Background
Cytokines are defined as short-range protein messengers with important functions in the regulation of the immune response and intercellular communications [
1]. These proteins have been shown to be overexpressed in the context of several diseases, including allergies, autoimmune disorders, cancer and some infectious diseases [
2‐
5]. A large number of therapeutic approaches aimed at inhibiting the activity of these molecules has been developed, and there are over than 20 cytokine-targeting pharmaceutical agents currently approved for clinical use [
6].
Interleukin (IL)-15, one of the members of this protein family, is a pro-inflammatory cytokine that is overexpressed in several inflammatory disorders such as Rheumatoid Arthritis (RA), psoriasis, ulcerative colitis and sarcoidosis [
7‐
11]. The participation of IL-15 in the pathogenesis of autoimmune diseases has been demonstrated by in vitro studies [
12,
13], murine animal models [
14] and clinical trials with an anti-human IL-15 antibody (Ab), AMG714 [
15]. In particular, IL-15 is an important player in the inflammatory processes of RA, where it recruits circulating memory T cells in the synovial membrane and may up regulate other pro-inflammatory cytokines through a variety of mechanisms [
16,
17]. Among these mechanisms are included the induction of tumour necrosis factor alpha (TNF-α) production through the activation of synovial T cells and macrophages via a cell contact-dependent mechanism [
18], as well as the activation of Th17 lymphocytes driving up the biosynthesis of IL-17 [
19].
One possible approach for inhibiting the activity of cytokines produced at pathogenic levels would be to actively immunize patients with the relevant cytokine coupled to a carrier protein or with the modified cytokine [
20,
21]. This strategy, aimed at inducing high titers of neutralizing polyclonal auto-Abs against a pathogenic cytokine in order to antagonize its harmful effects without interfering with other physiologic processes [
22,
23], would possibly exhibit less adverse events than passive immunization strategies, requiring much smaller number of doses, having a lower cost and not presenting the potential problem of anti-Ab response [
24,
25]. Extensive overviews of anti-cytokines vaccination have been published which based almost on the results obtained in animal models, demonstrate that cytokine vaccination may be an effective solution to the control of several autoimmune diseases [
26‐
31]. These data also suggest, based on the absence of severe side effects, that active anti-cytokine immunization represents a relatively safe solution [
32]. Taking into account these promising results, new clinical trials have been developed using
kinoids, which are approved by the Food and Drug Administration for clinical human use [
33].
The aim of the current research was to induce a neutralizing Ab response against self-IL-15 as a potential therapeutic strategy for diseases involving the overexpression of this cytokine. Although an anti-human IL-15 Ab, AMG714, has already been tested in clinical trials [
15], the cytokine itself has never been employed as a target for active vaccination. For our work, human IL-15 was expressed in
Escherichia coli following the procedure described by Santos et al. [
34]. The purified protein, denominated here as modified human IL-15 (mhIL-15), exhibits a scrambled disulfide bonds pattern and it has an additional Alanine residue at its N-terminus. In the present study, non-human primates (NHP)
Macaca fascicularis were immunized with mhIL-15 adjuvanted in aluminum hydroxide (Alum), Montanide ISA-51 VG or Incomplete Freund’s Adjuvant (IFA). The immune response of the monkeys was analyzed by serum antigen-specific Ab titers and the neutralizing capacity of the resulting sera was determined in CTLL-2, an IL-15-dependent cell line. The effect of these sera on the biological activity of human IL-2 and simian IL-15 was also explored. Additionally, we examined the effect of sera from macaques immunized with Alum-adjuvanted mhIL-15 on IL-15-mediated TNF-α production by synovial fluid cells from patients with RA. Finally, the effect of immunization with mhIL-15 on IL-15-dependent cell populations was studied.
Methods
Animals. Handling and husbandry
Twelve adult macaques (Macaca fascicularis) of either sex were used, weighting from 2 to 5 kg. All animals were purchased from the National Center for Animal Breeding (CENPALAB, Havana, Cuba) and maintained in the animal facility of the Center for Genetic Engineering and Biotechnology (CIGB, Havana, Cuba). An environmental temperature of 22–29 °C and a light/dark cycle of 12:12 h were maintained throughout the study. The animals were housed individually in stainless steel cages (90 × 60 × 60 cm) and randomized into groups of 3 to receive mhIL-15 in each adjuvant. Three animals were used as control (placebo group).
The monkeys were adapted to laboratory conditions for at least 4 weeks. They were fed with fresh tomatoes, guavas, bananas, and commercial chow (certificated granulated formula CMQ 1600 ALYco; CENPALAB, Havana, Cuba, containing 25 % of proteins, 3.5 % of crude fat and 3.8 % of crude fiber) twice a day with 150–300 g per monkey according to their ages and body weights. Water was provided ad libitum. The animals were anesthetized with an intramuscular injection of 10 mg/kg ketamine hydrochloride (Liorad Laboratories, Havana, Cuba) before immunization. Vital signs, temperature, heart rate, blood pressure and body weight were registered along the whole scheme before each immunization.
CTLL-2 cell line
CTLL-2 is a T cell-derived, IL-2 dependent cell line obtained from C57bl/6 mice. These cells were grown in RPMI medium 1640 (Thermo Fisher Scientific, USA) containing 2 mM L-glutamine (Thermo Fisher Scientific, USA), 50 μg/mL gentamicin (Sigma-Aldrich, USA), 10 % heat-inactivated fetal bovine serum (FBS, Capricorn Scientific, Germany) and 10 ng/ml recombinant human IL-2 (R&D, USA). Cells were incubated at 37 °C with 5 % CO2, 95 % humidity. CTLL-2 cells were harvested and used in log phase growth (Cell passage 5 after thawing; Cell viability: ≥95 %). Prior to use, the cells were washed 5 times with RPMI medium. The CTLL-2 cell bank was generated from cells directly obtained from ATCC (TIB-214).
Purification of the recombinant mhIL-15
Expression of recombinant mhIL-15 in
E. coli resulted in the formation of insoluble inclusion bodies. After extraction in buffer containing 8 M urea (Merck, USA) in phosphate-buffered saline (PBS, pH 7.4, Thermo Fisher Scientific, USA), mhIL-15 was purified using size-exclusion chromatography (SEC) followed by reverse phase (RP) - high performance liquid chromatography (HPLC). For SEC, we used a HiLoad 26/600 Superdex 200 preparative grade (60 cm × 26 mm, 34 μm, GE Healthcare, USA) column, which was operated at 4 mL/min. The mhIL-15-containing fraction, detected at 226 nm, was then loaded at 0.2 mL/min onto a C
4 column (1 × 25 cm, 10 μm, Vydac, USA). The proteins were separated using a mobile phase containing 0.1 % trifluoroacetic acid (Sigma-Aldrich, USA) and HPLC grade acetonitrile (Sigma-Aldrich, USA), with 0–80 % acetonitrile gradient over 70 min at 2.5 mL/min. The separation was monitored at 226 nm [
34].
Enzyme digestion of purified mhIL-15
Twenty micrograms of RP-HPLC purified mhIL-15 was suspended in 20 μL of 50 mM NH4HCO3 (Sigma-Aldrich, USA) pH 8.0 and incubated for 4 h at 37 °C with trypsin (Promega, USA) 1:100 (w/w) enzyme: mhIL-15 ratio. Afterwards, endoproteinase Glu-C (Roche Biochemical Reagents, USA) was added in tandem, in the same ratio as trypsin, and incubated for 2 h at 37 °C. Peptides were desalted by ZipTips (Millipore, USA), eluted in 3 μL of 60 % acetonitrile (Sigma-Aldrich, USA) in 1 % formic acid (Caledon, Canada) and injected in a hybrid quadrupole-time-of-flight (QTOF-2) mass spectrometer (Micromass, UK).
Mass spectrometry
Intact protein samples as well as peptide digests were analyzed by nano-electrospray ionization (ESI) - mass spectrometry (MS) with a QTOF-2 mass spectrometer (Micromass, UK). The samples were injected through a slightly pressurized borosilicate capillary (Thermo Scientific, USA). Capillary and cone voltages were set to 900 and 35 V, respectively. The mass range of 50–2000 Da was calibrated with a mixture of sodium iodide and cesium iodide (Sigma-Aldrich, USA). MS-MS was performed by selecting a 2–3 Th mass window in the first quadrupole and the precursors fragmented at collision energies between 25 and 35 eV to achieve enough structural information. Data acquisition and processing were performed with the MassLynx version 3.5 package (Micromass, UK).
Vaccine doses and schedule
All monkeys were screened for Abs against IL-15 proteins, and considered naive with respect to the antigen when specific Abs were undetectable by enzyme-linked immunosorbent assay (ELISA, titer < 1:50; see methods below). The animals were immunized subcutaneously at several sites of the interscapular region with 200 μg of mhIL-15 in a total volume of 0.5 mL adjuvanted with either Alum (1.8 mg/mL, Brenntag Biosector, Denmark), Montanide ISA-51 VG (50:50 v/v, SEPPIC, France) or IFA (50:50 v/v, Sigma, USA). Three immunizations were performed, spaced 1 month between the first and second, and 2 months between the second and third. In the case of the Alum-adjuvanted mhIL-15 group, there were two additional immunizations at months 8 (fourth dose) and 18 (fifth dose) after the third inoculation.
Blood samples were collected before beginning the scheme (pre-immune), 15 days after each immunization, and 3 and 6 months after the third dose. In the case of animals immunized with Alum-adjuvanted mhIL-15, samples were also taken 10 months after the fourth dose. Complement was inactivated by incubating the sera at 56 °C for 30 min and the sample were then stored at -20 °C until used. Group serum pools were used to evaluate the recognition of native or simian IL-15 by ELISA. For this purpose, equal volumes of serum from animals of the same group were mixed.
ELISA for serum anti-IL-15 Abs
Specific Abs titers against IL-15 and the recognition of native or simian IL-15 by immune sera were measured through an ELISA as indicated below. EIA 96-well plates (Costar, USA) were coated overnight at 25 °C with 1 μg/mL of mhIL-15, simian IL-15 (previously obtained at the laboratory of CIGB, Havana, Cuba) or native IL-15 (R&D, USA) in PBS pH 7.4. After 3 washes with 0.05 % Tween 20 (Calbiochem, Germany) in PBS, the plates were blocked with 1 % bovine serum albumin (BSA, Sigma-Aldrich, USA) in PBS for 1 h at 37 °C, followed by 3 washes. PBS, 0.05 % Tween 20 and 0.01 % BSA-diluted sera or pool of sera (starting dilution 1:1000 or fixed dilution 1:4000, respectively) were added to wells and incubated for 2 h at 37 °C. Wells were then washed 3 times and incubated with anti-monkey IgG (Fc specific)-peroxidase Ab (Sigma, USA) diluted 1: 10 000 in PBS. After incubating for 1 h at 37 °C, the plates were washed 5 times and incubated with 100 μL of substrate solution (Ultra 3, 3′, 5, 5′-Tetramethylbenzidine Liquid Substrate System, Thermo Scientific, USA) for 15 min. The reaction was stopped by adding 50 μL of 2 N sulphuric acid solution (R&D Systems, USA) and the absorbance at 450 nm was measured with an ELISA plate reader (Biotrak GE, Healthcare, USA). The 450 nm absorbance value corresponding to a PBS sample was subtracted from all the obtained diluted serum readings. Ab titer was considered as the highest serum dilution yielding at least twice the value of the optical density (OD) at 450 nm of the pre-immune serum from each animal. The data were processed using the GraphPad Prism program v6.05 (GraphPad Software, Inc.).
Effect of serum on the proliferation of CTLL-2 cells
To evaluate the neutralizing capacity of individual or pooled samples, twofold serial dilutions of heat-inactivated sera (starting dilution 1:100 or 1:25 respectively) were performed in 96-well plates (Costar, USA) in a volume of 30 μL of RPMI medium supplemented with 10 % FBS. MAB247 and MAB202 (R&D, USA), which are commercially available neutralizing anti-human IL-15 and anti-human IL-2 Abs respectively, were used as positive controls in a range of 1 μg/mL to 7.8 ng/mL (twofold serial dilutions). Then, previously washed CTLL-2 cells were added in amounts of 5 × 10
3 cells/well in 50 μL. Afterwards, 300 pg/mL of native human IL-15 (R&D, USA) or recombinant simian IL-15 or 50 ng/mL of human IL-2 (R&D, USA) in a volume of 20 μL was added to each well, and the plate was incubated for 72 h at 5 % CO
2 and 37 °C [
35]. After 72 h, yellow tetrazolium MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide, Sigma, USA) was added and the plates were further incubated for 4 h [
36]. Finally, 100 μL of a solution containing 10 % sodium dodecyl sulfate (Merck, Germany), 0.1 N HCl (Sigma-Aldrich, USA) and 50 % isopropyl alcohol (Pharmco-AAPER, USA) were added per well. Plates were read at 578 nm on a Multiscan (Sensident Scan, Merck, Germany). Curve Expert Program V.1.3.80 (
www.curveexpert.net/) was used to calculate the neutralizing titers of sera from immunized monkeys with the anti-IL-15 vaccine. These titers were expressed as the dilution of sera that is required for inhibiting the proliferation by at least 50 % (ID
50). The data were graphed using the GraphPad Prism program v6.05 (GraphPad Software, Inc.).
After obtaining written informed consent, synovial fluid from RA patients was extracted and incubated with 10 μg/ml hyaluronidase (Sigma, USA) for 45 min at 37 °C. Synovial fluid cells were obtained after centrifugation at 1200 g for 10 min. The cells were incubated in 96-well plates at 2 × 105 cells per well either with serum (dilution 1:1000), or 60 ng/ml of native IL-15 (R&D, USA), or a combination of both. After 48 h of incubation, the supernatants were collected and stored at -70 °C until further evaluation. TNF-α concentration was determined by ELISA (R&D Systems, USA) according to the manufacturer’s instructions. The data were graphed using the GraphPad Prism program v6.05 (GraphPad Software, Inc.).
Determination of macaque CD8+ and CD56+ cell populations from whole blood samples
One hundred microliters of blood containing 1 % Ethylenediaminetetraacetic acid (EDTA-Na2, Sigma-Aldrich, USA) as anticoagulant were gently homogenized with 2 mL of lysis solution (0.15 M NH4Cl (Sigma-Aldrich, USA), 1 mM KHCO3 (Sigma-Aldrich, USA) and 0.1 mM EDTA in 0.2 L of distilled water), keeping the samples in the dark for 15 min at 25 °C and mixing them every 5 min. After this time, the reaction was stopped by incubation on ice for 2 min, the cells were centrifuged at 1200 g for 5 min and the supernatant was discarded. The cell pellet was washed 3 times with 1 mL of cold PBS by gentle homogenization and centrifugation at 1200 g for 5 min. Afterwards, the cells were incubated on ice with 25 μL of Fluorescein isothiocyanate (FITC)-labelled anti-human CD8 monoclonal Ab clone 17D8 (Exalpha Biologicals, USA) diluted 1:3 and an anti-human CD56 monoclonal Ab clone MEM-188 (BioVendor, Czech Republic) diluted 1:25 in PBS, keeping the samples in the dark for 30 min. The cells were then washed 3 times as indicated above and the samples labeled with the anti-human CD56 Ab were incubated on ice for 30 min with anti-mouse IgG (whole molecule)-FITC Ab (Sigma, USA) diluted 1:30 in PBS. After washing the cells 3 times as described above, they were analyzed in a PARTEC Pass II flow cytometer (Partec, Germany) by collecting 20 000 events. The percentages of cells with CD8 and CD56 surface markers were obtained from the analysis of samples using FloMax software v2.4 (Partec, Germany).
Statistical analysis
The Shapiro-Wilk and Leveneʼs tests were used to verify normality and homogeneity of variance. The comparison of the levels of TNF-α and the percentages of CD8+ and CD56+ cells was performed with Studentʼs T test for paired samples. Statistical significance was set at p ≤ 0.05. In all cases, the SPSS/PASW (Statistical Package for the Social Sciences/ Predictive Analytics Software) Statistics for Windows version 18 (Chicago: SPSS Inc.) was used.
Discussion
In the current work, we evaluated a therapeutic vaccine composed of recombinant mhIL-15 as antigen. Our goal was to generate neutralizing antibodies which could inhibit IL-15 pathological effects. This vaccine could be used for treatment of autoimmune diseases, leukemia or transplant rejection, scenarios where uncontrolled expression of IL-15 is related to disease’s course [
39‐
41]. At first, the structurally modified recombinant protein was expressed in the host
E. coli. Recombinant mhIL-15 obtained by our group contains disulfide bridges between contiguous cysteines C
36-C
43 and C
86-C
89, unlike previous reported cysteines C
35-C
85 and C
42-C
88 for native IL-15 [
37]. However, it is noteworthy that IL-15 obtained by us has an Alanine residue at the N-terminus of the protein before the initial codon. Consequently, location of cysteines in the mhIL-15 sequence is displaced in one residue compared with native IL-15 [
37]. This structural modification is privileged due to the reducing environment in the cytoplasm of the bacterium, which does not favor formation of disulfide bonds. Additionally, we speculate that this modification can favor exposure of subdominant or cryptic epitopes that promote an effective Ab response against the native protein.
Selection of a suitable animal model is important for assessing immunogenicity of a recombinant protein. The NHP were selected because they are the specie of the greatest homology with humans in the amino acid sequence of IL-15, reporting a 97 % similarity between proteins of both species [
42]. The latter is suitable for testing the concept that through vaccination with mhIL-15, a rupture of the immune tolerance can be achieved. Also, there is a high similarity between simian and human IL-15 regarding biological activity and recognition of receptor subunits [
43] which could be advantageous to our approach. Thus, to assess the immunogenicity of IL-15 vaccine in NHP, we used three distinct adjuvants: Alum, Montanide and IFA. Immunization with mhIL-15 generates a response of anti-IL-15 Abs with titers superior to 1: 20000 after the third immunization in all groups. These results indicate a rupture of B cells tolerance as consequence of immunization and generation of specific Abs against the cytokine. Higher Abs titers were obtained in the group immunized with IFA, in correspondence with a potent immunostimulatory effect described for this adjuvant [
44], although it also caused toxicity in every animal of this group, presenting septic ulcers at the site of inoculation. We are aware that this toxicity hinders its use in humans; nevertheless, we incorporated it in our scheme as an experimental control based on previous results not shown in this work.
On the other hand, Alum is the most widely used adjuvants in human vaccines [
45], and its use elicits strong humoral immune responses primarily mediated by secreted antigen-specific Abs [
46]. This constitutes a favorable element, considering that the aim of active immunotherapy against cytokine is to obtain blocking Abs from the immune system of the treated patient. In addition, Alum is a poor inducer of cell-mediated immune responses and is unsuitable for vaccines that require a strong cellular immune response [
47]. Considering this elements and the fact that its use generated the response of anti-IL-15 Abs with higher neutralizing capacity, we selected Alum as adjuvant for active immunization with mhIL-15. However, taking into account the number of animals used in this study, it would be necessary to use additional animals per group to confirm the superiority of alum over other adjuvants like Montanide.
Due to the proliferation within some inflamed tissues, it is mandatory to avoid accumulation of T cells in most of the diseases where cytokines are chronically secreted. Therefore, it is critical when designing vaccines against cytokines to disrupt B-cell but not T-cell tolerance to self-cytokines, thereby eliciting production of neutralizing Abs in high titers [
1,
23]. In this work, we showed that immunization with mhIL-15 generated neutralizing Abs against native IL-15. However, it is still necessary to demonstrate that immunization with this cytokine does not elicit a specific cellular response.
Our results indicated that Abs response was self-regulated when Alum was used as adjuvant. In our scheme, Abs titers begin to decrease after three months post-immunization, which could be due to limited production of these Abs by the activated B cells in absence of specific T helper cells [
48]. Noteworthy, before a new re-immunization, the Abs response recovered to a similar extent of that achieved in previous immunizations.
These results suggest the generation of B memory cells, which are activated in response to a new immunization, so that it does not generate a response with sustained production of Abs, but rather a controlled response by immunization. Application of this vaccine would allow manipulation of treatments in such a way that may induce a controlled and not sustained Abs response against IL-15 in diseases such as RA which are characterized by periods of crisis and remissions [
49]. Particularly, the frequency of boosters could be optimized in this disease monitoring both Abs titers by ELISA and neutralizing activity in immune sera.
Another important result was recognition and neutralization of native IL-15 by Abs generated by immunization. This element is favorable if one considers that our aim with an anti-IL-15 vaccine is to develop a specific Abs response against native IL-15 capable of neutralizing this cytokine overexpression and its pathological effect. A native IL-15 containing disulfide bonds in correct positions was used in all test. Our results indicate that Abs present in immune sera from macaques neutralized native IL-15 activity; showing correspondence between Abs titers and neutralizing effects.
Although our strategy did not include the introduction of foreign immunodominant T-helper epitopes into native structure of the cytokine nor the fusion of the self-protein to a carrier, we demonstrated that immunization with mhIL-15 generated a specific neutralizing Abs response against native IL-15. We speculate that structural modifications of the mhIL-15 could favor an exposure of dominant epitopes that cooperates with B cells in generating a specific Abs response against IL-15. In previous studies, our group found that at least fusion of mhIL-15 with P64K protein as a carrier generates an antibody response that does not neutralize native IL-15 (unpublished results), but we do not rule out the possibility that fusion to another protein such as Keyhole limpet hemocyanin (KLH), Virus-like particles (VLP) or Ovalbumin (OVA) could develop a neutralizing Abs response against IL-15.
On the other hand, the specificity of neutralizing sera was determined in presence of IL-2, considering that CTLL-2 cells also proliferate with this cytokine. Although receptors for IL-2 and IL-15 share the β and γ
c subunits and some biological functions due to redundant effect have been described for these proteins [
50], in this study we demonstrate that sera generated by immunization with mhIL-15 does not inhibit IL-2-induced proliferation. In this cell line, no toxic effect caused by sera on CTLL-2 cells was observed, supporting the statement that the decrease on cell proliferation obtained in previous experiments with native IL-15, was due to the neutralizing capacity of Abs generated by immunization.
It has been proposed that an IL-15 antagonist could be useful for treating some autoimmune diseases in which IL-15 acts as proinflammatory cytokine. Particularly, high levels of IL-15 have been found in synovial fluids from RA patients [
51], and it is known that in response to IL-15, synovial T cells secrete TNF-α directly and induce TNF-α synthesis by macrophages through cognate interactions [
18,
52]. In this work, we demonstrated that immunization with mhIL-15 in Alum generates a neutralizing serum that slightly diminished levels of TNF-α in synovial cells, with or without IL-15 stimulation. Although, the number of tested patients is very small, these results suggest that this vaccine could be useful for treating RA taking into account that TNF-α is an important and validated target in RA, nevertheless additional experiments will be necessary to confirm this hypothesis.
Despite a high homology between human and simian IL-15 (97 % amino acid sequence identity), our results demonstrated that sera from animals immunized with mhIL-15 inhibited simian IL-15 biological activity in a CTLL-2 cell proliferation assay. This finding suggests that Abs against epitopes present in simian IL-15 were generated through vaccination, validating the use of this species as a model in evaluating the proposed strategy. In this sense, as security elements, we assessed the effects of immunization on cell populations that are important targets of IL-15, such as CD56
+ NK and CD8
+ T cells [
53,
54]. We found that vaccination with a mhIL-15 adjuvanted in Alum did not affect the percentage of cells with CD8 and CD56 markers.
Although in human two phenotypically and functionally distinct peripheral blood NK cell subsets have been described based on the expression of CD56 and CD16 [
55], in NHP the ability to investigate the role of NK cells in the models of disease has been greatly limited by the lack of appropriate phenotypic markers for this cellular population. In this study we used CD56 as a marker to assess NK cell. However, in previous studies in primates, the expression of CD56 was defined as a marker of a minor subset of NK cells [
56‐
59]. To confirm that vaccination do not affects the number of entire NK cells, it would be necessary further experiments before carry out a clinical trial with this approach. For this purpose we could use the human NK receptor monoclonal Abs for NKp80 and NKG2A, alone or in combination with anti-CD16 monoclonal Ab to identify the entire NK cell population in NHP. While anti-NKp80 recognized virtually all NK cells in macaques, anti-NKG2A proved to be significantly more specific than anti-NKp80 for simian NK cells. Nevertheless, the same specific recognition of NK cells could be achieved with anti-NKp80 if used in combination with anti-CD16 [
60].
This aspect is important in assessing the safety of the strategy we propose. While the goal is to apply this vaccine for therapeutic purposes in patients with elevated levels of IL-15, it is important to study a possible effect of immunization on the physiological activity of this cytokine in individual’s immune defense. Despite the fact that high affinity Abs against cytokines will not impair the physiology of normal tissues [
47] and that anti-cytokine vaccination have been demonstrated to be safe in experimental and clinical studies [
61‐
63], it would be necessary to demonstrate that immunization with IL-15 does not interfere with functionality of these cell populations.
In our research was not possible to study the variation on IL-15 levels in serum from immunized macaques because in physiological conditions exists many regulatory elements that allow the modest expression of IL-15 [
64]. In fact, in serum from healthy controls as well as in healthy NHP, the median IL-15 value was less than 2 pg/mL [
65,
66], so it is difficult to detect changes at this level. Therefore, it is tricky to study the variation on IL-15 levels in serum from the NHP used in the current work, although we agree that this is informative data and will be considered in the clinical trials of this therapeutic vaccine.
In parallel, all animals were monitored during the scheme by measuring temperature, body weight, heart rate and behavioral state. The biochemical parameters in blood were into the physiological limits established for these species. Only severe local lesions are observed in inoculation sites of animals immunized with IFA, some adverse events associated with use of this adjuvant [
67]. As future purposes of this work, it is necessary to demonstrate effectiveness of this vaccine in an animal model of the disease and in humans through clinical trials. Nevertheless, the use of NHP as a model can guide us on the clinical potential of this cytokine in humans due to the high homology between these species.
Acknowledgments
The authors thank Yolanda Gómez, Karen León, Carlos M. Díaz and Mey L. Reytor for the carefully revision of the manuscript and Ivette Raíces for statistical analyses. We would also like to thank Alejandro Martin and Alejandro Moro for linguistic advice.