Journal article
HIV-1 Tropism and Survival in Vertically Infected Ugandan Infants
The Journal of infectious diseases, Vol.197(10), pp.1382-1388
2008
DOI: 10.1086/587492
PMID: 18444795
Abstract
Background. Human immunodeficiency virus type 1 (HIV-1) may utilize the CXCR4 coreceptor (X4 virus), the CCR5 coreceptor (R5 virus), or both (dual/mixed [DM] virus). We analyzed HIV-1 coreceptor tropism in Ugandan infants enrolled in the HIVNET (HIV Network for Prevention Trials) 012 trial.
Methods. Plasma or serum was analyzed using a commercial coreceptor tropism assay. HIV env subtype was determined by phylogenetic methods.
Results. Tropism results were obtained for 57 samples from infants collected 6–14 weeks after birth. Fifty-two infants had only R5 virus, and 5 had either X4 or DM virus. The mothers of those 5 infants also had X4 or DM virus. In infants, subtype D infection was associated with high-level infectivity in CCR5-bearing cells and also with the detection of X4 or DM strains. High-level infectivity in CCR5-bearing cells was associated with decreased infant survival, but infection with X4 or DM virus was not. HIV clones from infants with DM viral populations showed different patterns of coreceptor use. V3 loop sequence- based algorithms predicted the tropism of some, but not all, env clones.
Conclusions. Complex patterns of HIV tropism were found in HIV-infected newborn infants. Subtype D infection was associated with X4 virus and with high-level replication in CCR5-bearing cells. High-level replication of R5 virus was associated with decreased infant survival.
Details
- Title: Subtitle
- HIV-1 Tropism and Survival in Vertically Infected Ugandan Infants
- Creators
- Jessica D CHURCH - Johns Hopkins University, Baltimore, Maryland, United StatesWei Huang - Monogram Biosciences, South San Francisco, California, United StatesNeil PARKIN - Monogram Biosciences, South San Francisco, California, United StatesSusan H ESHLEMAN - Johns Hopkins University, Baltimore, Maryland, United StatesAnthony MWATHA - Statistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Research Center, Seattle, Washington, United StatesJonathan TOMA - Monogram Biosciences, South San Francisco, California, United StatesEric STAWISKI - Monogram Biosciences, South San Francisco, California, United StatesDeborah DONNELL - Statistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson Cancer Research Center, Seattle, Washington, United StatesLaura A GUAY - Johns Hopkins University, Baltimore, Maryland, United StatesFrancis MMIRO - Makerere University-Johns Hopkins University (MUJHU) Research Collaboration, UgandaPhilippa MUSOKE - Makerere University, Kampala, UgandaJ. Brooks JACKSON - Johns Hopkins University, Baltimore, Maryland, United States
- Resource Type
- Journal article
- Publication Details
- The Journal of infectious diseases, Vol.197(10), pp.1382-1388
- DOI
- 10.1086/587492
- PMID
- 18444795
- NLM abbreviation
- J Infect Dis
- ISSN
- 0022-1899
- eISSN
- 1537-6613
- Publisher
- University of Chicago Press; Chicago, IL
- Language
- English
- Date published
- 2008
- Academic Unit
- Pathology; VPMA - Administration
- Record Identifier
- 9984047625502771
Metrics
12 Record Views