Available reports suggest that, Leishmania donovani antigen KMP-11 may be significant in the modulation of immune responses in visceral leishmaniasis (VL). This study evaluated vaccine prospect of presentation of KMP-11 antigen through murine dendritic cells against VL in infected BALB/c mice. We report here that immunization with KMP-11 delivered through bone marrow derived dendritic cells can lead to killing of L. donovani in infected BALB/c mice. Furthermore, the strategy to use KMP-11 as vaccine delivered through DCs can stimulate the production of IFN-g, IL-12, IL-2R and TNF-α with concomitant down-regulation of IL-10 and IL-4. Furthermore, anti-leishmanial defence function (ROS) of splenocytes was observed increased in the presence of DC-delivered KMP-11 vaccination accompanied with an increased p38-MAPK signalling in vaccinated splenocytes. We summarized from our data that KMP-11 delivered through DCs has potential for eliciting protective immunity through pro-inflammatory cytokines (IFN-γ, IL-12, IL-2, TNF-α) following an up-regulation in signalling event of p38-MAPK. Therefore the study suggests a new control strategy against VL in future.
Leishmania, a protozoan pathogen, is a causative agent of various forms of Leishmaniasis like cutaneous (CL), mucocutaneous (MCL), and visceral leish- maniasis (VL), of which VL is almost fatal if untreated [
Infection of Leishmania parasite in dendritic cells has been reported in several studies [
The outer membrane of Leishmania is covered by a dense glycocalyx consisting mostly lipophosphoglycan (LPG) [
Bone marrow cells from BALB/c mice were taken and cultured for 8 - 9 days in 6 well plates in the presence of murine recombinant GM-CSF (20 ng/ml) (BD Biosciences, USA) and antibiotics (Sigma, USA) in complete RPMI-5 media (supplemented with FSC 5%) [
Briefly, splenocytes were subjected to immunogen at 3 different concentrations (5, 10 & 20 µg/mL) for 48 h incubation followed by RPMI-MTT treatment (1 mg/mL) at 37˚C for 3 h then it was kept in isopropanolic solution for another 15 min and finally absorbance was taken at 570 nm [
The recombinant KMP-11 protein was obtained as described previously [
BALB/c mice were divided into 5 groups: (a) uninfected control, (b) infected control, (c) immunized with DC-KMP-11 and infected, (d) immunized with SLA and infected and (e) immunized with Con-A and infected. Mice were immunized by intramuscular injection in the hind thigh with sterile saline on days 1 and 15. On day 27, immunized mice were challenged with intra-cardial injection of 1 × 107 virulent strain of freshly transformed L. donovani (AG83) promastigotes. Finally, animals were sacrificed on 60 days after infection, and spleen from different groups were isolated to determine splenic parasite burden. The number of parasites present in the spleen was determined by microscopic evaluation of Giemsa-stained tissue imprints as described previously [
Briefly, a weighed portion of spleen from different groups of experimental mice 60 days after infection was dissected out and mildly homogenized in complete medium 199 (M199, Sigma USA) and re-suspended at a final concentration of
1 mg/mL in the same medium. Cells were washed, fixed in methanol and giemsa stained for enumeration and expression of parasite load as amastigotes/100 macrophage. To further determine the efficacy of DC-primed KMP-11 as vaccine, splenocytes were washed and stained with popidium iodide (PI) for FACS determination of percentage of killing in different groups of animals. The mean of fluorescence intensity of the cells were analyzed by flow cytometry FACS Calibur and CellQuest software.
Proliferation of splenocytes isolated on day 60 after infection from the infected groups of mice (n = 10) was measured in response to KMP-11 (10 µg/mL). Briefly, single cell suspensions of splenocytes were plated at a concentration of 0.1 × 106 cells in 96 well plates and were allowed to proliferate for 3 days at 37˚C in a 5% CO2 incubator in the presence or absence of KMP-11 antigen (10 µg/mL). Cell proliferation was determined by BrdU (5-bromo-2’ deoxyuridine) incorpo- ration on FACS Calibur. Soluble leishmania antigen (SLA) was used as control.
Subsequent experiments were performed to look at the potential of vaccination to drive CD4 T-cell cytokine response in splenocytes of vaccinated mice. Splenocytes were isolated by density gradient centrifugation over Ficoll-Paque (Pharmacia, Uppsala, Sweden). Cells (2 × 106/mL) were cultured in 12-well plates for 24 h with purified L. donovani protein (KMP-11). The culture conditions involved humidified 5% CO2 incubation at 35˚C ± 1˚C, 6 h prior to completion of incubation, the plate was supplemented with monensin containing golgi stop (2 µM/mL final concentration, Pharmingen). The cells were then harvested using ice-cold PBS plus azide, cytofixed using 2% formaldehyde. The cells were then permeabilized with a solution of saponin and stained for 30 min using antimouse cytokine antibodies directly conjugated with FITC (IFN-γ, IL-12 & IL-2R), APC (IL-4 and IL-10). PE and FITC labeled immunoglobulin control antibodies as well as a control of unstimulated peripheral blood mononuclear cells (PBMCs) were included in these experiments. The cells were acquired and analyzed within 24 h through FACS Calibur (Flow Cytometer, Becton Dickinson, USA) [
Measurements of reactive oxygen species (ROS) activity in splenocytes were accomplished with flow cytometry. Briefly, 100 µL of splenocyte blood was triggered with N-Formylmethionine-leucyl-phenylalanine (FMLP; 5 mg/mL) at 37˚C in a water bath for 10 min, followed by further incubation with 20 µL of 10 mm dihydrorhodamine-123 (DHR-123) at 37˚C in a water bath for 15 min to allow for the internalization of the later into the cell and converted into green fluorescent compound which binds to oxidative bursts produced by stimulated cells. Further incubation, erythrocytes were lysed at room temperature with 2 mL FACS lysing reagent, washed (1×PBS, 268 g, 5 min) and re-suspended in 450 mL PBS containing 1% paraformaldehyde. The ROS produced by the stimulated cells were measured as mean fluorescence intensity (MFI) and detected by flow cytometry (FACS Calibur).
All data were expressed as mean ± SE (standard error of the mean). One way analysis of variance with Tukey post-hoc test was carried out using Graph Pad Prism 5, USA software. A value of significance p < 0.05 was considered statistically significant.
DCs from bone marrow of BALB/c mice were obtained as described earlier. Finally, viable cells were counted by inverted microscopic analysis (Figures 1(a)-(c)) and assessed the yield of DCs by Flow Cytometry. DCs were positive for CD86 and DEC 205 (
It was observed that 10 µg/ml KMP-11 given with 1 × 106 DC resulted in highest viability of splenocytes (
The presence of antibodies (1:500 & 1:1000) against KMP-11 in successful treated VL patients sera was detected in western blot analysis with purified protein. We found that treated VL patients sera had antibody against KMP-11 antigen (
DC primed rKMP-11 immunization protects against VL. DC primed KMP-11 immunized animals were challenged with L. donovani and no. of intracellular parasites were compared on day 60 post infection in spleen from different groups of animals (
DCs count | |||
---|---|---|---|
KMP-11 (Concentration) | 0.5 × 106 | 1.0 × 106 | 2.0 × 106 |
5 µg/mL | 0.410 | 0.604 | 0.712 |
10 µg/mL | 0.414 | 0.812 | 0.452 |
20 µg/mL | 0.612 | 0.680 | 0.521 |
Immunization days | Immunized groups (% Killing) | Infected groups | |
---|---|---|---|
SLA | DC-KMP | ||
Day 10 | 100 | 400 | 35 |
Day 21 | 50 | 125 | 40 |
Day 42 | 55 | 115 | 25 |
Day 60 | 60 | 132 | 22 |
We observed enhanced T-cell proliferation from splenocytes in response to KMP-11 antigen in DC-KMP-immunized group compared to infected group (p < 0.001). Functional significance of splenocyte proliferation upon re-stimulation to KMP-11 antigen was determined by production of BrdU and IL-2R. Furthermore, the higher trend of proliferation triggered by KMP-11 was corroborated by higher production of BrdU (~9.7 fold, p < 0.001) andIL-2R (~2.1 fold, p < 0.01) compared to untreated infected control (
As functionally more splenocytes proliferated upon antigenic re-stimulation to KMP-11 antigen, we further extended our investigation to understand nature of immune response generated by vaccination. A total of 10 mice each was tested for this investigation from different study group. As shown in Figures 5(a)-(e) significant increase was observed in IFN-γ production in DC-KMP-11 immunized mice in comparison to un-immunized infected mice (p < 0.001). DC? KMP-11 immunization in response to rKMP-11 protein showed about 6.38 fold (p < 0.001) more IFN-γ, 4.40-fold (p < 0.001) more IL-12 and 3.26 fold (p < 0.001) more TNF-α, whereas cells from SLA vaccinated mice produced about 1.57, 2.36 (p < 0.05), and 1.79 (p < 0.01) fold more IFN-γ, IL-12 and TNF-α, respectively in comparison to controls (Figures 5(a)-(c)). In contrast, vaccination with DC primed KMP-11 inhibited the production of IL-10 by 5.81 (p < 0.001) and 1.08 fold (
Because reactive oxygen species are important leishmanicidal molecules, we examined if KMP-11 immunization contributed to L. donovani elimination by inducing ROS. It was observed that DC-KMP vaccination increased ROS production by about 3.54 fold in comparison with infected control (p < 0.001). These results suggest the requirement of ROS in KMP-11 mediated Leishmania killing. Because Leishmania suppresses the host protective response such as expression of ROS by modulating p38MAP kinase, we examined whether DC- KMP-11 immunization modulated p38MAP kinase in infected macrophages. We observed that p38MAPK which is associated with IL-12 production and development of protective immunity was significantly up-regulated in DC-KMP immunized groups of infected mice compared to non-vaccinated infected groups (p < 0.001). These results indicate that DC-KMP immunization enhances the protective responses by modulating the p38MAP-Kinase phosphorylation (
This study gives a new vaccine strategy of dendritic cell presented KMP-11 as immunogen for control against experimental VL. It was also apparent that KMP-11 antigen promoted the activation of DCs in particular compared to L. donovani infected mice that produced IL-12.
LPG linked KMP-11 is the major protein on the promastigote surface which plays a key role in immunity against L. donovani [
are linked with immune protection [
We earlier reported the cytokine response produced by KMP-11 antigen in DCs had an upliftment of IFN-γ and IL-12 production with down-regulation in IL-4 and IL-10 production. The information became the initial breakthrough in testing the efficiencies of KMP-11 antigen through dendritic cell.
There was ample evidence on the abilities of KMP-11 immunomodulation through DCs which clear Leishmania amastigotes in infected animals more effectively than un-immunized groups. The above encouraging findings on immunization and vaccine prospect of DC primed KMP-11 in the study prompted to look at the infected splenocytes. Previously, Padigel et al., and Jones et al. found the outcome of experimental leishmaniasis in mice is determined by a balance Th1 and Th2 cells [
KMP-11 primed in DCs triggered the release of IL-2 and IL-2R on day 60 after infection ensuring a higher durability for proliferation in T-cells. DC?KMP-11 immunization in response to rKMP-11 protein showed about 6.38 fold more IFN-γ, 4.40-fold more IL-12 and 3.26 fold more TNF-α, whereas cells from SLA vaccinated mice produced about 1.57, 2.36 and 1.79 fold more IFN-γ, IL-12 and TNF-α, respectively in comparison to controls. In contrast, vaccination with DC primed KMP-11 inhibited the production of IL-10 by 5.81 and 1.08 fold and reduced the production of IL-4 by 2.47 and 1.16 fold, respectively, compared to controls. The disease promoting cytokines such as IL-10 were down-regulated following immunization. Pro-inflammatory cytokines such as IFN-γ and TNF-α play a critical role in the induction of ROS during VL [
We also investigated about KMP-11 mediated alteration in signaling pathways that result in the production of pro-inflammatory cytokines such as IL-12. We have shown that the effector response in form of ROS and IL-12 was mainly because following priming DCs with KMP-11, the defective p38MAPK was restored in splenocytes. The p38MAPK inhibition increased parasite load, but impaired ROS production and IL-2 secretion. In conclusion, we report a new vaccine approach for control against VL.
This work was supported by the I.C.M.R, Ministry of Health and family welfare, Government of India. We are indebted to ICMR for the fellowship awarded to Rajesh Chaudhary to pursue this study. We are also thankful to Manish Ranjan, Ajay Raj and technical assistance by Santosh K. Singh and Santosh K. Sinha for their support.
Ethical approval was taken from Ethical Committee of this Institute (RMRIMS, Patna).
Chaudhary, R., Amit, A., Kumar, A., Dikhit, M.R., Pandey, K., Das, P. and Bimal, S. (2017) A New Vaccine Strategy of Dendritic Cell Presented Kinetoplastid Membrane (KMP-11) as Immunogen for Control against Experimental Visceral Leishmaniasis. Modern Re- search in Inflammation, 6, 15-28. https://doi.org/10.4236/mri.2017.63003