AI Article Synopsis

  • Testing HIV-1 RNA in plasma using PCR is the standard method for diagnosing the infection and monitoring treatment, but it can sometimes inaccurately reflect viral replication.
  • This study introduces a new assay to measure HIV-1 reverse transcriptase (RT) activity in blood samples, which may provide more accurate insights into viral status for patients.
  • The findings revealed a significant inverse relationship between HIV-1 RT levels and HIV-1 RNA levels, indicating that the new assay could be a valuable tool for assessing the functional virological status of HIV-1-infected individuals.

Article Abstract

Testing HIV-1 RNA in plasma by PCR is universally accepted as the ultimate standard to confirm diagnosis of HIV-1 infection and to monitor viral load in patients under treatment. However, in some cases, this assay could either underestimate or overestimate the replication capacity of a circulating or latent virus. In the present study, we performed the assessment of evaluating the HIV-1 reverse transcriptase (RT) activity by means of a new assay for the functional screening of the status of HIV-1 patients. To this purpose, we utilized, for the first time on blood samples, an adapted version of a real-time RT quantitative PCR assay, utilized to evaluate the HIV-1-RT inhibitory activity of compounds. The study analyzed blood samples from 28 HIV-1-infected patients, exhibiting a wide range of viremia and immunological values. Results demonstrated that plasma HIV-1 RT levels, expressed as cycle threshold values obtained with the assay under appraisal, were inversely and highly significantly correlated with the plasma HIV-1-RNA levels of the patients. Thus, an HIV-1 RT quantitative PCR assay was created which we describe in this study, and it may be considered as a promising basis for an additional tool capable of furnishing information on the functional virological status of HIV-1-infected patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763350PMC
http://dx.doi.org/10.3390/pathogens9121047DOI Listing

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