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Early and late effects of highly active antiretroviral therapy: a 2 year follow-up of antiviral-treated and antiviral-naive chronically HIV-infected patients
被引:16
作者:
Clerici, M
Seminari, E
Maggiolo, F
Pan, A
Migliorino, M
Trabattoni, D
Castelli, F
Suter, F
Fusi, ML
Minoli, L
Carosi, G
Maserati, R
机构:
[1] Univ Milan, Cattedra Immunol, DISP LITA Vialba, I-20174 Milan, Italy
[2] Univ Pavia, Clin Malattie Infett, IRCCS San Matteo, I-27100 Pavia, Italy
[3] Osped Riuniti Bergamo, I-24100 Bergamo, Italy
[4] Univ Brescia, Clin Malattie Infett & Trop, Spedali Civili, Brescia, Italy
[5] Osped Circolo, Busto Arsizio, Varese, Italy
来源:
关键词:
cytokines;
HAART;
HIV;
IL-7;
immunology;
virology;
D O I:
10.1097/00002030-200209060-00009
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background: Control of HIV replication can be observed in highly active antiretroviral therapy (HAART)-treated and, occasionally, in HAART-naive patients. The immunological correlates of these situations were examined in a longitudinal study. Design: A prospective study. Immunovirological analyses in 16 chronically HIV-infected, HAART-naive patients (time 0) who started HAART. Fifteen patients (short-term HAART) were re-evaluated after 24 months (time 1). Results were compared with those of 30 patients who received HAART for more than 12 months before the study period (long-term HAART) and were analysed at the same timepoints. Fifteen patients who were antiviral therapy naive (naive) at both timepoints were also studied. Results: Over a 24-month period CD4 and CD8 cell counts and viraemia remained unchanged in naive and long-term HAART patients; CD4 cell counts increased and viraemia diminished in short-term HAART individuals. Antigen-stimulated proliferation was unmodified in naive and short-term HAART patients, but improved in long-term HAART individuals. Gp160-stimulated IL-2 and IFN-gamma production was augmented in long-term HAART patients and marginally modified in other patients. IL-7 production was unmodified in naive individuals, augmented in short-term HAART patients, and diminished in long-term HAART patients. Chemokine production was similar in all patients. Naive patients showed the highest CD8 cell counts at both timepoints. Conclusion: HAART has a major impact on the outcome of HIV infection, even if functional immune modulation in HAART-treated patients is evident only after long periods of therapy. Low but detectable HIV replication in HAART-naive patients with preserved immune functions might not be associated with CD4 cell reduction, functional immune defects, or changes in viraemia. (C) 2002 Lippincott Williams Wilkins.
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页码:1767 / 1773
页数:7
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