ALTERATIONS IN PERIPHERAL-BLOOD MONONUCLEAR CELL CYTOKINE PRODUCTION IN RESPONSE TO PHYTOHEMAGGLUTININ IN MULTIPLE-SCLEROSIS PATIENTS

被引:17
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 33612
[2] UNIV S FLORIDA,COLL MED,DEPT NEUROL,TAMPA,FL 33612
关键词
D O I
10.1128/CDLI.2.6.766-769.1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is an autoimmune demyelinating disorder of the central nervous system (CNS). The disease is characterized by inflammatory lesions in the white matter of the CNS, consisting of a specific immune response to the myelin sheath. We investigated peripheral blood mononuclear cell (PBMC) cytokine production by enzyme-linked immunosorbent assays of 21 MS patients and 19 age-matched normal controls in response to the T-cell mitogen phytohemagglutinin (PHA). Peripheral blood mononuclear cells were cultured in medium alone or in medium with 5 mu g of PHA per ml for 48 h, and culture supernatants were collected for analysis. Cytokines selected for study were interleukin-10 (IL-10), gamma interferon (IFN-gamma), IL-2, and IL-4. All cytokine activities described were expressed as concentrations per 500,000 cells. We found that 48% (10 of 21) of the MS patients produced small but detectable levels of IL-10 in medium alone, compared with 26% (5 of 18) of the controls. We found that the MS patients produced significantly higher quantities of IL-10 protein than the controls in response to PHA (mean supernatant concentrations of IL-10 for patients and controls, 421 and 204 pg/ml, respectively [P < 0.05]). No significant differences were detected in the production of IL-2, IFN-gamma, and IL-4 between patients and controls in response to PHA, although patients appeared to display a trend toward decreased production of IFN-gamma.
引用
收藏
页码:766 / 769
页数:4
相关论文
共 32 条
[1]   T-CELLS RESPONSIVE TO MYELIN BASIC-PROTEIN IN PATIENTS WITH MULTIPLE-SCLEROSIS [J].
ALLEGRETTA, M ;
NICKLAS, JA ;
SRIRAM, S ;
ALBERTINI, RJ .
SCIENCE, 1990, 247 (4943) :718-721
[2]   ENCEPHALITOGENIC T-CELLS IN THE B10.PL MODEL OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS (EAE) ARE OF THE TH-1 LYMPHOKINE SUBTYPE [J].
ANDO, DG ;
CLAYTON, J ;
KONO, D ;
URBAN, JL ;
SERCARZ, EE .
CELLULAR IMMUNOLOGY, 1989, 124 (01) :132-143
[3]   REGULATORY T-CELL CLONES INDUCED BY ORAL TOLERANCE - SUPPRESSION OF AUTOIMMUNE ENCEPHALOMYELITIS [J].
CHEN, YH ;
KUCHROO, VK ;
INOBE, J ;
HAFLER, DA ;
WEINER, HL .
SCIENCE, 1994, 265 (5176) :1237-1240
[4]  
CORREALE J, 1995, J IMMUNOL, V154, P2959
[5]   ALTERATIONS IN LEVELS OF CD28(-)/CD8(+) SUPPRESSOR-CELL PRECURSOR AND CD45RO(+)/CD4(+) MEMORY T-LYMPHOCYTES IN THE PERIPHERAL-BLOOD OF MULTIPLE-SCLEROSIS PATIENTS [J].
CRUCIAN, B ;
DUNNE, P ;
FRIEDMAN, H ;
RAGSDALE, R ;
PROSS, S ;
WIDEN, R .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1995, 2 (02) :249-252
[6]   EXPRESSION OF MONOCYTE ACTIVATION ANTIGEN MO3 ON THE SURFACE OF PERIPHERAL-BLOOD MONOCYTES FROM PATIENTS WITH MULTIPLE-SCLEROSIS [J].
DOREDUFFY, P ;
DONOVAN, C ;
TODD, RF .
NEUROLOGY, 1992, 42 (08) :1609-1614
[7]   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
[8]   MS - A CNS AND SYSTEMIC AUTOIMMUNE-DISEASE [J].
HAFLER, DA ;
WEINER, HL .
IMMUNOLOGY TODAY, 1989, 10 (03) :104-107
[9]   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
[10]   CYTOKINE PRODUCTION BY PERIPHERAL-BLOOD MONOCYTES MACROPHAGES IN MULTIPLE-SCLEROSIS PATIENTS [J].
IMAMURA, K ;
SUZUMURA, A ;
HAYASHI, F ;
MARUNOUCHI, T .
ACTA NEUROLOGICA SCANDINAVICA, 1993, 87 (04) :281-285