HIV in body fluids during primary HIV infection: implications for pathogenesis, treatment and public health

被引:133
作者
Pilcher, CD
Shugars, DC
Fiscus, SA
Miller, WC
Menezes, P
Giner, J
Dean, B
Robertson, K
Hart, CE
Lennox, JL
Eron, JJ
Hicks, CB
机构
[1] Univ N Carolina, Sch Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Dent, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Publ Hlth, Chapel Hill, NC 27599 USA
[4] Duke Univ, Med Ctr, Durham, NC USA
[5] Emory Univ, Atlanta, GA 30322 USA
[6] Ctr Dis Control & Prevent, Atlanta, GA USA
关键词
acute infection; antiretroviral therapy; sexual transmission; semen; neurological/brain; oral medicine; viral load;
D O I
10.1097/00002030-200105040-00004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To describe initial viral dissemination to peripheral tissues and infectious body fluids during human primary HIV infection. Design: Observational cohort study. Methods: Blood plasma, cerebrospinal fluid (CSF), seminal plasma, cervicovaginal lavage fluid and/or saliva were sampled from 17 individuals with primary HIV infection (range of time from symptoms onset to sampling, 8-70 days) and one individual with early infection (168 days). Subjects' HIV-1 RNA levels in each fluid were compared with levels from antiretroviral-naive controls with established HIV infection. For study subjects, correlations were assessed between HIV-1 RNA levels and time from symptoms onset. Responses to antiretroviral therapy with didanosine + stavudine + nevirapine +/- hydroxyurea were assessed in each compartment. Results: HIV-1 RNA levels were highest closest to symptoms onset in blood plasma (18 patients) and saliva (11 patients). CSF HIV-1 RNA levels (five patients) appeared lower closer to symptoms onset, although they were higher overall in primary versus established infection. Shedding into seminal plasma (eight patients) and cervicovaginal fluid (two patients) was established at revels observed in chronic infection within 3-5 weeks of symptoms onset. High-level seminal plasma shedding was associated with coinfection with other sexually transmitted pathogens. Virus replication was suppressed in all compartments by antiretroviral therapy. Conclusions: Peak level HIV replication is established in blood, oropharyngeal tissues and genital tract, but potentially not in CSF, by the time patients are commonly diagnosed with primary HIV infection. Antiretroviral therapy is unlikely to limit initial virus spread to most tissue compartments, but may control genital tract shedding and central nervous system expansion in primary infection. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:837 / 845
页数:9
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