AI Article Synopsis

  • A nonradioactive reverse transcriptase (RT) assay was utilized to measure RT activity and the development of RT-blocking antibodies in SIV-infected macaques during primary infection and after seroconversion.
  • The RT assay proved to be about 40 times more sensitive than a traditional antigen capture immunoassay for detecting SIVsm in serum samples, detecting RT activity as low as 3 pg/ml.
  • The RT assay identified viral replication as early as days 6-8 with peak levels on day 10, while RT-blocking antibodies were detected between days 17-23 and significantly increased by days 62-77, highlighting the assay's potential for monitoring SIV infection.

Article Abstract

A nonradioactive reverse transcriptase (RT) assay was used to measure RT activity in serum during the viremia peak associated with primary infection and for measuring the generation and maintenance of RT activity-blocking antibody (RTb-ab) titers during and after seroconversion in SIV-infected macaques. The RT assay was compared to an antigen capture immunoassay designed for HIV-2/SIVsm and was found to be approximately 40 times more sensitive in detecting SIVsm in serum from infected macaques. The RT assay detected RT activity in serum corresponding to levels from 3 pg/ml. Earliest detection of viral replication using the RT assay was on day 6-8, with a peak at day 10 (up to 8000 pg/ml). The earliest detection of RTb-ab was seen on day 17-23, with established RTb-ab titers by day 29, followed by increasing titers of 15,000-120,000 by day 62-77. The usefulness of RT and RTb-ab for monitoring the course of SIV infection in monkey models is discussed.

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http://dx.doi.org/10.1089/aid.1997.13.601DOI Listing

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