- Original research
- Open Access
Longitudinal changes in HIV-specific IFN-γ secretion in subjects who received Remune™ vaccination prior to treatment interruption
© Huang et al; licensee BioMed Central Ltd. 2006
- Received: 10 October 2006
- Accepted: 28 November 2006
- Published: 28 November 2006
Despite the benefits of highly active antitretroviral therapy (HAART) for suppressing viral replication in HIV infection, virus persists and rebounds during treatment interruption (TI). This study explored whether HAART intensification with Remune™ vaccination before TI can boost HIV-1-specific immunity, leading to improved control of viremia off HAART.
Ten chronically HIV-infected adults were enrolled in this proof of concept study. After a 6-month HAART intensification phase with didanosine, hydroxyurea, granulocyte-macrophage colony-stimulating factor, (GM-CSF), and a first dose of Remune™ (HIV-1 Immunogen), HAART was discontinued. Patients continued to receive Remune™ every 3 months until the end of study. HAART was restarted if viral load did not fall below 50,000 copies/ml of plasma within 3 months or if CD4+ counts decreased to <200 cells/mm3. HIV-specific immunity was monitored with the interferon-γ (IFN-γ) ELISPOT assay.
All subjects experienced viral rebound during TIs. Although the magnitude and breadth of HIV-specific responses to HLA-restricted optimal peptide panels and Gag p55 peptide pools increased and viral load decreased by 0.44 log10 units from TI#1 to TI#2, no significant correlations between these parameters were observed. The patients spent 50.4% of their 36 months follow up off HAART.
Stopping HAART in this vaccinated population induced immune responses that persisted after therapy was restarted. Induction of HIV-specific immunity beyond IFN-γ secretion may be contributing to better control of viremia during subsequent TIs allowing for long periods off HAART.
- Viral Load
- Peripheral Blood Mononuclear Cell
- Major Histocompatibility Complex Class
- Simian Immunodeficiency Virus
- Treatment Interruption
The introduction of highly active antiretroviral therapy (HAART) to the management of patients infected with HIV has significantly decreased mortality and morbidity . Although HAART suppresses HIV replication in a significant proportion of HIV infected individuals, it is not able to eradicate viral infection [2, 3]. Serious side effects and emergence of drug resistant virus provide the impetus to explore alternatives to continuous HAART [4, 5].
HIV specific CD8+ T cells contribute to the control of HIV replication. The strongest evidence supporting this comes from an animal model of HIV infection, macaques infected with the simian immunodeficiency virus (SIV). In SIV infected macaques CD8+ T cell depletion results in increased viral load, which returns to pre-treatment values when CD8+ T cells reemerge . Several other observations support a role for CD8+ T cells in control of HIV. These include viral escape from the CTL responses [7–10], the temporal association between decline in viral load and the emergence of CTL responses in HIV primary infection (PI) [11, 12], the association of certain major histocompatibility complex (MHC) class I alleles and heterozygosity at loci coding for these alleles with rate of HIV disease progression [13, 14] and the association between HIV-specific CD8+ proliferative responses and long term non progressor status . Initiation of HAART in the chronic phase of infection generally results in a decline in the breadth and magnitude of the HIV-specific responses in association with viral load control [16, 17].
In order to boost HIV-specific immunity and limit exposure to antiretroviral drugs, treatment interruptions (TI) are being investigated. The rationale behind TI in HIV infection is that stopping treatment allows reemergence of autologous virus, which will boost virus specific immunity that can contribute to subsequent viral load control. In subjects who start HAART in acute HIV infection, the breadth and magnitude of HIV-specific immune responses is compromised compared with that seen later in infection [18–20]. In these individuals, TIs have been used after a period on HAART to expand HIV-specific immunity . This strategy of early initiation of HAART followed by a controlled TI increased HIV-specific immunity and transiently suppressed viral replication.
TI performed in the setting of chronic infection has been largely unsuccessful in stimulating immunity that controls viremia [22–24]. For this reason, therapeutic vaccination and immunomodulatory therapies, which boost HIV-specific immunity are currently being investigated for HAART treated chronically HIV-infected patients prior to TI to determine whether they induce HIV-specific immunity that improves viral load control off therapy. The use of therapeutic HIV immunization (Remune™ – HIV-1 Immunogen) in chronic HIV infection to induce HIV-specific lymphoproliferative responses (LPR) is well documented. [25–28].
We present results on within-subject changes in HIV-specific immunity induced in HIV infected patients (n = 10) in the chronic phase of infection who underwent therapy intensification and vaccination with Remune™ before multiple rounds of TI. We observed that the magnitude and breadth of HIV-specific responses detected in IFN-γ ELISPOT and intracellular cytokine secretion assays increased from on treatment time points pre-TI#1 to pre-TI#2. However, this increase in HIV-specific immune response did not correlate with the decrease in the viral load plateau seen during TI#1 to that seen during TI#2. Although our results show that HAART intensification and Remune™ vaccination were able to reduce and sustain lower VL plateau during consecutive cycles of TI, this reduction did not correlate with increases in HIV-specific responses measured.
Patient population and study design
Study Population Characteristics
MHC Class I
Before HAART Intensification
Before First Treatment Interruption (TI)
CD4 Cell Count (cells/mm3)
CD4 Cell %
CD4 Cell Count (cells/mm3)
CD4 Cell %
The treatment schedule included a 6-month HAART intensification phase, during which didanosine (ddI) and hydroxyurea (HU) were added to the existing regimen for the first 5 months and granulocyte-macrophage colony-stimulating factor (GM-CSF) for the first 3 months. Remune™ (10 units of p24 antigen – 100 μg total protein, in Incomplete Freund's Adjuvant) was given at month 5 of the treatment intensification phase when HU was stopped. All 10 patients completed another month of therapy intensification with ddI and were vaccinated with Remune™ at three-month intervals until the end of study. Patients were monitored for 36 months after the first TI. Blood samples were obtained at baseline, month 3, 6, of the HAART intensification phase, and every 3 months for 36 months thereafter for virological and immunological assessments. HAART and HU were resumed if VL did not decrease to <50 000 copies within 3 months or if the CD4+ counts decreased to <200 cells/mm3. HAART was again interrupted when viral load was <50 HIV-1 RNA copies/ml and CD4+ counts were >200 cells/mm3 measured on two occasions one month apart.
Plasma viremia was determined using the Roche Amplicor Assay (Roche Diagnostics, Mississauga, Ontario, Canada) with a detection limit of 500 HIV-1 RNA copies/ml of plasma. Samples falling below the detection limit were retested with the ultrasensitive method (Ultradirect; Roche Diagnostics) with a detection limit of 50 HIV-1 RNA copies/ml.
Genomic DNA for molecular HLA typing was prepared from Epstein-Barr virus (EBV)-transformed B cell lines using the QIAamp DNA blood kit (Qiagen, Mississauga, Ontario, Canada). Each patient was typed for HLA class I alleles using 95 primer sets amplifying defined MHC class I alleles (ABC SSP Unitray; PelFreez Clinical Systems, Brown Deer, Wisconsin, USA) 
Cells and Peptide Selection
Peripheral blood mononuclear cells (PBMC) were isolated from blood collected in acid citrate dextrose anticoagulant at each study visit by density gradient centrifugation (Ficoll-Paque, Pharmacia, Upsala, Sweden) and frozen in 90% fetal calf serum (GIBCO BRL Life Technologies, Burlington, Ontario, Canada), 10% dimethyl sulfoxide (DMSO, Sigma, St. Louis MO). The HIV epitopes used for PBMC stimulation were chosen from the Los Alamos HIV Molecular Immunology Database . Optimal peptides of 8 to 10 aa in length restricted to the MHC class I alleles expressed by the individuals being tested were synthesized to greater than 85% purity by solid phase synthesis using F-MOC chemistry (Sheldon Biotechnology Center, Montreal, Quebec, Canada). Twenty-mer peptides corresponding to HIV Gag p55 were obtained from the National Institute of Biological Standards and Controls (Potters Bar Hertz, UK). These were organized into pools containing peptides corresponding to HIV Gag p17, p24 and p15. Each peptide in these pools was present at a final concentration of 2.0 μg/ml. In addition, MHC restricted EBV- or cytomegalovirus (CMV)-derived 8- to 10-mer optimal peptides were also synthesized as described above and used as positive peptide control stimuli.
IFN-γ Enzyme-Linked Immunospot (ELISPOT) Assay
List of MHC class I-restricted peptides used as stimuli
MHC Restriction (s)
A3, A11, A6801
A3, A3.1, A11, A6801, A33, B7, B35
A3, A11, A31, B27, B35
B44, B57, Cw4
B18, B2601, B44, B70
A3, A6801, A11, Cw7
Data were analyzed by using GraphPad InStat statistical software, version 3.06 [(2003) GraphPad Software, San Diego, California, USA]. Two-tailed nonparametric Wilcoxon matched-pairs signed-ranks tests were used to assess differences in VL, the magnitude and breadth of HIV-specific responses, and the percentage of Gag p55-specific CD4+ and CD8+ T-cells between each TI. Nonparametric Spearman rank correlations were used to correlate the VL improvements with both increases in the magnitude of HIV-specific responses and changes in breadth of these responses between the 1st and 2nd TI. The total immune responses generated were expressed as the area under the curve (AUC) calculated from total HIV-specific responses over time for each patient. Nonparametric Spearman rank correlations were used to evaluate the correlation between the total HIV-specific immune responses and the number of days patients were able to stay off HAART. All tests for statistical significance were two-tailed and p values <0.05 were considered significant.
Changes in HIV-specific immune responses
To compare the fate of HIV-specific IFN-γ secretion between the study population and individuals in the chronic phase of infection on continuous HAART that suppresses viremia to undetectable levels but who do not undergo therapy intensification, vaccination or TI, nine historical controls of a similar age and absolute CD4 count to the study population were assembled. The continuously treated controls were screened with an MHC class I restricted HIV peptide panel at 2 on-HAART time points separated by a time interval similar to that between pre-TI#1 and pre-TI#2 time points in the study population (p = 0.45; Mann-Whitney test). The size of the peptide panels used for both the study population and the controls was similar. The magnitude of the IFN-γ responses in continuously treated controls to the peptide panels tested did not change significantly from the first to the second time point tested (data not shown). Furthermore, comparison of the magnitude of the change in IFN-γ responses from the first to the second time point differed significantly in these two populations (-240 ± 331 versus +457 ± 475 SFC/106 PBMC in the controls and the study population, respectively, p = 0.0028; Mann-Whitney test) (Figure 3D).
In order to determine whether changes in HIV-specific immunity occurred in the CD4+ or CD8+ cell compartments (or both) we also measured percent of HIV Gag p55 specific IFN-γ secreting CD4+ and CD8+ cells by ICS as described . Although changes in HIV-specific IFN-γ secretion responses detected by ICS displayed a similar trend in both compartments to that observed using the ELISPOT assay, none of these differences was statistically significant (not shown).
Timing of appearance and magnitude of HIV-specific immune responses with control of VL after HAART is withdrawn
The participants in this trial spent an average of 50.4% of the 36 months they were followed after stopping therapy for the first time off HAART. We therefore investigated whether there was a correlation between the percentage of time off HAART and the total HIV-specific immune responses to either the peptide panel tested or pools of peptides corresponding to HIV Gag p55. No significant association between these parameters was observed (not shown)
This report presents results on changes in HIV-specific immune responses in 10 subjects in the chronic phase of infection with undetectable HIV VL on HAART at study entry. All underwent 6 months of therapy intensification and received an initial dose of the therapeutic vaccine Remune™ before stopping HAART and all of them received Remune™ every 3 months for a total of 11 doses. Treatment was restarted if rebound VL did not decrease to <50 000 copies within 3 months or if the CD4+ counts decreased to <200 cells/μl during TI. HAART was again interrupted when viral load was <50 HIV-1 RNA copies/ml and CD4+ counts were >200 cells/mm3 on two occasions one month apart.
We found that the average VL plateau decreased significantly with TI#1 to TI#2. Although both magnitude of breadth of immune responses to the screening peptide panel and Gag p55 peptide pools increased significantly from TI#1 to TI#2, no correlation between changes in VL and changes in immune response were detected. Patients were able stay off HAART for 50.4% of the time over 36 months of follow up. No correlation between the percentage of days off HAART and the immune responses generated was detected.
Subject 14003 was able to maintain viral load to below 40 000 copies/ml after one TI and remained off therapy for the reminder of the study and was not included in the analysis (mean VL of 27 288 copies/ml over 968 days). The VL in subject 14008 remained below 42 000 copies/ml of plasma (mean VL of 13 937 copies/ml over 637 days) after 2 TIs. This individual was included in comparisons between TI#1 and TI#2, but no data was available for this individual for TI#3. It should be noted that the absence of statistical significance between the comparisons of breadth and magnitude of HIV-specific immune responses may be related to the small size of comparison groups.
The increase in the breadth and magnitude of IFN-γ responses to the peptide panel tested from the time point prior to TI#1 to the time point prior to TI#2 differs from the fate of these parameters for HIV-specific responses observed in chronically infected subjects on continuous HAART that suppresses VL to below 50 copies/ml of plasma. First, the magnitude of the IFN-γ responses in continuously treated controls did not change significantly from the first to second time tested and the change in magnitude of IFN-γ responses from the first to the second time point differed significantly in these two populations. This supports the conclusion that the study population interventions including treatment intensification, vaccination and TI led to expansion of HIV-specific immunity.
Several factors may account for the lack of correlation between the increase in the magnitude and breadth of HIV-specific immune responses measured by IFN-γ ELISPOT and VL decrease from TI#1 to TI#2. First, the use of optimal peptide panels and Gag peptide pools corresponding to reference strain HIV isolates rather than autologous sequences may underestimate the true extent of HIV specific immunity . Although the same set of stimuli were used to assess HIV-specific IFN-γ secretion at all time points, it is possible that the accumulation of viral sequences changes no longer recognized by HIV-specific cells with time reduces the correlation between this function of HIV-specific cells and VL control.
Second, the cytolytic activity of CD8+ T-cells is believed to be important in controlling the viral burden in HIV infection. Since IFN-γ secretion has been shown to be a surrogate for the level of CD8+ T-cell effector activity, IFN-γ ELISPOT and ICS are the standard techniques used to screen for antigen specific CTL . However, recent studies have shown that lysosomal-associated membrane protein-1 (LAMP-1 or CD107a) expression on the cell surface could be a better marker for CD8+ T-cell cytolysis. CD107a has been shown to be upregulated following antigenic stimulation coupled with degranulation and the release of perforin [34, 35]. Moreover, studies in chronic viral infection in murine models have shown that there is a hierarchical exhaustion of CD8+ T-cell functions. Virus-specific memory CD8+ T-cells progressively loose their functional capabilities in response to viral antigen recognition starting with the inability to secrete interleukin-2 (IL-2), and reduced proliferative and lytic activity. Next, the ability to secrete tumor-necrosis factor alpha (TNF-α) wanes . IFN-γ secretion is the CD8+ T cell function most resistant to exhaustion. Therefore, the measurement of HIV-specific IFN-γ-secreting CD8+ T-cells might reflect an incomplete picture of HIV-specific immune responses best associated with suppression of viral replication.
As well, recent reports have shown that the breadth and magnitude of HIV-specific IFN-γ responses to all expressed HIV genes do not correlate with either VL or with rate of CD4+ T cell decline [37, 38]. While it is fairly well established that HIV-specific CD8+ cells do mediate anti-viral activity, it may be that other functions of these cells correlate better with control of HIV replication than IFN-γ secretion. Studies with HIV infected long-term nonprogressors (LTNPs) showed that they have elevated HIV-specific proliferative capacity coupled to increased perforin expression when compared to HIV infected disease progressors . Moreover, LTNPs possess an enhanced CD8 T-cell functional profile compared with progressors including maintenance of polyfunctional responses such as TNF-α and IL-2 secretion in addition to other functions . Furthermore, aviremic patients treated during primary infection have increased HIV proliferative capacity as well as ability to maintain an HIV-specific IL-2-secreting CD4+ T-cell population when compared to viremic patients . These studies suggest that it is the quality (HIV-specific IL-2 secretion and proliferation in particular), rather than the quantity of HIV-specific responses that may be better immune correlates of viral control.
In summary our study showed that HAART intensification with GM-CSF, ddI and HU followed by Remune™ vaccination augmented HIV-specific IFN-γ secretion from TI#1 to T1#2 with a corresponding significant decrease in VL. However, no correlation could be established between these two phenomena. Patients were able to stay off HAART for 50.4% of the period of the study. TIs are an important part of the clinical management of HIV infected subjects because of the potential cost saving, reversion of drug-resistant virus to drug sensitive variants, and patients' request for a break from their medications. Therefore, the immunological and virological benefits observed in this proof of concept study warrant further studies with a larger patient population to identify potential protective HIV-specific immune responses induced by this therapeutic strategy of TI in combination with Remune™ vaccination. In addition, recent studies with Remune vaccination in chronic HIV-infected patients showed an induction of polyfunctional HIV-specific CD8+ T-cells with increased proliferative capacity, IL-2, MIP-1β, IFN-γ, and TNF-α secretion . Thus, future immune monitoring for T-cell responses vaccine trials should include not only IFN-γ secretion, but also polychromatic flow cytometry to assess proliferation, degranulation, other cytokine and chemokine secretion as well.
The authors wish to express their gratitude to the study participants. In addition the authors would like to thank the CTN 140 study group, Alefia Merchant and Nancy Simic for their technical expertise. This work was supported by grants from the Canadian Foundation for AIDS Research (CANFAR) # 013–521 and #015–509 and the Fonds de Recherche en Santé du Québec AIDS and Infectious Diseases Network. The CTN 140 investigator-initiated pilot trial (PI. E. Toma) was supported by grants from Canadian HIV Trials Network (CTN).
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