- Open Access
Mesenteric lymph node cells from neonates present a prominent IL-12 response to CpG oligodeoxynucleotide via an IL-15 feedback loop of amplification
© Ferret-Bernard et al; licensee BioMed Central Ltd. 2011
- Received: 2 August 2010
- Accepted: 30 September 2010
- Published: 2 February 2011
At birth, the immune system is still in development making neonates more susceptible to infections. The recognition of microbial ligands is a key step in the initiation of immune responses. It can be mimicked to stimulate the immune system by the use of synthetic ligands recognising pattern recognition receptors. In human and mouse, it has been found that neonatal cytokine responses to toll-like receptor (TLR) ligands differ in many ways from those of adults but the relevant studies have been limited to cord blood and spleen cells. In this study, we compared the responses in neonate and adult sheep to CpG oligodeoxynucleotides (ODN), a TLR9 ligand, in both a mucosal and a systemic organ. We observed that in response to CpG-ODN more IL-12 was produced by neonatal than adult sheep cells from mesenteric lymph nodes (MLN) and spleen. This higher IL-12 response was limited to the first 20 days after birth for MLN cells but persisted for a longer period for spleen cells. The major IL-12-producing cells were identified as CD14+CD11b+. These cells were poor producers of IL-12 in response to direct stimulation with CpG-ODN and required the cooperation of other MLN cells. The difference in response to CpG-ODN between neonates and adults can be attributed to both a higher proportion of CD14+CD11b+ cells in neonate lambs and their higher capacity to produce IL-15. The IL-15 increases IL-12 production by an amplifying feedback loop involving CD40.
- Spleen Cell
- Mesenteric Lymph Node
- Adult Sheep
- Commensal Flora
Immune responses in neonates differ from those in adults due to differences in the relative proportions, phenotypes and functional properties of their immune cells [1–4]. In infant and neonate mouse a Th2 bias has been reported that leads to a reduced capacity to respond efficiently to vaccines that rely on a Th1 immune response for their efficacy. Immunoprophylactic strategies have therefore to be adapted for neonates and properly targeted. Pattern recognition receptors are expressed by cells of the innate immune system and identify microbial components or cellular stress. Toll-like receptors (TLR) belong to this family of receptors, and are attractive targets for immunostimulation strategies; consequently, many synthetic molecules that mimic bacterial or viral components have been generated. Synthetic CpG oligodeoxynucleotides (CpG-ODN) resembling bacterial DNA have been extensively used to promote Th1 immune responses  and to control both systemic and mucosal infections. We observed that a single administration of CpG-ODN to neonate mice can greatly reduce infection by Cryptosporidium parvum by inducing the production IFNγ, a cytokine central to the control of this zoonotic parasite infecting intestinal epithelial cells [7, 8]. CpG-ODN have also been shown to be safe to use in veterinary species, [9, 10] and effective in ruminants for controlling bacterial [11, 12], parasitic  and viral infections . The potential of CpG-ODN for stimulating innate immune responses has been also demonstrated in neonate lambs in a study by Nichani et al. reporting that their administration can reduce viral shedding of bovine herpes virus-1 .
The specificities of the responses of human and mouse neonatal cells have been described. However, the relevant studies were limited to human cord blood cells and mouse spleen cells. Neonate small ruminants, being much bigger than rodent animal models, allow the recovery of large numbers of cells from various tissues facilitating investigations. In addition, data obtained in human or mouse cannot be directly extrapolated to veterinary species despite the conservation of TLR throughout evolution. This is because TLR responses to their agonists may differ between species due to differential expression among immune cell populations or differences in binding or signalling [16–18]. Exploiting the advantages of a large animal model, the goats, we previously investigated the cytokine response to various TLR ligands of cells isolated from neonatal and adult lymph nodes draining the intestine. The intestine is subjected to many changes after birth due to exposure to dietary antigens and colonization by the commensal flora. In response to TLR stimulation, neonate mesenteric lymph nodes (MLN) cells presented a stronger IFNγ and IL-12 response than their adult counterparts . Although CD8+ lymphocytes were identified as being responsible for the IFNγ production, the precise nature of the cells secreting IL-12 was not identified.
Using lambs as a model, we describe further investigations regarding the age-related differences of cytokine responses to TLR ligands. In particular, we aimed to determine until what age neonate MLN and spleen cells continued to produce more IL-12 than their adult counterparts in response to CpG-ODN stimulation and the reasons for the difference.
Animals and cell isolation
The Préalpes adult sheep (aged 6 ± 1 year), neonates (aged 6 to 14 days) and lambs (aged 20 days) used were reared in conventional but protected sanitary facilities (PFIE, INRA, F-37380 Nouzilly, France). Newborn lambs were not separated from their mothers until one day after birth, to allow them to suckle colostrum. They were then fed ad libitum with reconstituted milk. Experimental protocols were designed in compliance with French law (Décret 2001-464 29/05/01) and EEC regulations (86/609/CEE) concerning the care and use of laboratory animals. Euthanasia was performed after electric stunning according to AMVA guidelines (2007) on euthanasia. Cells from freshly removed MLN or spleen were isolated as previously described .
CpG-2006 5'TCGTCGTTTTGTCGTTTTGTCGTT3' and control-CpG-2006 (Ctl-ODN) 5'TGCTGCTTTTGTGCTTTTGTGCTT3' have a phosphorothioate backbone and were purchased from Sigma-Aldrich (Lyon, France). Recombinant human TGFβ1 and recombinant type I interferons (IFN) (IFNα hybrid, constructed with human IFN αA and αD is active in all mammalian species) were obtained from AbD Serotec (Oxford, UK). Recombinant human IL-15 was from Immunotools (Friesoythe, Germany). Recombinant ovine IL-12 and IL-10 were kindly provided by S. Wattegedera (Moredun Research Institute, Edinburgh, UK). Anti-CD40 mAb supernatant clone ILA156 originally produced by J. Naessens (ILRAD, Nairobi, Kenya) was provided by I. Schwartz-Cornil.
CpG-ODN stimulation and cytokine quantification by ELISA and by bioassay
Mesenteric lymph node (MLN) or spleen cells were stimulated for 48 h, at a density of 1.5 × 106/mL in complete RPMI 1640 medium (Gibco-Invitrogen, Cergy-Pontoise, France) supplemented with 10% FCS, 100 IU/mL penicillin, 100 μg/mL streptomycin sulphate and 50 μM β-mercaptoethanol (Merck Chemicals Ltd., Nottingham, UK) with Ctl-ODN (1 μM) or CpG-2006 (1 μM). In the IL-12 neutralisation assay, mouse anti-bovine IL-12 (clone CC301, Serotec) or its isotype control (mouse IgG2a, Caltag-Invitrogen) was added, at a concentration of 10 μg/mL, at the same time as the TLR agonist.
In some experiments, rhTGFβ1, rovIL-10, rh type I IFN or rhIL-15 was added to MLN cells at the same time as Ctl-ODN or CpG-2006. Culture supernatants were harvested and stored at -20°C until assayed for the detection of cytokines by ELISA. Intracellular staining for IL-12 (clone CC301, AbD Serotec) was performed on MLN cells cultured in complete RPMI medium with Ctl-ODN or CpG-2006 for 25 h. Brefeldin A (Sigma) was added to the cells at a concentration of 5 μg/mL, for the last 5 h of culture.
Pairs of antibodies against bovine cytokines were obtained from AbD Serotec; these antibodies have been shown to recognise ovine IL-12 [20, 21], IFNγ  and IL-10 [20, 22]. ELISA was carried out as previously described . Incubations were performed at 37°C for IL-10 ELISA and at room temperature for the other ELISA. To assess biologically active TGFβ1 secretion by ovine cells, we used the TGFβ1 Emax® ImmunoAssay System (Promega, Charbonnières-les-Bains, France) according to the manufacturer's instructions.
Type I IFN in cell supernatants were quantified using a cytopathic effect reduction assay with Madin-Darby bovine kidney cells challenged with vesicular stomatitis virus. An internal recombinant IFNα reference was included as described elsewhere . Each supernatant was tested over eight serial dilutions. Results are expressed as type I IFN units per mL.
Colistin treatment and Gram negative bacterial enumeration
Control and colistin-treated animals were separated from their mothers directly after birth and bottle-fed every 12 h for the first day with preheated ewe colostrum containing or not containing 50 000 IU/kg body weight of colistin (Virbac, Carros, France). Thereafter, they were fed daily ad libitum with reconstituted milk containing or not containing 100 000 IU/kg body weight of colistin (Virbac) until the age of 20 days. Mean body weights were used to prepare the milk containing colistin: 3 kg for 2- to 8-day-old, 4 kg for 9- to 14-day-old and 7 kg for 15- to 20-day-old lambs. Lambs were slaughtered at age 20 days and both MLN (for in vitro cell stimulation as previously described) and distal ileum contents were collected. To determine the total number of Gram -ve bacteria, serial dilutions of ileal content homogenised in PBS were plated onto Drigalski lactose agar (selective medium for the isolation of Gram -ve bacteria). The plates were incubated overnight at 37°C and colonies counted.
Cell sorting and flow cytometry
A high-speed MoFlo cell sorter (Dako, Trappes, France) was used to sort freshly isolated total MLN cells. In these experiments, cells were labelled with a mouse antibody specific for ovine CD14 (clone CAM36A, VMRD, Pullman, USA) and stained with a fluorochrome-conjugated goat anti-mouse immunoglobulin antibody (Caltag-Invitrogen). Lymph granulocytes in sheep display intermediate levels of CD14 expression . CD14+ cell sorting was therefore always performed after gating on non-granulocytic MLN cells according to SSC/FSC analysis, although most granulocytes were removed on the Histopaque gradient. Both CD14+ and CD14- cell fractions were cultured in vitro, with Ctl-ODN or CpG-2006, or were directly analysed by qRT-PCR.
For intracellular staining of IL-12, stimulated cells were cultured in the presence of Brefeldin A for the last 5 h. First, the following purified monoclonal antibodies directed against ovine markers were used for surface staining: CD11b (clone MM12A, VMRD), CD14 (clone CAM36A, VMRD), MHC class II (clone 28.1, AbD Serotec) and CD205 (clone CC98, AbD Serotec). Fixed and permeabilised cells were then incubated with the mouse anti-bovine/ovine IL-12 antibody (clone CC301, AbD Serotec).
Sorted CD14+ cells were fixed, post-fixed, dehydrated in a graded series of ethanol solutions and embedded in Epon resin (Sigma). Ultrathin sections were cut, stained and examined under a Jeol 1010 transmission electron microscope (Jeol, Croissy-sur-Seine, France).
RNA isolation and real-time RT-PCR
RNA was extracted with the NucleoSpin RNA II kit (Macherey-Nagel, Hoerdt, France), according to the manufacturer's instructions and quantified using Nanodrop (Thermo Fisher Scientific, Courtaboeuf, France). Purified RNA was reverse-transcribed using oligo(dT) primers and M-MLV reverse transcriptase (Promega). Primer pairs were designed using Primer 3 software (Additional file 1, Table S1). Each primer was designed on different exons to span the intervening intron and thus avoid amplification from contaminating genomic DNA. For each primer pair, all qPCR displayed an efficiency of between 90% and 110%. Diluted cDNA was combined with primers and IQ SYBRGreen Supermix (Bio-Rad, Hercules, USA) according to the manufacturer's recommendations and real-time assays were run on a Bio-Rad Chromo 4 (Bio-Rad). The specificity of the qPCR reactions was assessed by analysing the melting curves of the products and size verification of the amplicons. To minimise sample variations, we used identical numbers of cells and high quality RNA. Hypoxanthine phosphoribosyltransferase (HPRT) mRNA levels were used to normalise RNA quantification.
Non-parametric Mann-Whitney (two groups) and Kruskal-Wallis (three or more groups) statistical tests were used to compare unpaired values. In case of paired values, paired t-tests were performed.
IL-12 and IFNγ responses of neonatal and adult MLN cells to CpG-ODN stimulation
Age-dependent IL-12 responses of MLN and spleen cells to CpG-ODN stimulation
Effect of Gram negative intestinal flora on the response of neonatal MLN cells to CpG-ODN
IL-12-producing cells among lamb bulk MLN cells
CD14 + and CD14- cells purified by flow cell sorting from neonate and adult MLN were stimulated with CpG-2006. The absence of CD14+ cells inhibited greatly IL-12 secretion not only in neonate (67 ± 7%) but also in adult (85 ± 8%) samples, indicating the essential role of these cells in both groups (Figure 4D). Some CD14- cells participated in the residual IL-12 secretory activity (33 ± 7%) in neonates and (15 ± 8%) in adults. We cultured the same numbers of neonate or adult sorted CD14+ cells in the presence of CpG for 48 h but very little or no IL-12 was detected. Therefore, CD14+ are poor IL-12-producing cells in the absence of CD14- cells, suggesting an indirect activation mechanism (Figure 4D). Flow cytometry analyses also revealed that the proportion of CD14+ cells among bulk MLN cells was twice as high in neonates as in adults (Figure 4E). Although we did not observe a direct correlation between the proportion of CD14+ cells in the MLN and the IL-12 response to CpG-2006 (data not shown), this quantitative difference may nevertheless contribute to the higher responsiveness of neonatal MLN cells to CpG-ODN.
Effects of TGFβ1, IL-10 and type I IFN on the cytokine response to CpG-ODN
We next searched for differences that may affect the signal provided by CD14- cells to CD14+ cells for IL-12 production. It has been reported that type I IFN either stimulate or inhibit IL-12 production by myeloid cells [29, 30]. TLR9-triggering of plasmacytoid DC (pDC) induces the secretion of large amounts of type I IFN . We investigated exactly how type I IFN influence IL-12 secretion by CD14+ MLN from neonates and adults stimulated by CpG-2006. Interestingly, rhIFN (IFNα hybrid) displayed suppressive properties on both neonate and adult MLN cells (Figure 5E). We performed a type I IFN bioassay on supernatants from neonate and adult MLN cells after CpG-2006 stimulation to test whether the lower IL-12 response in adults was associated with higher levels of type I IFN, but no difference in type I IFN concentrations were observed (Figure 5F).
Role of IL-15 in the IL-12 response of MLN cells to CpG-ODN
Neonates are more sensitive to infections in particular when exposed to poor sanitary conditions before their immune system is fully developed. It is therefore important to develop immunoprophylactic strategies dedicated to neonates. With the discovery of TLRs and their importance in the initiation of immune responses to invading pathogens, a large set of new synthetic adjuvants has been developed including CpG-ODN for use against infectious disease and cancer [33–35]. In human and mouse, the age-dependent response to TLR has only been documented in cord blood cells and spleen cells, respectively [36–38]. The size of small ruminants facilitates investigation of these responses in different organs including mucosal tissues and their draining lymph nodes [19, 28].
Here, we report that cells isolated from the MLN and spleen in neonate lambs produced more IL-12 than their equivalents in adults in response to CpG-2006. This higher IL-12 production was responsible in large part for the higher IFNγ response in neonatal stimulated MLN cells as revealed by in vitro IL-12 neutralisation assay. We next examined the age until which neonate cells produced more IL-12 than adults and found that this stronger IL-12 response was restricted to about the first two weeks of life: from age 20 days MLN from lambs produced similar amounts of IL-12 as those from adults. Interestingly, spleen cells from 20-day-old lambs continued to produce more IL-12 in response to CpG-ODN suggesting that a rapid and specific change in TLR agonist responsiveness occurs in MLN. During this period, the dietary regimen of lambs was similar with reconstituted milk provided ad libitum. As MLN drain the intestinal tissue, we thought that the progressive installation of the commensal flora might have influenced TLR9 responsiveness. Indeed, Gram -ve bacteria are important for lymphoid tissue development . We set up a protocol to control Gram -ve bacteria by feeding lambs with reconstituted milk containing the antibiotic colistin. Although dramatically reducing Gram -ve bacterial counts in the intestine of 20-day-old lambs, this treatment did not significantly affect the capacity of MLN cells to produce IL-12. We next investigated the role of regulatory cytokines, including IL-10 and TGFβ1 produced in large amounts in intestinal tissue. These cytokines effectively suppressed IL-12 production by MLN cells stimulated with CpG-2006. Although, in response to CpG-2006 stimulation in vitro, they were produced in similar amounts by MLN cells whatever the age of the animal and only detected for some animals. Adult MLN cells activated with CpG-ODN presented a slightly higher sensitivity to these cytokines at certain concentrations. Therefore we cannot exclude that for some animals it may participate to the lower IL-12 response of adults. Booth et al.  identified a CD5-CD21 + B cell population in the ileal Peyer's patches (iPP) in adult sheep. These cells reduce the expression of IFNγ and IL-12 by iPP cells stimulated with CpG-ODN by producing large amount of IL-10. However, in agreement with our results the authors did not observe any similar regulatory mechanism in the MLN . To continue, we needed to identify the cell population responsible for IL-12 production. Intracellular IL-12 staining revealed that cells expressing CD14 and CD11b were the main producers. These cells have a dendritic morphology and resemble sheep bone marrow-derived DC [26, 27]. Possibly, these myeloid cells originate from blood monocytes and differentiate into inflammatory DC. These DC are known to produce abundant IL-12 and potently stimulate Th1 responses . We observed that the percentage of CD14+ cells was higher in MLN of neonates than of adults. This might contribute to the higher IL-12 response of neonate MLN but we did not observe a direct correlation between the percentage of CD14+ cells in MLN and the level of IL-12 produced after CpG stimulation; consequently, we do not think that this is the complete explanation. CD14+ cells respond poorly to direct CpG-2006 stimulation but require the cooperation of other cells to release IL-12. It has been reported that Mycobacterium bovis-induced IL-12 secretion by bovine DC is enhanced by WC1+ γδ T cells . Moreover, Hedges et al. observed that bovine γδ T cells express different TLR including TLR9 and respond directly to some pathogen-associated molecular patterns like LPS and peptidoglycan, however in this study the response of γδ T cells to CpG-ODN was not investigated . Therefore in our experimental model γδ T cells may cooperate with CD14+ cells for the IL-12 response to CpG-ODN. Another population, pDC have been shown to cooperate with the IL-12 response of conventional DC (cDC) to CpG-ODN . Activated pDC produce alpha IFN, cytokines that in our experimental model inhibited the IL-12 response of MLN cells stimulated with CpG-2006. After stimulation, we found only a low level of type I IFN activity. This is probably because CpG-2006 is a class B-ODN and this class induces type I IFN much more weakly than do class A- and class C-ODN. However, the level of type I IFN activity released by neonates and adults being equivalent, this cannot explain the difference in IL-12 production observed. Kuwajima et al. showed that CpG-treated IL-15-deficient mice produced little IL-12 . They observed that CpG-stimulated cDC were the main producers of both IL-15 and IL-12, but cDC did not produce IL-12 in the absence of pDC. After CpG-2006 stimulation, we observed a much stronger concurrent upregulation of IL-12p40 and IL-15 mRNA in MLN cells from neonate than adult sheep suggesting that in adults IL-15 availability may be insufficient for the full activation. We therefore added exogenous IL-15 to CpG-stimulated adult MLN cell and observed an increase in IL-12 production of up to a three-fold. When a CD40 mAb was added to the culture medium, it reduced IL-12 production by half. This is consistent with the findings of Kuwajima et al.  who observed that IL-15-induced CD40 expression by cDC and interaction between CD40 on cDC and CD40 ligand on pDC led to IL-12 production by cDC. IL-15 therefore plays a key role in the innate response to CpG and seems to act via a feedback amplification loop. We recently demonstrated that IL-15 is also an important molecule for NK cells in neonates, another innate immune cell population . Indeed, NK cells from one week-old neonate calves expanded in presence of IL-15, but not IL-2, presented both a higher cytotoxicity than their equivalents from older animals in direct lysis assay and a higher IFNγ response to IL-12 when associated with NKp46 receptor stimulation.
Here, we demonstrate the potential of CpG-ODN to induce a preferential Th1-type cytokine and IL-15 response in neonate lambs. CpG oligonucleotides are therefore potentially useful molecules for enhancing the efficacy of vaccines against intracellular pathogens affecting these animals.
We would like to thank T Chaumeil and E Guitton for supplying us with animals and for helping us with the neonates and during the antibiotic treatment protocol. We would also like to thank Y Le Vern for expert technical assistance with cell sorting and A Brée for her help with bacteriology procedures. We are grateful to S Wattegedera for providing recombinant ovine cytokines, which were produced at the Moredun Research Institute with funding from the Scottish Executive Environment and Rural Affairs Department (SEERAD) in collaboration with the BBSRC/SEERAD Immunological Toolbox initiative. We are thankful to I Schwartz-Cornil (INRA Jouy-en-Josas) for providing anti CD40 mAb supernatant originally produced by J Naessens (ILRAD, Nairobi, Kenya).
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