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dc.contributor.authorPugatch, David
dc.contributor.authorSullivan, John L.
dc.contributor.authorPikora, Cheryl A.
dc.contributor.authorLuzuriaga, Katherine
dc.date2022-08-11T08:08:47.000
dc.date.accessioned2022-08-23T16:08:23Z
dc.date.available2022-08-23T16:08:23Z
dc.date.issued1997-09-18
dc.date.submitted2008-11-26
dc.identifier.citation<p>J Infect Dis. 1997 Sep;176(3):643-8.</p>
dc.identifier.issn0022-1899 (Print)
dc.identifier.doi10.1086/514085
dc.identifier.pmid9291310
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32435
dc.description.abstractHuman 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.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9291310&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1086/514085
dc.subjectAntibody-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
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleDelayed 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
dc.typeJournal Article
dc.source.journaltitleThe Journal of infectious diseases
dc.source.volume176
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1005
dc.identifier.contextkey673221
html.description.abstract<p>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.</p>
dc.identifier.submissionpathgsbs_sp/1005
dc.contributor.departmentPediatrics
dc.source.pages643-8


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