DIFFERENTIAL IGG AVIDITY TO RUBELLA-VIRUS STRUCTURAL PROTEINS

被引:17
作者
MAURACHER, CA
MITCHELL, LA
TINGLE, AJ
机构
[1] UNIV BRITISH COLUMBIA,DEPT PEDIAT,VANCOUVER V6T 1W5,BC,CANADA
[2] UNIV BRITISH COLUMBIA,DEPT PATHOL,VANCOUVER V6T 1W5,BC,CANADA
关键词
ANTIBODY AVIDITY; RUBELLA INFECTION; VIRAL-SPECIFIC IMMUNE RESPONSES;
D O I
10.1002/jmv.1890360310
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Avidity maturation of IgG antibody responses directed against the structural proteins of rubella virus (E1, E2, and C) as well as whole rubella virus (RV) was assessed at sequential time intervals in 7 individuals following serologically confirmed wild rubella infection. Individual structural proteins were purified from tissue culture supernatants by differential centrifugation, followed by preparative SDS-PAGE under non-reducing conditions. Avidity of IgG anti-rubella responses was measured by using the 8 M urea elution technique and results expressed as an elution ratio [ER(%)]. A low mean ER(%) of 23% was determined for E1-specific IgG responses during the 10-20 day period following onset of clinical rubella, with subsequent maturation of avidity ER(%) values to 52%, 75%, and 84% at 3 months, 1 year, and 2 years, respectively, post-rubella. In contrast, IgG anti-E2 responses showed minimal avidity maturation with ER(%) values of 20%, 29%, 30%, and 31% over the same time intervals. Similarly, responses to the capsid protein (C) remained at low avidity ER(%) values of 21%, 29%, 36%, and 35% over the 2 year follow-up period. The avidity maturation values for IgG directed against whole RV preparations paralleled observations for E1-specific responses with ER(%) values of 23%, 52%, 85%, and 87%, respectively. These data support the need to assess individual protein-specific antibody avidities in order to more fully understand viral-specific immune responses.
引用
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页码:202 / 208
页数:7
相关论文
共 22 条
[1]  
CHAYE HH, UNPUB CELLULAR HUMOR
[2]   NUCLEOTIDE-SEQUENCE AND INVITRO EXPRESSION OF RUBELLA-VIRUS 24S SUBGENOMIC MESSENGER-RNA ENCODING THE STRUCTURAL PROTEIN-E1, PROTEIN-E2 AND PROTEIN-C [J].
CLARKE, DM ;
LOO, TW ;
HUI, I ;
CHONG, P ;
GILLAM, S .
NUCLEIC ACIDS RESEARCH, 1987, 15 (07) :3041-3057
[3]   SOME MONOCLONAL-ANTIBODIES RAISED WITH A NATIVE PROTEIN BIND PREFERENTIALLY TO THE DENATURED ANTIGEN [J].
FRIGUET, B ;
DJAVADIOHANIANCE, L ;
GOLDBERG, ME .
MOLECULAR IMMUNOLOGY, 1984, 21 (07) :673-677
[4]   RUBELLA-VIRUS ANTIGENS - LOCALIZATION OF EPITOPES INVOLVED IN HEMAGGLUTINATION AND NEUTRALIZATION BY USING MONOCLONAL-ANTIBODIES [J].
GREEN, KY ;
DORSETT, PH .
JOURNAL OF VIROLOGY, 1986, 57 (03) :893-898
[5]   RECENT RUBELLA-VIRUS INFECTION INDICATED BY A LOW AVIDITY OF SPECIFIC IGG [J].
HEDMAN, K ;
SEPPALA, I .
JOURNAL OF CLINICAL IMMUNOLOGY, 1988, 8 (03) :214-221
[6]   MEASUREMENT OF AVIDITY OF SPECIFIC IGG FOR VERIFICATION OF RECENT PRIMARY RUBELLA [J].
HEDMAN, K ;
ROUSSEAU, SA .
JOURNAL OF MEDICAL VIROLOGY, 1989, 27 (04) :288-292
[7]   THE ROLE OF GLYCOSYLATION ON HEMAGGLUTINATION AND IMMUNOLOGICAL REACTIVITY OF RUBELLA-VIRUS [J].
HOTERRY, L ;
COHEN, A .
ARCHIVES OF VIROLOGY, 1984, 79 (3-4) :139-146
[8]   CHANGES IN ANTIBODY AVIDITY AFTER VIRUS-INFECTIONS - DETECTION BY AN IMMUNOSORBENT-ASSAY IN WHICH A MILD PROTEIN-DENATURING AGENT IS EMPLOYED [J].
INOUYE, S ;
HASEGAWA, A ;
MATSUNO, S ;
KATOW, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 20 (03) :525-529
[9]   ANTIGEN-PRESENTING B-CELLS AND HELPER T-CELLS COOPERATIVELY MEDIATE INTRAVIRIONIC ANTIGENIC-COMPETITION BETWEEN INFLUENZA-A VIRUS SURFACE GLYCOPROTEINS [J].
JOHANSSON, BE ;
MORAN, TM ;
KILBOURNE, ED .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (19) :6869-6873
[10]  
KLENK HD, 1990, IMMUNOCHEMISTRY VIRU, V2, P25