Increased expression of CD25, CD83, and CD86, and secretion of IL-12, IL-23, and IL-10 by human dendritic cells incubated in the presence of Toll-like receptor 2 ligands and Giardia duodenalis
© Obendorf et al.; licensee BioMed Central Ltd. 2013
Received: 9 October 2013
Accepted: 1 November 2013
Published: 4 November 2013
Effects of Giardia duodenalis on dendritic cell (DC) functions may contribute to the pathogenesis of chronic giardiasis. G. duodenalis lysate has been shown to inhibit the activation of murine DCs through the ligands of various Toll-like receptors (TLRs), including TLR2 and TLR4. Our study aimed at translating these findings to human DCs.
As described previously for murine DCs, also human DCs were only weakly activated by the parasite itself. LPS-stimulated DCs incubated in the presence of G. duodenalis lysate produced less IL-12/23p40 (p = 0.002), IL-12p70 (p = 0.011), and IL-23 (p = 0.004), but more IL-10 (p = 0.006) than cells incubated in the absence of the parasite. Concomitantly, the expression of CD25, CD83, CD86, and HLA-DR was reduced on G. duodenalis- incubated DCs as compared to control cells. In contrast, human DCs stimulated through TLR2 in combination with TLR1 or TLR6 and G. duodenalis lysate secreted significantly more IL-12/23p40 (p = 0.006), IL-23 (p = 0.002), and IL-10 (p = 0.014) than cells stimulated through TLR2 ligands alone. Ligands for TLR2/TLR1 or TLR2/TLR6 also induced enhanced extracellular expression of CD25, CD83, and CD86 (p < 0.05).
In contrast to murine DCs, human DCs incubated in the presence of G. duodenalis and stimulated through TLR2 show increased activation as compared to cells incubated in the absence of the parasite. Thus, TLR2 ligands, e.g., delivered by probiotic lactobacilli, might be beneficial in human giardiasis through an adjuvant effect on the induction of cellular immune responses against G. duodenalis.
KeywordsDendritic cells Giardia duodenalis Toll-like receptors CD25 CD83 CD86 IL-12 IL-23 IL-10
Giardia duodenalis is the most frequent parasitic agent of gastroenteritis worldwide and has been targeted as part of the WHO “Neglected Disease Initiative” since 2006 . In East Africa, for example, we and others have observed prevalences of >60% in children younger than five years [2, 3]. Notably, chronic (or recurrent) giardiasis in children has been associated with malnutrition, wasting, and stunting as well as reduced cognitive functions at a later age .
The pathogenesis of chronic giardiasis is poorly understood and both parasitic and host factors might be involved. The parasite is non-invasive but stays in the intestinal lumen where it adheres to epithelial cells. Since CD4+ T helper cells are involved in protection against G. duodenalis, chronic infection might result from insufficient antigen presentation that does not lead to the development of protective cellular immunity. Dendritic cells (DCs) might be critically involved in the induction of anti-Giardia immune responses as they are able to reach with their cellular protrusions into the gut lumen and sample antigen . Following antigen-uptake, DCs may process and present specific peptides to naïve T lymphocytes, and DCs activated through ligands of pattern-recognition receptors (PRRs), e.g., Toll-like receptors (TLRs), C-type lectins, and nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs), are essential for the induction of specific cellular immunity . A recently published study with murine DCs has shown that G. duodenalis lysate may interfere with the activation of DCs through TLR2 or TLR4 in vitro. Signals through both receptors might be relevant for the induction of anti-Giardia immune responses because G. duodenalis by itself only weakly activates murine DCs . In vivo, bacteria belonging to the gut flora might deliver the required stimuli to G. duodenalis-processing DCs since TLR2 may recognize lipoproteins derived from Gram-positive while TLR4 binds LPS of Gram-negative bacteria .
The present study aimed at translating the previous findings from murine to human DCs. To monitor DC activation, we focused on the expression of typical surface markers and cytokine production . Regarding cytokines, we analyzed the secretion of members of the IL-12 family. IL-12 is a pro-inflammatory cytokine, which consists in its biologically active form, IL-12p70, of a light chain (IL-12p35) and a heavy chain (IL-12p40), and favors the differentiation of Th1 cells . IL-12p40 (together with a p19 subunit) may also be part of IL-23, which drives the development of T helper cells that secrete IL-17 (Th17) . In addition, we analyzed the secretion of the anti-inflammatory cytokine, IL-10.
Preparation of G. duodenalis lysate
G. duodenalis strain WB-C6 (ATCC 50803) trophozoites were propagated in TYI-S-33 medium as previously described . Parasites were harvested and washed by centrifugation through PBS. Pellets were resuspended in PBS, and the parasites counted and diluted to a concentration of 108 parasites/ml. Lysates were prepared by subjecting the suspensions in three consecutive freezing-thawing cycles.
Generation of human DCs
DCs were generated as described previously . Briefly, peripheral blood mononuclear cells were isolated from buffy coats obtained from healthy donors (German Red Cross, Berlin). CD14+ monocytes were separated with magnetic microbeads (Miltenyi Biotec, Bergisch-Gladbach, Germany) and cultured at 3x106 cells/well in 6-well cell culture dishes (Nunc, Roskilde, Denmark) for six days in medium consisting of RPMI 1640 supplemented with 2 mM L-glutamine, 10 mM HEPES, penicillin (1,000 U/ml)-streptomycin (1,000 μg/ml) (all from Gibco, Invitro-gen, Karlsruhe, Germany), 50 μM 2-mercaptoethanol (Sigma, Taufkirchen, Germany), 10% fetal calf serum (Biochrom, Berlin, Germany), 1000 U/ml human rGM-CSF (sargramostim, Leukine®, Berlex, Richmond, CA, USA), and 100 U/ml human rIL-4 (R&D Systems, Wiesbaden-Nordenstadt, Germany). On days 2 and 4, fresh medium and cytokines were added to the wells.
Incubation of human DCs with G. duodenalis lysate and TLR ligands
On day 6, DCs were harvested and transferred to 96-well round-bottom trays (Nunc) at 105 cells/well. The TLR stimuli Pam2CSK4 and Pam3CSK4 (100 ng/ml; Invivogen, Toulouse, France) or LPS (1 μg/ml; derived from Escherichia coli 0111:B4, Sigma) were added and the cells incubated in the presence or absence of G. duodenalis lysate (equivalent to five trophozoites/cell). Immature cells kept in medium were equally incubated in the presence or absence of G. duodenalis lysate.
Flow cytometric analyses
The phenotype of DCs was monitored by flow cytometry with PE- or FITC-labeled anti-human mAbs against HLA-DR, CD14, CD25, CD86 (all BD Pharmingen), CD83 (Caltag Laboratories, Hamburg, Germany), or the appropriate isotype controls, as previously described . Cells were fixed with 10% formalin/PBS (v/v) before analysis on a FACScan® cytometer with CELLQuest®Pro software (BD Pharmingen). Percentages of positive cells and median fluorescence intensities (MFIs) were calculated.
Analysis of cytokine secretion by DCs
Cell-free supernatants of cell cultures were harvested after 48 h and stored at -80°C until analysis by sandwich ELISAs for IL-12p40, IL-12p70, and IL-10 (all U-CyTech, Utrecht, The Netherlands), or IL-23 (eBioscience). Samples with known cytokine concentrations provided by the manufacturers of the ELISA kits were included in each analysis and used to create standard curves. Only values within the linear section of these curves were considered. The level of detection was 5 pg/ml for all assays.
Data were analyzed statistically with the nonparametric Wilcoxon matched-pairs signed rank test using GraphPad Prism version 6.0a for Mac OS X. Differences were considered statistically significant for p < 0.05.
We incubated human immature monocyte-derived DCs in the presence or absence of G. duodenalis lysate with the TLR4 ligand LPS or with ligands binding to TLR2/TLR1 or TLR2/TLR6, i.e., Pam3CSK4 and Pam2CSK4, respectively, since TLR2 is expressed together with either TLR1 or TLR6 . Control cells were kept in the absence of TLR ligands. Two days later, supernatants were collected and the cells harvested.
DC activation markers expressed by human DCs incubated in the presence of ligands for TLR4, TLR2/TLR1, or TLR2/TLR6, and in the presence or absence of G. duodenalis lysate
LPS + Gd
Pam3CSK + Gd
Pam2CSK4 + Gd
84 [73, 90]#
82 [66, 88]*
8 [3, 21]
20 [7, 30]*
10 [3, 27]
21 [9, 35]*
90 [85, 95]
84 [80, 93]*
18 [12, 51]
35 [22, 59]*
23 [15, 51]
39 [24, 63]*
98 [97, 99]
96 [93, 97]*
51 [48, 61]
67 [59, 79]*
56 [48, 71]
70 [61, 86]*
99 [98, 99]
97 [95, 98]*
88 [84, 97]
90 [86, 97]
88 [84, 96]
92 [84, 97]
Thus, while we could translate the previous murine data regarding the inhibition of LPS-stimulated DCs through G. duodenalis to the human cell system, we observed the opposite for DCs stimulated through TLR2. Exposure of TLR2-activated DCs to G. duodenalis considerably enhanced the expression of crucial surface molecules and the secretion of cytokines belonging to the IL-12 family.
In contrast to TLR4 ligands and in contrast to murine DCs, TLR2 ligands may augment the antigen-presenting functions of human DCs in giardiasis. Although the LPS-induced cytokine responses were comparably stronger than those induced by the TLR2 ligands, which might be due to the concentrations of the stimuli used, we feel that the data together, i.e., opposite results for cytokine secretion and also surface molecule expression for the stimuli tested, may argue for an additive effect of TLR2 and G. duodenalis on human DC functions. In contrast, G. duodenalis apparently may interfere with immune responses induced by human DCs activated through TLR4 agonists.
Probiotic Lactobacillus spp. are recognized by human DCs through TLR2 and NOD2 , and may induce – dependent on TLR2 – the secretion of IL-12, IL-10, and type I interferons as shown for murine DCs . In a Gerbil model, interestingly, lactobacilli interfere with G. duodenalis infection in vivo, and this effect could partly depend on TLR2 signaling. Although this remains to be investigated, our demonstration that G. duodenalis can augment TLR2-mediated DC function suggests that TLR2 ligands might be of considerable interest in the management of clinical giardiasis. Since an anti-giardial effect by Lactobacillus spp. on murine giardiasis is also evident when the bacteria are administered together with anti-giardial drugs  or in malnourished animals , clinical studies are warranted in which the potential benefit of lactobacilli in the treatment of human giardiasis patients may be evaluated as a combination of bacteria with standard therapy, e.g., metronidazole or tinidazole, but also in therapy-refractory chronic giardiasis.
We thank Petra Gosten-Heinrich for excellent technical assistance. This study was supported by the Charité – Universitätsmedizin Berlin and in part by a grant to T.A. (01KI1019) from the National Research Platform for Zoonosis, which is funded by the German Federal Ministry of Education and Research (BMBF).
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