Immunogenicity and protective efficacy of DNA vaccine against visceral leishmaniasis in BALB/c mice

Sukhbir Kaur, Tejinder Kaur, Jyoti Joshi

Parasitology Laboratory, Department of Zoology, Panjab University, Chandigarh 160014, India.

Immunogenicity and protective efficacy of DNA vaccine against visceral leishmaniasis in BALB/c mice

Sukhbir Kaur✉, Tejinder Kaur, Jyoti Joshi

Parasitology Laboratory, Department of Zoology, Panjab University, Chandigarh 160014, India.

The current study was designed to examine the protective efficacy of DNA vaccines based on gp63 and Hsp70 against murine visceral leishmaniasis. Inbred BALB/c mice were immunized subcutaneously twice at an interval of three weeks with pcDNA3.1(+) encoding T cell epitopes of gp63 and Hsp70 individually and in combination. Animals were challenged intracardially with 107promastigotes ofLeishmania donovani10 days post immunization and sacrificed 1, 2 and 3 months post challenge. The immunized animals revealed a significant reduction (P＜ 0.05) in splenic and hepatic parasite burden as compared to the infected controls. Maximum reduction in parasite load (P＜ 0.05) was observed in animals treated with a combination of pcDNA/gp63 and pcDNA/Hsp70. These animals also showed heightened DTH response, increased IgG2a, elevated Th1 cytokines (IFN-γ and IL-2) and reduced IgG1 and IL-10 levels. Thus, mice immunized with the cocktail vaccine exhibited significantly greater protection in comparison to those immunized with individual antigens.

visceral leishmaniasis, DNA vaccine, T-cell epitopes, gp63, Hsp70

Introduction

Leishmaniasis is a group of diseases comprised of three clinical entities： visceral leishmaniasis (VL), cutaneous leishmaniasis (CL) and muco-cutaneous leishmaniasis (MCL). The severest form of leishmaniasis is VL, or kala-azar, which is usually fatal if left untreated[1]. In India, the state of Bihar and adjoining areas of West Bengal, Jharkhand and Uttar Pradesh account for about half of the world's burden of VL[2]. Intensive efforts have been devoted to vaccine development against the disease because of the lack of effective and low-cost treatments and the irreversibility of tissue damage during infection. Because DNA vaccines elicit a strong Th1 bias in the immune response, they appear particularly promising in the case ofLeishmania[3]. Indeed, the superior efficacy, compared to their recombinant counterparts, of DNAvaccines encoding gp63, PSA-2 and LACK demonstrated the potential of this approach[4-8]. DNA vaccines induce a full spectrum of immune responses that include cytolytic T cells, helper T cells and antibodies[9]. The ability of plasmid DNA encoding specific antigen to induce both CD4+and CD8+T cells suggests that this approach will be of particular use for protection against diseases that require cell-mediated immunity, such as leishmaniasis. In a study by Rafati, the protective potential of an immunogenic gene, known asSPase(signal peptidase type I) fromLeishmania major(L. major), was evaluated using three different vaccination strategies (DNA/DNA, protein/ protein, and DNA/protein) againstL. majorinfection. The results suggested that a DNA/DNA strategy induced greater protection than the other two approaches[10]. The membrane protease gp63 is present in promastigotes of allspecies and is one of the parasite receptors for host monoclonal antibodies. Parasite mutants lacking the protein are avirulent[11]. It induced Th1 type of immune responses when used as vaccine in human models[5]. Recombinant BCG expressing theLeishmaniasurface antigen gp63 induced a protective immune response againstL. majorinfection in BALB/c mice[12]. In fact, gp63 or leishmaniolysin was the first recombinant antigen used to vaccinate against leishmaniasis.

Hsp70 has been shown to be a potent activator of innate immunity. AnLeishmania donovani(L. donovani) antigen belonging to the Hsp70 family is recognized by sera from the majority of patients with visceral leishmaniasis[13].Leishmania infantum(L. infantum) Hsp70 has been described as an immunodominant antigen in both humans and dogs suffering from VL. It has been found to be a major target of the humoral immune response duringLeishmaniainfections[14]. In addition, Hsp70 has been found to activate the complement system[15]and in the development of protective immune response. In our previous study, we reported the protective efficacy of a gp63 and Hsp70 cocktail vaccine against experimental murine VL[16], but the vaccine did not provide complete protection fromLeishmaniainfection. DNA vaccines may be able to induce a better immunity than protein vaccine; thus, in this study, the immunogenicity and efficacy of DNA vaccines encoding gp63 along with Hsp70 as an adjuvant was tested and compared with the protein counterparts to define the most promising antigen againstL. donovani.

Materials and methods

Parasite

Promastigotes ofL. donovani, strain MHOM/IN/80/ Dd8 were grown at ambient temperature of 22°C+1°C in RPMI-1640 medium supplemented with 10% FCS. TheL. donovanistrain was maintained by serial subcultures in the same medium after every 48-72 hours.

Animals

Inbred BALB/c mice of either sex, weighing 20-25 g, were obtained from the Central Animal House of Panjab University, Chandigarh, India. They were fed with water and foodad libitum. The ethical clearance to conduct the experiments was obtained from Institutional Animal Ethics Committee, Panjab University, Chandigarh and the study was done according to the established guidelines of CPCSEA (110/CAH).

Preparation of vaccines

Isolation of genomic DNA

Approximately 2×108log phase promastigotes were harvested by centrifugation at 2,000gfor 15 mintues at 4ºC. The pellet was washed once with phosphate buffer saline (PBS, pH 7.2) and finally suspended in the same. Totally 1×106promastigotes were taken in 800 µL of lysis buffer provided with the genomic DNA extraction kit (Zymo Research, USA). The isolated DNA was quantitated by NanodropTM.

PCR

The T cell epitopes of genes encoding gp63 (GenBank accession No. M60048) and Hsp70 (GenBank accession No. X85798) were identified using "MHC Pred" online software. The T cell epitopes were identified on the basis of prediction score for both mouse alleles,i.e.IAd and IEd. The primers were designed from the gene sequences available in the database using IDT "Scitools". The restriction enzyme sites forBamHI andHindIII and kozak sequences were added in the primers. The following primers were designed for amplification of 612 bp sequence of Hsp70： forward primer, 5'-GCA GGA TCC GCC ACC ATG GGC AAC GAG ATC-3' and reverse primer - 5'-GCG CAG CTC GAG TTA GAG GTC CTG GAA GAT-3'. The following primers were designed for amplification of 576 bp sequence of gp63： forward primer, 5'-GCA GGA TCC GCC ACC ATG GAC AAG CGC-3' and reverse primer 5'-CAG CTC GAG TTA GTG CCC TTC TCC TCC-3'. The following conditions were used for the amplification of the coding region of T cell epitopes of Hsp70 and gp63. Initial denaturation was performed at 94ºC for 10 minutes and then for 1 minute. Annealing was carried out for one minute at 55.4ºC for Hsp70 and 57ºC for gp63. Extension was carried out at 72ºC for 1 minute and final extension was done at the same temperature for 10 minutes. PCR was carried out for 40 cycles.

Preparation of DNA vaccine

DNA vaccines were prepared with pcDNA3.1 (+) vector. The fragments of genes encoding gp63 and Hsp70 were amplified using primers. The cloning of these fragments was done according to the manufacturer's instructions (Lucigen). Briefly, the PCR products were run on agarose gel electrophoresis and the desired DNA fragments were isolated and purified from the gel using a commercial DNA purification kit (Geneaid, Taiwan, China) following the manufacturer's instructions to avoid any contamination of unused primers and primer dimers. The purified DNA was quantified using NanodropTM.

Restriction digestions of PCR products and plasmid DNA were performed per the manufacturer's instructions (MBI Fermentas, Germany). The reaction mixture was mixed gently and incubated at 37°C. Double digestion of PCR products and the plasmid was carried out withBamH1 andHindIII. The double digested plasmid DNA and PCR products were electrophoresedand purified from the rest of the reaction mixtures with Gel Extraction kit (Geneaid) using the manufacturer’s protocol. Ligation reactions were set up using the linearized pcDNA3.1(+) and double digested PCR products. The ligation mixture was incubated at 16°C for 16 hours in water bath.

Transformation efficiency of the competent cells was checked by transforming them with an uncut plasmid and calculating the cfu/μg of DNA. The transformation efficiency of 1×108cfu/μg DNA and above was taken as a good competent cell preparation. Transformation ofE. coliDH5α cells was carried out per the instructions given by Sambrook and Russell[50]. The presence of thegp63andHsp70genes in pcDNA3.1(+) vector was determined by restriction enzyme digestion (data not shown) and then by PCR primers. Furthermore, thein vitroexpression of the inserted genes in vector pcDNA3.1 was checked by transfection of plasmid constructs in J774.2 cell lines from mouse macrophages.

In vivoimmunization and challenge infection

Immunization and infection of mice

Each group had 6 BALB/c mice. They were immunized by subcutaneous injections of 100 µg of pcDNA/ gp63 and pcDNA/Hsp70, free or in combination. Group I animals were immunized with gene encoding gp 63 alone, Group II were immunized with genes encoding Hsp70 alone and the animals in Group III were given the combination of both genes. Two injections were given at an interval of 3 weeks. Animals receiving only PBS served as unimmunized infected controls. Ten days after the booster, the immunized and unimmunized infected control mice were intracardially challenged with 107promastigotes.

Assessment of parasite load

Animals were sacrificed on 30, 60 and 90 days post infection/challenge. The livers and spleens of all animals were removed and weighed. Impression smears of the liver and spleen were made and the parasite load was assessed in terms ofL. donovanUnits (LDU) by the method of Bradley and Kirkley[17].

Delayed type hypersensitivity (DTH) responses to Leishmania

All groups of mice were challenged in the right foot pad with a subcutaneous injection of leishmanin. The left foot pads were inoculated with PBS. After 48 hours, the thickness of the right and left foot pad was measured using a pair of Vernier calipers. Results were expressed as mean ± S.D. of percentage increase in the thickness of the right foot pad as compared to the left footpad of mice[18-19].

ELISA

The specific serum immunoglobulin G (IgG) isotype antibody response was measured by conventional ELISA using commercially available kits (Bangalore Genei, India). ELISA plates were coated with crude antigen. Serum samples were added at two fold serial dilutions, followed by washes and addition of isotype specific HRP-conjugated secondary antibodies (rabbit anti-mouse IgG1 or IgG2a) after which the substrate and chromogen were added and absorbance was read on an ELISA plate reader at 450 nm.

For determination of vaccine-induced cytokine production, the lymphocytes from spleens of mice were cultured in 24 well plates in 1 mL of RPMI-1640 containing 20 mmol/L NaHCO3, 10 mmol/L HEPES, 10 U/ mL of penicillin, 100 µg/mL streptomycin, 2 mmol/LL-glutamine and 10% fetal calf serum. Cells were stimulated with 50 µg/mL of 63 kDa, 70 kDa or 63+70 kDa proteins. Cells were then incubated at 37ºC for 72 hours and supernatant was collected and stored at -20ºC. This was then assayed for IL-2, IL-4, IL-10 and IFN-γ by using ELISA kits (BenderMed Systems, Diaclone).

Statistical analysis

All the experiments were performed three times independently. All the data were analyzed using twoway analysis of variance (ANOVA). Post hoc test was used for multiple comparisons. The results were considered statistically significant whenP＜ 0.05.

Results

Parasite load

The splenic parasite load increased significantly (P＜ 0.05) from 30 to 60 days post infection and then decreased significantly (P＜ 0.05) from 60 to 90 days post infection in the unimmunized infected mice. However, in the immunized animals, the splenic parasite burden declined significantly (P＜ 0.05) from 30 to 90 days post challenge. A significant reduction in parasite load was observed in animals immunized with pcDNA/gp63 as compared to the infected controls. The pcDNA/Hsp70 genetic vaccine also caused a decline in the parasite burden. However, mice immunized with the cocktail DNA vaccine showed the least parasite burden as compared to those immunized with individual genetic vaccines (Fig. 1A).

The hepatic parasite load decreased significantly from 30 to 90 days post challenge/infection. However, the decrease was more significant (P＜ 0.05) in immunized animals as compared to the unimmunized infected mice. Similar to parasite burden of the spleen, minimum parasite load was observed in mice immunized with the combination of pcDNA/gp63 and pcDNA/Hsp70 (Fig. 1B).

Fig. 1Parasite load in terms ofL. donovanunits (LDU) in BALB/c mice immunized with different vaccine formulations. Infected micevs.mice immunized with Hsp70 or mice immunized with gp63 or mice immunized with gp63+Hsp70 or mice immunized with pcDNA/Hsp70 or mice immunized with pcDNA/gp63 or mice immunized with pcDNA/gp63+pcDNA/Hsp70; *P＜ 0.05.

DTH response to leishmanin

Immunization with vaccine containing pcDNA/gp63 and pcDNA/Hsp70 induced the highest level of DTH response which was significantly higher as compared to mice immunized with individual DNA vaccines (P ＜0.05), suggesting the generation of cell-mediated immune responses. The DTH responses in immunized animals were significantly higher than the unimmunized infected and unimmunized uninfected animals (P＜ 0.05). In immunized animals, the DTH responses were significantly increased from 30 to 90 days post challenge (Fig. 2).

Parasite-specific IgG1 and IgG2a isotypes

IgG1 and IgG2a antibody responses were also evaluated by ELISA using specific anti-mouse isotype antibodies. Mice immunized with combination of DNA vaccines revealed the highest level of Th1 regulated antibody, IgG2a. Th2 regulated antibody, IgG1, was the lowest in mice immunized with pcDNA/gp63 and pcDNA/Hsp70. IgG1 levels were significantly higher in the unimmunized infected animals as compared to the immunized mice (P＜ 0.05). Both IgG1 and IgG2a levels increased from 30 to 90 days post challenge (Fig. 3).

Vaccine induced cytokine responses

Th1 specific cytokines, that is, IFN-γ and IL-2 , were significantly higher in immunized mice as compared to the unimmunized infected and unimmunized uninfected animals (P＜ 0.05). Maximum concentrations of these cytokines were found in animals immunized with the combination of DNA vaccines in comparison to those immunized by pcDNA/gp63 or pcDNA/Hsp70 individually (Fig. 4). The difference within the groups was significant (P＜ 0.05).

Fig. 2DTH responses in BALB/c mice immunized with different vaccine formulations. Infected mice vs mice immunized with Hsp70 or mice immunized with gp63 or mice immunized with gp63+Hsp70 or mice immunized with pcDNA/Hsp70 or mice immunized with pcDNA/gp63 or mice immunized with pcDNA/gp63+pcDNA/Hsp70; *P＜ 0.05.

Th2 regulated cytokines IL-4 and IL-10 levels were the lowest in mice immunized with combination of pcDNA/ gp63 and pcDNA/Hsp70 (Fig. 5). Mice immunized with individual genetic vaccines showed significantly greater levels of these cytokines as compared to those immunized with the combination of antigens (P＜ 0.05).

Discussion

Fig. 3Levels ofLeishmania-specific antibodies (A： IgG2a , B： IgG1) in serum samples on different days post challenge in BALB/c mice immunized with different vaccine formulations.

Fig. 4Concentration of Th1 cytokines (A： IFN-γ, B： IL-2) in the supernatants of cultures of splenocytes of all groups of animals. The splenocytes were prepared from spleen collected on different days post challenge in BALB/c mice immunized with different vaccine formulations. Infected mice vs mice immunized with Hsp70 or mice immunized with gp63 or mice immunized with gp63+Hsp70 or mice immunized with pcDNA/ Hsp70 or mice immunized with pcDNA/gp63 or mice immunized with pcDNA/gp63+pcDNA/Hsp70; *P＜ 0.05.

DNA vaccination was introduced in 1990 by a study that demonstrated the induction of protein expression upon direct intramuscular injection of plasmid DNA in myocytes[20]. Several features of DNA vaccines have made them an attractive alternative to conventional methods of vaccination. These include the ability of DNA vaccines to express native protein antigensin situfor recognition by B cells and presentation by MHC class I and II molecules to prime helper T cells and CTLs (cytotoxic T lymphocytes), elicit robust immune responses in animal species, and be efficiently manufactured and well characterized[21]. DNA vaccines have been shown to induce a preferentially Th1 immune response, which is necessary for elimination of intracellular parasites[22-24]. DNA plasmids are good priming agents since they are internalized by antigen presenting cells and can induce antigen presentation via MHC class I or II. DNA plasmid backbones are immunogenic due to the presence of stimulatory unmethylated CpG motifs that readily induce Th-1 cytokine expression, leading to cell mediated immunity. Because cytokines or co-stimulatory cell surface molecules play a crucial role in generation of effector T-cell subsets and in determining the magnitude of response, plasmid DNA encoding various cytokines, or co-stimulatory molecules like IL-12, IFN-γ, GM- CSF, and TGF-β, etc. have been used to enhance or bias the immune response generated by DNA vaccination[25]. Cationic liposomes containing solubleLeishmaniaantigens and CpG ODNs have been reported to induce Th1 immune response and protection against leishmaniasis[26]. Recombinant gp63 has been found to be a potential vaccine candidate for CL[12]. It has been shown to be immunogenic and shows extensive cross reactions among differentLeishmaniaspecies[27]. gp63 has been found to stimulate expression of Th1 related cytokines which is a known indicator of protective immunity against leishmaniasis[28]. Also, genetic adjuvants have been found to increase the protective efficacy of DNA vaccines. AL. donovaniantigen, belonging to Hsp70 family, has been described which is recognized by sera from patients with VL[13]. Hsp70 acts as chaperones and the adjuvant effect of Hsp70 has been demonstrated after immunization withPlasmodiumpeptides[29]andL. infantum[30]. It has been used as an adjuvant along with DNA immunization with P4[31]. Therefore, the present study was conducted to test the protective efficacy of a DNA vaccine encoding gp63 along with gene encoding Hsp70 as an adjuvant against visceral leishmaniasis. The existence of drug-resistant strains ofL. donovaniand the increased prevalence of VL among HIV-positive patients have provided a new impetus to the search for a vaccine[32]. In a previous study, we worked on the immunoprophylactic potential of a gp63 and Hsp70 cocktail vaccine inL. donovaniinfected BALB/c mice[16]. The vaccine imparted significantprotection against the disease, but it could not eliminate the parasite completely. Therefore, to impart complete protection againstL. donovani, we vaccinated the mice subcutaneously with DNA vaccines comprising of a T-cell epitopic region of gp63 and Hsp70 genes individually and in combination. Subcutaneous route was chosen because, compared to the intramuscular route, the subcutaneous route is easier and safer to administer. Earlier workers have also reported protection against VL and CL with the help of DNA vaccines inoculated subcutaneously in mice[23,33]. The protective efficacy of the three vaccines in our study was assessed by the percentage reduction in the hepatic and splenic parasite load and immunogenicity was assessed through the detection of delayed type hypersensitivity responses, production of anti-leishmanial antibodies (IgG1 and IgG2a) and cytokines such as IFN-γ, IL-2, IL-4 and IL-10.

Fig. 5Concentration of Th2 cytokines (A： IL-4, B： IL-10) in the supernatants of cultures of splenocytes of all groups of animals. The splenocytes were prepared from spleen collected on different days post challenge in BALB/c mice immunized with different vaccine formulations. Infected mice vs mice immunized with Hsp70 or mice immunized with gp63 or mice immunized with gp63+Hsp70 or mice immunized with pcDNA/Hsp70 or mice immunized with pcDNA/gp63 or mice immunized with pcDNA/gp63+pcDNA/Hsp70; *P＜ 0.05.

In the present study, immunization of mice with gp63 and Hsp70 based DNA vaccines conferred significant protection against a progressive infection withL. donovani. The genetic vaccine comprising both pcDNA/ gp63 and pcDNA/Hsp70 significantly protected the BALB/c mice againstL. donovaniinfection and reduced the parasite load in the liver by 99.13% and in the spleen by 97.35%. The level of protection was enhanced in comparison to the protein vaccines used in our previous study where, in the animals immunized with a cocktail vaccine of gp63 and Hsp70, the parasite load declined by 82.21% to 92.61% as compared to the infected controls[16]. Similar to our study, Mazumderet al.[34]also reported durable protection againstL. donovanichallenge till 12 weeks post vaccination with CpG based gp63 vaccine. Similarly, cocktail DNA vaccine encoding cysteine proteinase I, II and III with solid nanoparticles imparted protection in mice againstL. majorinfection[35]. In another study, C57BL/6 mice were vaccinated subcutaneously with a mixture of plasmid DNAs encoding theLeishmaniaAgs LACK, LmSTI1, and TSA (AgDNA), which led to a complete protection against the development of dermal lesions, and a 100-fold reduction in peak dermal parasite loads compared with controls[51]. Moreover, Guhaet al.[52]observed that immunization with HbR-DNA (hemoglobin receptor-DNA) induces complete protection against virulentL. donovaniinfection in both BALB/c mice and hamsters.

The humoral responses to the vaccines were characterized by analyzing the distribution of IgG1 and IgG2a specific antibodies in the sera of immunized and control animals. ELISA results show that immunized groups developed higher level of antibody responses than control animals. IgG1 response is an indicator of Th2 type of immune response and IgG2a antibody response corresponds to Th1 response which is protective. Among the immunized groups, the highest IgG1 response was induced in mice immunized with pcDNA/Hsp70 followed by gp63 pcDNA/gp63 and the least antibody response was observed in the animals immunized with the combination of both the vaccines. In contrast, the IgG2a antibody production was found to be the maximum in mice immunized with pcDNA/gp63+ pcDNA/ Hsp70 genetic vaccine indicating towards the generation of Th1 response. This corresponds to a previous study where mice injected i.m. with 100 LgL. mexicanacDNA demonstrated high levels of IgG2a isotype antibody and low levels of IgG1 antibody[36]. Abdianet al.[37]also reported higher antibody levels in BALB/c mice immunized with LPG3 based DNA/DNA vaccine as compared to the DNA/protein vaccine approach.

A typical DTH reaction is characterized by activation and recruitment, predominantly of T cells and macrophages, at the intradermal injection site in a previously sensitized host[38]. Peak DTH responses were observed in animals immunized with the combination of pcDNA/gp63 and pcDNA/Hsp70 and these were followed by animals immunized with pcDNA/gp63 DNA vaccine. The immunized mice developed a strong cell mediated immune response and thereby resisted the challenge by parasites. The results demonstrated a positive correlation between enhanced DTH response and reduced parasite load for all groups. These results correspond with an earlier study where mongrel dogs infected withL.chagasiamastigotes and vaccinated with NH36-DNA vaccine developed a significant increase in DTH reactions[39].

The immune response (Th1 or Th2) generated by various vaccine formulations was assessed by quantifying the cytokines (IFN-γ, IL-2 and IL-10) produced by splenocytes of vaccinated animals. Mice immunized with pcDNA/gp63 and pcDNA/Hsp70 in combination showed a greater concentration of IFN-γ, the Th1 specific cytokine, in comparison to mice immunized with the individual genes. High levels of IFN-γ indicate the development of a protective Th1 immune response. Similar to our study, Gurunathanet al.[23]observed that the control of disease progression and parasitic burden in mice vaccinated with LACK DNA was associated with enhancement of antigen-specific IFN-γ production. This IFN-γ is found to come from natural killer cells and is thought to play an important role as a component of innate immune mechanism for the activation of macrophages[40]. Immunization of animals significantly increased the concentration of IL-2 in comparison to the infected controls. Similarly, the IL-2 levels were also found to be maximum in animals immunized with the combination of pcDNA/ gp63 and pcDNA/Hsp70 plasmids. IL-2 plays a critical role in priming naive CD4+ T cells to become IL-4 or IFN-γ producers[41]and it is a principal T cell growth factor for Th1 type of immune response. In contrast, IL-4 and IL-10 response was found to be maximum in infected control animals but declined significantly in immunized mice. The lowest concentrations of these two cytokines were observed in the animals immunized with the combination of pcDNA/ gp63 and pcDNA/Hsp70. IL-10 represents the main macrophage-deactivating cytokine and plays an important regulatory role in the progression of VL[42]. Our results are consistent with those obtained from the murine leishmaniasis model of both cutaneous and visceral diseases where expression of IFN-γ is associated with control of infection[43,44]. Studies on cytokine profiles in canine VL have established the predominance of theLeishmania-specific Th1 response in asymptomatic dogs and the role of IFN-γ as the key cytokine involved in the activation of macrophages and the killing of the intracellular amastigotes[45]. High levels of IL-10 in infected control animals supported the view that upregulation of this cytokine is accompanied by disease progression and depressed Th1 type of cell mediated immunity with decreased production of IFN-γ and IL-12[46-47]. Previous studies have also confirmed that IL-10 suppresses Th1 response, which plays a protective role against active VL[48]. Cytotoxic T lymphocyte activity of splenocytes was observed in mice immunized either withL. mexicanagp63 cDNA or SLA and long-lived CTL activity was observed in immunized and/or re-challenged mice but not naive mice infected with the parasite[35]. In BALB/ c mice,the intramuscular injection of aL. majorgp63 plasmid DNA construct resulted in partial protection againstLeishmaniainfection, where IFN- γ but not IL-4 was produced by immune CD4+ cells upon restimulation with parasite antigens, suggesting a bias towards a Th1 response[49-50].

Vaccination is the most cost-effective way of controlling infectious diseases. A successful vaccine would be one which is able to generate a long lasting immunity. DNA vaccines, in this regard, are more stable and have lower production costs compared to recombinant vaccines. These vaccines induce stronger and more durable immune responses through triggering innate immune responses. In the present study, the genes encoding T cell epitopes of gp63 and Hsp70 have been used for the first time. Moreover, the immune response generated suggests them as promising candidates for vaccine trials but further studies are needed in higher animal models before coming to a logical conclusion.

Acknowledgments

The authors acknowledge the support provided by the Indian Council of Medical Research, Department of Health Research, India for providing financial support for this study under project ref. 5/8-7(77)/2006-ECD-||.

[1] Ravindran R, Ali N. Progress in vaccine research and possible effector mechanisms in visceral leishmaniasis[J].Curr Mol Med, 2004, 4(6)： 697-709.

[2] Sundar S, Chatterjee M. Visceral leishmaniasis-current therapeutic modalities[J].Indian J Med Res, 2006, 123(3)： 345-352.

[3] Dumonteil E, RSM Jesus, EO Javier, et al. DNA vaccines induce partial protection against[J].Leishmania Mexicana Vaccine, 2003, 21(17-18)： 2161-2168.

[4] Gurunathan S, Prussin C, Sacks DL, et al. Vaccine requirements for sustained cellular immunity to an intracellular parasitic infection[J].Nat Med, 1998, 4(12)： 1409-1415.

[5] Olobo JO, Anjili CO, Gicheru MM, et al. Vaccination of vervet monkeys against cutaneous leishmaniasis using recombinantLeishmania major“surface glycoprotein”(gp63)[J].Vet Parasitol, 1995, 60(3-4)： 199-212.

[6] Rafati S, Kariminia A, Seyde-Eslami S, et al. Recombinant cysteine proteinases-based vaccines againstLeishmania majorin Balb/c mice： the partial protection relies on interferon gamma producing CD8+T Lymphocyte activation[J].Vaccine, 2002, 20(19-20)： 2439-2447.

[7] Sjolander A, Baldwin TM, Curtis JM, et al. Vaccination with recombinant parasite surface antigen 2 fromLeishmania majorinduces a Th1 type of immune response but does not protect against infection[J].Vaccine, 1998, 16(20)： 2077-2084.

[8] Sjolander A, Baldwin TM, Curtis JM, et al. Induction of a Th1 immune response and simultaneous lack of activation of a Th2 response are required for generation of immunity to leishmaniasis[J].J Immunol, 1998, 160(8)： 3949-3957.

[9] Kowalczyk DW, Ertl HCJ. Immune responses to DNA vaccines.Cell Mol Life Sci,1998, 55(5)： 751-770.

[10] Rafati S, Ghaemimanesh F, Zahedifard F. Comparison of potential protection induced by three vaccination strategies (DNA/DNA, Protein/Protein and DNA/ Protein) againstLeishmania majorinfection using signal peptidase type I in BALB/c mice[J].Vaccine, 2006, 24(16)： 3290-3297.

[11] Russell DG, Alexander J. Effective immunization against cutaneous leishmaniasis with defined membrane antigens reconstituted into liposomes[J].J Immunol, 1988, 140(4)： 1274-1279.

[12] Abdelhak S, Louzir H, Timm J, et al. Recombinant BCG expressing theLeishmaniasurface antigen gp63 induces protective immunity againstLeishmania majorinfection in BALB/c mice[J].Microbiol, 1995, 141 (Pt 7)： 1585-1592.

[13] Macfarlane J, Blaxter ML, Bishop RP, et al. Identification and characterization of aLeishmania donovaniantigen belonging to the 70 kDa heat shock protein family[J].Eur J Biochem, 1990, 190(2)： 377-384.

[14] Quijada L, Requena JM, Soto M, et al. Analysis of the antigenic properties of theL. infantumHsp70： design of synthetic peptides for specific serodiagnosis of human leishmaniasis[J].Immunol Lett, 1998, 63(3)： 169-174.

[15] Prohaszka Z, Singh M, Nagy K, Kiss E, et al. Heat shock protein 70 is a potent activator of the human complement system[J].Cell Stress Chaperone, 2002, 7(1)： 17-22.

[16] Kaur T, Sobti RC, Kaur S. Cocktail of gp63 and Hsp70 induces protection againstLeishmania donovaniin BALB/c mice[J].Parasite Immunol, 2011, 33(2)： 95-103.

[17] Bradley DJ, Kirkley J. Regulation ofLeishmaniapopulations within host I. the variable course ofLeishmania donovaniinfections in mice[J].Clin Exp Immunol, 1977, 30(1)： 119-129.

[18] Nagill R, Kaur S. Enhanced efficacy and immunogenicity of 78 kDa antigen formulated in various adjuvants against murine visceral leishmaniasis[J].Vaccine, 2010, 28(23)： 4002-4012.

[19] Kaur S, Kaur T, Garg N, et al. Effect of dose and route of inoculation on the generation of CD4+ Th1/Th2 type of immune response in murine visceral leishmaniasis[J].Parasitol Res, 2008, 103(6)： 1413-1419.

[20] Wolff JA, Malone RW, Williams P, et al. Direct gene transfer into mouse musclein vivo[J]. Science, 1990, 247(4949 Pt 1)： 1465-1468.

[21] Donnelly JJ, Liu MA, Ulmer JB. Antigen Presentation and DNA vaccines[J].Am J Respir Crit Care Med, 2000, 162(4 Pt 2)： S190-S193.

[22] Campos-Neto A, Webb JR, Greeson K, et al. Vacination with plasmid DNA encoding TSA/LmSTII leishmanial fusion proteins confer protection againstLeishmania majorinfection in Balb/c mice[J].Infect Immun, 2002, 70(6)：2828-2836.

[23] Gurunathan S, Sacks DL, Brown DR, et al. Vaccination with DNA encoding the immunodominant LACK parasite antigen confers protective immunity to mice infected withLeishmania major[J]. J Exp Med, 1997, 186(7)：1137-1147.

[24] Seder RA, Hill AVS. Vaccine against intracellular infections requiring cellular immunity.Nature, 2000, 406： 793-8.

[25] Gurunathan S, Klinman DM, Seder RA. DNA vaccines：immunology, application and optimization[J].Annu Rev Immunol, 2000, 18： 927-974.

[26] Heravi Shargh V, Jaafari MR, Khamesipour A, et al. Cationic liposomes contatining solubleLeishmaniaantigens (SLA) plus CpG ODNs induce protection against murine model of leishmanaisis[J].Parasitol Res, 2012, 111(1)： 105-114.

[27] Jaffe CL, Bennett E., Grimaldi G Jr, et al. Production and characterization of species specific monoclonal antibodiesagainstLeishmania donovanifor immunodiagnosis[J].J Immunol, 1984, 133(1)： 440-447.

[28] Habibi GR, Khamesipour A, McMaster WR, et al. Cytokine gene expression in healing and non-healing cases of cutaneous leishmaniasis in response toin vitrostimulation with recombinant gp63 using semi-quantitative RT-PCR[J].Scand J Immunol, 2001, 54(4)： 414-420.

[29] Barrios C, Lussow AR, Van Embden J, et al. Mycobacterial heat-shock proteins as carrier molecules. II. The use of the 70 kDa mycobacterial heat shock protein as carrier for conjugated vaccines can circumvent the need for adjuvants and Bacillus Calmette Gue´rin priming[J].Eur J Immunol, 1992, 22(6)： 1365-1372.

[30] Rico AI, Del Real G, Soto M, et al. Characterization of the immunostimulatory properties ofLeishmania infantumHsp70 by fusion to theEscherichia colimaltose- binding protein in normal and nu/nu BALB/c mice[J].Infect Immun, 1998, 66(1)： 347-352.

[31] Campbell K, Diao H, Ji J, et al. DNA immunization with the gene encoding p4 nuclease ofLeishmania amazonensisprotects mice against cutaneous leishmaniasis[J].Infect Immun, 2003, 71(11)： 6270-6278.

[32] Afrin F, Anam K, Ali N. Induction of partial protection againstLeishmania donovaniby promastigote antigens in negatively charged liposomes[J].J Parasitol, 2000, 86(4)： 730-735.

[33] Aguilar-Be I, Zardo RD, Paraguai de Souza E, et al. Crossprotective efficacy of a prophylacticLeishmania donovaniDNA vaccine against visceral and cutaneous murine leishmaniasis[J].Infect Immun, 2005, 73(2)： 812-819.

[34] Mazumder S, Maji M, Das A, et al. Potency, efficacy and durability of DNA/DNA, DNA/Protein and Protein/ Protein based vaccination using gp63 againstLeishmania donovaniin BALB/c Mice[J].PLoS ONE, 2011, 6：e14644.

[35] Doroud D, Zahedifard F, Vatanara A, et al. Delivery of a cocktail vaccine encoding cysteine proteinases I, II and III with solid lipid nano particles potentiates protective immunity againstLeishmania majorinfection[J].J Con Rel, 2011, 153(2)： 154-162.

[36] Ali SA, Rezvan H, Mcardle SE, et al. CTL responses toLeishmania mexicanagp63-cDNA vaccine in a murine model[J].Parasite Immunol, 2009, 31(7)： 373-383.

[37] Abdian N, Gholami E, Zahedifard F,. Evaluation of DNA/ DNA and prime-boost vaccination using LPG3 againstLeishmania majorinfection in susceptible BALB/c mice and its antigenic properties in human leishmaniasis[J].Exp Parasitol.2011, 127(3)： 627-636.

[38] Black CA. Delayed type hypersensitivity： current theories with an historic perspective[J].Dermatol Online J, 1999, 5(1)： 7.

[39] Borja-Cabrera GP, Santos FB, Nico D, et al. The Leishmune Nucleoside hydrolase DNA vaccine as an aid in immunotherapy of canine visceral leishmaniasis[J].Pro vaccinol, 2012, 6： 64-73.

[40] Nylen S, Maasho K, Soderstrom K. LiveLeishmaniapromastigotes can directly activate primary human natural killer cells to produce interferon -gamma[J].Clin Exp Immunol, 2003, 131(3)： 457-467.

[41] Seder RA, Paul W E. Acquisition of lymphokine- producing phenotype by CD4+T cells[J].Annu Rev Immunol, 1994, 12： 635-673.

[42] Tripathi P, Singh V, Naik S. Immune response toLeishmania： paradox rather than paradigm[J].FEMS Immunol Med Microbiol, 2007, 51(2)： 229-242.

[43] Heinzel FP, Sadick MD, Holaday BJ, et al. Reciprocal expression of interferon gamma or interleukin 4 during the resolution or progression of murine leishmaniasis. Evidence for expansion of distinct helper T cell subsets[J].J Exp Med, 1989, 169(1)： 59-72.

[44] Squires KE, Schreiber RD, McElrath MJ, et al. Experimental visceral leishmaniasis： role of endogenous IFN-gamma in host defence and tissue granulomatous response[J].J Immunol, 1989, 143(12)： 4244-4249.

[45] Carrillo E, Moreno J. Cytokine profiles in canine visceral leishmaniasis[J].Vet Immunol Immunopathol, 2009, 128(1-3)： 67-70.

[46] Carvalho EM, Bacellar O, Barral A, et al. Antigen- specific immunosuppression in visceral leishmaniasis is cell mediated[J].J Clin Invest, 1989, 83(3)： 860-864.

[47] Ghalib HW, Piuvezam MR, Skeiky YA, et al. Interleukin 10 production correlates with pathology in humanLeishmania donovaniinfections[J].J Clin Invest, 1993, 92(1)： 324-329.

[48] Murphy ML, Wille U, Villegas EN, et al. IL-10 mediates susceptibility toLeishmania donovaniinfection[J].Eur J Immunol, 2001, 31(10)： 2848-2856.

[49] Walker PS, Scharton-Kersten T, Rowton ED, et al. Genetic immunization with glycoprotein 63 cDNA results in a helper T cell type 1 immune response and protection in a murine model of leishmaniasis[J].Hum Gene Ther, 1998, 9(13)： 1899-1907.

[50] Xu D, Liew FY. Protection against leishmaniasis by injection of DNA encoding a major surface glycoprotein, gp63, ofL. major[J].Immunology,1995, 84(2)： 173-176.

[51] Sambrook J, Russell DW. Molecular Cloning： A Laboratory Manual, 3rd Edition. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2001.

[52] Méndez S, Gurunathan S, Kamhawi S, et al. The potency and durability of DNA and proteinbased vaccines against Leishmania major evaluated using lowdose, intradermal challenge[J].J Immunol,2001, 166(8)： 5122-5128.

[53] Guha R, Gupta D, Rastogi R, et al. Vaccination withLeishmaniaHemoglobin Receptor-Encoding DNA Protects Against Visceral Leishmaniasis[J].Sci Translational Med, 2013, 5(202)： 202ra121.

✉Corresponding author： Sukhbir Kaur, Parasitology Laboratory, Department of Zoology, Panjab University, Chandigarh 160014, India. Tel/Fax： 0172-541942/+91172-2747725, E-mail： puzoology@yahoo.com.

© 2016 by the Journal of Biomedical Research. All rights reserved.

Received 01 September 2015, Revised 05 November 2015, Accepted 16 December 2015, Epub 10 March 2016

R382.2+2, Document code： A.

The authors reported no conflict of interests.

10.7555/JBR.30.20150125