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    Delayed generation of antibodies mediating human immunodeficiency virus type 1-specific antibody-dependent cellular cytotoxicity in vertically infected infants. WITS Study Group. Women and Infants Transmission Study

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    Authors
    Pugatch, David
    Sullivan, John L.
    Pikora, Cheryl A.
    Luzuriaga, Katherine
    UMass Chan Affiliations
    Department of Pediatrics
    Program in Immunology and Virology
    Graduate School of Biomedical Sciences
    Graduate School of Biomedical Sciences
    Document Type
    Journal Article
    Publication Date
    1997-09-18
    Keywords
    Antibody-Dependent Cell Cytotoxicity; Cells, Cultured; Disease Progression; *Disease Transmission, Vertical; Female; HIV Antibodies; HIV Envelope Protein gp160; HIV-1; Humans; Infant; Infant, Newborn; Labor, Obstetric; Leukocytes, Mononuclear; Male; Pregnancy; Pregnancy Complications, Infectious
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    https://doi.org/10.1086/514085
    Abstract
    Human immunodeficiency virus type 1 (HIV-1)-specific antibody-dependent cellular cytotoxicity (ADCC) antibody titers were serially measured from birth to 24 months in the plasma of 14 intrapartum-infected and 10 uninfected infants born to HIV-1-infected women. The mean ADCC antibody titers measured at birth in infected and uninfected infants were similar (10(-3.9) and 10(-4.0), respectively), suggesting that ADCC antibodies did not protect infants from the intrapartum transmission of HIV-1. In infected infants, ADCC titers at birth did not predict subsequent clinical disease course. The active production of HIV-1-specific ADCC antibodies was detected in most infected infants only after 12 months of age, well after the loss of passively acquired maternal ADCC antibody. The delayed production of ADCC antibodies in infancy may account, in part, for the less efficient control of viral replication and more rapid disease progression following vertical infection compared with that in adults.
    Source

    J Infect Dis. 1997 Sep;176(3):643-8.

    DOI
    10.1086/514085
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/32435
    PubMed ID
    9291310
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    ae974a485f413a2113503eed53cd6c53
    10.1086/514085
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