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Cytokines in Systemic Lupus Erythematosus 2011

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Volume 2011 |Article ID 980286 |

Katsuhisa Miyake, Mitsuteru Akahoshi, Hitoshi Nakashima, "Th Subset Balance in Lupus Nephritis", BioMed Research International, vol. 2011, Article ID 980286, 7 pages, 2011.

Th Subset Balance in Lupus Nephritis

Academic Editor: Brian Poole
Received27 Jun 2011
Accepted05 Jul 2011
Published28 Aug 2011


Lupus nephritis, which has various histological patterns and variable clinical outcomes, is one of the most important complications of systemic lupus nephritis (SLE). This pathogenetic mechanism in each histologically different type of lupus nephritis (LN) remains unclear. Although SLE is suggested to be a Th2-driven disease, elevation of both Th1 and Th2 cytokines occurs in both humans and mice, suggesting that SLE is a complex disease driven by different lymphocyte subsets with high heterogeneity of clinical manifestations and organ involvement. Recent findings in LN elucidate an essential role for the Th1, IL-17 producing T cells and Th17 cells in the development of diffuse proliferative lupus nephritis (DPLN), and Th2 cytokine in that of membranous lupus nephritis (MLN). These data support the hypothesis that individual Th1/Th2 balance is one of the critical determinants for histopathology of LN.

1. Introduction

Systemic lupus erythematosus (SLE) is an autoimmune disease, which is characterized by tissue deposition of circulating immune complexes leading to release of inflammatory mediators, influx of inflammatory cells, and clinically apparent disease [1]. It is a prototypic systemic disease and has the potential to involve the multiple organ system in contrast to autoimmune diseases such as multiple sclerosis and type 1 diabetes mellitus [2]. The renal involvement, called lupus nephritis (LN), is one of the most serious complications, and shows the phenotypic and histological heterogeneity. In particular, two polar morphologic forms, diffuse proliferative lupus nephritis (DPLN, World Health Organization (WHO) class IV) and membranous lupus nephritis (MLN, WHO class V) are representative of histological findings in LN [35]. DPLN is the most common, severe, and important form of LN. Hematuria and proteinuria are present in all DPLN patients with active disease, and the nephrotic syndrome, hypertension, and renal insufficiency are all frequently seen. Affected patients typically have significant hypocomplementemia (especially C3) and elevated anti-DNA levels, especially during active disease [6]. Patients with DPLN usually have an unfavorable prognosis with a high percentage of eventually progressing to a renal failure despite aggressive treatment [7]. On the other hand MLN patients would be predicted to have proteinuria as the most prominent clinical feature and an indolent course similar to that seen with idiopathic membranous glomerulonephritis (MGN). It is intriguing that two polar morphologic forms exit in the same disease, and what causes the morphologic form determination. Human IgG molecules are classified into four IgG subclasses according to the immunologically distinct constant region of the heavy chain [8]. The IgG is the most important Ig isotype in immunopathogenesis for LN, and accordingly, different IgG subclasses have distinct physicochemical and biological properties. Although it should be recalled that glomerular deposited IgG subclasses have a role for determination of morphological form, it was demonstrated that distribution of subclass in glomerular IgG deposition was not associated with the different histological expressions of DPLN and MLN [9] (Figure 1).

It is widely recognized that naïve CD4+ T cells become activated and differentiate into various effector T cell subsets after encountering a specific antigen, T helper type 1 (Th1), Th2, and Th17 cells, characterized by distinct patterns of cytokine production. Th1 cells produce mainly interferon- (IFN-γ), interleukin-2 (IL-2), and tumor necrosis factor- (TNF-α), and promote cell-mediated immunity. Th2 cells secreting IL-4, IL-5, and IL-10 and are associated with humoral immune responses and induce antibody production [10]. Th17 cells produced IL-17 and drives inflammatory responses. Exaggeration of responses by Th1, Th2, and Th17 cells can induce tissue inflammation and another subset of regulatory T cells (Treg cells) controls these effector T cells for maintenance of the immune response and prevention of autoimmunity and tissue inflammation. Various types of Treg cells have been described that mediate these regulatory functions. It has been demonstrated that an imbalance between Th1 and Th2 cytokine production is much concerned with the induction and development of several autoimmune diseases. The polarized situation between Th1 and Th2 cells is established to be important in animal models and human autoimmune diseases [11].

Although a relationship between SLE activity and cytokine productions was abundantly reported, cytokine profiles concerned with LN, especially each histologic phenotype have not been sufficiently discussed. In this review we focus on Th subset, which exerts significant effect on the determination of morphological form in LN.

2. Th1 Subset

A large number of studies suggested that SLE is a Th2-driven disease [12, 13]. However, elevation of both Th1 and Th2 cytokines occurs in both humans and mice suggesting that SLE is a complex disease driven by different lymphocyte subsets [14] with heterogeneity of clinical manifestations and organ involvement.

In human LN, a relationship between histological classification and Th1/Th2 balance was suggested. Immunohistological study for nephritis showed the large number of infiltrating macrophages, Th1 cells, CD40 positive cells, and osteopontin in DPLN, but not in MLN [15]. CD40-CD40L interaction and osteopontin function are known to be involved in early Th1-mediated cellular immunity [1618]. IL-12 is a 70 kDa heterodimer (IL12p70) produced by macrophages and dendritic cells (DC). In conjunction with IL-18, it promotes IFN-γ production, and leads to polarization of peripheral cells toward a Th1 phenotype. In LN both serum and urinary IL-12p70 elevation was reported and which reflected IL-12 production in glomeruli [19]. Although there was no significant difference in the serum values of IL-12p70 between DPLN and MLN, significant difference was shown in the urinary value of IL-12p70. It was also demonstrated that the value of peripheral IFN- /IL-4 ratio in DPLN was much greater than that in MLN, and these results are coincident with our previous report [20, 21] (Figures 2 and 3). The fact that activity index for DPLN was correlated with the value of IFN- /IL-4 ratio indicates IFN-γ plays a principal role in the development of DPLN [21]. It was also shown that large amounts of IL-18 have been found within serum and glomeruli of humans LN. However, there was no difference between them in DPLN and MLN [19].

MRL/MpJ-lpr/lpr (MRL/lpr) mice have proven particularly valuable for the investigation of SLE pathogenesis [22]. MRL/lpr mice develop a lupus-like autoimmune disease characterized by severe panisotypic hypergammaglobulinemia, autoantibody production, lymphadenopathy, and immune complex- (IC-)associated nephritis. Because MLR/lpr nephritis involves the glomerulus, interstitium, and vascular components, and shows infiltration of macrophages and T cells, it is considered a suitable histological model for human DPLN. Moreover, like human DPLN, MLR/lpr nephritis is associated with Th1 responses [23]. MRL/lpr mice deficient in the IFN-γ or its receptor developed significantly reduced DPLN [24, 25]. IL-12 deficiency in MRL/lpr mice delayed DPLN and diminished systemic pathology [26]. It was also demonstrated that IL-18 accelerated DPLN, and that DPLN was exacerbated by the synergistic action of IL-12 and IL-18, a combination known to promote Th1 cell development [27]. Th2 cytokine IL-10 deficient MRL/lpr mice developed severe DPLN [28]. These results indicate Th1-dependent mechanism plays a role in the pathogenesis of DPLN.

3. Th2 Subset

In human LN, MLN is a representative of secondary MGN. It was suggested a predominant Th2 cytokine response is associated with MGN pathogenesis [21, 29, 30]. The deposits stain uniformly with a predominance of IgG4 in idiopathic MGN [31, 32], and it was suggested that MGN occurs in individuals who generate IgG4 to M-type phospholipase A2 receptor (PLA2R) [33]. IgG4 is a Th2-dependent IgG subclass, and IL-4 directs naïve human B cells to switch to IgG4 and IgE production [34]. In addition the fact that chronic graft versus host diseases (cGVHD), in which Th2 immune response occurs predominantly, occasionally associates with MGN not diffuse proliferative glomerulonephritis (DPGN), supports the notion that predominant Th2 cytokine response is associated with MGN pathogenesis [35, 36]. While MLN shows apparently different IgG subclass distribution of deposit [9], and IgG eluted from the glomerular deposits in the patient with MLN does not recognize PLA2R [33]. However, it was also suggested a predominant Th2 cytokine response is associated with MLN pathogenesis [20, 29, 32]. Association study between MLN and IFN-γ gene using microsatellite polymorphisms demonstrated that half of the MLN patients were homozygous of the allele of lower amount of IFN-γ production. This result suggested that the immune response of SLE patient bearing lower amount of IFN-γ production genotype is tend to be predominant to Th2. It was suggested that genetically determined IFN-γ production should influence on the histological finding of LN [37].

In murine LN, MRL/lpr mice disrupted the WSX-1 gene developed disease essentially identical with human MLN, accompanied by marked impairment of Th1-type immune responses with Th2-type immune deviation [38] (Figure 4). WSX-1 is a class I cytokine receptor expressed mainly on T lymphocytes. The initial mounting of Th1 responses depends on the function of the WSX-1 gene, which encodes a subunit of the IL-27R with homology to IL-12R [39]. It is indicated that the phenotypic shift from DPLN to MLN in MRL/lpr mouse occurred because the loss of WSX-1 impaired the Th1 response and concomitantly enhanced the Th2 response. These results suggested that Th2-dependent mechanism plays a role in the pathogenesis of MLN.

4. IL-17 Producing T Cells and Th17 Subset

IL-17 is mostly produced by CD4+, CD8+, CD4/CD8, and γ/δ T-cells, and Th17 cells. In human LN, it was reported that IL-17 expressing T-cells migrate to the kidney and contribute to inflammatory processes [40]. Expressions of costimulatory marker CD80 and CD134 on IL-17 producing T cells in the peripheral blood in SLE patients was increased as compared to healthy controls. The presence of CD134+ T-cells in the kidney suggests that these cells after ligation with CD134L expressed by endothelial cells migrate to the kidney and might contribute to inflammatory processes through IL-17 secretion. However, no significant difference in the expressions was seen between in patients with DPLN and MLN. In murine LN, relevant amounts of IL-17 are produced, and IL-17 producing T-cells largely infiltrate the nephritic kidneys of NZB/NZWF1 mice [41]. By contrast, treatment with anti-CD3 monoclonal antibodies delayed the renal damage with concurrent defect of IL-17 production in both serum and glomeruli [42]. In MRL/lpr mice IL-17 producing T-cells arises from CD3+/CD4/CD8 subset. Therefore, this cell population is considered an active mediator of renal cytotoxicity.

  IL-6 promotes the proliferation of renal mesangial cells and activates naïve T cell differentiation towards Th17 cooperated with transforming growth factor- (TGF- ) [43]. Also it primes the differentiation of B cells into antibody-producing cells. In human LN, infiltrating inflammatory cells in the kidney, mainly macrophages and monocytes, are the main source of IL-6. In addition to the high IL-6 serum levels, significant overexpression of IL-6 is found in DPLN whereas healthy kidneys show little IL-6 expression [44]. In murine LN, blocking IL-6 with anti-IL-6 antibodies was able to reduce kidney pathology in MRL/lpr [45] and NZB/NZW mice [46] whereas mice with IL-6 overexpression develop mesangial proliferative glomerulonephritis [47]. IL-6-deficient MRL/lpr mice showed delayed onset of proteinuria and hematuria compared to control mice. The absence of IL-6 resulted in significant reduction of infiltrating macrophages in the kidney, a decrease in renal IgG and C3 deposition, and a reduction of CD4+ and CD8+ lymphocytes [48]. These results indicate that IL-6 is a strong promoter for DPLN.

5. Treg Subset

Treg cells are a heterogeneous population of CD4+/ CD8+/CD25+ cells differentiated in two subsets. The Foxp3 population includes both IL-10-producing Treg cells and Th3 cells that produce TGF-β. This cytokine plays crucial roles in the differentiation to CD4+CD25+FoxP3+Treg. By contrast, Foxp3+ Treg cells play a protective role in autoimmunity. The expression of Foxp3 prevents T-cells from differentiating into Th17 proinflammatory effector T-cells [49]. On the other hand TGF-β, together with IL-6, promotes the differentiation of Th17 cells and suppresses FoxP3, leading to a reduction in Treg cells [43]. In human LN, the proportion of Treg cells in PBMCs and serum and urinary TGF-β1 levels were evaluated. TGF-β1 is the main immunemodulating member of TGF-β protein. The results demonstrated a significant decrease in the frequency of CD4+CD25high and CD4+CD25+FoxP3+ T cells in LN patients. This decreased Treg cells might enhance autoimmune response. This decrease was accompanied with lower serum TGF-β1 levels and higher urinary TGF-β1 levels [50]. It was described that urinary TGF-β reflects the grade of interstitial fibrosis in glomerular disease and also the mesangial matrix increase in proliferative glomerulonephritis [51]. The elevated excretion of TGF-β was also shown in the patient with focal glomerulosclerosis [52]. These results make us conceive the idea that Th17 cells and Treg cells may compete with each other in the process of development of LN, and nevertheless this Th17/Treg balance TGF-β production may be activated.

In murine LN, depletion of CD4+/CD25+ cells in NZB/NZWF1 accelerates the onset of DPLN whereas their transfer into CD4/CD25 KO mice delays the DPLN development [53]. The treatment of antimouse thymocyte globulin (ATG) in conjunction with TGF-β1 for MRL/lpr mice demonstrated inhibition of progression of proteinuria and improvement in long-time survival accompanied with reduced renal histological findings. It was suggested that ATG followed TGF-β1 treatment induced the differentiation for CD4+CD25+FoxP3+Treg [54].

Also IL-10 elevation occurs in different clinical conditions associated to SLE. Although this cytokine has been extensively studied, it remains unclear whether elevation of IL-10 is a cause of LN or not. Recently IL-10 is not considered as a lineage specific cytokine, because it has been shown that not only Th2 cells but also Th1 cells, Th17, and Treg cells can produce IL-10. We conceive that the overexpression of IL-10 in SLE might reflect IL-10-producing Treg cells activation against intrinsic defect of the cytokine homeostasis.

6. Conclusions

It is interesting that there are two distinct phenotypes, DPLN and MLN, in histological findings of lupus nephritis despite of being based on the same disease. Although the determinants that account for these differences were still equivocal, recent studies have supported that Th1, IL-17 producing T cells and Th17 cells play a principal role for DPLN. While Th2 cells may contribute to development of MLN. Individual Th1/Th2 balance may be one of the critical determinants for histopathology of LN. Similarly Treg cells control effector T cells for maintenance of the immune response, and Treg/Th17 balance may be another determinant for development of LN.


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