ALTERATIONS IN LEVELS OF CD28(-)/CD8(+) SUPPRESSOR-CELL PRECURSOR AND CD45RO(+)/CD4(+) MEMORY T-LYMPHOCYTES IN THE PERIPHERAL-BLOOD OF MULTIPLE-SCLEROSIS PATIENTS

被引:75
作者
CRUCIAN, B
DUNNE, P
FRIEDMAN, H
RAGSDALE, R
PROSS, S
WIDEN, R
机构
[1] UNIV S FLORIDA,COLL MED,DEPT MED MICROBIOL IMMUNOL,TAMPA,FL
[2] UNIV S FLORIDA,COLL MED,DEPT NEUROL,TAMPA,FL
关键词
D O I
10.1128/CDLI.2.2.249-252.1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A comprehensive peripheral blood immunophenotype analysis of 16 multiple sclerosis (MS) patients was performed by three-color flow cytometric analysis, and the results were compared with those for age-matched healthy controls, The cell subsets quantified included T cells (CD3(+)), B cells (CD19(+)), NK cells (CD56(+)), CD4(+) and CD8(+) T cells, cytotoxic (CD28(+)) and suppressor precursor (CD28(-)) CD8(+) T cells, CD45RA(+) and CD45RO(+) T cells (CD4(+) and CD8(+)), and CD5(+) T and B cells. Analysis of MS patients' peripheral blood revealed essentially normal levels of total T, B, and NK cells. In agreement with results obtained by other investigators, it was found that MS patients had an increased CD4/CD8 ratio, primarily due to a decrease in CD8(+) T cells. MS patients were found to have a significantly decreased level of suppressor precursor (CD28(-)) CD8(+) T cells compared with that of controls but to have normal levels of cytotoxie (CD28(+)) CD8(+) T cells. These data indicate that MS patients do not have a general decrease in CD8(+) T cells but that they have a specific decrease in the suppressor precursor subset only and normal levels of cytotoxic CD8(+) T cells. MS patients also had a significant increase in memory (CD45RO(+)) CD4(+) T cells and displayed a trend towards a decrease in naive (CD45RA(+)) T cells in the peripheral blood.
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页码:249 / 252
页数:4
相关论文
共 30 条
[1]   LOSS OF FUNCTIONAL SUPPRESSION IS LINKED TO DECREASES IN CIRCULATING SUPPRESSOR INDUCER (CD4+2H4+) T-CELLS IN MULTIPLE-SCLEROSIS [J].
CHOFFLON, M ;
WEINER, HL ;
MORIMOTO, C ;
HAFLER, DA .
ANNALS OF NEUROLOGY, 1988, 24 (02) :185-191
[2]   CO-STIMULATION VIA CD28 INDUCES ACTIVATION OF A REFRACTORY SUBSET OF MRL-LPR/LPR T-LYMPHOCYTES [J].
CLEMENTS, JL ;
WINSLOW, G ;
DONAHUE, C ;
COOPER, SM ;
ALLISON, JP ;
BUDD, RC .
INTERNATIONAL IMMUNOLOGY, 1993, 5 (11) :1451-1460
[3]   PHENOTYPIC AND FUNCTIONAL-CHARACTERISTICS OF ACTIVATED CD8+ CELLS - A CD11B-CD28- SUBSET MEDIATES NONCYTOLYTIC FUNCTIONAL SUPPRESSION [J].
FREEDMAN, MS ;
RUIJS, TCG ;
BLAIN, M ;
ANTEL, JP .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1991, 60 (02) :254-267
[4]   INDUCTION OF HYPORESPONSIVENESS IN HUMAN T-LYMPHOCYTES DESPITE THEIR EXPRESSION OF BOTH THE CORECEPTOR CD28 AND ITS LIGAND B7 [J].
FRICCIUS, H ;
SIEGELSHUBENTHAL, P ;
REHBEIN, A ;
SCHLOTZ, E ;
PAWELEC, G .
CELLULAR IMMUNOLOGY, 1993, 151 (02) :283-290
[5]   CD21+ (B2 ANTIGEN+) CELL DECREMENT AND CD4+CD29+ (HELPER-INDUCER) CELL INCREMENT SUGGEST AN ACTIVATION OF CELL IMMUNE REACTIVITY IN MULTIPLE-SCLEROSIS [J].
GAMBI, D ;
PORRINI, AM ;
GIAMPIETRO, A ;
MACOR, S .
JOURNAL OF NEUROIMMUNOLOGY, 1991, 33 (02) :97-102
[6]   T-CELL AND B-CELL RESPONSES TO MYELIN BASIC-PROTEIN AND ENCEPHALITOGENIC EPITOPES [J].
GOULD, KE ;
SWANBORG, RH .
JOURNAL OF NEUROIMMUNOLOGY, 1993, 46 (1-2) :193-198
[7]   MS - A CNS AND SYSTEMIC AUTOIMMUNE-DISEASE [J].
HAFLER, DA ;
WEINER, HL .
IMMUNOLOGY TODAY, 1989, 10 (03) :104-107
[8]   IMMUNOHISTOCHEMICAL ANALYSIS OF THE CELLULAR INFILTRATE IN MULTIPLE-SCLEROSIS LESIONS [J].
HAUSER, SL ;
BHAN, AK ;
GILLES, F ;
KEMP, M ;
KERR, C ;
WEINER, HL .
ANNALS OF NEUROLOGY, 1986, 19 (06) :578-587
[9]   SYSTEMIC LYMPHOBLASTOID INTERFERON THERAPY IN CHRONIC PROGRESSIVE MULTIPLE-SCLEROSIS .2. IMMUNOLOGICAL EVALUATION [J].
KASTRUKOFF, LF ;
OGER, JJF ;
TOURTELLOTTE, WW ;
SACKS, SL ;
BERKOWITZ, J ;
PATY, DW .
NEUROLOGY, 1991, 41 (12) :1936-1941
[10]  
KOIDE J, 1990, J IMMUNOL, V144, P32