Does HLA-dependent chimerism underlie the pathogenesis of juvenile dermatomyositis?

被引:54
作者
Reed, AM
McNallan, K
Wettstein, P
Vehe, R
Ober, C
机构
[1] Mayo Clin & Mayo Grad Sch Med, Dept Med, Div Rheumatol E15, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Grad Sch Med, Dept Pediat, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Grad Sch Med, Dept Immunobiol, Rochester, MN 55905 USA
[4] Univ Minnesota, Div Pediat Rheumatol, Minneapolis, MN 55455 USA
[5] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
关键词
D O I
10.4049/jimmunol.172.8.5041
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Juvenile dermatomyositis (JDM) is a multisystem autoimmune disease that at times resembles chronic graft-vs-host disease. This led us to suggest that nonself cells may play a role in the disease process. In this study we examined the relationship between HLA genotype and the presence of maternally derived chimeric cells in JDM patients and healthy controls, and assessed immunologic activity in the chimeric cells. We identified chimeric cells more often in children with JDM (60 of 72) than in their unaffected siblings (11 of 48) or in healthy controls (5 of 29). The presence of chimerism in the JDM patients, their healthy siblings, and unaffected control children was associated with a HLA-DQA1*0501 allele in the mother (p = 0.011). Further, we show that maternally transferred chimeric T cells are responsive to the host's (JDM childs') lymphocytes (33.75 +/- 8.4 IFN-gamma-producing cells from JDM cells vs 5.0 +/- 1.25 from maternal cells), and that this is a memory response. These combined data indicate that chimeric cells play a direct role in the JDM disease process and that the mother's HLA genotype facilitates the transfer and/or persistence of maternal cells in the fetal circulation.
引用
收藏
页码:5041 / 5046
页数:6
相关论文
共 27 条
[11]   Maternal-fetal immunology and autoimmune disease - Is some autoimmune disease auto-alloimmune or allo-autoimmune? [J].
Nelson, JL .
ARTHRITIS AND RHEUMATISM, 1996, 39 (02) :191-194
[12]   Microchimerism and human autoimmune diseases [J].
Nelson, JL .
LUPUS, 2002, 11 (10) :651-654
[13]   Microchimerism and HLA-compatible relationships of pregnancy in scleroderma [J].
Nelson, JL ;
Furst, DE ;
Maloney, S ;
Gooley, T ;
Evans, PC ;
Smith, A ;
Bean, MA ;
Ober, C ;
Bianchi, DW .
LANCET, 1998, 351 (9102) :559-562
[14]   Human leukocyte antigen matching and fetal Loss: results of a 10 year prospective study [J].
Ober, C ;
Hyslop, T ;
Elias, S ;
Weitkamp, LR ;
Hauck, WW .
HUMAN REPRODUCTION, 1998, 13 (01) :33-38
[15]   Variation in the HLA-G promoter region influences miscarriage rates [J].
Ober, C ;
Aldrich, CL ;
Chervoneva, I ;
Billstrand, C ;
Rahimov, F ;
Gray, HL ;
Hyslop, T .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (06) :1425-1435
[16]   HLA-DQB1 AND HLA-DQA1 TYPING BY PCR AMPLIFICATION WITH SEQUENCE-SPECIFIC PRIMERS (PCR-SSP) IN 2 HOURS [J].
OLERUP, O ;
ALDENER, A ;
FOGDELL, A .
TISSUE ANTIGENS, 1993, 41 (03) :119-134
[17]  
Reed AM, 1998, J RHEUMATOL, V25, P1000
[18]   Association of the HLA-DQA1*0501 allele in multiple racial groups with juvenile dermatomyositis [J].
Reed, AM ;
Stirling, JD .
HUMAN IMMUNOLOGY, 1995, 44 (03) :131-135
[19]   MOLECULAR GENETIC-STUDIES OF MAJOR HISTOCOMPATIBILITY COMPLEX GENES IN CHILDREN WITH JUVENILE DERMATOMYOSITIS - INCREASED RISK ASSOCIATED WITH HLA-DQA1-0501 [J].
REED, AM ;
PACHMAN, L ;
OBER, C .
HUMAN IMMUNOLOGY, 1991, 32 (04) :235-240
[20]   Chimerism in children with juvenile dermatomyositis [J].
Reed, AM ;
Picornell, YJ ;
Harwood, A ;
Kredich, DW .
LANCET, 2000, 356 (9248) :2156-2157