POLYMERASE CHAIN-REACTION, VIRUS ISOLATION AND ANTIGEN-ASSAY IN HIV-1-ANTIBODY-POSITIVE MOTHERS AND THEIR CHILDREN

被引:94
作者
SCARLATTI, G
LOMBARDI, V
PLEBANI, A
PRINCIPI, N
VEGNI, C
FERRARIS, G
BUCCERI, A
FENYO, EM
WIGZELL, H
ROSSI, P
ALBERT, J
机构
[1] KAROLINSKA INST,DEPT IMMUNOL,S-10401 STOCKHOLM 60,SWEDEN
[2] KAROLINSKA INST,DEPT VIROL,S-10401 STOCKHOLM 60,SWEDEN
[3] UNITA SOCIO SANIT LOCALE 751,MILAN,ITALY
[4] UNIV ROME TOR VERGATA,DEPT PAEDIAT,ROME,ITALY
[5] NATL BACTERIOL LAB,DEPT VIROL,S-10521 STOCKHOLM,SWEDEN
[6] UNIV MILAN,DEPT PAEDIAT 1,I-20122 MILAN,ITALY
[7] UNIV MILAN,DEPT PAEDIA 4,I-20122 MILAN,ITALY
[8] UNIV MILAN,DIV NEONATOL OBSTET & GYNECOL MANGIAGALLI,I-20122 MILAN,ITALY
关键词
VERTICAL TRANSMISSION; MOTHER-TO-CHILD; PERINATAL; HIV-1; AIDS; POLYMERASE CHAIN REACTION; VIRUS ISOLATION; ANTIGENEMIA;
D O I
10.1097/00002030-199110000-00003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Diagnosis of perinatal HIV-1 infection is complicated by the persistence of maternal antibodies and the conflicting reports on polymerase chain reaction (PCR) reactivity in children born to HIV-1-seropositive mothers. We have compared PCR with other diagnostic methods for perinatal HIV-1 infection and have attempted also to identify maternal markers which correlate with risk of transmission. PCR was the most sensitive method for early diagnosis of perinatal transmission of HIV-1, but the PCR-positive children (n = 11) developed at least one additional sign of infection. The PCR-negative children (n = 76) were clinically healthy, virus isolation negative, and their serum was HIV-1-antigen-negative. All children who had become seronegative (n = 36) were both PCR- and isolation-negative. Antigenaemia in the mothers correlated significantly with higher risk of perinatal transmission of HIV-1, while no other parameters (clinical stage, lymphocyte subsets, PCR and isolation) showed such a correlation. This indicates that the level of virus expression may be of key importance for the risk of vertical transmission of HIV-1 infection.
引用
收藏
页码:1173 / 1178
页数:6
相关论文
共 30 条
[1]   RAPID DEVELOPMENT OF ISOLATE-SPECIFIC NEUTRALIZING ANTIBODIES AFTER PRIMARY HIV-1 INFECTION AND CONSEQUENT EMERGENCE OF VIRUS VARIANTS WHICH RESIST NEUTRALIZATION BY AUTOLOGOUS SERA [J].
ALBERT, J ;
ABRAHAMSSON, B ;
NAGY, K ;
AURELIUS, E ;
GAINES, H ;
NYSTROM, G ;
FENYO, EM .
AIDS, 1990, 4 (02) :107-112
[2]   SIMPLE, SENSITIVE, AND SPECIFIC DETECTION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN CLINICAL SPECIMENS BY POLYMERASE CHAIN-REACTION WITH NESTED PRIMERS [J].
ALBERT, J ;
FENYO, EM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (07) :1560-1564
[3]  
ASJO B, 1986, LANCET, V2, P660
[4]   A PROSPECTIVE-STUDY OF INFANTS BORN TO WOMEN SEROPOSITIVE FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 [J].
BLANCHE, S ;
ROUZIOUX, C ;
MOSCATO, MLG ;
VEBER, F ;
MAYAUX, MJ ;
JACOMET, C ;
TRICOIRE, J ;
DEVILLE, A ;
VIAL, M ;
FIRTION, G ;
DECREPY, A ;
DOUARD, D ;
ROBIN, M ;
COURPOTIN, C ;
CIRARUVIGNERON, N ;
LEDEIST, F ;
GRISCELLI, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (25) :1643-1648
[5]  
BORKOWSKY W, 1987, LANCET, V1, P1168
[6]  
BRINCHMAN JE, 1990, J VIROL, V65, P2019
[7]   VERTICAL TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS IS CORRELATED WITH THE ABSENCE OF HIGH-AFFINITY AVIDITY MATERNAL ANTIBODIES TO THE GP120 PRINCIPAL NEUTRALIZING DOMAIN [J].
DEVASH, Y ;
CALVELLI, TA ;
WOOD, DG ;
REAGAN, KJ ;
RUBINSTEIN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3445-3449
[8]   POLYMERASE CHAIN-REACTION COMPARED WITH CONCURRENT VIRAL CULTURES FOR RAPID IDENTIFICATION OF HUMAN IMMUNODEFICIENCY VIRUS-INFECTION AMONG HIGH-RISK INFANTS AND CHILDREN [J].
EDWARDS, JR ;
ULRICH, PP ;
WEINTRUB, PS ;
COWAN, MJ ;
LEVY, JA ;
WARA, DW ;
VYAS, GN .
JOURNAL OF PEDIATRICS, 1989, 115 (02) :200-203
[9]  
HEWLETT IK, 1990, J ACQ IMMUN DEF SYND, V3, P714
[10]   SERUM ENHANCEMENT OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) INFECTION CORRELATES WITH DISEASE IN HIV-INFECTED INDIVIDUALS [J].
HOMSY, J ;
MEYER, M ;
LEVY, JA .
JOURNAL OF VIROLOGY, 1990, 64 (04) :1437-1440