Polymorphism in MICA rather than HLA-B/C genes is associated with psoriatic arthritis in the Jewish population

被引:81
作者
González, S
Brautbar, C
Martínez-Borra, J
López-Vazquez, A
Segal, R
Blanco-Gelaz, MA
Enk, CD
Safriman, C
López-Larrea, C
机构
[1] Hosp Cent Asturias, Dept Immunol, E-3006 Oviedo, Spain
[2] Univ Hosp, Hadassah Med Ctr, Dept Dermatol, Jerusalem, Israel
[3] Univ Hosp, Hadassah Med Ctr, Dept Rheumatol, Jerusalem, Israel
[4] Hebrew Univ Jerusalem, Sch Med, Lautenberg Ctr Gen & Tumor Immunol, IL-91010 Jerusalem, Israel
[5] Hadassah Univ Hosp, Tissue Typing Unit, IL-91120 Jerusalem, Israel
[6] Univ Oviedo, Funct Biol Dept, Asturias, Spain
关键词
psoriasis; PsA; MICA gene; arthritis;
D O I
10.1016/S0198-8859(01)00242-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The aim of this study was to examine whether the association of psoriatic arthritis (PsA) with human leukocyte antigen (HLA) class I genes is secondary to linkage disequilibrium with a nearby gene. We examined a sample of the Jewish population to investigate whether HLA-B/C and DR polymorphism is associated with:susceptibility, or whether other closely related class I loci, such as the major histocompatibility complex class I chain-related gene A (MICA) and tumor necrosis factor (TNF), might play a role in disease development. Comparisons of different populations with different HLA profiles would be of value in identifying the candidate genes involved in PSA. Fifty two patients with PsA and 73 random: matched controls from a Jewish population were selected and DNA typed by polymerase chain reaction-single-strand oligonucleotide probe (PCR-SSOP) (HLA-C), PCR sequence-specific primers (PCR-SSP) (HLA-B, DR), radioactive PCR (MICA-TM polymorphism in the transmembrane region), and PCR-RFLP (TNF). Some findings can be concluded from the study: (1) the frequency of HLA-B*5701, B*3801, B*39, B*27, Cw*0602, Cw*07, DRB1*0402, and DRB1*0701 were not found to be significantly increased in PsA; (2) no significant differences of TNF alpha' promoter alleles at positions -308 and -238 were found between PsA and healthy controls; (3) the trinucleotide repeat polymorphism MICA-A3 was present at a higher frequency in PsA patients, (p, < 0.009, RR = 3.34, EF = 0.39); and (4) MICA-A9 polymorphism was found in linkage disequilibrium with HLA-B alleles (B*5701, B*3801) described to be associated with PsA in Caucasians. These results suggest that the MICA gene or other nearby gene(s) may be involved in the development of PsA, and it would thus appear that psoriasis vulgaris (PsV) and PsA are associated with different MHC susceptibility genes. Human Immunology 62, 632- 638 (2001). (C) American Society for Histocompatibility and Immunogenetics, 2001. Published by Elsevier Science Inc.
引用
收藏
页码:632 / 638
页数:7
相关论文
共 34 条
[1]   A 2ND LINEAGE OF MAMMALIAN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I GENES [J].
BAHRAM, S ;
BRESNAHAN, M ;
GERAGHTY, DE ;
SPIES, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6259-6263
[2]   HLA B-13, B17, B37 AND CW6 IN PSORIASIS-VULGARIS - ASSOCIATION WITH AGE OF ONSET [J].
BRENNER, W ;
GSCHNAIT, F ;
MAYR, WR .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1978, 262 (03) :337-339
[3]   COMPREHENSIVE, SEROLOGICALLY EQUIVALENT DNA TYPING FOR HLA-B BY PCR USING SEQUENCE-SPECIFIC PRIMERS (PCR-SSP) [J].
BUNCE, M ;
FANNING, GC ;
WELSH, KI .
TISSUE ANTIGENS, 1995, 45 (02) :81-90
[4]   HLA-A, -B, -C polymorphism in a UK Ashkenazi Jewish potential bone marrow donor population [J].
Cox, ST ;
Marsh, SGE ;
Scott, I ;
Clayton, J ;
Argüello, JR ;
McWhinnie, AJ ;
Prokupek, B ;
Holman, R ;
Madrigal, JA ;
Little, AM .
TISSUE ANTIGENS, 1999, 53 (01) :41-50
[5]   GENETICS AND HLA ANTIGENS [J].
EASTMOND, CJ .
BAILLIERES CLINICAL RHEUMATOLOGY, 1994, 8 (02) :263-276
[6]   THE GENETICS OF PSORIASIS [J].
ELDER, JT ;
NAIR, RP ;
GUO, SW ;
HENSELER, T ;
CHRISTOPHERS, E ;
VOORHEES, JJ .
ARCHIVES OF DERMATOLOGY, 1994, 130 (02) :216-224
[7]  
Espinoza LR, 1998, SPONDYLARTHRITIDES, P97
[8]   ELEVATED TUMOR-NECROSIS-FACTOR-ALPHA (TNF-ALPHA) BIOLOGICAL-ACTIVITY IN PSORIATIC SKIN-LESIONS [J].
ETTEHADI, P ;
GREAVES, MW ;
WALLACH, D ;
ADERKA, D ;
CAMP, RDR .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1994, 96 (01) :146-151
[9]   NATURAL-HISTORY OF PSORIATIC-ARTHRITIS [J].
GLADMAN, DD .
BAILLIERES CLINICAL RHEUMATOLOGY, 1994, 8 (02) :379-394
[10]   THE ROLE OF HLA ANTIGENS AS INDICATORS OF DISEASE PROGRESSION IN PSORIATIC-ARTHRITIS - MULTIVARIATE RELATIVE RISK MODEL [J].
GLADMAN, DD ;
FAREWELL, VT .
ARTHRITIS AND RHEUMATISM, 1995, 38 (06) :845-850