HIV-1-specific immune responses in subjects who temporarily contain virus replication after discontinuation of highly active antiretroviral therapy

G M Ortiz, D F Nixon, A Trkola, J Binley, X Jin, S Bonhoeffer, P J Kuebler, S M Donahoe, M A Demoitie, W M Kakimoto, T Ketas, B Clas, J J Heymann, L Zhang, Y Cao, A Hurley, J P Moore, D D Ho, M Markowitz, G M Ortiz, D F Nixon, A Trkola, J Binley, X Jin, S Bonhoeffer, P J Kuebler, S M Donahoe, M A Demoitie, W M Kakimoto, T Ketas, B Clas, J J Heymann, L Zhang, Y Cao, A Hurley, J P Moore, D D Ho, M Markowitz

Abstract

Therapeutic intervention with highly active antiretroviral therapy (HAART) can lead to suppression of HIV-1 plasma viremia to undetectable levels for 3 or more years. However, adherence to complex drug regimens can prove problematic, and subjects may temporarily discontinue HAART for variable periods. We studied 6 HIV-1-infected individuals who stopped therapy. Off HAART, levels of viremia were suppressed to fewer than 500 copies/mL in 2 subjects for more than 12 and more than 24 months, respectively, and in 1 subject for 4 months on 1 occasion. Three subjects failed to contain plasma viremia. Broad and strong HIV-1-specific immune responses were detected in subjects with prolonged suppression of viral replication. This longitudinal study suggests that containment of HIV-1 replication to low or undetectable levels after discontinuation of HAART is associated with strong virus-specific immune responses. Boosting of HIV-1-specific immune responses should be considered as an adjunctive treatment strategy for HIV-1-infected individuals on HAART.

Figures

Figure 1
Figure 1
Longitudinal study of virological and immunological parameters in subjects nos. 6 and 8. Plasma viremia is shown in a and e. The horizontal bars at the top of a and e represent the estimation of adherence to HAART. Filled bars reflect full adherence; gray bars intermittent adherence; and open bars no drug therapy. The frequency of HIV-1–specific CTLp/106 PBMCs is shown in b and f. Binding antibody titers to gp120 and p24 are shown in c and g. Neutralizing antibody titers to previral isolates (pre-ID90) and postviral isolates (post-ID90) are shown in d and h.
Figure 2
Figure 2
Longitudinal study of virological and immunological parameters in subjects nos. 11 and 12. Plasma viremia, measured by RT-PCR, is shown in a and e. The horizontal bars at the top of a and e represent the estimation of adherence to HAART. Filled bars reflect full adherence; gray bars intermittent adherence; and open bars no drug therapy. The frequency of HIV-1–specific CTLp/106 PBMCs is shown in b and f. Binding antibody titers to gp120 and p24 are shown in c and g. Neutralizing antibody titers to previral isolates (pre-ID90) and postviral isolates (post-ID90) are shown in d and h.
Figure 3
Figure 3
Longitudinal study of virological and immunological parameters in subjects nos. 11, 3005, and 31. Plasma viremia was measured by RT-PCR (a and c) or bDNA (e). The horizontal bars at the top of a, c, and e represent the estimation of adherence to HAART. Filled bars reflect full adherence; gray bars intermittent adherence; and open bars no drug therapy. The frequency of HIV-1–specific SFC/106 PBMCs is shown in b, d, and f.

Source: PubMed

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