Abstract Interleukin-15 (IL-15) enhances the effector mechanisms of anti-HIV immune responses and thus is considered a potential adjuvant of HIV-1 vaccine. However, there are a lack of data concerning the relationships between IL-15 expression and regulation in HIV-1-infected patients and the course of disease progression. We found that IL-15, but not IL-15Rα, is expressed at significantly higher levels in the CD14(+) monocytes [stimulated or not with interferon (IFN)-γ] of long-term nonprogressors (LTNP) than in those of HIV-1 progressors or healthy controls. There was no between-group difference in the amounts of soluble IL-15 released from the cells. We also found that like the healthy controls, the LTNP expressed the IL-15 and IL-15Rα genes in a more coordinated manner than the progressors. Our findings show that there are significant differences in IL-15 expression between patients with different courses of HIV infection, and that the coordinated expression of the IL-15 and IL-15Rα genes is dysregulated in patients with progressive disease. They also provide important information concerning the mechanisms of infection and the potential use of IL-15 as a therapeutic agent.

Expression of Interleukin-15 and Interleukin-15Rα in Monocytes of HIV Type 1-Infected Patients with Different Courses of Disease Progression / M. Tarkowski, L. Ferraris, S. Martone, F. Strambiodecastillia, D. Misciagna, R.I. Mazzucchelli, E. Lattuada, G. Paraninfo, M. Galli, A. Riva, The ELVIS Study Group. - In: AIDS RESEARCH AND HUMAN RETROVIRUSES. - ISSN 0889-2229. - 28:7(2012 Jul), pp. 693-701.

Expression of Interleukin-15 and Interleukin-15Rα in Monocytes of HIV Type 1-Infected Patients with Different Courses of Disease Progression

M. Tarkowski
Primo
;
L. Ferraris
Secondo
;
F. Strambiodecastillia;D. Misciagna;M. Galli;A. Riva;
2012

Abstract

Abstract Interleukin-15 (IL-15) enhances the effector mechanisms of anti-HIV immune responses and thus is considered a potential adjuvant of HIV-1 vaccine. However, there are a lack of data concerning the relationships between IL-15 expression and regulation in HIV-1-infected patients and the course of disease progression. We found that IL-15, but not IL-15Rα, is expressed at significantly higher levels in the CD14(+) monocytes [stimulated or not with interferon (IFN)-γ] of long-term nonprogressors (LTNP) than in those of HIV-1 progressors or healthy controls. There was no between-group difference in the amounts of soluble IL-15 released from the cells. We also found that like the healthy controls, the LTNP expressed the IL-15 and IL-15Rα genes in a more coordinated manner than the progressors. Our findings show that there are significant differences in IL-15 expression between patients with different courses of HIV infection, and that the coordinated expression of the IL-15 and IL-15Rα genes is dysregulated in patients with progressive disease. They also provide important information concerning the mechanisms of infection and the potential use of IL-15 as a therapeutic agent.
English
CD8(+) T-CELLS ; NATURAL-KILLER-CELLS ; CD95/FAS-INDUCED APOPTOSIS ; ANTIRETROVIRAL THERAPY ; PERFORIN EXPRESSION ; TRANS-PRESENTATION ; INFECTED MACAQUES ; INTERFERON-GAMMA ; DNA VACCINE ; NK CELLS
Settore MED/03 - Genetica Medica
Articolo
Sì, ma tipo non specificato
lug-2012
28
7
693
701
Pubblicato
Periodico con rilevanza internazionale
info:eu-repo/semantics/article
Expression of Interleukin-15 and Interleukin-15Rα in Monocytes of HIV Type 1-Infected Patients with Different Courses of Disease Progression / M. Tarkowski, L. Ferraris, S. Martone, F. Strambiodecastillia, D. Misciagna, R.I. Mazzucchelli, E. Lattuada, G. Paraninfo, M. Galli, A. Riva, The ELVIS Study Group. - In: AIDS RESEARCH AND HUMAN RETROVIRUSES. - ISSN 0889-2229. - 28:7(2012 Jul), pp. 693-701.
none
Prodotti della ricerca::01 - Articolo su periodico
11
262
Article (author)
si
M. Tarkowski, L. Ferraris, S. Martone, F. Strambiodecastillia, D. Misciagna, R.I. Mazzucchelli, E. Lattuada, G. Paraninfo, M. Galli, A. Riva, The ELVIS Study Group
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/168334
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