Mechanisms of Resistance of HIV-1 Primary Isolates to Complement-Mediated Lysis
Virology, ISSN: 0042-6822, Vol: 246, Issue: 2, Page: 370-378
1998
- 37Citations
- 5Captures
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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
- Citations37
- Citation Indexes37
- 37
- CrossRef30
- Captures5
- Readers5
Article Description
Previous studies suggested that HIV-1 primary isolates (PI) were resistant to complement-mediated lysis (CML), while virus produced in certain T cell lines and virus taken directly from the plasma of HIV + persons were both susceptible to CML. The purpose of this study was to investigate the mechanism(s) of PI resistance. PI were resistant to CML using pooled seropositive serum as an antibody source. Additionally, PI obtained from two patients at several times over 2 years were resistant to CML using autologous antibody. PI were also resistant to CML induced by monoclonal antibodies which neutralize a broad range of PI. Resistance to CML was associated with low binding of antibody to PI but was not due to low gp120 levels. Cell-line-derived virus and PI were equally sensitive to CML induced by antibody to host-cell proteins, suggesting that PBMC do not contribute properties to virions which make them more physically resistant to CML in general but that PI resistance is restricted to CML induced by antiviral antibody. These studies show that PI are resistant to CML mediated by various antiviral antibodies and indicate that low binding of antibody to virus is an important factor contributing to resistance.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0042682298992054; http://dx.doi.org/10.1006/viro.1998.9205; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0032486586&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/9657955; https://linkinghub.elsevier.com/retrieve/pii/S0042682298992054; https://dx.doi.org/10.1006/viro.1998.9205
Elsevier BV
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