F. Coutlee et al., ABSENCE OF PROLONGED IMMUNOSILENT INFECTION WITH HUMAN-IMMUNODEFICIENCY-VIRUS IN INDIVIDUALS WITH HIGH-RISK BEHAVIORS, The American journal of medicine, 96(1), 1994, pp. 42-48
PURPOSE: The presence in some individuals of a prolonged phase of infe
ction with human immunodeficiency virus type 1 (HIV-1) before seroconv
ersion remains controversial. This study was undertaken to determine w
ith a sensitive in vitro amplification technique, the polymerase chain
reaction (PCR), whether seronegative individuals with high-risk behav
iors could harbor HTV-1 sequences in their peripheral blood mononuclea
r cells (PBMCs) and remain seronegative for more than 6 months. PATIEN
TS AND METHODS: Seronegative individuals who engaged in unprotected an
ogenital intercourse with HIV-1-infected partners or with more than 10
individuals per year, and seronegative individuals who shared needles
with seropositive partners, were recruited prospectively over 18 mont
hs. HTV-1 DNA and RNA sequences were detected in PBMCs of these indivi
duals with three PCR assays using SK38/SK39, SK145/SK431, and SK68/SK6
9. Seronegative but PCR-positive patients were also evaluated with p24
antigen capture assay, radioimmunoprecipitation assay, and Western bl
ot. The latter patients were followed prospectively to reproduce PCR-p
ositive results and monitor serologic responses. RESULTS: Sixty-one me
n and 18 women, with an average age of 34.1 +/- 7.6 years, were recrui
ted: 56 were homosexual men, 18 were heterosexual women, and 5 were he
terosexual men. Amplification reactions for HIV-1 of 104 PBMC specimen
s from 79 patients with negative or indeterminate serologies revealed
that 4 patients (5.1%) were positive with PCR for HIV-1 DNA and RNA at
the time of enrollment. Positive amplification reactions could not be
reproduced in prospective samples for one patient. The analysis of a
variable human genomic locus in this patient's PBMCs demonstrated that
the first PCR-positive sample and following PCR-negative samples orig
inated from different patients, suggesting a specimen mix-up. Two of t
he three PCR-positive seronegative patients had symptoms suggestive of
acute retroviral disease. Sera from all three patients contained p24
antigen. Two patients seroconverted within 1 month whereas one patient
could not be followed prospectively. CONCLUSION: Prolonged infection
with HIV-1 without seroconversion was not found in our population of p
atients at very high risk for HIV-1 infection. All PCR-positive patien
ts seroconverted in less than 1 month.