Intracellular antiviral activity of low-dose ritonavir in boosted protease inhibitor regimens.

Author: AbdiAdnan Mohamed, BonoraStefano, CalcagnoAndrea, D'AvolioAntonio, De NicolòAmedeo, Di PerriGiovanni, SimieleMarco

Paper Details 
Original Abstract of the Article :
Protease inhibitors are largely used for the treatment of HIV infection in combination with other antiretroviral drugs. Their improved pharmacokinetic profiles can be achieved through the concomitant administration of low doses of ritonavir (RTV), a protease inhibitor currently used as a booster, in...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4068548/

データ提供:米国国立医学図書館(NLM)

Ritonavir's Intracellular Antiviral Activity: A New Perspective on Boosted Protease Inhibitor Regimens

Protease inhibitors (PIs) are a mainstay in the treatment of HIV infection, often used in combination with other antiretroviral drugs. This study investigates the intracellular antiviral activity of ritonavir, a drug commonly used to boost the effectiveness of other PIs.

Ritonavir's Intracellular Effects: More Than a Booster

The researchers found that ritonavir, even when administered at low doses, accumulates inside cells, including lymphocytes and monocytes, which are important cells in the immune system. This intracellular concentration of ritonavir may contribute to its antiviral activity, going beyond its role as a booster for other PIs.

A New Look at Ritonavir's Role in HIV Treatment

The study highlights the need for further research into the intracellular antiviral activity of ritonavir. This could lead to a better understanding of how ritonavir works in boosted PI regimens and potentially inform the development of more effective and safer treatment strategies for HIV infection.

Dr. Camel's Conclusion

This research takes us on a journey into the hidden depths of intracellular activity, revealing a new facet of ritonavir's role in HIV treatment. The findings suggest that ritonavir's effects may extend beyond its role as a booster, potentially providing direct antiviral benefits. This opens up exciting avenues for further research and development of new approaches to HIV treatment.

Date :
  1. Date Completed 2016-03-21
  2. Date Revised 2021-10-21
Further Info :

Pubmed ID

24798279

DOI: Digital Object Identifier

PMC4068548

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Languages

English

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