KLARESKOG, L ;
OUCHTERLONY, O .
JOURNAL OF IMMUNOLOGICAL METHODS, 1988, 110 (01) :29-36
[5]   T-CELL ANTIGENIC SITES TEND TO BE AMPHIPATHIC STRUCTURES [J].
DELISI, C ;
BERZOFSKY, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (20) :7048-7052
[6]   STRATEGIES FOR EPITOPE ANALYSIS USING PEPTIDE-SYNTHESIS [J].
GEYSEN, HM ;
RODDA, SJ ;
MASON, TJ ;
TRIBBICK, G ;
SCHOOFS, PG .
JOURNAL OF IMMUNOLOGICAL METHODS, 1987, 102 (02) :259-274
[7]  
GOOD MF, 1988, J IMMUNOL, V140, P1645
[8]   A JUXTA-MEMBRANE EPITOPE ON THE HUMAN ACETYLCHOLINE-RECEPTOR RECOGNIZED BY T-CELLS IN MYASTHENIA-GRAVIS [J].
HARCOURT, GC ;
SOMMER, N ;
ROTHBARD, J ;
WILLCOX, HNA ;
NEWSOMDAVIS, J .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (04) :1295-1300
[9]  
HECHT TT, 1983, J IMMUNOL, V131, P1049
[10]   MYASTHENIA-GRAVIS - STIMULATION OF ANTIRECEPTOR AUTOANTIBODIES BY AUTOREACTIVE T-CELL LINES [J].
HOHLFELD, R ;
KALIES, I ;
KOHLEISEN, B ;
HEININGER, K ;
CONTITRONCONI, B ;
TOYKA, KV .
NEUROLOGY, 1986, 36 (05) :618-621