HIV associated cell death: Peptide-induced apoptosis restricts viral transmission
Frontiers in Immunology, ISSN: 1664-3224, Vol: 14, Page: 1096759
2023
- 18Usage
- 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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Usage18
- Downloads13
- Abstract Views5
- Captures18
- Readers18
- 18
Article Description
The human immunodeficiency virus (HIV) is still a global pandemic and despite the successful use of anti-retroviral therapy, a well-established cure remains to be identified. Viral modulation of cell death has a significant role in HIV pathogenesis. Here we sought to understand the major mechanisms of HIV-induced death of lymphocytes and the effects on viral transmission. Flow cytometry analysis of lymphocytes from five latent HIV-infected patients, and HIV IIIB-infected MT2 cells demonstrated both necrosis and apoptosis to be the major mechanisms of cell death in CD4 and CD4/CD8 lymphocytes. Significantly, pro-apoptotic tumor necrosis factor (TNF) peptide (P13) was found to inhibit HIV-related cell death and reduced viral transmission. Whereas pro-necrotic TNF peptide (P16) had little effect on HIV-related cell death and viral transmission. Understanding mechanisms by which cell death can be manipulated may provide additional drug targets to reduce the loss of CD4 cells and the formation of a viral reservoir in HIV infection.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85149654320&origin=inward; http://dx.doi.org/10.3389/fimmu.2023.1096759; http://www.ncbi.nlm.nih.gov/pubmed/36911666; https://www.frontiersin.org/articles/10.3389/fimmu.2023.1096759/full; https://mouseion.jax.org/stfb2023/72; https://mouseion.jax.org/cgi/viewcontent.cgi?article=1066&context=stfb2023; https://dx.doi.org/10.3389/fimmu.2023.1096759; https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1096759/full
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