Antiretroviral resistance in viral isolates from HIV-1-transmitting mothers and their infants
AIDS, ISSN: 0269-9370, Vol: 20, Issue: 13, Page: 1707-1712
2006
- 10Citations
- 42Usage
- 18Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations10
- Citation Indexes8
- CrossRef6
- Policy Citations2
- Policy Citation2
- Usage42
- Abstract Views42
- Captures18
- Readers18
- 18
Article Description
OBJECTIVE: To characterize concordance of resistance mutations to antiretroviral drugs (ART) in mother-infant pairs. DESIGN: Case series of HIV-transmitting mothers and infants in the Women and Infants Transmission Study, where delivery occurred between April 1994 and December 1999. METHODS: Reverse transcriptase and protease genes were sequenced in stored viral isolates from 32 mother-infant pairs. Mutations were coded as 'pure mutants' where only mutant virus was detected or as 'mixtures' where a mixed mutant/wild-type population was identified. ART resistance mutations were compared for concordance between mothers and their infants. RESULTS: Maternal mutations associated with resistance to nucleoside reverse transcriptase inhibitor (NRTI) and minor protease inhibitor (PI) drugs were typically concordant with that of infant, while those associated with non-nucleoside reverse transcriptase inhibitors (NNRTI) and major PI drugs were not. Of five NRTI-associated maternal mutations observed, three pure mutants corresponded with mutant in the infant, while two wild-type-predominant mixtures corresponded with infant wild type. The only NNRTI-associated mutation observed, K103N, was not transmitted, nor were the two major PI-associated mutations, L90M and V82I/V. Transmission of minor PI-associated mutations was consistent with the sole observed or dominant variant for 20 of 21 mutations. CONCLUSIONS: For NRTI- and minor PI-associated mutations, transmission was consistent with relative quantity of variants in maternal virus. However, where NNRTI- and major PI-associated mutations were present in three cases, they were not transmitted, even where only mutant virus was detectable in maternal isolates. This is consistent with evidence of loss of transmission with resistance to NNRTI and PI drugs. © 2006 Lippincott Williams & Wilkins.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=33748044608&origin=inward; http://dx.doi.org/10.1097/01.aids.0000242816.80462.81; http://www.ncbi.nlm.nih.gov/pubmed/16931934; https://journals.lww.com/00002030-200608220-00003; https://ir.lib.uwo.ca/epidempub/31; https://ir.lib.uwo.ca/cgi/viewcontent.cgi?article=1030&context=epidempub; https://insights.ovid.com/crossref?an=00002030-200608220-00003
Ovid Technologies (Wolters Kluwer Health)
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