Longitudinal studies of viral sequence, viral phenotype, and immunologic parameters of human immunodeficiency virus type 1 infection in perinatally infected twins with discordant disease courses

被引:34
作者
Hutto, C
Zhou, Y
He, J
Geffin, R
Hill, M
Scott, W
Wood, C
机构
[1] UNIV MIAMI,SCH MED,DEPT PEDIAT,MIAMI,FL 33136
[2] UNIV MIAMI,SCH MED,DEPT MICROBIOL & IMMUNOL,MIAMI,FL 33136
[3] UNIV MIAMI,SCH MED,DEPT NEUROL,MIAMI,FL 33136
[4] UNIV MIAMI,SCH MED,DEPT BIOCHEM & MOLEC BIOL,MIAMI,FL 33136
关键词
D O I
10.1128/JVI.70.6.3589-3598.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Perinatal human immunodeficiency virus type 1 (HIV-1) infections cause a broad spectrum of clinical disease and are variable in both the age of the patient at onset of serious disease and the progression of the clinical course, Heterozygotic perinatally infected twins with a marked difference in their clinical courses were monitored during the first 2 years of life, Twin B, the second-born twin, developed AIDS by 6 months of age and died at 22 months of age, while twin A remained minimally symptomatic through the first 2 years, Sequential blood specimens were obtained from the twins in order to characterize the immunologic properties of the children and the phenotypes and genotypes of the HIV-1 isolates at various times, Twin A developed neutralizing antibodies and a high-level antibody mediated cellular cytotoxicity (ADCC) response, while twin B had no neutralizing antibody and a much lower ADCC response, The virus isolates obtained from the two children at various time points proliferated equally well in peripheral blood mononuclear cells, were non-syncytium inducing, and could not infect established T-cell lines, They differed in their ability to infect primary macrophages, In parallel to the biological studies, the HIV-1 tnt and part of the env gene sequences of the longitudinal isolates at four time points were determined, Sequences of virus from both twins at different time points were highly conserved; the viruses evolved at a similar rate until the last analyzed time point, at which there was a dramatic increase in sequence diversity for the sicker child, especially in the tnt gene, Our results show that the viruses isolated at different times do not have significant changes in growth properties, The absence or low levels of neutralizing antibodies may correlate with disease progression in the twins.
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页码:3589 / 3598
页数:10
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共 43 条
[1]  
AUSUBEL FM, 1990, CURRENT PROTOCOLS MO
[2]   RELATION OF THE COURSE OF HIV-INFECTION IN CHILDREN TO THE SEVERITY OF THE DISEASE IN THEIR MOTHERS AT DELIVERY [J].
BLANCHE, S ;
MAYAUX, MJ ;
ROUZIOUX, C ;
TEGLAS, JP ;
FIRTION, G ;
MONPOUX, F ;
CIRARUVIGNERON, N ;
MEIER, F ;
TRICOIRE, J ;
COURPOTIN, C ;
VILMER, E ;
GRISCELLI, C ;
DELFRAISSY, JF ;
TARDIEU, M ;
NOSEDA, G ;
HURAUX, JM ;
LEVINE, M ;
VILMER, E ;
DECREPY, A ;
SIMON, F ;
KRIVINE, A ;
FRANCOUAL, C ;
DIMARIA, L ;
COURPOTIN, C ;
MONCOMBLE, CC ;
BURGARD, M ;
ROUZIOUX, C ;
GIRAULT, D ;
STEPHAN, JL ;
BLANCHE, S ;
TERRIS, J ;
VEBER, F ;
FIRTION, G ;
HENRION, R ;
CIRARUVIGNERON, N ;
BRUNER, C ;
MATHIEU, FP ;
HERVE, F ;
ALLISY, C ;
DANDINE, M ;
LABRUNE, P ;
VIAL, M ;
LACHASSINE, E ;
GAUDELUS, J ;
FLOCH, C ;
MAZY, F ;
MEIER, F ;
ROBIN, M ;
ALLEMON, MC ;
TALON, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (05) :308-312
[3]   LONGITUDINAL-STUDY OF 94 SYMPTOMATIC INFANTS WITH PERINATALLY ACQUIRED HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION - EVIDENCE FOR A BIMODAL EXPRESSION OF CLINICAL AND BIOLOGICAL SYMPTOMS [J].
BLANCHE, S ;
TARDIEU, M ;
DULIEGE, AM ;
ROUZIOUX, C ;
LEDEIST, F ;
FUKUNAGA, K ;
CANIGLIA, M ;
JACOMET, C ;
MESSIAH, A ;
GRISCELLI, C .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1990, 144 (11) :1210-1215
[4]   A SINGLE AMINO-ACID SUBSTITUTION IN THE V1 LOOP OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 GP120 ALTERS CELLULAR TROPISM [J].
BOYD, MT ;
SIMPSON, GR ;
CANN, AJ ;
JOHNSON, MA ;
WEISS, RA .
JOURNAL OF VIROLOGY, 1993, 67 (06) :3649-3652
[5]  
BROLIDEN K, 1993, CLIN EXP IMMUNOL, V93, P56
[6]   HOST RANGE, REPLICATIVE, AND CYTOPATHIC PROPERTIES OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ARE DETERMINED BY VERY FEW AMINO-ACID CHANGES IN TAT AND GP120 [J].
CHENGMAYER, C ;
SHIODA, T ;
LEVY, JA .
JOURNAL OF VIROLOGY, 1991, 65 (12) :6931-6941
[7]   ISOLATES OF HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 FROM THE BRAIN MAY CONSTITUTE A SPECIAL GROUP OF THE AIDS VIRUS [J].
CHENGMAYER, C ;
WEISS, C ;
SETO, D ;
LEVY, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (21) :8575-8579
[8]   MACROPHAGE-TROPIC HUMAN-IMMUNODEFICIENCY-VIRUS ISOLATES FROM DIFFERENT PATIENTS EXHIBIT UNUSUAL V3 ENVELOPE SEQUENCE HOMOGENEITY IN COMPARISON WITH T-CELL-TROPIC ISOLATES - DEFINITION OF CRITICAL AMINO-ACIDS INVOLVED IN CELL TROPISM [J].
CHESEBRO, B ;
WEHRLY, K ;
NISHIO, J ;
PERRYMAN, S .
JOURNAL OF VIROLOGY, 1992, 66 (11) :6547-6554
[9]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VARIANTS WITH INCREASED REPLICATIVE CAPACITY DEVELOP DURING THE ASYMPTOMATIC STAGE BEFORE DISEASE PROGRESSION [J].
CONNOR, RI ;
HO, DD .
JOURNAL OF VIROLOGY, 1994, 68 (07) :4400-4408
[10]   HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 EVOLUTION IN-VIVO TRACKED BY DNA HETERODUPLEX MOBILITY ASSAYS [J].
DELWART, EL ;
SHEPPARD, HW ;
WALKER, BD ;
GOUDSMIT, J ;
MULLINS, JI .
JOURNAL OF VIROLOGY, 1994, 68 (10) :6672-6683