Intrathecal administration of antibodies against LFA-1 and against ICAM-1 suppresses experimental allergic encephalomyelitis in rats

被引:44
作者
Kawai, K
Kobayashi, Y
Shiratori, M
Sobue, G
Tamatani, T
Miyasaka, M
Yoshikai, Y
机构
[1] NAGOYA UNIV,SCH MED,DIS MECHANISM & CONTROL RES INST,LAB GERMFREE LIFE,NAGOYA,AICHI 466,JAPAN
[2] JT INC,PHARMACEUT BASIC RES LAB,TOKYO 113,JAPAN
[3] OSAKA UNIV,SCH MED,BIOMED RES CTR,DEPT BIOREGULAT,OSAKA 565,JAPAN
关键词
D O I
10.1006/cimm.1996.9989
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The effects of intracerebroventricular administration of mAbs against LFA-1 and ICAM-1 on both active and passive experimental allergic encephalomyelitis (EAE) in rats were examined. Lewis rats were immunized with guinea pig myelin basic protein (MBP) or MBP 68-86 peptide in complete Freund's adjuvant to induce active EAE, or they were injected with encephalitogenic MBP-reactive lymphocytes for adoptive transferred EAE. LFA-1-specific mAbs and/or ICAM-1-specific mAbs or a control mAb or PBS were injected into the lateral ventricles via implanted needles. Intracerebroventricular administration of the specific mAbs together on Days 0, 2, 4, and 6 or on Days 4, 6, 8, and 10 after immunization almost completely suppressed the clinical signs of the actively induced EAE with reduced numbers of the infiltrating cells and reduced percentages of W3/25(+) and 1A-29(+) cells in the central nervous system (CNS) of the rats. Pretreatment with both specific mAbs from 14 to 11 days prior to immunization also exhibited a considerable protective effect. However, daily injection from Day 10 to 13 after immunization did not suppress the clinical signs. In rats with adoptive transferred EAE, daily treatment from Day 0 to Day 4 after cell transfer completely abolished clinical signs of EAE, although comparison of histological findings was not remarkable. In conclusion, intrathecal administration of antibodies against LFA-1 and ICAM-1 may be useful for the treatment of human demyelinating diseases, such as multiple sclerosis. (C) 1996 Academic Press, Inc.
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页码:262 / 268
页数:7
相关论文
共 34 条
[1]   INHIBITION OF EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS BY AN ANTIBODY TO THE INTERCELLULAR-ADHESION MOLECULE ICAM-1 [J].
ARCHELOS, JJ ;
JUNG, S ;
MAURER, M ;
SCHMIED, M ;
LASSMANN, H ;
TAMATANI, T ;
MIYASAKA, M ;
TOYKA, KV ;
HARTUNG, HP .
ANNALS OF NEUROLOGY, 1993, 34 (02) :145-154
[2]  
AZUMA T, 1987, MOL IMMUNOL, V24, P287
[3]   SURFACE EXPRESSION OF ALPHA-4 INTEGRIN BY CD4 T-CELLS IS REQUIRED FOR THEIR ENTRY INTO BRAIN PARENCHYMA [J].
BARON, JL ;
MADRI, JA ;
RUDDLE, NH ;
HASHIM, G ;
JANEWAY, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (01) :57-68
[4]   ANTIADHESION MOLECULE THERAPY IN EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS [J].
CANNELLA, B ;
CROSS, AH ;
RAINE, CS .
JOURNAL OF NEUROIMMUNOLOGY, 1993, 46 (1-2) :43-56
[5]   CHARACTERIZATION OF ICAM-2 AND EVIDENCE FOR A 3RD COUNTER-RECEPTOR FOR LFA-1 [J].
DEFOUGEROLLES, AR ;
STACKER, SA ;
SCHWARTING, R ;
SPRINGER, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (01) :253-267
[6]   LARGE-SCALE PREPARATION OF MYELIN BASIC PROTEIN FROM CENTRAL NERVOUS-TISSUE OF SEVERAL MAMMALIAN SPECIES [J].
DEIBLER, GE ;
KIES, MW ;
MARTENSON, RE .
PREPARATIVE BIOCHEMISTRY, 1972, 2 (02) :139-+
[7]   ICAM-1 (CD54) - A COUNTER-RECEPTOR FOR MAC-1 (CD11B CD18) [J].
DIAMOND, MS ;
STAUNTON, DE ;
DEFOUGEROLLES, AR ;
STACKER, SA ;
GARCIAAGUILAR, J ;
HIBBS, ML ;
SPRINGER, TA .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :3129-3139
[8]   T-CELL RECEPTOR CROSS-LINKING TRANSIENTLY STIMULATES ADHESIVENESS THROUGH LFA-1 [J].
DUSTIN, ML ;
SPRINGER, TA .
NATURE, 1989, 341 (6243) :619-624
[9]   MOLECULAR-CLONING OF ICAM-3, A 3RD LIGAND FOR LFA-1, CONSTITUTIVELY EXPRESSED ON RESTING LEUKOCYTES [J].
FAWCETT, J ;
HOLNESS, CLL ;
NEEDHAM, LA ;
TURLEY, H ;
GATTER, KC ;
MASON, DY ;
SIMMONS, DL .
NATURE, 1992, 360 (6403) :481-484
[10]  
HARDING CV, 1991, J IMMUNOL, V147, P767