MHC CLASS-II COMPATIBILITY IN ABORTED FETUSES AND TERM INFANTS OF COUPLES WITH RECURRENT SPONTANEOUS-ABORTION

被引:48
作者
OBER, C
STECK, T
VANDERVEN, K
BILLSTRAND, C
MESSER, L
KWAK, J
BEAMAN, K
BEER, A
机构
[1] UNIV CHICAGO,COMM EVOLUT BIOL,CHICAGO,IL 60637
[2] UNIV HLTH SCI CHICAGO MED SCH,DEPT MICROBIOL & IMMUNOL,N CHICAGO,IL 60064
关键词
HLA SHARING; HLA-DQA1; RECURRENT SPONTANEOUS ABORTION;
D O I
10.1016/0165-0378(93)90063-N
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Maternal-fetal histocompatibility for alleles at HLA class II loci, HLA-DQA1 and HLA-DQB1, was examined in 40 abortuses and 31 liveborn children of 68 couples with a history of idiopathic recurrent spontaneous abortion (RSAB) who underwent leukocyte immunization prior to the index pregnancy. Significantly more couples with RSAB shared two HLA-DQA1 alleles as compared with fertile control couples (0.18 vs. 0.03, respectively; P = 0.031). There were no differences in HLA sharing between couples with RSAB who experienced a repeat abortion in the index pregnancy as compared with couples with RSAB who were delivered of a liveborn child. Non-significant deficits of abortuses who were compatible for alleles at the HLA-DQA1 (6 observed vs. 8.5 expected; P = 0.225) and the HLA-DQB1 (7 observed vs. 9.2 expected; P = 0.254) loci were observed. A significant deficit of HLA-DQA1 compatible liveborn children was observed (1 observed vs. 5.5 expected; P = 0.0069). The overall deficit of HLA-DQA1 compatible fetuses (7 observed vs. 14.0 expected; P = 0.0018) after approximately 8 weeks gestation suggests that HLA-DQA1 compatible fetuses may be aborted early in pregnancy, prior to the time when fetal tissue can be recovered for genetic studies.
引用
收藏
页码:195 / 207
页数:13
相关论文
共 29 条
[1]  
Beer A.E., 1976, IMMUNOBIOLOGY MAMMAL
[2]  
Beer A. E., 1988, EARLY PREGNANCY LOSS, P337
[3]  
BEER AE, 1985, EXP CLIN IMMUNOGENET, V2, P137
[4]   POLYMORPHIC DNA REGION ADJACENT TO THE 5'-END OF THE HUMAN INSULIN GENE [J].
BELL, GI ;
KARAM, JH ;
RUTTER, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09) :5759-5763
[5]  
BODMER JG, 1991, HUMAN IMMUNOL, V34, P4
[6]   PRENATAL-DIAGNOSIS USING DNA POLYMORPHISMS - REPORT ON 95 PREGNANCIES AT RISK FOR SICKLE-CELL DISEASE OR BETA-THALASSEMIA [J].
BOEHM, CD ;
ANTONARAKIS, SE ;
PHILLIPS, JA ;
STETTEN, G ;
KAZAZIAN, HH .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 308 (18) :1054-1058
[7]   RAPID TYPING OF HLA-DQB1 DNA POLYMORPHISM USING NONRADIOACTIVE OLIGONUCLEOTIDE PROBES AND AMPLIFIED DNA [J].
BUGAWAN, TL ;
ERLICH, HA .
IMMUNOGENETICS, 1991, 33 (03) :163-170
[8]   PATERNAL MONONUCLEAR CELL IMMUNIZATION THERAPY FOR REPEATED MISCARRIAGE - PREDICTIVE VARIABLES FOR PREGNANCY SUCCESS [J].
COWCHOCK, FS ;
SMITH, JB ;
DAVID, S ;
SCHER, J ;
BATZER, F ;
CORSON, S .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1990, 22 (1-2) :12-17
[9]  
ERLICH HA, 1989, PCR TECHNOLOGY PRINC, P193
[10]  
GILL TJ, 1979, AM J PATHOL, V95, P464