Skip to main content

Interleukin-35 pathobiology in periodontal disease: a systematic scoping review

Abstract

Background

Interleukin (IL)-35 is a novel anti-inflammatory cytokine that is produced by regulatory T cells. IL-35 mediates immunological functions and plays a protective role in several diseases such as asthma and rheumatoid arthritis. However, the role of IL-35 in gingivitis and periodontitis remains unclear. The aim of this study was to systematically review the literature and collecting the available evidence regarding the role of IL-35 in pathogenesis of periodontal disease.

Methods

A systematic search of electronic databases including MEDLINE, Google Scholar, Cochrane Library, Web of Science, and Scopus was conducted in November 2020 to identify studies addressing the Interleukin-35 pathobiology in periodontal disease. The identified studies were subjected to pre-identified inclusion criteria. The retrived papers were assessed by the authours independently and consensus was reached in cases where disagreement occurred. Articles written in languages other than English, case reports, letters to editors, conference abstracts, theses, and dissertations were excluded from the review.

Results

A total of 176 possibly relevant articles were identified through the search strategy. Finally, 15 papers which met the criteria of eligibility were included in this review by consensus. The included articles were classified based on their design and level of evidence.Three subclinical study, ten cross sectional investigation and two randomized clinical trials constituted the final set of studies in this review. At preclinical level, Il-35 showed inhibitory characteristics regarding alveolar bone resorption of animal periodontitis models. The results of observatory human studies confirmed the presence of high levels of IL-35 in saliva, GCF, serum, and gingival biopsies of patients suffering from inflammatory periodontal disease. Moreover, two included clinical trials showed that non-surgical periodontal therapy could downregulate IL-35 production in chronic periodontitis patients.

Conclusion

Interleukin-35 has an undeniable role in pathobiology of inflammatory periodontal disease. Further well-controlled studies are needed to better elucidate the functional pattern of IL-35 in pathogeneisis of gingival and periodontal disease.

Peer Review reports

Background

Studies revealed that periodontitis is the sixth most common disease globally. The prevalence of periodontitis is high, and approximately 10% of the global population has been affected by severe periodontitis[1]. As such, it affects the tooth supporting tissues leading to attachment loss and—if left untreated—to tooth loss. It represents a multifactorial disease primarily caused by pathogenic bacteria, which triggers and maintains a host-mediated process [2, 3]. The interplay between the imbalance within the microbial community and a dysregulated host immune response—known as dysbiosis—including some systemic and environmental modifying risk-factors leads to destruction of periodontal tissues, i.e., the periodontal ligament and alveolar bone [4]. Several studies have documented that cell-produced cytokines play a critical role in this process [5, 6], as they up- and down- regulated the local cell environment.

Different types of cells, such as fibroblasts, macrophages, and lymphocytes secrete a plethora of cytokines, especially during the active phases of periodontitis. Among the first cytokines discovered within the context of periodontal inflammation were the interleukin-1 (IL-1), IL-6, and tumor necrosis factor (TNF)families [7].

These cytokines are primarily recognized as pro-inflammatory cytokines exhibiting mainly pleiotropic effects on lymphocyte promotion and tissue destruction [8]. Further studies have documented some important related cytokines such as IL-1 receptor antagonist (IL-1Ra), IL-10, IL-4, IL-11, and transforming growth factor-beta [TGFB] with anti-inflammatory functions within the destructive processes [9]. It has been shown that both pro-inflammatory and anti-inflammatory cytokines play a critical role in the pathogenesis of periodontitis, thereby influencing destruction, repair, and remodeling of periodontal tissues [10, 11]. In this context, IL-35 is a rather newly discovered cytokine with shown anti-inflammatory capacities [12]. It is mainly produced by regulatory T cells (Treg) and formed from a heterodimer of IL-12p35 subunits and Epstein-Barr virus induced gene 3 (EBI3) [13]. The binding of IL-35 and its receptors, IL-12Rβ2, gp130, or a heterodimer of IL-12Rβ2:gp130 activates the Janus kinase–signal transducer and activator of transcription (JAK-STAT) pathway and induces immunosuppression[14].In this regard, in a gene polymorphism analyses study among Japanese subjects, the authors reported that the frequencies of variant alleles of IL-12Rβ2 were significantly higher in aggressive periodontitis patients as compared with healthy controls or chronic periodontitis patients.

It has been documented that IL-35 mainly suppresses proliferation of T cells by blocking mitosis in G1 phase without provoking apoptosis [15, 16]. IT can also induce the development of IL-35-producing T cells (iTr35), which are subsets of regulatory T cells (Treg) [16] and inhibits IL-17 production by inhibiting T-helper-17 (Th17) cell induction and, thus, plays a protective role in several diseases, whose pathogenesis is closely associated with the Th17/Treg imbalance, such as experimental colitis, asthma, inflammatory bowel disease, and rheumatoid arthritis [17,18,19,20].

IL-35 is also secreted by B cells and induces the conversion of human B cells into Breg cells to inhibit antimicrobial immunity through production of IL-35. This cytokine may also play a crucial role in the immune suppression function of Breg cells[21, 22].

Moreover, a recently published experimental study’s findings revealed that IL-35 prevents bone loss in rheumatoid arthritis disease [23]. IL-35 has also been detected in periodontal tissues, gingival crevicular fluid (GCF) of different types of periodontal disease [24,25,26] and some evidence supports its important role in the pathogenesis of periodontitis [27, 28]. The iTr35 cells also negatively regulate various immune responses mediated by Th1, Th17, and cytotoxic T lymphocyte cells. It has been documented that all of these immune cells are involved in pathogenesis of periodontitis [12, 29,30,31,32].

Previously it has been documented that through the production of IL-10, IL-35, and transforming growth factor b (TGF-b), Breg cells suppress immunopathology by prohibiting the expansion of pathogenic T cells and other pro-inflammatory lymphocytes[33]. Recently the results of a human study approved that the frequency of Breg cells was positively correlated to serum levels of IL10, IL35, and TGFβ1 in peripheral blood samples of periodontitis patients[34].

Periodontitis may be viewed as an infectious disease with a number of specific characteristics[35]. Pathogens of the subgingival microbiota can interact with host tissues and activate related immune responses. Recent studies suggested that IL-35 may promote infectious tolerance in some ways [21, 36,37,38]. In this regard the results of an animal study showed that the mice which did not express IL-35 displayed a strikingly improved resistance to infection with the intracellular bacterial pathogen Salmonella typhimurium[37]. These experimental samples showed superior containment of the bacterial growth and prolonged survival both after primary infection and upon secondary challenge after vaccination, compared to control group. This ability of Il-35 should be also considered in the way of describing the role of IL-35 in pathogenesis of periodontal disease.

To the best of our knowledge, there is no systematically collected evidence in the literature in this regard, especially in the field of periodontology. Hence, this study aimed to systematically review the existing literature regarding the role of IL-35 in pathogenesis of periodontal disease.

Methods

Scoping review approach and related question

A literature review using a scoping review approach, which is commonly used to elaborate and better understand the available evidence on a given topic, identify gaps in the literature and assess the need for further research [39]. Arksey and O’Malley explained the required methodological framework stages for a scoping review [39] and served as the methodological basis for this work. The main modified focus question of this study was as follows: ‘’What is known from the available literature about the role of IL-35 in the pathogenesis and controlling of periodontal disease?’’.

Search strategy

Our literature search applied a wide range of computerized databases, including MEDLINE, Google Scholar, Cochrane Library, Web of Science, and Scopus. The following search terms included relevant keywords in various forms and combinations are used in the study: Periodontitis, gingivitis, and interleukin-35 and interleukin-35 receptors (IL-12Rβ2, gp130). Full details of the search strings used in this review are shown in additional file 1. It should be noted that the search syntax was adapted to each database based on their specific instructions.

Eligibility criteria

Retrieved titles and abstracts obtained from the search, along with the full texts (if necessary), were assessed by two independent reviewers (OF and MD). Any inconsistencies in this regard were solved by a constructive discussion. After completing this initial search, the reference lists of the selected articles were also reviewed to identify additional relevant studies not found during the original electronic search. All letters, narrative reviews, and duplicate articles were excluded. The search strategy was not restricted by the publication date. Hence, all relevant evidence that met the inclusion criteria by November 20, 2020, was assessed. The process of selection articles for the final review is illustrated in Fig. 1.

Fig. 1
figure1

Flowchart of the process for study selection

Screening of studies and data extraction

Two authors (OF and MD) searched the databases independently. The two sets of articles were then compared. Disagreements were resolved through discussion or, if necessary, by including a third researcher (PS) to make the final decision. Duplicate articles were also excluded from the review. One researcher (OF) extracted the data, and another author (PS) checked its accuracy and completeness. The final set of selected articles and the relevant data based on the study research question is summarized in Table 1.

Table 1 General characteristics and main outcomes of the included studies

Exclusion criteria

Articles written in languages other than English, studies focusing on medically compromised individuals, case reports/case series, letters to editors, opinions, conference abstracts, commentaries, theses, and dissertations were excluded from the review.

Results

Study selection

A total of 176 possibly relevant articles were identified through the search strategy. After completing the screening titles and abstracts and eliminating duplicates, 23 studies were retrieved, and their full-text versions were collected for further assessment. A manual search for the reference lists of the 23 studies revealed no additional qualifying paper. Out of these 23 studies were subjected to full article review eligibility, and eight articles were excluded. The reasons for excluding full-text articles are as follows: The English versions of the full-text articles were not available (n = 3), the articles were not suitable for our research question (n = 2), and articles consisting of literature reviews without any original data (n = 3). Finally, 15 articles were found to be eligible and could be included in this review. Additional details on the data search are shown in the flowchart (Fig. 1).

Results of included studies

We classified and presented the results of fifteen articles included in this review based on their design and level of evidence[40]. In the first subchapter, we presented the results of two in vitro cell studies and one animal (preclinical) study. In the second subchapter, including the most articles, we described the results of ten cross-sectional studies. Finally, in the last subchapter, the results and outcomes of two human randomized control trials (RCT) regarding the effect of non-surgical periodontal treatment on levels of IL-35 were presented. The detailed characteristics of included studies are summarized in Table 1.

Animal and In vitro cell studies

In the first in vitro cell study by Shindo et al., who used human periodontal ligament cells stimulated with IL-17A [41]. In this research, the authors reported that IL-35 produced from regulatory T cells might inhibit progression of periodontitis by decreasing IL-17A-induced levels of IL-6 and IL-8. Another in vitro cell study, using cultured mouse monocyte line RAW cells, osteoclastogenesis function of IL-35 was assessed [42]. They stimulated RANKL-treated RAW cells with or without IL-35 to determine whether IL-35 affects RANKL-dependent osteoclastogenesis. The results showed that IL-35 and RANKL induced osteoclastogenesis synergistically. In the last study in this category, an interventional animal study was conducted on mice with ligature-induced periodontitis[43]. In this study, the researchers evaluated the effect of locally or systemically administered IL-35 on alveolar bone resorption measured by micro-computed tomography and scanning electron microscopy. The results of this project revealed that IL-35 inhibited alveolar bone resorption in periodontitis mice. Furthermore, IL-35 induced less detection of Th17 lymphocytes and down regulation of Th17-related cytokines, along with higher detection of Treg lymphocytes and upregulation of Treg-related cytokines in periodontitis-affected tissues. The authors of this article also reported that in periodontitis-affected mice treated with IL-35, the mRNA and protein levels of RANKL were significantly lower and conversely the expressed and secreted levels of OPG were significantly higher comparing to mice without IL_35 treatment.

Association studies with cross-sectional design

Ten of the studies included in this review were mainly association studies with a cross-sectional design. Almost all of these studies compared the level of IL-35 in various tissue samples, such as peripheral blood, serum, gingival crevicular fluid (GCF), and periodontal tissue biopsies in periodontitis patients with a healthy control group. Among these, nine studies were conducted among systemically healthy individuals, and only one study was conducted among patients with Type 2 diabetes mellitus. The study results among patients with diabetes showed that neither type 2 diabetes mellitus nor chronic periodontitis differentially has affected serum levels of IL-35 [44]. However, the results of all the studies among systematically healthy individuals showed that the levels of IL-35 were higher in tissue samples of periodontitis patients comparing to non-infected samples. In this regard, eight studies focused on chronic types of periodontal disease, including gingivitis and periodontitis. However, Kalburgi et al. examined IL-35 mRNA expression in gingival tissue samples of patients with aggressive periodontitis, patients with chronic periodontitis, and healthy controls using reverse transcriptase polymerase chain reaction (RT-PCR). The results showed that IL-35 mRNA expression was highest in subjects with chronic periodontitis compared to the subjects with aggressive periodontitis and the least seen in healthy patients[26]. Among the included studies, only one paper reported that IL-35 elevated level was also associated with the severity of chronic periodontitis[45]. Unfortunately, due to substantial heterogeneity in sampling methods, severity of disease, and laboratory tests used in these observational studies, the post hoc analysis such as meta-analysis was not feasible [46].

Randomized control clinical studies

Only two human interventional studies on IL-35 (patho) biology in periodontal disease were identified [47, 48]. Both were randomized controlled clinical trials and assessed the effect of non-surgical periodontal treatment (NSPT) on IL-35 level among patients with chronic periodontitis. The first study was conducted among forty patients with chronic periodontitis who were randomly divided into two equal groups [48]. The control group received scaling root planning (SRP), and the test group treated with SRP followed by Er, Cr: YSGG laser. The results of this trial showed that all clinical parameters and GCF levels of immunological factors (IL-1β, IL-6, IL-35) significantly reduced in both groups compared with the baseline (P < 0.05), but no significant change was detected among the groups.

In the second study, 60 participants were divided into three equal groups, including healthy, gingivitis, and chronic periodontitis patients [47]. Only the subjects in periodontitis group underwent SRP treatment completed in two sessions within 24 h in accordance with the Quirynen’s one stage, full mouth debridement protocol. The study findings revealed that the mean IL-35 concentration in GCF samples of patients with chronic periodontitis was significantly higher than the other groups at baseline. Furthermore, the results confirmed a significant reduction in IL-35 concentration of GCF samples obtained from patients with periodontal disease six weeks after NSPT. It should be noted that this reduction of IL-35 concentration was consistent with the decrease in clinical parameters, including periodontal pocket depth (PPD), Clinical attachment level (CAL), plaque index (PI), gingival index (GI) and bleeding index (BI) in patients with periodontal disease. As there is a high level of heterogeneity in periodontal disease definitions, treatment protocols, and laboratory tests used in these studies, it was not appropriate to apply meta-analysis.

Discussion

IL-35 has been introduced as an anti-inflammatory cytokine in various diseases and conditions, such as experimental colitis, allergic asthma, and collagen-induced autoimmune arthritis [15, 17, 49]. IL-35 is—relatively spoken—a newcomer among suppressive cytokines[12]. The results of many studies showed the role of Th1 and Th17 cells and their cytokine profiles in periodontal disease [31, 50,51,52,53]. Based on the results of various studies, abnormal cellular immunity occurs in chronic periodontitis and elevated peripheral Th17 and Th1 cells might be simultaneously associated with the development of periodontal disease[31, 50]. It is interesting that IL-35 inhibits Th17 and Th1 cells and may play a protective role in periodontal disease[22, 54].

In this study, we tried to collect all available data in the literature about the role of IL-35 in pathobiology of periodontal disease. An in-depth analysis of the role of IL-35 could provide novel avenues for diagnosing, monitoring, and treating periodontitis.

In vitro and preclinical animal studies provided critical information about the function of IL-35 and the interaction of other immunological factors with this newly found agent. A study by Shindo et al. suggested an anti-inhibitory action for IL-35 in pathogenesis of periodontitis [41] and reported that IL-35 could inhibit the production of inflammatory cytokines such as IL-6 and IL-8. In this line, the results of an interventional animal study also considered an inhibitory effect for IL-35 in pathogenesis of alveolar bone resorption [43]. Another in vitro cell study suggested that IL-35 may also induce osteoclastogenesis by a synergistic correlation with RANKL [42]. It should be noted that in this study, the researchers just evaluated one type of cells (RAW264). However as they declared in their report, bone marrow derived-macrophages include many cell populations, mainly lymphocytes, which may affected by IL-35 in various manners [42]. In this regard, the results from the cross-sectional and RCTs were more consistent. All of these studies, except one conducted on patients with diabetes, confirmed the higher levels of IL-35 in tissue samples of patients with periodontal disease.

In only one study evaluating serum levels of IL-35 in patients with periodontal disease, included type 2 diabetic individuals with a control group, the results were inconsistent with the others[44]. The authors of this study reported that, despite significant associations of serum concentration of IL-35 with certain periodontal and inflammatory indices, neither type 2 diabetes mellitus nor chronic periodontitis affected the serum levels of these cytokines differently. This contradictory result may be related to the evaluation of this biomarker in the serum, not with GCF or a gingival biopsy.

In this way, the results of two interventional randomized clinical trials proved that treatment of chronic periodontitis and controlling periodontal tissues' inflammation could reduce the concentration of IL-35 in GCF. The exact function of IL-35 in etiopathogenesis of periodontal disease is not clear, but it is suggested to be produced by Treg cells as negative feedback regulation[12]. Previous research has revealed that in chronic periodontitis, the expression of Treg cells is significantly increased compared to gingivitis and healthy condition [55, 56]. These cells are recruited by immune system for arresting tissue destruction and containing the disease. Hence, a reduction in inflammatory load reduces the expression of Treg cells. Therefore, IL-35 levels in GCF also decrease. This may explain the significant reduction in GCF IL-35 levels in chronic patients with periodontal disease after NSPT was performed in two included RCTs [47, 48].

The results of the included studies in this review do not contradict previous reports on the protective role of IL-35 in pathogenesis of inflammatory diseases. Loss of IL-35 activity in animal models leads to worsening and progression of various inflammatory diseases such as encephalomyelitis [57, 58]. In this regard, samples lacking functional IL-35 showed greater severity of the disease[59, 60]. Conversely, when IL-35 was administered as a therapeutic agent in collagen-induced rheumatoid arthritis-affected mice, a significant reduction of pathological inflammation was observed[20]. In this scope, there is only one study in periodontology conducted by Cafferata et al. examining the effect of IL-35 administration on the alveolar bone resorption in periodontitis mice [43]. They concluded that IL-35 is beneficial in the regulation of periodontitis. Particularly, IL-35 inhibited alveolar bone resorption, and this inhibition was closely associated with modulation of the periodontal Th17/Treg imbalance.

Most of the studies included in this review had a cross-sectional design (level III) and thus indicated an overall low level of evidence to prove the definitive role of IL-35 in periodontitis[40]. Further longitudinal and controlled clinical trials are required to clarify the detailed functional pattern of IL-35 in various periodontal diseases. Future research in the IL-35 field could develop new innovative treatment methods to control periodontal.

Conclusion

In summary, these scoping review results confirmed the presence of high levels of IL-35 in saliva, GCF, serum, and gingival biopsies of patients with clinically diagnosed inflammatory periodontal disease. Elevated levels of IL-35 in periodontal tissues might be associated with the severity of periodontitis. At preclinical level, IL-35 showed inhibitory characteristics regarding alveolar bone resorption of periodontitis models. Moreover, non-surgical periodontal therapy could downregulate IL-35 production in patients with chronic periodontal disease.

Availability of data and materials

The datasets supporting the conclusions of this article are included within the article and its additional file.

Abbreviations

IL:

Interleukin

TNF:

Tumor necrosis factor

IL-1Ra:

Interleukin 1 receptor antagonist

TGFB:

Transforming growth factor-beta

Treg:

Regulatory T cells

EBI3:

Epstein-Barr virus induced gene 3

Th17:

T-helper-17

RCT:

Randomized control trials

GCF:

Gingival crevicular fluid

RT-PCR:

Reverse transcriptase polymerase chain reaction

NSPT:

Non-surgical periodontal treatment

SRP:

Scaling root planning

PPD:

Periodontal pocket depth

CAL:

Clinical attachment level

PI:

Plaque index

GI:

Gingival index

BI:

Bleeding index

References

  1. 1.

    Frencken JE, Sharma P, Stenhouse L, Green D, Laverty D, Dietrich T. Global epidemiology of dental caries and severe periodontitis–a comprehensive review. J Clin Periodontol. 2017;44:S94–105.

    PubMed  Article  PubMed Central  Google Scholar 

  2. 2.

    Bartold PM, Van Dyke TE. An appraisal of the role of specific bacteria in the initial pathogenesis of periodontitis. J Clin Periodontol. 2019;46(1):6–11.

    PubMed  PubMed Central  Article  Google Scholar 

  3. 3.

    Fakheran O, Khodadadi-Bohlouli Z, Khademi A: Effect of vitamin D level on periodontal treatment outcomes: a systematic review. Gen Dent 2019:64–67.

  4. 4.

    Van Dyke TE. Bartold PM. Reynolds EC: The Nexus Between Periodontal Inflammation and Dysbiosis. Frontiers in Immunology; 2020. p. 11.

    Google Scholar 

  5. 5.

    Pan W, Wang Q, Chen Q. The cytokine network involved in the host immune response to periodontitis. Int J Oral Sci. 2019;11(3):1–13.

    Article  Google Scholar 

  6. 6.

    Graves D. Cytokines that promote periodontal tissue destruction. J Periodontol. 2008;79:1585–91.

    PubMed  Article  Google Scholar 

  7. 7.

    Hanada T, Yoshimura A. Regulation of cytokine signaling and inflammation. Cytokine Growth Factor Rev. 2002;13(4–5):413–21.

    PubMed  Article  Google Scholar 

  8. 8.

    Hajishengallis G, Korostoff JM: Revisiting the Page & Schroeder model: the good, the bad and the unknowns in the periodontal host response 40 years later. Periodontology 2000 2017, 75(1):116–151.

  9. 9.

    Takashiba S, Naruishi K, Murayama Y. Perspective of cytokine regulation for periodontal treatment: fibroblast biology. J Periodontol. 2003;74(1):103–10.

    PubMed  Article  PubMed Central  Google Scholar 

  10. 10.

    Yucel-Lindberg T, Båge T: Inflammatory mediators in the pathogenesis of periodontitis. Exp Rev Mol Med 2013, 15.

  11. 11.

    Hienz SA, Paliwal S, Ivanovski S: Mechanisms of bone resorption in periodontitis. Journal of immunology research 2015, 2015.

  12. 12.

    Sawant DV, Hamilton K, Vignali DA. Interleukin-35: expanding its job profile. J Interferon Cytokine Res. 2015;35(7):499–512.

    PubMed  PubMed Central  Article  Google Scholar 

  13. 13.

    Devergne O, Birkenbach M, Kieff E. Epstein-Barr virus-induced gene 3 and the p35 subunit of interleukin 12 form a novel heterodimeric hematopoietin. Proc Natl Acad Sci. 1997;94(22):12041–6.

    PubMed  Article  Google Scholar 

  14. 14.

    Pope RM, Shahrara S. Possible roles of IL-12-family cytokines in rheumatoid arthritis. Nat Rev Rheumatol. 2013;9(4):252–6.

    PubMed  Article  Google Scholar 

  15. 15.

    Collison LW, Workman CJ, Kuo TT, Boyd K, Wang Y, Vignali KM, Cross R, Sehy D, Blumberg RS, Vignali DA. The inhibitory cytokine IL-35 contributes to regulatory T-cell function. Nature. 2007;450(7169):566–9.

    PubMed  Article  Google Scholar 

  16. 16.

    Collison LW, Chaturvedi V, Henderson AL, Giacomin PR, Guy C, Bankoti J, Finkelstein D, Forbes K, Workman CJ, Brown SA. IL-35-mediated induction of a potent regulatory T cell population. Nat Immunol. 2010;11(12):1093–101.

    PubMed  PubMed Central  Article  Google Scholar 

  17. 17.

    Wirtz S, Billmeier U, Mchedlidze T, Blumberg RS, Neurath MF. Interleukin-35 mediates mucosal immune responses that protect against T-cell–dependent colitis. Gastroenterology. 2011;141(5):1875–86.

    PubMed  PubMed Central  Article  Google Scholar 

  18. 18.

    Li Y, Wang Y, Liu Y, Wang Y, Zuo X, Li Y, Lu X: The possible role of the novel cytokines il-35 and il-37 in inflammatory bowel disease. Mediators of Inflammation 2014, 2014.

  19. 19.

    Gao P, Su Z, Lv X, Zhang J: Interluekin-35 in asthma and its potential as an effective therapeutic agent. Med Inflamm, 2017.

  20. 20.

    Niedbala W. Wei Xq, Cai B, Hueber AJ, Leung BP, McInnes IB, Liew FY: 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. Eur J Immunol. 2007;37(11):3021–9.

    PubMed  Article  PubMed Central  Google Scholar 

  21. 21.

    Shen P, Roch T, Lampropoulou V, O’Connor RA, Stervbo U, Hilgenberg E, Ries S, Jaimes Y, Daridon C, Li R. IL-35-producing B cells are critical regulators of immunity during autoimmune and infectious diseases. Nature. 2014;507(7492):366–70.

    PubMed  PubMed Central  Article  Google Scholar 

  22. 22.

    Wang R-X, Yu C-R, Dambuza IM, Mahdi RM, Dolinska MB, Sergeev YV, Wingfield PT, Kim S-H, Egwuagu CE. Interleukin-35 induces regulatory B cells that suppress autoimmune disease. Nat Med. 2014;20(6):633–41.

    PubMed  PubMed Central  Article  Google Scholar 

  23. 23.

    Li Y, Li D, Wu S, Jiang S, Lin T, Xia L, Shen H, Lu J. Interleukin-35 upregulates OPG and inhibits RANKL in mice with collagen-induced arthritis and fibroblast-like synoviocytes. Osteoporos Int. 2016;27(4):1537–46.

    PubMed  Article  PubMed Central  Google Scholar 

  24. 24.

    Köseoğlu S, Sağlam M, Pekbağrıyanık T, Savran L, Sütçü R. Level of interleukin-35 in gingival crevicular fluid, saliva, and plasma in periodontal disease and health. J Periodontol. 2015;86(8):964–71.

    PubMed  Article  PubMed Central  Google Scholar 

  25. 25.

    Mitani A, Niedbala W, Fujimura T, Mogi M, Miyamae S, Higuchi N, Abe A, Hishikawa T, Mizutani M, Ishihara Y. Increased expression of interleukin (IL)-35 and IL-17, but not IL-27, in gingival tissues with chronic periodontitis. J Periodontol. 2015;86(2):301–9.

    PubMed  Article  PubMed Central  Google Scholar 

  26. 26.

    Kalburgi NB, Muley A, Shivaprasad B, Koregol AC: Expression profile of IL-35 mRNA in gingiva of chronic periodontitis and aggressive periodontitis patients: a semiquantitative RT-PCR study. Dis Mark 2013, 35.

  27. 27.

    Jin Y, Liu D, Lin X. IL-35 may maintain homeostasis of the immune microenvironment in periodontitis. Exp Ther Med. 2017;14(6):5605–10.

    PubMed  PubMed Central  Google Scholar 

  28. 28.

    Jing L, Kim S, Sun L, Wang L, Mildner E, Divaris K, Jiao Y, Offenbacher S. IL-37-and IL-35/IL-37-producing plasma cells in chronic periodontitis. J Dent Res. 2019;98(7):813–21.

    PubMed  PubMed Central  Article  Google Scholar 

  29. 29.

    Liu W, Zeng Q, Wen Y, Tang Y, Yan S, Li Y, Zhou L, Luo R: Inhibited interleukin 35 expression and interleukin 35–induced regulatory T cells promote type II innate lymphoid cell response in allergic rhinitis. Ann Allergy Asthma Immunol 2021, 126(2):152–161. e151.

  30. 30.

    Bello RO, Chin VK. Abd Rachman Isnadi MF, Abd Majid R, Atmadini Abdullah M, Lee TY, Amiruddin Zakaria Z, Hussain MK, Basir R: The role, involvement and function (s) of interleukin-35 and interleukin-37 in disease pathogenesis. Int J Mol Sci. 2018;19(4):1149.

    Article  Google Scholar 

  31. 31.

    Chen X-T, Chen L-L, Tan J-Y, Shi D-H, Ke T, Lei L-H. Th17 and Th1 lymphocytes are correlated with chronic periodontitis. Immunol Invest. 2016;45(3):243–54.

    PubMed  Article  Google Scholar 

  32. 32.

    Sommer M, Dalia R, Nogueira A, Cirelli J, Vinolo M, Fachi J, Oliveira C, Andrade T, Mendonça F, Santamaria M Jr. Immune response mediated by Th1/IL-17/caspase-9 promotes evolution of periodontal disease. Arch Oral Biol. 2019;97:77–84.

    PubMed  Article  PubMed Central  Google Scholar 

  33. 33.

    Rosser EC, Mauri C. Regulatory B cells: origin, phenotype, and function. Immunity. 2015;42(4):607–12.

    Article  Google Scholar 

  34. 34.

    Hetta HF, Mwafey IM. Batiha GE-S, Alomar SY, Mohamed NA, Ibrahim MA, Elkady A, Meshaal AK, Alrefai H, Khodeer DM: Cd19+ cd24hi cd38hi regulatory b cells and memory b cells in periodontitis: Association with pro-inflammatory and anti-inflammatory cytokines. Vaccines. 2020;8(2):340.

    PubMed Central  Article  PubMed  Google Scholar 

  35. 35.

    Slots J: Periodontitis: facts, fallacies and the future. Periodontology 2000 2017, 75(1):7–23.

  36. 36.

    Burlingham WJ, Al-Adra DA, Olson BM, McNeel DG, Sullivan JA. Infectious Tolerance as seen with 2020 vision: the role of IL-35 and Extracellular Vesicles. Front Immunol. 1867;2020:11.

    Google Scholar 

  37. 37.

    Sullivan JA, Tomita Y, Jankowska-Gan E, Lema DA, Arvedson MP, Nair A, Bracamonte-Baran W, Zhou Y, Meyer KK, Zhong W: Treg-cell-derived IL-35-coated extracellular vesicles promote infectious tolerance. Cell Reports 2020, 30(4):1039–1051. e1035.

  38. 38.

    Rojas García C, Campos Mora M, Cárcamo I, Villalón N, Elhusseiny A, Contreras Kallens P, Refisch A, Gálvez Jirón F, Emparán I, Montoya Riveros A: T regulatory cells-derived extracellular vesicles and their contribution to the generation of immune tolerance. 2020.

  39. 39.

    Arksey H, O’Malley L. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. 2005;8(1):19–32.

    Article  Google Scholar 

  40. 40.

    Burns PB, Rohrich RJ, Chung KC. The levels of evidence and their role in evidence-based medicine. Plast Reconstr Surg. 2011;128(1):305.

    PubMed  PubMed Central  Article  Google Scholar 

  41. 41.

    Shindo S, Hosokawa Y, Hosokawa I, Shiba H. Interleukin (IL)-35 suppresses IL-6 and IL-8 production in IL-17A-stimulated human periodontal ligament cells. Inflammation. 2019;42(3):835–40.

    PubMed  Article  Google Scholar 

  42. 42.

    Kamiya Y, Kikuchi T, Goto H, Okabe I, Takayanagi Y, Suzuki Y, Sawada N, Okabe T, Kondo S. Hayashi J-i: IL-35 and RANKL Synergistically Induce Osteoclastogenesis in RAW264 Mouse Monocytic Cells. Int J Mol Sci. 2020;21(6):2069.

    PubMed Central  Article  Google Scholar 

  43. 43.

    Cafferata EA, Terraza-Aguirre C, Barrera R, Faúndez N, González N, Rojas C, Melgar-Rodríguez S, Hernández M, Carvajal P, Cortez C. Interleukin-35 inhibits alveolar bone resorption by modulating the Th17/Treg imbalance during periodontitis. J Clin Periodontol. 2020;47(6):676–88.

    PubMed  Article  Google Scholar 

  44. 44.

    Maboudi A, Eghbalian-Nouzanizadeh A, Seifi H, Bahar A, Mohadese M, Mohammadpour RA, Abediankenari S, Poorbaghi SL, Sepehrimanesh M. Serum levels of interleukin-23 and 35 in patients with and without type 2 diabetes mellitus and chronic periodontitis. Caspian J Intern Med. 2019;10(3):295.

    PubMed  PubMed Central  Google Scholar 

  45. 45.

    Cai S, Liu X, Li H, Feng L, Cao L, Huang J, Liang Y, Zeng J, Shi B. Elevated interleukin (IL)-35-related sCD14 but not IL-23 is associated with the severity of chronic periodontitis. Int J Clin Exp Med. 2017;10(2):4119–28.

    Google Scholar 

  46. 46.

    Chess LE, Gagnier JJ. Applicable or non-applicable: investigations of clinical heterogeneity in systematic reviews. BMC Med Res Methodol. 2016;16(1):19.

    PubMed  PubMed Central  Article  Google Scholar 

  47. 47.

    Raj SC, Panda SM, Dash M, Patnaik K, Mohanty D, Katti N, Mahapatra A, Mishra D, Praharaj K. Association of human interleukin-35 level in gingival crevicular fluid and serum in periodontal health, disease, and after nonsurgical therapy: A comparative study. Contemporary clinical dentistry. 2018;9(2):293.

    PubMed  PubMed Central  Article  Google Scholar 

  48. 48.

    Üstün K, Hatipoğlu M, Daltaban Ö, Felek R, Firat M. Clinical and biochemical effects of erbium, chromium: yttrium, scandium, gallium, garnet laser treatment as a complement to periodontal treatment. Niger J Clin Pract. 2018;21(9):1150–7.

    PubMed  PubMed Central  Google Scholar 

  49. 49.

    Huang C-H. Loo EX-L, Kuo I-C, Soh GH, Goh DL-M, Lee BW, Chua KY: Airway inflammation and IgE production induced by dust mite allergen-specific memory/effector Th2 cell line can be effectively attenuated by IL-35. J Immunol. 2011;187(1):462–71.

    PubMed  Article  Google Scholar 

  50. 50.

    Arun K, Talwar A, Kumar T. T-helper cells in the etiopathogenesis of periodontal disease: A mini review. Journal of Indian Society of Periodontology. 2011;15(1):4.

    PubMed  PubMed Central  Article  Google Scholar 

  51. 51.

    Zhao L, Zhou Y, Xu Y, Sun Y, Li L, Chen W. Effect of non-surgical periodontal therapy on the levels of Th17/Th1/Th2 cytokines and their transcription factors in Chinese chronic periodontitis patients. J Clin Periodontol. 2011;38(6):509–16.

    PubMed  Article  PubMed Central  Google Scholar 

  52. 52.

    Bi CS, Li X, Qu HL, Sun LJ, An Y, Hong YL, Tian BM, Chen FM. Calcitriol inhibits osteoclastogenesis in an inflammatory environment by changing the proportion and function of T helper cell subsets (Th2/Th17). Cell Prolif. 2020;53(6):e12827.

    PubMed  PubMed Central  Article  Google Scholar 

  53. 53.

    Huang H, Chen D, Lippuner K, Hunziker EB: Induced Experimental Periimplantitis and Periodontitis: What are the Differences in the Inflammatory Response? Experimental periimplantitis and periodontitis in dogs. Journal of oral implantology 2020.

  54. 54.

    Teng D-K, Liu Y, Lv Y-F, Wang L, Zhang W, Wang J-P, Li Y. Elevated interleukin-35 suppresses liver inflammation by regulation of T helper 17 cells in acute hepatitis B virus infection. Int Immunopharmacol. 2019;70:252–9.

    PubMed  Article  PubMed Central  Google Scholar 

  55. 55.

    Nakajima T, Ueki-Maruyama K, Oda T, Ohsawa Y, Ito H, Seymour G, Yamazaki K. Regulatory T-cells infiltrate periodontal disease tissues. J Dent Res. 2005;84(7):639–43.

    PubMed  Article  Google Scholar 

  56. 56.

    Garlet GP, Cardoso CR, Mariano FS, Claudino M, De Assis GF, Campanelli AP, Ávila-Campos MJ, Silva JS. Regulatory T cells attenuate experimental periodontitis progression in mice. J Clin Periodontol. 2010;37(7):591–600.

    PubMed  Article  PubMed Central  Google Scholar 

  57. 57.

    Tirotta E, Duncker P, Oak J, Klaus S, Tsukamoto MR, Gov L, Lane TE. Epstein-Barr virus-induced gene 3 negatively regulates neuroinflammation and T cell activation following coronavirus-induced encephalomyelitis. J Neuroimmunol. 2013;254(1–2):110–6.

    PubMed  Article  PubMed Central  Google Scholar 

  58. 58.

    Liu J-Q, Liu Z, Zhang X, Shi Y, Talebian F, Carl JW, Yu C, Shi F-D, Whitacre CC, Trgovcich J. Increased Th17 and regulatory T cell responses in EBV-induced gene 3-deficient mice lead to marginally enhanced development of autoimmune encephalomyelitis. J Immunol. 2012;188(7):3099–106.

    PubMed  PubMed Central  Article  Google Scholar 

  59. 59.

    Egwuagu CE, Yu C-R, Sun L, Wang R. Interleukin 35: Critical regulator of immunity and lymphocyte-mediated diseases. Cytokine Growth Factor Rev. 2015;26(5):587–93.

    PubMed  PubMed Central  Article  Google Scholar 

  60. 60.

    Zhang Y-L, Zhou X-Y, Guo X-Y, Tu J-W. Association between serum interleukin-35 levels and severity of acute pancreatitis. Int J Clin Exp Med. 2015;8(5):7430.

    PubMed  PubMed Central  Google Scholar 

  61. 61.

    Costantini E, Sinjari B, Piscopo F, Porreca A, Reale M, Caputi S, Murmura G. Evaluation of salivary cytokines and Vitamin D levels in periodontopathic patients. Int J Mol Sci. 2020;21(8):2669.

    PubMed Central  Article  Google Scholar 

  62. 62.

    Okada K, Fujimura T, Kikuchi T, Aino M, Kamiya Y, Izawa A, Iwamura Y, Goto H, Okabe I, Miyake E. Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4+ T cells. PeerJ. 2017;5:e2999.

    PubMed  PubMed Central  Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

Isfahan University of Medical Sciences and Clinician-Scientist Program office (Project ID: IR.MUI.REC. 396722).

Author information

Affiliations

Authors

Contributions

OF: Conceptualization, Methodology, Formal analysis, Investigation, Software, Writing—Original Draft, MD: Conceptualization, Methodology, Formal analysis, Investigation, Writing—Review & Editing, Supervision. PS: Conceptualization, Formal analysis, Investigation, Writing—Review & Editing, Supervision. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Omid Fakheran.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Full details of the search protocol used in this systematic review.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Schmidlin, P.R., Dehghannejad, M. & Fakheran, O. Interleukin-35 pathobiology in periodontal disease: a systematic scoping review. BMC Oral Health 21, 139 (2021). https://doi.org/10.1186/s12903-021-01515-1

Download citation

Keywords

  • Interleukin-35
  • Periodontal disease
  • Systematic review