MYELIN PROTEOLIPID PROTEIN - MINIMUM SEQUENCE REQUIREMENTS FOR ACTIVE INDUCTION OF AUTOIMMUNE ENCEPHALOMYELITIS IN SWR/J AND SJL/J MICE

被引:54
作者
TUOHY, VK
SOBEL, RA
LU, ZJ
LAURSEN, RA
LEES, MB
机构
[1] EK SHRIVER CTR,DEPT BIOCHEM,WALTHAM,MA
[2] BOSTON UNIV,DEPT CHEM,BOSTON,MA 02215
[3] MASSACHUSETTS GEN HOSP,NEUROL SERV,BOSTON,MA 02114
[4] MASSACHUSETTS GEN HOSP,IMMUNOPATHOL UNIT,BOSTON,MA 02114
[5] MASSACHUSETTS GEN HOSP,NEUROPATHOL UNIT,BOSTON,MA 02114
[6] HARVARD UNIV,SCH MED,DEPT NEUROL,BOSTON,MA 02115
[7] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
关键词
MYELIN PROTEOLIPID PROTEIN; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; T-CELL EPITOPE; ENCEPHALITOGENIC; DEMYELINATION; MULTIPLE SCLEROSIS;
D O I
10.1016/0165-5728(92)90175-K
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Proteolipid protein (PLP) is the major protein constituent of mammalian central nervous system myelin. We have previously identified two different PLP encephalitogenic T cell epitopes in two mouse strains. Murine PLP peptides 103-116 YKTTICGKGLSATV and 139-151 HCLGKWLGHPDKF are encephalitogenic determinants in SWR/J (H-2q) and SJL/J (H-2s) mice, respectively. The purpose of the present study was to determine the minimum sequence requirements for each of these PLP encephalitogens. In SWR/J mice, at least two distinct overlapping peptides can induce experimental autoimmune encephalomyelitis (EAE). The eleven residue sequences PLP 105-115 TTICGKGLSAT and PLP 106-116 TICGKGLSATV are encephalitogenic in SWR/J mice, but PLP 106-115 TICGKGLSAT, the decapeptide indigenous to both sequences, is non-encephalitogenic. In contrast, the shortest PLP sequence capable of inducing EAE in SJL/J mice is the nonapeptide 141-149 LGKWL-GHPD. These data indicate that encephalitogenic determinants of PLP are short contiguous peptide sequences similar in length and diversity to those of MBP.
引用
收藏
页码:67 / 74
页数:8
相关论文
共 39 条
[31]  
TUOHY VK, 1988, J IMMUNOL, V140, P1868
[32]  
TUOHY VK, 1989, J IMMUNOL, V142, P1523
[33]  
TUOHY VK, 1989, ANN NEUROL, V26, P297
[34]   THE DEVELOPMENT AND CHARACTERIZATION OF ENCEPHALITOGENIC CLONED T-CELLS SPECIFIC FOR MYELIN PROTEOLIPID PROTEIN [J].
VANDERVEEN, RC ;
TROTTER, JL ;
HICKEY, WF ;
KAPP, JA .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 26 (02) :139-145
[35]  
WHITHAM RH, 1991, J IMMUNOL, V146, P101
[36]  
WHITHAM RH, 1991, J IMMUNOL, V147, P3803
[37]   ANTIGEN RECOGNITION IN AUTOIMMUNE ENCEPHALOMYELITIS AND THE POTENTIAL FOR PEPTIDE-MEDIATED IMMUNOTHERAPY [J].
WRAITH, DC ;
SMILEK, DE ;
MITCHELL, DJ ;
STEINMAN, L ;
MCDEVITT, HO .
CELL, 1989, 59 (02) :247-255
[38]   T-CELL EPITOPE OF THE AUTOANTIGEN MYELIN BASIC-PROTEIN THAT INDUCES ENCEPHALOMYELITIS [J].
ZAMVIL, SS ;
MITCHELL, DJ ;
MOORE, AC ;
KITAMURA, K ;
STEINMAN, L ;
ROTHBARD, JB .
NATURE, 1986, 324 (6094) :258-260
[39]   MULTIPLE DISCRETE ENCEPHALITOGENIC EPITOPES OF THE AUTO-ANTIGEN MYELIN BASIC-PROTEIN INCLUDE A DETERMINANT FOR I-E CLASS-II-RESTRICTED T-CELLS [J].
ZAMVIL, SS ;
MITCHELL, DJ ;
POWELL, MB ;
SAKAI, K ;
ROTHBARD, JB ;
STEINMAN, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :1181-1186