Determination of mRNA expression for IFN-γ and IL-4 in lymphocytes from children with IDDM by RT-PCR technique

被引:8
作者
Karlsson, MGE [1 ]
Ludvigsson, J [1 ]
机构
[1] Linkoping Univ Hosp, Fac Hlth Sci, Div Pediat, Dept Hlth & Environm, S-58185 Linkoping, Sweden
关键词
IDDM; Th-lymphocytes; IFN-gamma; IL-4; mRNA; glutamic acid decarboxylase;
D O I
10.1016/S0168-8227(98)00014-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin-dependent diabetes mellitus (IDDM) is characterized by infiltration of T-lymphocytes in the islets of Langerhans. Antigens are presented to Th-lymphocytes which can be divided into Th1- and Th2-lymphocytes, producing interferon-gamma (IFN-gamma) and interleukin-4 (IL-4) respectively. The aim of our study was to determine the messenger-RNA (mRNA) for these cytokines by RT-PCR in antigen-stimulated lymphocytes from children with newly diagnosed IDDM. The expression of mRNA for IL-4, and to a lesser degree IFN-gamma, is increased in lymphocytes stimulated with tetanus toroid (TT). Loss of activity after freezing and thawing could be compensated for, by increased amplification, while the use of EDTA or sodium heparin in the blood samples did not influence the results. In a pilot application, the lymphocytes from children with newly diagnosed IDDM were stimulated with a peptide of glutamic acid decarboxylase (GAD) (a.a. 247-279) known to have a similar aminoacid sequence as the Coxsackie B virus (a.a. 32-47). Increased IFN-gamma mRNA could be seen in two out of four children, whereas IL-4 showed a less pronounced mRNA expression. No increased mRNA expression for IFN-gamma and IL-4 could be seen in healthy HLA-matched controls. Further studies are needed to confirm whether increased IFN-gamma, mRNA in Th1-like lymphocytes stimulated with this specific GAD-peptide play a role in the cell-mediated immune response seen in children early after the onset of IDDM. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 30
页数:10
相关论文
共 22 条
[1]  
ARAI N, 1989, J IMMUNOL, V142, P274
[2]   RESPONSE OF PERIPHERAL-BLOOD MONONUCLEAR-CELLS TO GLUTAMATE-DECARBOXYLASE IN INSULIN-DEPENDENT DIABETES [J].
ATKINSON, MA ;
KAUFMAN, DL ;
CAMPBELL, L ;
GIBBS, KA ;
SHAH, SC ;
BU, DF ;
ERLANDER, MG ;
TOBIN, AJ ;
MACLAREN, NK .
LANCET, 1992, 339 (8791) :458-459
[3]   CELLULAR-IMMUNITY TO A DETERMINANT COMMON TO GLUTAMATE-DECARBOXYLASE AND COXSACKIE-VIRUS IN INSULIN-DEPENDENT DIABETES [J].
ATKINSON, MA ;
BOWMAN, MA ;
CAMPBELL, L ;
DARROW, BL ;
KAUFMAN, DL ;
MACLAREN, NK .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :2125-2129
[4]   REVELATION OF SPECIFICITY OF 64K AUTOANTIBODIES IN IDDM SERUMS BY HIGH-RESOLUTION 2-D GEL-ELECTROPHORESIS - UNAMBIGUOUS IDENTIFICATION OF 64K TARGET ANTIGEN [J].
BAEKKESKOV, S ;
WARNOCK, G ;
CHRISTIE, M ;
RAJOTTE, RV ;
LARSEN, PM ;
FEY, S .
DIABETES, 1989, 38 (09) :1133-1141
[5]   AUTOANTIBODIES IN NEWLY DIAGNOSED DIABETIC CHILDREN IMMUNOPRECIPITATE HUMAN PANCREATIC-ISLET CELL-PROTEINS [J].
BAEKKESKOV, S ;
NIELSEN, JH ;
MARNER, B ;
BILDE, T ;
LUDVIGSSON, J ;
LERNMARK, A .
NATURE, 1982, 298 (5870) :167-169
[6]   IDENTIFICATION OF THE 64K AUTOANTIGEN IN INSULIN-DEPENDENT DIABETES AS THE GABA-SYNTHESIZING ENZYME GLUTAMIC-ACID DECARBOXYLASE [J].
BAEKKESKOV, S ;
AANSTOOT, HJ ;
CHRISTGAU, S ;
REETZ, A ;
SOLIMENA, M ;
CASCALHO, M ;
FOLLI, F ;
RICHTEROLESEN, H ;
CAMILLI, PD .
NATURE, 1990, 347 (6289) :151-156
[7]   INSITU CHARACTERIZATION OF AUTOIMMUNE PHENOMENA AND EXPRESSION OF HLA MOLECULES IN THE PANCREAS IN DIABETIC INSULITIS [J].
BOTTAZZO, GF ;
DEAN, BM ;
MCNALLY, JM ;
MACKAY, EH ;
SWIFT, PGF ;
GAMBLE, DR .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (06) :353-360
[8]  
CASTANO L, 1990, ANNU REV IMMUNOL, V8, P647, DOI 10.1146/annurev.iy.08.040190.003243
[9]   STRUCTURE OF THE HUMAN IMMUNE INTERFERON GENE [J].
GRAY, PW ;
GOEDDEL, DV .
NATURE, 1982, 298 (5877) :859-863
[10]   HUMAN CU/ZN SUPEROXIDE-DISMUTASE CDNA - ISOLATION OF CLONES SYNTHESIZING HIGH-LEVELS OF ACTIVE OR INACTIVE ENZYME FROM AN EXPRESSION LIBRARY [J].
HALLEWELL, RA ;
MASIARZ, FR ;
NAJARIAN, RC ;
PUMA, JP ;
QUIROGA, MR ;
RANDOLPH, A ;
SANCHEZPESCADOR, R ;
SCANDELLA, CJ ;
SMITH, B ;
STEIMER, KS ;
MULLENBACH, GT .
NUCLEIC ACIDS RESEARCH, 1985, 13 (06) :2017-2034