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3rd International AIDS Society Conference on HIV Pathogenesis and TreatmentRio de Janeiro - July 24 - 27, 2005 |
SPECIAL PROGRAM OF ASSISTED REPRODUCTION FOR HIV-INFECTED MEN
IAS Conf HIV Pathog Treat 2005 Jul 24-27;3rd: Abstract No. MoPp0204
A. Kiessling A., Desmarais B., Yin H.-Z., Eyre R., Steinberg J.
Bedford Research Foundation, Somerville, United States of America
INTRODUCTION: Assisted reproductive technologies (ART) can help HIV-infected men safely father children. But many ART programs are reluctant to treat HIV-infected men because of concerns about handling HIV-infected semen. A sensitive RT-PCR assay for virus and virus-infected cells allows eliminatiion of HIV-infected specimens and identification of specimens with an undetectable viral burden which can be shipped to ART clinics, thus eliminating concerns about handling infected specimens.
METHODS: Semen specimens are overnight-shipped to the laboratory for testing. Part of the specimen is added to guanidium isothiocyanate at a concentration that lyses virus and non-sperm cells; HIVgag was detected by a triple bracket-nested RT-PCR assay that could detect 210 copies of viral RNA/ml semen, and/or one infected cell. Sperm, cryopreserved prior to testing, from specimens with an undetectable viral burden were shipped to ART clinics.
RESULTS: From 1999 to June, 2004, 442 semen specimens from 133 men on successful anti-retroviral therapy were tested for HIV; 104 tested positive and were discarded. Men with two positive specimens in a row were further evaluated for prostatitis, or for modification of their anti-retroviral therapy. Sixty seven couples proceeded to ART, resulting in 29 pregnancies, 38 babies born, all mothers and babies tested negative for HIV antibody.
CONCLUSIONS: Testing semen for HIV can eliminate specimens with a detectable viral burden, and allow the use of tested specimens in ART clinics near the couples' home. Moreover, adjusting treatment regimens of HIV-infected men to eliminate virus production by semen producing organs may also prevent disease progression.
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Prevention | MoPp0204 | Ann Kiessling
10.7 262 10.7 Sexual transmission
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