Association of maternal histocompatibility at class II HLA loci with maternal microchimerism in the fetus

被引:33
作者
Berry, SM
Hassan, SS
Russell, E
Kukuruga, D
Land, S
Kaplan, J
机构
[1] Wayne State Univ, Dept Obstet & Gynecol, Div Maternal Fetal Med, Detroit, MI 48201 USA
[2] Wayne State Univ, Dept Pathol, Div Maternal Fetal Med, Detroit, MI 48201 USA
[3] Wayne State Univ, Dept Pediat, Div Maternal Fetal Med, Detroit, MI 48201 USA
[4] Wayne State Univ, Ctr Mol Med & Genet, Detroit, MI 48201 USA
关键词
D O I
10.1203/01.PDR.0000129656.10005.A6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
For investigating the possible influence of maternal-fetal HLA compatibility on maternal microchimerism, DNA samples from blood of 120 maternal-fetal pairs were genotyped at two polymorphic loci: glutathione-S-transferase M1 (GSTM1) and angiotensin-converting enzyme (ACE). Informative pairs (mother heterozygous/fetus homozygous at one of the two loci) were then tested by quantitative real-time PCR for the noninherited maternal allele(s) and genotyped at the HLA-A, B, and C class I loci and/or at the DRB1 and/or DQB1 class 11 loci. Small numbers of maternal cells were detected in the circulation of 16 of the 30 informative second- and third-trimester fetuses. Comparison with HLA data suggested an association between micro-chimerism and maternal compatibility at the class II DRB1 and/or DQB1 HLA loci and with the maternal HLA-DQB1*0301 allele. There was no relationship between maternal microchimerism and maternal-fetal HLA compatibility at other HLA loci or with gestational age, fetal anomalies, or red cell or platelet isoimmunity.
引用
收藏
页码:73 / 78
页数:6
相关论文
共 17 条
[1]   Chimeric cells of maternal origin in juvenile idiopathic inflammatory myopathies [J].
Artlett, CM ;
Ramos, R ;
Jiminez, SA ;
Patterson, K ;
Miller, FW ;
Rider, LG .
LANCET, 2000, 356 (9248) :2155-2156
[2]   CIRCULATING LYMPHOCYTE SUBSETS IN 2ND-TRIMESTER AND 3RD-TRIMESTER FETUSES - COMPARISON WITH NEWBORNS AND ADULTS [J].
BERRY, SM ;
FINE, N ;
BICHALSKI, JA ;
COTTON, DB ;
DOMBROWSKI, MP ;
KAPLAN, J .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (04) :895-900
[3]   Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum [J].
Bianchi, DW ;
Zickwolf, GK ;
Weil, GJ ;
Sylvester, S ;
DeMaria, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :705-708
[4]   Long-term fetal microchimerism in peripheral blood mononuclear cell subsets in healthy women and women with scleroderma [J].
Evans, PC ;
Lambert, N ;
Maloney, S ;
Furst, DE ;
Moore, JM ;
Nelson, JL .
BLOOD, 1999, 93 (06) :2033-2037
[5]  
HALL JM, 1995, BLOOD, V86, P2829
[6]  
Lo YMD, 2000, CLIN CHEM, V46, P1301
[7]  
Lo YMD, 1996, BLOOD, V88, P4390
[8]   Microchimerism of maternal origin persists into adult life [J].
Maloney, S ;
Smith, A ;
Furst, DE ;
Myerson, D ;
Rupert, K ;
Evans, PC ;
Nelson, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (01) :41-47
[9]   Microchimerism and autoimmune disease [J].
Nelson, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (17) :1224-1225
[10]   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