Article ID Journal Published Year Pages File Type
3369682 Journal of Clinical Virology 2009 4 Pages PDF
Abstract

BackgroundThe optimum collection procedure for the evaluation of HIV-1 burden in ulcer secretions has not been well defined.ObjectivesThe objective of this study was to compare ulcer swabs and ulcer lavages for the detection and quantitation of HIV-1 RNA in genital ulcers.Study designA convenience sample of the first 84 HIV-positive participants in a randomized double blind placebo controlled trial of acyclovir episodic treatment among men with genital ulcer disease were included in this evaluation. At baseline, participants were screened for HIV, syphilis and HSV-2 by serology and for ulcer etiology by PCR. Ulcer specimens were collected by using (1) a non-traumatic washing procedure with 10 ml of PBS, and (2) sterile dry swabs. Ulcer samples were tested with HIV-1 Amplicor 1.5 Ultra Sensitive Assay with a lower threshold of 50 copies/ml.ResultsOf ulcer samples 35 (41.7%) had HIV detected by ulcer lavage and 32 (38.1%) by swabs (p = 0.68). Overall, 45 (53.6%) were positive by one or both methods. The overall proportion of agreement was 73% (61/84). The chance-corrected proportion of agreement was 0.46 (95% CI: 0.26, 0.65) as estimated by the Kappa statistic. The log mean viral load from lavages (1.49 log10 copies/ml, 95% CI: 1.17–1.81) did not differ significantly from that of swabs (1.41 log10 copies/ml, 95% CI: 1.16–1.71) (p = 0.29) with a mean difference of 0.08 log copies/ml (SD 0.96).ConclusionUlcer lavage and ulcer swab performed in moderate agreement in the detection and quantitation of HIV RNA from ulcer specimens.

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Life Sciences Immunology and Microbiology Applied Microbiology and Biotechnology
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