About this Journal Submit a Manuscript Table of Contents
Clinical and Developmental Immunology
Volume 2011 (2011), Article ID 697340, 10 pages
http://dx.doi.org/10.1155/2011/697340
Review Article

The Role of the IL-12 Cytokine Family in Directing T-Cell Responses in Oral Candidosis

Tissue Engineering and Reparative Dentistry, School of Dentistry, Cardiff University, Heath Park, Cardiff CF14 4XY, UK

Received 14 June 2010; Accepted 3 September 2010

Academic Editor: John J. Taylor

Copyright © 2011 Xiao-Qing Wei et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Candida albicans is an opportunistic fungal pathogen that normally exists as a harmless commensal in humans. In instances where host debilitation occurs, Candida can cause a range of clinical infections, and whilst these are primarily superficial, effecting mucosal membranes, systemic infections can develop in severely immunocompromised individuals. The mechanism of host immunity during commensal carriage of C. albicans has been intensively studied. In this paper, we present the most recent information concerning host recognition of C. albicans leading to cytokine production and the subsequent T-cell responses generated in response to C. albicans. Particular focus is given to the role of the IL-12 cytokine family including IL-12, IL-23, IL-27, and IL-35, in host immunity to Candida. T-cells are considered crucial in the regulation of immunity and inflammation. In this regard, the role of Th1/2, helper cells, together with the recently identified Th17 and Treg cells in candidosis will be discussed. Understanding the detailed mechanisms that underlie host immunity to Candida not only will be of benefit in terms of the infections caused by this organism but could also be exploited in the development of therapeutic interventions for other diseases.

1. Introduction

Candida albicans is normally a harmless commensal fungus of humans and has been shown to colonise up to 70% of individuals without any detriment to health [1, 2]. During commensal carriage, a balance exists between the body’s own defence systems and the continued persistence of the organism at a level that does not induce disease. However, in instances where there is disruption to this equilibrium, either through environmental factors that promote the growth of Candida or through a weakening of the host’s immune system, then proliferation of Candida and subsequent infection can arise. Clear examples of this occur in HIV-infected individuals or those patients receiving chemotherapy for treatment of cancer [35]. In these situations, a depletion of host T-cell function and that of other cells involved in establishing an appropriate immune response occurs with the result that candidosis can ensue.

Candidosis most frequently presents as superficial lesions of moist mucosal membranes, particularly those of the vagina and oral cavity. However, in severely immunocompromised individuals and particularly where there is neutropenia, systemic infections can develop which are often fatal. Most immunocompetent individuals have an underlying acquired immunity which is thought to prevent dissemination of mucosal candidal colonisation through the body. Individuals who are existing carriers of Candida are however deemed to be at an increased risk of developing systemic forms of the disease. The type of immune response generated is key in determining whether C. albicans clearance, infection, or commensal carriage occurs.

Oral candidosis is not a single disease entity and four distinct clinical forms of primary infection are recognised. Pseudomembranous candidiasis frequently occurs in newborn babies and in these instances is associated with an immature immune system. In older individuals the condition occurs when there is mild debilitation or local immunosuppression in the host as seen in asthma sufferers who use a corticosteroid inhaler as part of their treatment regime [6]. With the advent and escalation of HIV infection and AIDS, chronic forms of pseudomembranous candidosis are evident, which frequently reoccur despite administration of antifungals.

Acute erythematous candidosis is an infection that presents as a painful reddened lesion on the dorsum of the tongue and is associated with an overgrowth of Candida following broad spectrum antibiotics. Such lesions tend to resolve spontaneously after antibiotic therapy has been completed [7]. Chronic erythematous candidosis is the most prevalent form of oral candidosis affecting over 65% of denture wearers, often asymptomatically. It is thought that poor denture hygiene contributes to the infection that occurs on the palate beneath the upper fitting surface of the denture. Chronic hyperplastic candidosis is another chronic infection that presents as a white lesion on the oral mucosa, most frequently bilaterally on the buccal mucosa. The infection is particularly significant as it is associated with malignant change at the lesional site, although the role of Candida in this process remains unclear [8].

In addition to these primary infections, secondary oral infections are recognised and include angular cheilitis and median rhomboid glossitis. Angular cheilitis presents as lesions in the angles of the mouth from which Candida albicans is frequently recovered, often in combination with the bacterium Staphylococcus aureus [9]. Median rhomboid glossitis presents as a chronic tongue lesion within which Candida is detected by biopsy in over 85% of cases.

Chronic mucocutaneous candidiasis (CMC) is a collective term for a range of syndromes that result in the persistent occurrence of severe and diffuse cutaneous candidal infections. These infections manifest on the skin, nails, and mucous membranes (including the oral cavity) of CMC patients. Invariably, there is an underlying dysfunction in cell-mediated immunity that leads to the occurrence of CMC [10].

Neutrophils and macrophages are major components of the innate immune response and play an important role in the control of mucosal C. albicans colonisation. These cells are responsible for the phagocytosis of Candida and can kill the fungus through release of reactive oxygen species (ROS). Cytokines produced by T-cells, such as IFN- and IL-17 will promote neutrophil and macrophage activity against Candida [11, 12]. Neutrophils and macrophages recognise C. albicans via pattern recognition receptors (PRRs) and following recognition will also produce an array of cytokines and chemokines.

Dendritic cells (DCs) function as professional antigen presenting cells (APCs) that detect the presence of Candida at mucosal sites. DCs will interact with the fungus and become activated, with phagocytosis being the first action of the activated cell. After phagocytosis, DCs migrate to the nearest lymph node where the Candida antigen is processed and presented by the DCs to naïve CD4+ T-cells [1318]. The naïve T-cells then differentiate into mature effective T-cells under the direction of the DCs [19]. Examples of such differentiated T-cells include T-helper 1 (Th1), T-helper 2 (Th2), T-helper 17 (Th17), and regulatory T-cells (Tregs). The latter serve to control T-cell responses to avoid an overreactive immune response [20], and in this manner, an inducible Treg cell development can balance pathogenic and physiologic host immune responses [2124].

Activated DCs produce a variety of cytokines to direct T-cell differentiation, and the IL-12 family of cytokines (IL-12, IL-23, IL-27, and IL-35) would appear to play an important role in this T-cell differentiation [2527]. It is the relative level and type of cytokines that are expressed by the DCs into the local environment that will ultimately determine type of T-cell response (Th1, Th2, and Th17) generated. In this paper, we will discuss the role that members of the IL-12 cytokine family play in the host immune responses and their possible relationship in effecting either tolerance of fungal colonisation or the development of oral infection.

2. Candida albicans Recognition by Host DCs

As previously mentioned, the main function of DCs is to act as professional APCs that link the innate and adaptive host immune responses in combating host invading pathogens. Human peripheral blood-derived DCs are the main source of mucosal DCs, and it is these immature cells that will initially recognise Candida through various surface protein antigens and mannose and -glucans in the fungal cell wall [5].

The initial antigen recognition by DCs is mediated through the expression of pattern-recognition receptors (PRRs) on the surface of DCs. The nature of this interaction between DCs and the fungus is the key factor in determining whether immune activation or tolerance occurs [8]. The first group of PRRs identified were the toll-like receptors (TLRs) and to date, 10 of these TLRs have been identified in humans, with TLR2, TLR4 TLR6, and TLR9 implicated in host cell recognition of C. albicans [2830]. TLRs are type I membrane proteins and are either homodimer or heterodimer receptors, recognising various pathogen antigens including proteins, cell wall sugars, or DNA/RNA molecules (collectively referred to as pathogen-associated molecular patterns or PAMPs). Recently a new group of type II cell membrane molecules have been linked to the recognition of fungi by host cells, and these are referred to as C-type lectin-like receptors (CTLLRs) [31]. Dectin-1 and 2 are examples of CTLLRs and interact, respectively, with the -glucan and mannose components exposed in the C. albicans cell wall [32, 33]. Binding of dectin-1 to -glucan components of C. albicans will trigger host immune cell responses, and signalling is thought to be mediated through the Syk kinase pathway and the transmembrane adaptor caspase recruitment domain 9 (CARD9) leading to induction of the cytokines IL-23 and IL-6, but not IL-12 [34]. Interestingly in CMC patients, a CARD9 point mutation that leads to the generation of a premature termination codon (Q295X) has recently been identified [35].

Synergistic effects of dectin-1 with TLR2 and TLR4 signalling have been shown to enhance proinflammatory cytokine production by human peripheral blood monocytes (PBMCs) [36]. Recently, mutation in the human dectin-1 gene was identified in 4 women within a single family, who were all suffering from vulvovaginal candidosis. Monocytes isolated from these homozygote mutant patients all exhibited significantly reduced binding to C. albicans. These cells also produced less IL-6 and IL-17 cytokines [37].

3. The Role of the IL-12 Cytokine Family in Host Immunity

Many cytokines can be produced by APCs, although it is those belonging to the IL-12 family that would appear to be significant in controlling T-cell differentiation. This family of cytokines consists of at least 4 heterodimeric protein members and includes the cytokines IL-12, IL-23, IL-27 and IL-35 (Figure 1).

697340.fig.001
Figure 1: Schematic representation of structure of members of the IL-12 famil.

The IL-12 cytokine is composed of two protein subunits called p35 and p40 and was the first cytokine shown to be able to drive the differentiation of naïve T-cells into Th1 cells [38, 39]. The IL-23 cytokine also shares the same p40 subunit as IL-12, but in IL-23 this is combined with a p19 subunit. IL-23 was discovered almost 10 years after IL-12 [40] and has also been implicated in the later stages of Th1 cell differentiation. Followup studies have subsequently shown that IL-23 is in fact, functionally distinct from IL-12, as it not only acts on Th1 cells, but also stimulates Th17 cells to produce IL-17 [30, 41]. Interestingly, IL-23 also acts on macrophages to drive osteoclast development in inflammation-mediated bone pathology [42].

The IL-27 cytokine comprises of a p40-related protein referred to as EBi3 (Epstein-Barr virus induced gene 3) together with a subunit known as p28, (a p35-related protein). The EBi3 gene was first identified in 1996, following its expression during B-lymphocytes infection with the Epstein Barr Virus. The gene product is a secreted glycoprotein related to p40 [43]. Later, during research investigating IL-6 homologous proteins, its partner subunit, p28 was discovered. The p28, protein was only found to be efficiently secreted when coupled with EBI3. Following this discovery, the heterodimeric protein of EBi3 and p28 was named IL-27 [44].

Initially, the function of IL-27 was again thought to be similar to IL-12 in driving early stage Th1 cell development. Further study has however shown that IL-27 is also able to induce IL-10 production from Treg cells which can inhibit Th17 responses [45, 46]. In this regard, IL-27 can suppress inflammation in inflammatory mouse disease models including the collagen induced arthritis (CIA) mouse model [46, 47].

In addition to associating with p28 in IL-27, the EBi3 subunit can also couple with p35 to facilitate secretion of the latter [48]. The function of the EBi3/p35 heterodimer was not known until relatively recently when studies using a recombinant EBi3/p35 protein in a rheumatoid arthritis mouse model [46] showed that joint inflammation was effectively resolved by the recombinant protein. It was suggested that the therapeutic mechanism of this recombinant protein was through induction of Treg cell development and IL-10 expression with the subsequent suppression of Th1 and Th17 responses [46]. Furthermore, in the absence of EBi3 or p35 subunit production, Treg cells are unable to resolve gut inflammation in mouse inflammatory bowel disease (IBD) [49]. EBi3 and p35 are both highly expressed by mouse Treg cells, thus seemingly providing a key component of the immune regulating function of these cells. In cases where Treg cells are deficient in either the EBi3 or p35 genes, a reduced ability to suppress effector T-cell proliferation is evident [49].

The EBi3/p35 heterodimeric protein has since been named IL-35 [49], and whilst the functional effect of IL-35 in mouse models has clearly been seen, the role of this particular cytokine in immune regulation of humans still remains unclear.

3.1. The Role of IL-12 in Candidosis

A critical role of IL-12 in the immune response during human fungal infection has been reported. The 1 subunit of the IL-12 receptor is utilised by both IL-12 and IL-23 for cell signalling transduction and is encoded by the IL12RB1 gene. Recently, two unrelated Mexican patients were found to share a common mutation in the IL12RB1, gene and both were found to suffer from uncontrolled Bacille Calmette-Guérin (BCG) and C. albicans infection resulting in their early deaths by the ages of 4 and 16 years [50].

DC maturation is essential in the generation of an immune response following C. albicans stimulation. Human PBMC populations contain a large number of immature DCs and when stimulated with C. albicans, IL-12p40 mRNA expression is not detected [51]. However, in vitro derived and matured DCs from PBMC do respond to C. albicans stimulation with subsequent IL-12 production, which in turn stimulates Th1 cell differentiation [52].

The importance of IL-12p40 in controlling fungal infection has been shown in C. albicans infected mouse models. Mannoprotein from the fungal pathogen Cryptococcus neoformans appears to protect mice from subsequent intravenous challenge with C. albicans. However neutralisation of the IL-12 cytokine using a rat anti-IL-12 antibody removes this protective effect, indicating an involvement of IL-12 in the process [53]. An IL-12 recombinant protein fused with C. albicans antigen (enolase) has also been reported as being able to protect mice during C. albicans infection [54].

Both mucosal and systemic models of mouse candidosis have been developed [5557]. Based on these, it has been shown that IL-12p40 deficient mice exhibit significantly higher levels of C. albicans colonisation than their wild-type littermates. However, systemic infection with intravenously inoculation of C albicans appears unaffected by IL-12p40 deficiency [58].

3.2. The Role of IL-23 in Candidosis

Conceivably, the results obtained with the IL-12p40 gene knockout mice described above may also be the result of deficiencies in IL-23 production, since IL-12 and IL-23 share a protein subunit (IL-12p40). Recently, studies have shown that IL-23 may indeed play a key role in controlling vaginal candidosis, with the IL-23 cytokine, together with IL-6 readily detected in vaginal secretions of infected women [12, 59]. Even though DCs isolated from patients with candidosis demonstrate reduced maturation, they do have the ability to produce IL-23 and IL-6 [19], which seemingly can play a direct role in the maintenance of Th17 responses [6062].

Candida infection in both immune competent and immunosuppressed mice generally leads to enhanced IL-23p19 expression. Immune competent mice produce a much higher and more prolonged expression of IL-23p19 mRNA at mucosal tissue sites compared with those mice that are immunosuppressed [12]. Mice that are Th17 and IL-17 receptor deficient develop an inappropriate immune response [63], and other results indicate that over production of IL-23 and IL-17 can impair the host immune system in its ability to combat C. albicans infection, despite mice exhibiting inflammation [41].

3.3. Involvement of IL-27 and IL-35 in Candidosis

IL-27 and IL-35 are cytokines that regulate the production of IL-17 and IL-10 from Th17 and Treg cells, respectively. IL-27 and IL-35 both suppress IL-17 production by Th17 cells and promote IL-10 production by Treg or T suppressor cells [45, 46]. Although IL-27 can enhance APC and DC maturation by stimulation of MHC I and II expression in human THP-1 monocytic cells [64], an autocrine-mediated regulation has, as yet, not been demonstrated.

IL-12p35 knockout mice tend to have lower fungal burden and show no overt disease during oral C. albicans infection [63]. Since IL-12p35 is a component of IL-35, the result of this study demonstrated that the immunosuppressive effect of IL-35 can be countered by gene disruption, resulting in enhanced immunity against fungi infection. To date, there has been limited laboratory research into the role that IL-27 and IL-35 may have in the immune response to candidosis. Recent experiments performed in our laboratory (unpublished data) have shown that when THP-1 cells are challenged with heat killed C. albicans, an enhanced expression of EBi3 (a subunit of both IL-27 and IL-35) occurs compared with exposure to bacterial lipopolysaccharide alone (Figure 2(a)). Furthermore we have found that clinical strains of C. albicans exhibit strain variation in their ability to induce EBi3 mRNA expression in the THP-1 cells (Figure 2(b)). Prechallenging of THP-1 cell with heat killed C. albicans also leads to a detectable level of IL-27 expression after initial low dose LPS stimulation (Figure 2(c)), which can be explained by enhanced expression of TLR2 and TLR4 (Figure 2(d)).

fig2
Figure 2: Heat-killed Candida albicans (HKC) stimulated THP-1 cell for Ebi3 and TLR2/4 expression. (a) THP-1 cells were stimulated with  HKC /mL and 100 ng/mL LPS for indicated time. The Ebi3 mRNA was detected by RT-PCR. The RNA equal loading was shown by -Actin RT-PCR. (b) THP-1 cells were stimulated with two clinical strains of C. albicans (S1 and S2) for overnight. The Ebi3 expression was presented by band density ratios of Ebi3 over β-Actin. (c) IL-27 cytokineS were measured by a human IL-27 ELISA (R&D system) in a cell culture with pretreated THP-1 cell with indicated increase density of heat killed Candida followed by low dose LPS stimulation. (d) TLR2 and 4 mRNA expression was increased by  HKC /mL.

4. T-cell Immunity in Controlling Fungal Infection

As previously mentioned, the binding of PRRs to PAMPs on the Candida cell surface activates DCs and other professional APCs. Activated APCs can phagocytose C. albicans and present its antigens with MHC II to T-cell receptors (TCRs) of naïve CD4+ T-cells. The interaction of the DC and T-cell usually occurs within lymphoid tissue immediately after migration of the APC from the site of infection. APC binding with naïve CD4+ T-cells will result in the directed differentiation and proliferation of various T-cell subsets. The type of subset of T-helper cells that is developed is dependent on the cytokine environment supplied by the APC which will have a major bearing on the ensuing immune response.

Three signals are provided by the APC to the naïve CD4+ T-cell. The first is through interaction of the presented antigen and the TCR. The second is provided by costimulatory molecules on the APCs which bind to costimulatory receptors on T-cells. The third signal involves the production of cytokines by the APCs, which activate appropriate receptors on T-cell surfaces and induce T-cell differentiation [6568]. Many cytokines can be produced by activated APCs, and these can either be pro- or anti-inflammatory [33, 34, 69]. Results from animal models clearly show that T-cells are pivotal in the control of Candida colonisation of the host [7072].

Protective adaptive immune responses to Candida were initially thought to be mediated by CD4+ Th1 cells [15, 72], with Th2 cells associated with a failure to protect resulting in Candida infection [4, 73]. More recently, Th17-mediated immunity has been highlighted as a protective mechanism against Candida infection [74, 75].

4.1. Th1 and Th2 Cell Responses in Candidosis

By definition, a Th1 cell is a CD4+ T-cell that has the ability to respond to a specific antigen and produce the cytokines IFN , IL-2, and TNF . Similarly, Th2 cells are CD4+ T-cells that produce the cytokines IL-4, IL-5, IL-13, and IL-25 in response to antigen stimulation. It has been demonstrated that Th1 cells play an important role in the defence of mice against C. albicans infection [76, 77]. Studies that have neutralised IL-4 (a Th2 cytokine) production in mice resulted in an induced Th1 response with an associated resistance to C. albicans infection [78]. In addition, IFN receptor-deficient mice exhibit a greater susceptibility to C. albicans systemic infection. In cases where human peripheral blood derived DCs are stimulated with C albicans and cocultured with autologous CD4+ T-cells, a Th1 response is also elicited [52]. Defects in these Th1 cell responses lead to a significant impairment in host defences against Candida [79].

Although a protective role of Th1 responses has convincingly been showed in both humans and mice, contrasting results concerning Th1 or Th2 cytokine production at mucosal infection sites have been reported [71], and in some patients with candidosis, these cytokines may not even be detectable [80]. These findings may however be a result of different assay sensitivities in respective laboratories.

4.2. Th17 in Candidosis

Th17 cells produce the cytokines IL-17A, IL-17F, IL-21, and IL-22 [81]. Evidence for the importance of Th17 cells in protecting against Candida infection has been through experiments involving mice deficient in production of Th17 cells, the expression of IL-17, or for the receptor for IL-17. In such studies, the deficient mice exhibit greater susceptibility to oral infection with C. albicans [63]. Furthermore, human PBMCs from patients with chronic mucosal candidosis have been shown to exhibit reduced Th17 cell responses compared with PBMCs from healthy individuals after challenge with C. albicans [82, 83].

Mouse dectin-1 activated DCs direct Th17 cell development in vitro, and in a mouse candidosis model, CARD9-dependent Th17 development has been demonstrated [34]. IL-22 in mice plays a protective role against C. albicans infection when Th1 responses are impaired [84]. In addition, C. albicans-specific Th17 cells are readily detected in healthy individuals with a C. albicans mediated induction of Th17 responses observed via DCs [12]. Human monocyte derived DCs stimulated with the generally nonpathogenic Saccharomyces cerevisiae yeast induce cell-mediated Th1 responses, while C. albicans yeast or hyphae pulsed DCs shifted T-cell responses towards Th17 [85].

Hyphae of C. albicans have been shown to stimulate human monocyte-derived DCs to produce IL-23 and not IL-12. This is in contrast with C. albicans yeast which stimulate IL-12 production, with IL-23 only generated in response to high yeast concentrations. Such findings would suggest that it is the hyphal form of C. albicans that is responsible for triggering Th17 responses in vivo. Interestingly, human memory cells specific for C. albicans are derived from Th17 subsets that express the chemokine receptors CCR6 and CCR4 for skin and mucosal homing [86]. The exact function of this chemokine receptor expression in the control of in vivo Th17 cell migration does however remain unclear. Moreover, PBMCs from a CMC patient were found to produce lower levels of IL-17A and IL-22 in response to C. albicans stimulation compared with cells from a healthy individual. A decreased number of CCR6+ CD4+ T-cells have also been found in CMC patients [87].

4.3. Regulatory T-cells in Candidosis

Regulatory T-cells (Treg) are CD4+CD2 T-cells which can suppress CD4+ T effective cells, including the proliferation and differentiation of Th1 and Th17 cells. Such a suppression leads to reduced inflammatory responses against Candida in mucosal and disseminated infections [19, 28].

Candida albicans might be able to induce immune tolerance through interaction with DCs via Toll/IL-1 receptor domain-containing adaptor inducing IFN- (TRIF) and STAT3-dependent signal transduction that activates Treg differentiation. Treg cells express TLR2 and proliferate under stimulation with TLR2 ligands and TCR activation. Moreover TLR mice are more resistant to C. albicans infection and demonstrate significantly reduced IL-10 production. This would suggest that Treg cell function may be regulated directly by C. albicans to avoid unnecessary inflammatory responses [28, 29]. The balance between Th17 and Treg cells in mucosal tissue has been suggested as the determining factor for either commensal carriage or infection with C. albicans [13, 88]. However, human and animal models have yet to show any direct evidence that an over production of Treg cells and enhanced Treg function leads to C. albicans infection. Indirectly, Treg involvement in candidosis has been demonstrated using TNFα receptor-related gene (GITR) knockout mice. The wild-type mouse is associated with high expression of CD4+CD25+ T-cells (Treg). The GITR knockout mice have enhanced resistance to systemic C. albicans infection with an accompanying highly developed Th1 cell phenotype. Furthermore DCs produce elevated IL-12 levels when added to cultures of CD4+CD25+ T-cells from GITR knockout mice, when compared with wild-type mice [89]. This finding indicates that Treg cells may serve to suppress the protective Th1 role in candidosis. As previously mentioned, the cytokine IL-35 consists of the subunits EBi3 and IL-12p35 and would appear to promote Treg differentiation [46] and therefore control Treg immune suppression [49]. Mice deficient in the IL-12p35 gene are highly resistant to oropharyngeal candidosis [63], which again provides indirect evidence for the role of Treg in suppressing T-cell defensive responses against C. albicans infection.

T-cell responses can be generated by coculture of a pathogen’s antigen with peripheral blood monocytes. After several days of culture, the antigen-specific T-cells can be recalled to produce cytokines, such as the Th1 cell cytokine IFN [90]. We have isolated human PBMC from a healthy donor and recalled the T-cell response using heat killed C. albicans. Predominant Th1 and Th17 responses based on the cytokine profiles were seen at days 1, 3, and 7 after culturing PBMC with heat killed C. albicans (Figure 3).

fig3
Figure 3: Peripheral blood monocytes from a healthy individual responded to C. albicans stimulation for Th1 cytokine (IFNγ) production, Th17 cytokine (IL-17) production, but not Th2 cytokine (IL-4) production. The cytokines were measured with CBA kit (BD bioscience).

5. Summary

DCs are the key immune surveillance cells at mucosal sites and mediate their surveillance through cell surface expression of pattern recognition receptors (PRRs). The colonisation of mucosal surfaces by C. albicans can be detected through interaction of PRRs and surface antigens on Candida, which will ultimately lead to cell signalling and phagocytosis. Activated DCs migrate to local lymph nodes where the processed Candida antigens are presented to naïve CD4+ T-cells. T-helper and Treg cells will differentiate under the direction of cytokines produced by the DCs. The IL-12 cytokine family are largely involved in driving this T-helper cell development which in turn is essential for subsequent macrophage and neutrophil killing of C. albicans. Both Th1 and Th17 responses are considered protective, whilst Th2 and Treg responses may have a suppressive effect on host immunity against candidosis. The cytokine IL-12 drives Th1 development, whilst IL-23 is involved in directing and maintaining Th17 function. IL-27 has two effects in terms of regulating CD4+ T-cell responses. On one hand, IL-27 assists IL-12 in the early stage development of Th1 cells; however, like IL-35, IL-27 also serves to suppress Th17 activity. The role of IL-12 cytokines in immune function against Candida is still not completely understood, and our current knowledge particularly for the novel IL-12 family members, IL-27 and IL-35, needs to be enhanced. Additional research is warranted in order to understand the molecular mechanism of host against C. albicans infection, which will not only benefit in the treatment of candidosis but could also offer therapeutic options in the treatment of other inflammatory conditions.

References

  1. J. Schulze and U. Sonnenborn, “Yeasts in the gut: from commensals to infectious agents,” Deutsches Arzteblatt, vol. 106, no. 51-52, pp. 837–842, 2009. View at Publisher · View at Google Scholar · View at PubMed
  2. T. F. Meiller, B. Hube, L. Schild et al., “A novel immune evasion strategy of Candida albicans: proteolytic cleavage of a salivary antimicrobial peptide,” PLoS ONE, vol. 4, no. 4, Article ID e5039, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  3. S. Thaweboon, B. Thaweboon, T. Srithavaj, and S. Choonharuangdej, “Oral colonization of Candida species in patients receiving radiotherapy in the head and neck area,” Quintessence International, vol. 39, no. 2, pp. e52–e57, 2008. View at Scopus
  4. A. Vultaggio, L. Lombardelli, M. G. Giudizi et al., “T cells specific for Candida albicans antigens and producing type 2 cytokines in lesional mucosa of untreated HIV-infected patients with pseudomembranous oropharyngeal candidiasis,” Microbes and Infection, vol. 10, no. 2, pp. 166–174, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  5. L. de Repentigny, D. Lewandowski, F. Aumont, Z. Hanna, and P. Jolicoeur, “Oral mucosal cell response to Candida albicans in transgenic mice expressing HIV-1,” Methods in Molecular Biology, vol. 470, pp. 359–368, 2009. View at Publisher · View at Google Scholar · View at Scopus
  6. M. S. Thomas, A. Parolia, M. Kundabala, and M. Vikram, “Asthma and oral health: a review,” Australian Dental Journal, vol. 55, no. 2, pp. 128–133, 2010. View at Publisher · View at Google Scholar · View at PubMed
  7. A. Akpan and R. Morgan, “Oral candidiasis,” Postgraduate Medical Journal, vol. 78, no. 922, pp. 455–459, 2002. View at Publisher · View at Google Scholar · View at Scopus
  8. D. W. Williams, K. L. Bartie, A. J. Potts, M. J. Wilson, M. J. Fardy, and M. A. Lewis, “Strain persistence of invasive Candida albicans in chronic hyperplastic candidosis that underwent malignant change,” Gerodontology, vol. 18, no. 2, pp. 73–78, 2001. View at Scopus
  9. V. Sharon and N. Fazel, “Oral candidiasis and angular cheilitis,” Dermatologic Therapy, vol. 23, no. 3, pp. 230–242, 2010. View at Publisher · View at Google Scholar · View at PubMed
  10. C. H. Kirkpatrick and H. R. Hill, “Chronic mucocutaneous candidiasis,” Pediatric Infectious Disease Journal, vol. 20, no. 2, pp. 197–206, 2001. View at Publisher · View at Google Scholar · View at Scopus
  11. L. Lin, A. S. Ibrahim, X. Xu et al., “Th1-Th17 cells mediate protective adaptive immunity against Staphylococcus aureus and Candida albicans infection in mice,” PLoS Pathogens, vol. 5, no. 12, Article ID e1000703, 2009. View at Publisher · View at Google Scholar · View at PubMed
  12. Y. Wu, Z. Tan, Z. Liu, D. Xia, and J. Li, “Local IL-23 expression in murine vaginal candidiasis and its relationship with infection and immune status,” Journal of Huazhong University of Science and Technology. Medical Sciences, vol. 26, no. 2, pp. 245–247, 2006. View at Scopus
  13. P. Bonifazi, T. Zelante, C. D'Angelo et al., “Balancing inflammation and tolerance in vivo through dendritic cells by the commensal Candida albicans,” Mucosal Immunology, vol. 2, no. 4, pp. 362–374, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  14. T. Jouault, A. Sarazin, M. Martinez-esparza, C. Fradin, B. Sendid, and D. Poulain, “Host responses to a versatile commensal: PAMPs and PRRs interplay leading to tolerance or infection by Candida albicans,” Cellular Microbiology, vol. 11, no. 7, pp. 1007–1015, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  15. M. L. Gil and D. Gozalbo, “Role of Toll-like receptors in systemic Candida albicans infections,” Frontiers in Bioscience, vol. 14, pp. 570–582, 2009. View at Scopus
  16. C. Antonopoulos, M. Cumberbatch, J. B. Mee et al., “IL-18 is a key proximal mediator of contact hypersensitivity and allergen-induced Langerhans cell migration in murine epidermis,” Journal of Leukocyte Biology, vol. 83, no. 2, pp. 361–367, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  17. P. Verdijk, E. H. J. G. Aarntzen, W. J. Lesterhuis et al., “Limited amounts of dendritic cells migrate into thet-cell area of lymph nodes but have high immune activating potential in melanoma patients,” Clinical Cancer Research, vol. 15, no. 7, pp. 2531–2540, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  18. A. Del Prete, W. Vermi, E. Dander et al., “Defective dendritic cell migration and activation of adaptive immunity in PI3Kγ-deficient mice,” EMBO Journal, vol. 23, no. 17, pp. 3505–3515, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  19. K. R. Ryan, M. Hong, P. D. Arkwright et al., “Impaired dendritic cell maturation and cytokine production in patients with chronic mucocutanous candidiasis with or without APECED,” Clinical and Experimental Immunology, vol. 154, no. 3, pp. 406–414, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  20. S. Goriely and M. Goldman, “Interleukin-12 family members and the balance between rejection and tolerance,” Current Opinion in Organ Transplantation, vol. 13, no. 1, pp. 4–9, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  21. A. A. Hasan, A. M. Ghaemmaghami, L. Fairclough, A. Robins, H. F. Sewell, and F. Shakib, “Allergen-driven suppression of thiol production by human dendritic cells and the effect of thiols on T cell function,” Immunobiology, vol. 214, no. 1, pp. 2–16, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  22. G. Oldenhove, N. Bouladoux, E. A. Wohlfert et al., “Decrease of Foxp3+ Treg Cell Number and Acquisition of Effector Cell Phenotype during Lethal Infection,” Immunity, vol. 31, no. 5, pp. 772–786, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  23. J. B. McLachlan, D. M. Catron, J. J. Moon, and M. K. Jenkins, “Dendritic Cell Antigen Presentation Drives Simultaneous Cytokine Production by Effector and Regulatory T Cells in Inflamed Skin,” Immunity, vol. 30, no. 2, pp. 277–288, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  24. K. Loser and S. Beissert, “Dendritic Cells and T Cells in the Regulation of Cutaneous Immunity,” Advances in Dermatology, vol. 23, pp. 307–333, 2007. View at Publisher · View at Google Scholar · View at Scopus
  25. S. Goddard, J. Youster, E. Morgan, and D. H. Adams, “Interleukin-10 Secretion Differentiates Dendritic Cells from Human Liver and Skin,” American Journal of Pathology, vol. 164, no. 2, pp. 511–519, 2004. View at Scopus
  26. K. Gee, C. Guzzo, N. F. C. Mat, W. Ma, and A. Kumar, “The IL-12 family of cytokines in infection, inflammation and autoimmune disorders,” Inflammation and Allergy—Drug Targets, vol. 8, no. 1, pp. 40–52, 2009. View at Publisher · View at Google Scholar · View at Scopus
  27. S. Siegemund, N. Schütze, M. A. Freudenberg, M. B. Lutz, R. K. Straubinger, and G. Alber, “Production of IL-12, IL-23 and IL-27p28 by bone marrow-derived conventional dendritic cells rather than macrophages after LPS/TLR4-dependent induction by Salmonella Enteritidis,” Immunobiology, vol. 212, no. 9-10, pp. 739–750, 2008. View at Publisher · View at Google Scholar · View at PubMed
  28. R. P. M. Sutmuller, M. H. M. G. M. Den Brok, M. Kramer et al., “Toll-like receptor 2 controls expansion and function of regulatory T cells,” Journal of Clinical Investigation, vol. 116, no. 2, pp. 485–494, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  29. M. G. Netea, R. Sutmuller, C. Hermann et al., “Toll-Like Receptor 2 Suppresses Immunity against Candida albicans through Induction of IL-10 and Regulatory T Cells,” The Journal of Immunology, vol. 172, no. 6, pp. 3712–3718, 2004. View at Scopus
  30. A. Miyazato, K. Nakamura, N. Yamamoto et al., “Toll-like receptor 9-dependent activation of myeloid dendritic cells by deoxynucleic acids from Candida albicans,” Infection and Immunity, vol. 77, no. 7, pp. 3056–3064, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  31. G. D. Brown and S. Gordon, “Immune recognition. A new receptor for beta-glucans,” Nature, vol. 413, pp. 36–37, 2001.
  32. H. S. Goodridge and D. M. Underhill, “Fungal Recognition by TLR2 and Dectin-1,” Handbook of Experimental Pharmacology, no. 183, pp. 87–109, 2008. View at Scopus
  33. B. N. Taylor, M. Saavedra, and P. L. Fidel Jr., “Local Th1/Th2 cytokine production during experimental vaginal candidiasis: potential importance of transforming growth factor-β,” Medical Mycology, vol. 38, no. 6, pp. 419–431, 2000. View at Scopus
  34. S. LeibundGut-Landmann, O. Groß, M. J. Robinson et al., “Syk- and CARD9-dependent coupling of innate immunity to the induction of T helper cells that produce interleukin 17,” Nature Immunology, vol. 8, no. 6, pp. 630–638, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  35. E.-O. Glocker, A. Hennigs, M. Nabavi et al., “A homozygous CARD9 mutation in a family with susceptibility to fungal infections,” The New England Journal of Medicine, vol. 361, no. 18, pp. 1727–1735, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  36. G. Ferwerda, F. Meyer-Wentrup, B.-J. Kullberg, M. G. Netea, and G. J. Adema, “Dectin-1 synergizes with TLR2 and TLR4 for cytokine production in human primary monocytes and macrophages,” Cellular Microbiology, vol. 10, no. 10, pp. 2058–2066, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  37. B. Ferwerda, G. Ferwerda, T. S. Plantinga et al., “Human dectin-1 deficiency and mucocutaneous fungal infections,” The New England Journal of Medicine, vol. 361, no. 18, pp. 1760–1767, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  38. E. E. Murphy, G. Terres, S. E. Macatonia et al., “B7 and interleukin 12 cooperate for proliferation and interferon γ production by mouse T helper clones that are unresponsive to B7 costimulation,” Journal of Experimental Medicine, vol. 180, no. 1, pp. 223–231, 1994. View at Publisher · View at Google Scholar · View at Scopus
  39. S. E. Macatonia, C.-S. Hsieh, K. M. Murphy, and A. O'Garra, “Dendritic cells and macrophages are required for Th1 development of CD8+ t cells from αβ TCR transgenic mice: IL-12 substitution for macrophages to stimulate IFN-γ production is IFN-γ-dependent,” International Immunology, vol. 5, no. 9, pp. 1119–1128, 1993. View at Scopus
  40. B. Oppmann, R. Lesley, B. Blom et al., “Novel p19 protein engages IL-12p40 to form a cytokine, IL-23, with biological activities similar as well as distinct from IL-12,” Immunity, vol. 13, no. 5, pp. 715–725, 2000. View at Scopus
  41. T. Zelante, A. De Luca, P. Bonifazi et al., “IL-23 and the Th17 pathway promote inflammation and impair antifungal immune resistance,” The European Journal of Immunology, vol. 37, no. 10, pp. 2695–2706, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  42. L. Chen, X.-Q. Wei, B. Evans, W. Jiang, and D. Aeschlimann, “IL-23 promotes osteoclast formation by up-regulation of receptor activator of NF-B (RANK) expression in myeloid precursor cells,” The European Journal of Immunology, vol. 38, no. 10, pp. 2845–2854, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  43. O. Devergne, M. Hummel, H. Koeppen et al., “A novel interleukin-12 p40-related protein induced by latent Epstein-Barr virus infection in B lymphocytes,” Journal of Virology, vol. 70, no. 2, pp. 1143–1153, 1996. View at Scopus
  44. S. Pflanz, J. C. Timans, J. Cheung et al., “IL-27, a heterodimeric cytokine composed of EBI3 and p28 protein, induces proliferation of naive CD8+ T cells,” Immunity, vol. 16, no. 6, pp. 779–790, 2002. View at Publisher · View at Google Scholar · View at Scopus
  45. G. Murugaiyan, A. Mittal, R. Lopez-Diego, L. M. Maier, D. E. Anderson, and H. L. Weiner, “IL-27 is a key regulator of IL-10 and IL-17 production by human CD8+ T cells,” The Journal of Immunology, vol. 183, no. 4, pp. 2435–2443, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  46. W. Niedbala, X.-Q. Wei, B. Cai et al., “IL-35 is a novel cytokine with therapeutic effects against collagen-induced arthritis through the expansion of regulatory T cells and suppression of Th17 cells,” European The Journal of Immunology, vol. 37, no. 11, pp. 3021–3029, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  47. J. Furuzawa-Carballeda, M. I. Vargas-Rojas, and A. R. Cabral, “Autoimmune inflammation from the Th17 perspective,” Autoimmunity Reviews, vol. 6, no. 3, pp. 169–175, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  48. O. Devergne, M. Birkenbach, and E. Kieff, “Epstein-Barr virus-induced gene 3 and the p35 subunit of interleukin 12 form a novel heterodimeric hematopoietin,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 22, pp. 12041–12046, 1997. View at Publisher · View at Google Scholar · View at Scopus
  49. L. W. Collison, C. J. Workman, T. T. Kuo et al., “The inhibitory cytokine IL-35 contributes to regulatory T-cell function,” Nature, vol. 450, no. 7169, pp. 566–569, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  50. S. Pedraza-Sanchez, M. T. Herrera-Barrios, R. Aldana-Vergara et al., “Bacille Calmette-Guerin infection and disease with fatal outcome associated with a point mutation in the interleukin-12/interleukin-23 receptor beta-1 chain in two Mexican families,” International Journal of Infectious Diseases, vol. 14S3, pp. e256–e260, 2010.
  51. H. S. Kim, E. H. Choi, J. Khan et al., “Expression of genes encoding innate host defense molecules in normal human monocytes in response to Candida albicans,” Infection and Immunity, vol. 73, no. 6, pp. 3714–3724, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  52. M. Pepe, E. Jirillo, and V. Covelli, “In vitro infection of human monocyte-derived dendritic cells with Candida albicans: receptorial involvement and therapeutic implications,” Current Pharmaceutical Design, vol. 12, no. 32, pp. 4263–4269, 2006. View at Publisher · View at Google Scholar · View at Scopus
  53. D. Pietrella, P. Lupo, F. Bistoni, and A. Vecchiarelli, “An early imbalance of interleukin 12 influences the adjuvant effect of mannoproteins of cryptococcus neoformans,” Cellular Microbiology, vol. 6, no. 9, pp. 883–891, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  54. C. Montagnoli, S. Sandini, A. Bacci, L. Romani, and R. La Valle, “Immunogenicity and protective effect of recombinant enolase of Candida albicans in a murine model of systemic candidiasis,” Medical Mycology, vol. 42, no. 4, pp. 319–324, 2004. View at Publisher · View at Google Scholar · View at Scopus
  55. H. Ishibashi, K. Uchida, Y. Nishiyama, H. Yamaguchi, and S. Abe, “Oral administration of itraconazole solution has superior efficacy in experimental oral and oesophageal candidiasis in mice than its intragastric administration,” Journal of Antimicrobial Chemotherapy, vol. 59, no. 2, pp. 317–320, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  56. K. V. Clemons, G. M. Gonzalez, G. Singh et al., “Development of an orogastrointestinal mucosal model of candidiasis with dissemination to visceral organs,” Antimicrobial Agents and Chemotherapy, vol. 50, no. 8, pp. 2650–2657, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  57. A. B. Van Spriel, I. E. Van den Herik-Oudijk, and J. G. J. Van de Winkel, “Neutrophil FcγRI as target for immunotherapy of invasive candidiasis,” The Journal of Immunology, vol. 166, no. 12, pp. 7019–7022, 2001. View at Scopus
  58. C. S. Farah, Y. Hu, S. Riminton, and R. B. Ashman, “Distinct roles for interleukin-12p40 and tumour necrosis factor in resistance to oral candidiasis defined by gene-targeting,” Oral Microbiology and Immunology, vol. 21, no. 4, pp. 252–255, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  59. A. Lev-Sagie, P. Nyirjesy, N. Tarangelo et al., “Hyaluronan in vaginal secretions: association with recurrent vulvovaginal candidiasis,” American Journal of Obstetrics and Gynecology, vol. 201, no. 2, pp. 206–e1, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  60. G. Layh-Schmitt and R. A. Colbert, “The interleukin-23/interleukin-17 axis in spondyloarthritis,” Current Opinion in Rheumatology, vol. 20, no. 4, pp. 392–397, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  61. F. Annunziato, L. Cosmi, F. Liotta, E. Maggi, and S. Romagnani, “The phenotype of human Th17 cells and their precursors, the cytokines that mediate their differentiation and the role of Th17 cells in inflammation,” International Immunology, vol. 20, no. 11, pp. 1361–1368, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  62. G. Perona-Wright, S. J. Jenkins, R. A. O'Connor et al., “A pivotal role for CD40-mediated IL-6 production by dendritic cells during IL-17 induction in vivo,” The Journal of Immunology, vol. 182, no. 5, pp. 2808–2815, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  63. H. R. Conti, F. Shen, N. Nayyar et al., “Th17 cells and IL-17 receptor signaling are essential for mucosal host defense against oral candidiasis,” Journal of Experimental Medicine, vol. 206, no. 2, pp. 299–311, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  64. X. M. Feng, N. Liu, S. G. Yang et al., “Regulation of the class II and class I MHC pathways in human THP-1 monocytic cells by interleukin-27,” Biochemical and Biophysical Research Communications, vol. 367, no. 3, pp. 553–559, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  65. K.-C. Sheng, D. S. Pouniotis, M. D. Wright et al., “Mannan derivatives induce phenotypic and functional maturation of mouse dendritic cells,” Immunology, vol. 118, no. 3, pp. 372–383, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  66. M. Roudbary, S. Roudbar Mohammadi, M. Bozorgmehr, and S. M. Moazzeni, “The effects of Candida albicans cell wall protein fraction on dendritic cell maturation,” Iranian The Journal of Immunology, vol. 6, no. 2, pp. 67–74, 2009. View at Scopus
  67. F. Skrzypek, E. Cenci, D. Pietrella, A. Rachini, F. Bistoni, and A. Vecchiarelli, “Dectin-1 is required for human dendritic cells to initiate immune response to Candida albicans through Syk activation,” Microbes and Infection, vol. 11, no. 6-7, pp. 661–670, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  68. C. K. Baumgartner and L. P. Malherbe, “Regulation of CD4 T-cell receptor diversity by vaccine adjuvants,” Immunology, vol. 130, no. 1, pp. 16–22, 2010. View at Publisher · View at Google Scholar · View at PubMed
  69. F. De Bernardis, G. Santoni, M. Boccanera et al., “Local anticandidal immune responses in a rat model of vaginal infection by and protection against Candida albicans,” Infection and Immunity, vol. 68, no. 6, pp. 3297–3304, 2000. View at Publisher · View at Google Scholar · View at Scopus
  70. T. A. Myers, J. E. Leigh, A. R. Arribas et al., “Immunohistochemical evaluation of T cells in oral lesions from human immunodeficiency virus-positive persons with oropharyngeal candidiasis,” Infection and Immunity, vol. 71, no. 2, pp. 956–963, 2003. View at Publisher · View at Google Scholar · View at Scopus
  71. J. E. Leigh, C. Steele, F. Wormley, and P. L. Fidel Jr., “Salivary cytokine profiles in the immunocompetent individual with Candida-associated denture stomatitis,” Oral Microbiology and Immunology, vol. 17, no. 5, pp. 311–314, 2002. View at Publisher · View at Google Scholar · View at Scopus
  72. A. Mencacci, A. Bacci, E. Cenci et al., “Interleukin 18 restores defective Th1 immunity to Candida albicans in caspase 1-deficient mice,” Infection and Immunity, vol. 68, no. 9, pp. 5126–5131, 2000. View at Publisher · View at Google Scholar · View at Scopus
  73. A. Mencacci, K. Perruccio, A. Bacci et al., “Defective antifungal T-helper 1 (TH1) immunity in a murine model of allogeneic T-cell-depleted bone marrow transplantation and its restoration by treatment with TH2 cytokine antagonists,” Blood, vol. 97, no. 5, pp. 1483–1490, 2001. View at Publisher · View at Google Scholar · View at Scopus
  74. J. Z. Liu, M. Pezeshki, and M. Raffatellu, “Th17 cytokines and host-pathogen interactions at the mucosa: dichotomies of help and harm,” Cytokine, vol. 48, no. 1-2, pp. 156–160, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  75. S. M. Levitz, “Th17 Cells Bounce off the Fungal Wall,” Cell Host and Microbe, vol. 5, no. 4, pp. 311–313, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  76. J.-H. Lee, J. Y. Lee, J. H. Park et al., “Immunoregulatory activity by daucosterol, a β-sitosterol glycoside, induces protective Th1 immune response against disseminated Candidiasis in mice,” Vaccine, vol. 25, no. 19, pp. 3834–3840, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  77. E. Rosati, L. Scaringi, P. Cornacchione et al., “Activation of cytokine genes during primary and anamnestic immune response to inactivated C. albicans,” Immunology, vol. 89, no. 1, pp. 142–151, 1996. View at Scopus
  78. A. Mencacci, E. Cenci, A. Bacci, F. Bistoni, and L. Romani, “Host immune reactivity determines the efficacy of combination immunotherapy and antifungal chemotherapy in candidiasis,” Journal of Infectious Diseases, vol. 181, no. 2, pp. 686–694, 2000. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  79. M. G. Netea, B. J. Kullberg, and J. W. M. Van Der Meer, “Severely impaired IL-12/IL-18/IFNγaxis in patients with hyper IgE syndrome,” European Journal of Clinical Investigation, vol. 35, no. 11, pp. 718–721, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  80. J. E. Leigh, C. Steele, F. L. Wormley Jr. et al., “Th1/Th2 cytokine expression in saliva of HIV-positive and HIV-negative individuals: a pilot study in HIV-positive individuals with oropharyngeal candidiasis,” Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology, vol. 19, no. 4, pp. 373–380, 1998. View at Scopus
  81. W. Ouyang, J. K. Kolls, and Y. Zheng, “The Biological Functions of T Helper 17 Cell Effector Cytokines in Inflammation,” Immunity, vol. 28, no. 4, pp. 454–467, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  82. J. D. Milner, J. M. Brenchley, A. Laurence et al., “Impaired TH17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome,” Nature, vol. 452, no. 7188, pp. 773–776, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  83. M. Zhou, B. Yang, R. Ma, and C. Wu, “Memory Th-17 cells specific for C. albicans are persistent in human peripheral blood,” Immunology Letters, vol. 118, no. 1, pp. 72–81, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  84. A. De Luca, T. Zelante, C. D'Angelo et al., “IL-22 defines a novel immune pathway of antifungal resistance,” Mucosal Immunology, vol. 3, no. 4, pp. 361–373, 2010. View at Publisher · View at Google Scholar · View at PubMed
  85. L. Rizzetto, M. Kuka, C. De Filippo et al., “Differential IL-17 production and mannan recognition contribute to fungal pathogenicity and commensalism,” The Journal of Immunology, vol. 184, no. 8, pp. 4258–4268, 2010. View at Publisher · View at Google Scholar · View at PubMed
  86. E. V. Acosta-Rodriguez, L. Rivino, J. Geginat et al., “Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells,” Nature Immunology, vol. 8, no. 6, pp. 639–646, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  87. K. Eyerich, S. Foerster, S. Rombold et al., “Patients with chronic mucocutaneous candidiasis exhibit reduced production of Th17-associated cytokines IL-17 and IL-22,” Journal of Investigative Dermatology, vol. 128, no. 11, pp. 2640–2645, 2008. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  88. A. De Luca, C. Montagnoli, T. Zelante et al., “Functional yet balanced reactivity to Candida albicans requires TRIF, MyD88, and IDO-dependent inhibition of Rorc,” The Journal of Immunology, vol. 179, no. 9, pp. 5999–6008, 2007. View at Scopus
  89. M. Agostini, E. Cenci, E. Pericolini et al., “The glucocorticoid-induced tumor necrosis factor receptor-related gene modulates the response to Candida albicans infection,” Infection and Immunity, vol. 73, no. 11, pp. 7502–7508, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  90. J. J. Zaunders, M. L. Munier, N. Seddiki et al., “High levels of human antigen-specific CD8+ T cells in peripheral blood revealed by stimulated coexpression of CD25 and CD134 (OX40),” The Journal of Immunology, vol. 183, no. 4, pp. 2827–2836, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus