HERPES-SIMPLEX VIRUS-2 (HSV-2) TYPE-SPECIFIC ANTIBODY CORRELATES OF PROTECTION IN INFANTS EXPOSED TO HSV-2 AT BIRTH

被引:36
作者
ASHLEY, RL
DALESSIO, J
BURCHETT, S
BROWN, Z
BERRY, S
MOHAN, K
COREY, L
机构
[1] UNIV WASHINGTON,DEPT LAB MED,SEATTLE,WA 98105
[2] UNIV WASHINGTON,DEPT PEDIAT,SEATTLE,WA 98105
[3] UNIV WASHINGTON,DEPT OBSTET & GYNECOL,SEATTLE,WA 98105
[4] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98105
关键词
NEONATAL; HERPES HOMINIS; SEROLOGY; TRANSPLACENTAL IMMUNITY;
D O I
10.1172/JCI115888
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Western blot analysis was used to compare the herpes simplex virus (HSV)-2 antibody profiles of 40 infants < 2 wk of age who had been exposed to maternal genital HSV-2 at birth. 4 mothers were HSV seronegative at delivery and seroconverted to HSV-2 ("primary infection"), 9 had HSV-1 antibodies and seroconverted to HSV-2 ("nonprimary first episode infection"), and 27 were HSV-2 seropositive ("recurrent infection"). Neonatal herpes infections developed in 1 of 4 infants of women with primary infection, in 3 of 9 infants of women with nonprimary first episode infection, and in none of the 27 infants of women with recurrent HSV-2. Antibodies to HSV-2 proteins gG-2, VP5, and ICP35 were detected in 83, 89, and 72% of the 36 uninfected infants, respectively. None of the four infected infants had detectable antibodies to gG-2 and only one (25%) had antibodies to VP5 or ICP35. The more limited profiles of the 13 infants born to mothers with first episodes of HSV-2 were then analyzed separately; these profiles were similar among infected and uninfected infants except for gG-2, which elicits antibodies that are type specific for HSV-2. None of the infected infants versus seven of nine (78%) uninfected infants were gG-2 seropositive. These comparisons suggest that maternal type-specific antibodies may play a role in preventing neonatal infection after exposure to HSV-2.
引用
收藏
页码:511 / 514
页数:4
相关论文
共 24 条
[1]  
ASHLEY R, 1988, J MED VIROL, V4908, P703
[2]  
ASHLEY R, 1988, J INFECT DIS, V157, P319
[3]   GENITAL HERPES INFECTIONS [J].
ASHLEY, RL .
CLINICS IN LABORATORY MEDICINE, 1989, 9 (03) :405-420
[4]   COMPARISON OF WESTERN BLOT (IMMUNOBLOT) AND GLYCOPROTEIN-G-SPECIFIC IMMUNODOT ENZYME ASSAY FOR DETECTING ANTIBODIES TO HERPES-SIMPLEX VIRUS TYPE-1 AND TYPE-2 IN HUMAN-SERA [J].
ASHLEY, RL ;
MILITONI, J ;
LEE, F ;
NAHMIAS, A ;
COREY, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (04) :662-667
[5]  
ASHLEY RL, 1990, 30TH INT C ANT AG CH, P198
[6]   POSTEXPOSURE SERUM PROPHYLAXIS OF NEONATAL HERPES-SIMPLEX VIRUS-INFECTION OF MICE [J].
BARON, S ;
WORTHINGTON, MG ;
WILLIAMS, J ;
GAINES, JW .
NATURE, 1976, 261 (5560) :505-506
[7]   CHARACTERIZATION OF POST-TRANSLATIONAL PRODUCTS OF HERPES-SIMPLEX VIRUS GENE 35 PROTEINS BINDING TO THE SURFACES OF FULL CAPSIDS BUT NOT EMPTY CAPSIDS [J].
BRAUN, DK ;
ROIZMAN, B ;
PEREIRA, L .
JOURNAL OF VIROLOGY, 1984, 49 (01) :142-153
[8]   NEONATAL HERPES-SIMPLEX VIRUS-INFECTION IN RELATION TO ASYMPTOMATIC MATERNAL INFECTION AT THE TIME OF LABOR [J].
BROWN, ZA ;
BENEDETTI, J ;
ASHLEY, R ;
BURCHETT, S ;
SELKE, S ;
BERRY, S ;
VONTVER, LA ;
COREY, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (18) :1247-1252
[9]  
KOHL S, 1982, J IMMUNOL, V128, P1107
[10]  
KOHL S, 1989, PEDIATR INFECT DIS J, V8, P67