Abstract
Sjögren’s Syndrome (SjS) results in loss of salivary and lacrimal gland excretion due to an autoimmune attack on these secretory glands. Conventional SjS treatments address the symptoms, but not the cause of disease. Recognizing this deficit of treatments to reverse SjS disease, studies were pursued using the fimbriae from enterotoxigenic E. coli, colonization factor antigen I (CFA/I), which has anti-inflammatory properties. To determine if CFA/I fimbriae could attenuate SjS-like disease in C57BL/6.NOD-Aec1Aec2 (SjS) females, the Lactococcus lactis (LL) 301 strain was developed to chromosomally express the cfaI operon. Western blot analysis confirmed CFA/I protein expression, and this was tested in SjS females at different stages of disease. Repeated dosing with LL 301 proved effective in mitigating salivary flow loss and in reducing anti-nuclear antibodies (ANA) and inflammation in the submandibular glands (SMGs) in SjS females and in restoring salivary flow in diseased mice. LL 301 treatment reduced proinflammatory cytokine production with concomitant increases in TGF-β+ CD25+ CD4+ T cells. Moreover, LL 301 treatment reduced draining lymph and SMG follicular T helper (Tfh) cell levels and proinflammatory cytokines, IFN-γ, IL-6, IL-17, and IL-21. Such evidence points to the therapeutic capacity of CFA/I protein to suppress SjS disease and to have restorative properties in combating autoimmune disease.
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Introduction
Sjögren’s Syndrome (SjS) is a chronic, progressive autoimmune disease characterized by inflammatory cell infiltration of the salivary and lacrimal glands, resulting in acinar epithelial cell atrophy, cell death, and loss of exocrine function (reviewed in1,2,3). The disease incidence is estimated to be 0.1–3% of the general population4,5,6 occurring primarily in postmenopausal women4,5,7. SjS is a debilitating disease affecting as many as 3.1 million individuals in the US1,2,3,5,6 with women being nine times more likely to be afflicted than men2,4,5,7. The etiology of SjS remains unclear. The C57BL/6.NOD-Aec1Aec2 mouse model was derived based on the observation of SjS-like disease in diabetic NOD mice8,9,10,11. The responsible genes associated with SjS, but free from those responsible for diabetes, were inserted into B6 mice to recapitulate SjS10. This model has the advantage of exhibiting many of the salivary gland pathology observed with human SjS patients, and increased production of anti-nuclear antibodies (ANAs). Hence, studies with various mouse models, including the C57BL/6.NOD-Aec1Aec2 mouse, are beginning to define both the innate and adaptive immune responses during development and onset of SjS-like disease8,9,10.
The development of therapeutics for SjS poses significant challenges, in part because of the heterogeneity of clinical disease. Few studies have addressed the critical issue of identifying interventions to stop or reverse the destructive autoimmune process. Currently, no therapeutics address the cause of SjS, but instead treatments consist of replacement therapies such as artificial saliva and eye lubricants or immunosuppressive agents12,13. B cell-directed therapies, e.g., Rituximab (anti-CD20 mAb), have yielded promising, but conflicting results14,15,16,17,18, and are unable to alleviate patients’ dryness and fatigue19,20. CTLA-4 protein (Abatacept) showed some reduction in gland pathology21, and enhancement of salivary flow in a limited number of SjS patients22. Abatacept was recently shown to reduce serum IL-21 and follicular T helper (Tfh) cells in SjS patients23,24, and to reduce SjS symptoms25,26.
Originally conceived as a diarrheal vaccine for humans27,28,29,30, colonization factor antigen I (CFA/I) from enterotoxigenic E. coli (ETEC) was found by our lab to be potently effective in suppressing experimental models for multiple sclerosis31,32,33, arthritis34,35,36,37, and type 1 diabetes38,39. In fact, purified CFA/I fimbriae, given orally or nasally, can effectively attenuate inflammation36. The cfa1 operon has been successfully engineered into a Lactococcus lactis strain, and referred to as L. lactis-CFA/I (LL-CFA/I). By retaining its inhibitory activity, oral administration of LL-CFA/I protects against arthritis37. Of note, our results show that LL-CFA/I can attenuate genetically induced SjS via the stimulation/reactivation of diverse regulatory T cells (Tregs) producing TGF-β and IL-1040. Moreover, LL-CFA/I was found to be therapeutic for ongoing SjS.
The use of L. lactis for delivery of biologics and CFA/I protein has several advantages: (1) oral dosing of targeted biological immunotherapy which traditionally require infusion or frequent injections; (2) controllable dosing as L. lactis does not colonize the human gastrointestinal tract41,42, and our own studies in mice confirm its transient presence in tissues for < 48 h; and (3) pharmacodynamically optimized delivery of constitutively expressed CFA/I protein for engagement of microbiome-associated immune regulatory pathway. The fact that L. lactis does not colonize the gut41,43 is ideal for an immunotherapeutic as it enables a ‘tunable’ therapeutic strategy wherein identification of key mechanism-driving biomarkers, as discussed herein in the context of CFA/I protein, become critical for effective and efficient clinical development. Importantly, L. lactis, in the context of synthetic biology approaches to deliver CFA/I, allows for utilization of precision targeting methods, not capable using natural commensal strain strategies.
To advance clinical translation, an L. lactis line was generated to chromosomally express cfaI (referred to as LL 301), and LL 301 showed equivalent efficacy to LL-CFA/I, the precursor L. lactis line that expresses CFA/I from an episomal plasmid. Chromosomal insertion of the cfa/I operon increases stability of the line, as propagation no longer requires antibiotic selection, and relieves concerns regarding episomal transfer in vivo. When testing LL 301 in the genetic model for SjS using C57BL/6.NOD-Aec1Aec2 mice, our results show that prophylactic treatments proved effective in salivary flow mitigation, and therapeutic interventions restored salivary flow. Such changes from the diseased state were accomplished via the stimulation of Tregs and suppression of effector T (Teff) cells including Tfh cells.
Results
Oral intervention with LL 301 retains salivary flow in SjS mice
LL 301 was generated to have a Lactococcus lactis strain expressing CFA/I protein without reliance upon episomal expression as in L. lactis-CFA/I (LL-CFA/I). A ΔthyA L. lactis was produced by double homologous recombination via insertion of the cfaI operon replacing the thymidylate synthase (thyA) gene. Production levels of the major subunit, CfaB, by LL 301 was confirmed as evidenced by Western blot analysis (Fig. 1A).
In evaluating LL 301’s efficacy relevant to LL-CFA/I to mitigate salivary flow loss in C57BL/6.NOD-Aec1Aec2 (SjS) mice, baseline individual saliva flow rate (SFR) for all groups of 6 week (wk)-old females were obtained. Treatments of SjS mice were initiated at 10 weeks of age dosing at 3-week intervals for a total of six doses with PBS or one of three doses of LL 301: 5 × 107 (low), 5 × 108 (medium), or 5 × 109 (high) CFUs (Fig. 1B, C). As a positive control, one group of mice was given 5 × 107 CFUs of LL-CFA/I. SFR measurements were conducted at 28 weeks of age, three weeks after the last dose (Fig. 1D, E). Both the high dose LL 301 and LL-CFA/I proved significantly effective in retaining salivary flow relative to PBS-dosed mice (Fig. 1E). Treatments with the medium dose of LL 301 also proved effective in reducing the frequency of mice exhibiting ANA titers (Fig. 1F).
LL 301 treatment reduces proinflammatory cytokine production with a concomitant increase in anti-inflammatory cytokines
The mitigation of SFR loss would be expected to result from inflammatory cell arrest. The study was terminated at week 29, and the levels of IFN-γ- and IL-17-producing CD4+ T cells in the spleen were measured. The high dose LL 301 and LL-CFA/I effectively reduced the percentage of IFN-γ+ CD4+ T cells (Fig. 2A). Changes in IL-17+ CD4+ T cells were observed only for the LL 301 medium dose (Fig. 2B); however, increases in IL-10+ CD4+ T cells were obtained with the LL 301 medium dose and with LL-CFA/I (Fig. 2C). The percentage of TGF-β+ CD4+ T cells also increased in SjS mice treated with LL 301 high dose and LL-CFA/I (Fig. 2D).
Additional cytokine analysis was performed on anti-CD3 plus anti-CD28 mAb treatments to measure if head and neck lymph nodes (HNLNs), mesenteric LNs (MLNs) and splenic T cells exhibit anti-inflammatory cytokine capacity. All of the HNLN and MLN treatment groups showed significant reduction in IFN-γ production compared to PBS-dosed SjS mice (Fig. 2E). The LL 301 medium dose treatment group showed significant reduction of IFN-γ production (Fig. 2E). IL-17 was significantly reduced by all LL 301 treatment doses by HNLN lymphocytes and by splenic lymphocytes from the LL-CFA/I-treated mice (Fig. 2F). IL-6 production was also significantly reduced by HNLN lymphocytes from SjS mice treated with the LL 301 low and high doses, and LL-CFA/I-treated mice showed significant reduction in IL-6 from the HNLN, MLN, and splenic lymphocytes (Fig. 2G). IL-10 production remained relatively unchanged among the three lymphoid tissues except for the HNLN lymphocytes from the LL 301 high dose and LL-CFA/I groups showed a significant reduction (Fig. 2H).
Salivary flow is mitigated by LL 301 treatments and not with WT LL
Given the positive outcome of the previous findings using LL 301, the study was repeated using a medium (5 × 108 CFUs) and high (5 × 109 CFUs) doses of LL 301 compared to groups of SjS females treated with WT LL (5 × 108 CFUs) and PBS vehicle (Fig. 3A). Treatments were initiated at 5 weeks of age and additional doses administered at 3 week intervals until 17 weeks of age (Fig. 3B). SFRs were measured for individual mice, and showed that both doses of LL 301 were effective mitigating salivary flow in contrast to WT LL or PBS-vehicle treated SjS females (Fig. 3C). No significant differences in SFR were observed between PBS- and WT LL-treated SjS females. H&E staining was performed on paraffin-embedded submandibular glands (SMGs) from individual mice of each treatment group (Fig. 3D), and foci area and number of foci were quantified (Fig. 3E, F). The medium LL 301 dose showed ~ 50% reduction in foci area compared to vehicle- or WT LL-treated SjS mice (Fig. 3E). Both doses of LL 301 proved effective in reducing the number of foci in the SMGs, and the LL 301 high dose also significantly lessened the number of SMG foci relative to WT LL-treated mice (Fig. 3F).
Additional analysis was conducted to determine if LL 301 was capable of eliciting regulatory T cells (Tregs). No significant differences in splenic Foxp3+ CD4+ T cells or Foxp3+ CD25+ CD4+ T cells were observed relative to vehicle-treated mice (Fig. 4A, B); however, the LL 301 medium dose effectively enhanced Foxp3+ CD25+ CD4+ T cells relative to WT LL-treated SjS females (Fig. 4B). The CD25+ CD4+ T cells were further analyzed for expression of TGF-β, and the LL 301 medium dose showed significantly increased percentages of splenic TGF-β+ CD25+ CD4+ T cells relative to PBS- or WT LL-treated SjS females (Fig. 4C, D). Neither dose of LL 301 impacted the frequency of IL-17+ CD4+ T cells (Fig. 4E) or IL-17 production from restimulated splenic lymphocytes (Fig. 4G). In contrast, the high dose of LL 301 reduced the percentage of splenic IFN-γ+ CD4+ T cells (Fig. 4F) and reduced IFN-γ production from restimulated splenic lymphocytes compared to vehicle- or WT LL-treated mice (Fig. 4H).
Oral treatment with LL 301 is therapeutic in restoring salivary flow, and reducing inflammatory cytokine production.
To discern LL 301’s therapeutic potential (Fig. 5A), groups of SjS females were measured for their SFRs at 16 weeks of age, and then the mice were equally distributed among the three treatment groups (Fig. 5B). At 18 and 22 weeks of age, mice were treated with PBS, 3 × 109 CFUs WT LL, or 3 × 109 CFUs LL 301, and SFRs measured again at 24 weeks of age (Fig. 5A). After just two doses of LL 301, SjS females showed a significant increase in their SFRs, but not those treated with PBS nor WT LL (Fig. 5C). Although there were no significant differences in the number of foci in their SMGs relative to PBS-treated mice (Fig. 5D), the foci area was significantly increased in WT LL-treated mice (Fig. 5E). Upon termination of the mice at 24 weeks of age, splenic lymphocytes were examined for the presence of Tregs, but no differences in Foxp3+ CD4+ T cells nor Foxp3+ CD25+ CD4+ T cells were found (Fig. 5F, G). However, treatment with LL 301 and WT LL did show significant reductions in the percentage of IL-17+ CD4+ and IFN-γ+ CD4+ T cells (Fig. 5H, I). Total lymphocytes from the HNLNs, MLNs, and spleen were restimulated, and collected supernatants measured for IL-17 and IFN-γ production. Significant reductions in HNLN and MLN IL-17 were observed by LL 301- and WT LL-treated groups (Fig. 5J, K). HNLN IFN-γ production was also significantly reduced by the LL 301- and WT LL-treated groups (Fig. 5M). Splenic IL-17 and IFN-γ levels remained unchanged.
Treatment with LL 301 suppresses Tfh cells in SjS mice
Tfh cells aid B cells by supporting the formation of germinal centers for maturation of antibody responses, and patients with primary SjS exhibit increased circulating Tfh cells44. Given this finding, analyses were conducted to ascertain LL 301’s capacity to inhibit Tfh cells in SjS females. Groups of 6 week-old females were orally dosed with PBS or 5 × 109 CFUs LL 301, and additional doses were administered at 3-week intervals. Upon termination of the study at 31 weeks of age, Tfh cell analyses were performed. HNLN lymphocytes were gated on TCRβ+ CD4+ T cells and stained for Tfh cells (Fig. 6A, B). Significant reductions in CXCR5+ PD-1+ CD4+ T cells were observed for those SjS females treated with LL 301 relative PBS-treated mice (Fig. 6A–C). Since Tfh cells produce IL-21, analysis of the IL-21+ CD4+ T cells revealed their percentages were also significantly reduced in the HNLNs from LL 301-treated SjS females (Fig. 6D). The diminished Tfh cell response subsequent LL 301 treatment is consistent with the observed significant increase in TGF-β+ CD4+ T cells compared to PBS controls (Fig. 6E). HNLN lymphocytes were subsequently stimulated in vitro with anti-CD3 plus anti-CD28 mAbs, and collected culture supernatants from LL 301-treated SjS females showed significantly reduced levels of IFN-γ, IL-6, IL-17, IL-21, and GM-CSF relative to those T cells from PBS controls (Fig. 6F–J). IL-10 levels were significantly increased in for HNLN lymphocytes from LL 301-treated SjS mice (Fig. 6K).
SMGs from LL 301- and PBS-treated SjS females were also evaluated for the presence of Tfh cells and Tregs. SMG lymphocytes were gated on TCRβ+ CD4+ T cells and stained for Tfh cells expressing CXCR5 and BCL-6 (Fig. 7A, B). The percentages of CXCR5+ CD4+ and BCL6+ CD4+ T cells were significantly less in the LL 301-treated group compared to PBS-dosed mice (Fig. 7A–D). Likewise, the CXCR5+ BCL6+ CD4+ T cells were also significantly reduced in SMGs from LL 301-treated mice (Fig. 7E). LL 301 treatment positively impacted Treg presence noted by the increased percentage of Foxp3+ CD4+ T cells in the SMGs relative to those from PBS-treated mice (Fig. 7F). SMG lymphocytes from LL 301-treated SjS females that were restimulated with anti-CD3 plus anti-CD28 mAbs showed a reduction in proinflammatory IL-6 production relative to those lymphocytes from PBS control mice (Fig. 7G).
Discussion
SjS remains problematic with no current therapies addressing the deficits in regulatory cells to defend against autoimmune attack. The development of oral therapeutics that stimulate Tregs and other regulatory cells to treat autoimmune diseases has the potential to reverse disease. Past studies using CFA/I fimbriae as an oral therapeutic have demonstrated the capabilities of such protein to limit inflammatory T cells in a number of autoimmune disease settings31,32,33,34,35,36,37,38,39,40. Hence, the development of LL 301 enabling CFA/I protein expression from the Lactococcus chromosome averts episomal loss, and represents a cell line that can be tested in humans. The advantage of using L. lactis as a delivery vehicle is because of its generally regarded as safe (GRAS) status41,and has already been approved for use in foods45,46 and treating diseases45,46,47,48,49,50,51. Another advantage of lactococcal expression is that it avoids the tedious process of isolating and purifying intact CFA/I fimbriae. Moreover, bacterial delivery is more potent and efficient requiring less CFA/I protein to suppress autoimmune disease36,37.
The production of CFA/I protein by the LL 301 strain is similar to that of LL-CFA/I. As a result, LL 301 should be as effective as LL-CFA/I, which has previously been shown to protect against collagen-induced arthritis37 and SjS40. Thus, a comparison study was performed in young SjS females, and showed that LL 301 mitigated salivary flow loss as with LL-CFA/I over the course of 18 weeks. Treatment with the medium dose of LL 301 also lessened the development of ANA responses consistent with previous observations subsequent treatment with LL-CFA/I40. LL 301 proved effective in reducing the frequency of proinflammatory IFN-γ+ and IL-17+ CD4+ T cells with concomitant increases in anti-inflammatory IL-10+ and TGF-β+ CD4+ T cells. Reductions in Th1 and Th17 cytokines were primarily observed in the HNLNs, which directly drains the salivary glands. IL-10 production was also reduced in the HNLNs, which may have been attributed to lesser proinflammatory cytokines being induced during the polyclonal stimulation of T cells. Further study was pursued to ascertain the influence of LL 301 upon earlier phase of SjS development until 18 weeks of age. Using 3-week intervals beginning at 5 weeks of age, SjS females showed saliva flow mitigation when treated with either 5 × 108 or 5 × 109 CFUs of LL 301 unlike PBS- and WT LL-treated females noted by their significant reductions in saliva flow. Histological examination of the SMGs further confirmed that LL 301 could reduce the number of foci and foci area of inflammation. Thus, mitigation of the saliva flow was attributed to lessened disease pathology. As with LL-CFA/I40, LL 301 showed Treg augmentation, particularly by Foxp3+ CD25+ CD4+ T cells relative to WT LL-treated SjS females. Further inquiry revealed that the CD25+ CD4+ T cells contain a subset of TGF-β+ T cells that also contain anti-inflammatory activity. The capacity to induce or convert Tregs in SjS may be critical. SjS patients have been shown to exhibit deficits in Tregs in their labial salivary glands52,53 and peripheral blood52,53,54. Human Tregs from SjS patient were also found to be unresponsive to IL-2 stimulation due to reduced phosphorylation of STAT555, but were able to reduce IL-17+ CD4+ T cells56.
Foxp3 expression varied with times of detection subsequent treatment with LL 301. Our evidence also showed that Tregs did not always express Foxp3, although increases in TGF-β+ Foxp3- CD4+ T cells were detected. Such evidence of Treg variability has also been previously seen upon Salmonella-CFA/I treatment of mice induced with arthritis, whereas both IL-10+ Foxp3+ CD39+ CD4+ T cells and TGF-β+ Foxp3- CD39+ CD4+ T cells were co-induced, and were also found to be interconvertible35. Adoptive transfer of Foxp3GFP+ CD39+ CD4+ T cells showed a reduction in Foxp3GFP+ and IL-10 expression, and vice versa, adoptive transfer of Foxp3GFP- CD39+ CD4+ T cells showed conversion into IL-10+ Foxp3GFP+ CD39+ CD4+ T cells35. Importantly, both Treg subsets were needed to adoptively transfer protection. Such interconversion of Tregs demonstrate these cells are dynamic and vary in their expression of Foxp3 as others have also shown57,58. Few experimental studies have examined Tregs in SjS animal models. Low-dose IL-2 proved effective in stimulating Foxp3+ CD25+ CD4+ T cells to lessen salivary flow loss in NOD mice59,60.
An important finding from the current studies is that LL 301 can intervene with ongoing SjS. Two doses of LL 301 proved sufficient in restoring salivary flow. Although it was less able to impact SMG pathology due to the damage already caused by disease, LL 301 did prove effective in reducing proinflammatory IFN-γ+ and IL-17+ CD4+ T cells despite no significant change in Foxp3+ CD25+ CD4+ T cells. However, these data show that LL 301’s impact is immediate since only two doses were used. This discovery has significant clinical implications since diagnosis of SjS often comes long after the disease is well-established, and having a therapeutic available to interrupt further pathological changes is encouraging. Additional study will be needed to assess whether long-term treatments can prevent further tissue damage.
Tfh cells have also been implicated in contributing to SjS disease exacerbation in their role to expand autoimmune B cells in salivary glands23,24,61,62. Normally found associated with B cell follicles, Tfh cells are believed to aid B cells in their expansion and differentiation into plasma cells and memory B cells63,64. IL-2 impacts both Tregs and conventional CD4+ T cells, but can suppress Tfh cell differentiation63,64. In contrast, IL-6 reduces the expression of IL-2Rβ to facilitate Tfh cell expansion65. The presented data demonstrates that LL 301 increases Treg presence in lymphoid tissues and in the SMGs. The increased Tregs had a noted effect in reducing the Tfh cells in both the HNLNs and in the SMG. LL 301 also reduced the percentage of IL-21-producing CD4+ T cells, a cytokine associated with Tfh cells63,64. The production of IL-21 by HNLN T cells was also notably reduced. The reduced Tfh cell presence associated with reduced IL-6 production by both the HNLNs and SMG lymphocytes is indicative that LL 301 is exerting a regulatory effect upon these inflammatory cells. Furthermore, the observed Tfh phenotypes in the SjS mice appeared heterogeneous as others have ascertained63,64. In the HNLNs, these were found to be CXCR5+ PD-1+ CD4+ T cells, but their expression of PD-1 by SMG Tfh cells appeared unchanged with or without LL 301 treatment, and primarily were CXCR5+ Bcl-6+ CD4+ T cells. Bcl-6 is a transcription factor, and its activity is essential for Tfh cell differentiation, maintenance, and function63. As such, Bcl-6, was markedly expressed by SMG Tfh cells from diseased SjS females, and, LL 301 treatment reduced this population.
In summary, LL 301 proved effective in reducing inflammatory cell infiltration into the SMGs via the stimulation of Tregs and their action by the production of TGF-β and IL-10. Importantly, LL 301 can act therapeutically by reducing inflammatory cell infiltration into the SMGs and restore salivary flow. This study reveals the presence of Tfh cells in diseased C57BL/6.NOD-Aec1Aec2 mice, and oral LL 301 treatments markedly reduced Tfh cells in both the HNLNs and SMGs. Such findings further demonstrate that orally administered CFA/I protein can intervene to reduce inflammatory diseases. Moreover, our findings support strategies for a robust pharmacodynamic and biomarker assessment plan to speed future clinical development endeavors.
Methods
Generation of Lactococcus lactis 301 strain and culture conditions
The CFA/I expression cassette was integrated in L. lactis genome using standard double homologous recombination methods66,67. The cfa/I expression operon was synthesized (Blue Heron Biotech, Bothell, WA), and cloned into the pRISE1.2 plasmid (Rise Therapeutics, MD), which contains a temperature-sensitive origin of replication. After transformation into L. lactis, cells were initially grown at 30 °C, and then the temperature was shifted to 37 °C to select for integrant cells. The integration occurred at the thymidylate synthase (thyA) locus, hence replacing thyA from the L. lactis chromosome. The purpose of targeting and deleting the thyA gene is to allow for containment; that is, the CFA/I expressing L. lactis will not propagate without thymidine supplementation68. Stability of the integration event was confirmed by growing the selected clones under non-selective conditions in M17 media supplemented with 20 µg/ml thymidine for 100 generations. WT L. lactis (LL) was used as a negative control in treating SjS mice. Western blot analysis was performed to confirm expression of CFA/I protein. Purified recombinant CFA/I fimbriae was obtained as previously described36, and detected using a rabbit anti-CFA/1 fimbriae antibody (produced in-house). The rabbit anti-CFA/I fimbriae antibody was detected with horseradish peroxidase conjugated goat anti-rabbit IgG (H + L) (Jackson ImmunoResearch, West Grove, PA).
The generation of L. lactis-CFA/I was described previously37. Briefly, starter small cultures were grown overnight 30 °C, and next day large culture induced with 0.5 µg/mL nisin (Sigma-Aldrich, St. Louis, MO). Four hours after induction, LL-CFA/I was gently washed twice with sterile PBS prior to oral gavage.
Mice and oral gavage
Using a genetic model for SjS10, C57BL/6.NOD-Aec1Aec (SjS) female mice were bred and used for these studies. All mice were housed under specific pathogen-free conditions, and provided with food and water ad libitum. Prior to oral administration of lactococcal strains, SjS mice were pretreated orally with sterile 10% sodium bicarbonate solution to neutralize stomach acid. After 10 min, mice proceeded to receive oral gavage with sterile PBS or the indicated doses (5 × 107 to 5 × 109 CFUs) of WT LL, LL 301, or LL-CFA/I. All of the studies involving animals adhered to the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health; were carried out in accordance with relevant guidelines and regulations for ethical and humane treatment of animals; and approved by the University of Florida Institutional Animal Care and Use Committee. The presented study is reported in accordance with ARRIVE guidelines.
Measurement of salivary flow rate (SFR)
Individual mice were weighed and given an intraperitoneal (IP) injection of 100 μl of a mixture containing isoproterenol (Sigma-Aldrich) (0.2 mg/1 ml of PBS) and pilocarpine hydrochloride (Sigma-Aldrich) (0.05 mg/1 ml in PBS). To measure stimulated flow rates, saliva was collected for 10 min from the oral cavity of each mouse using a micropipette as previously described40. To calculate SFRs, the volume of each saliva sample was measured.
Histology
To assess the degree of inflammation of salivary glands, tissues were fixed in 10% phosphate-buffered formalin (Leica Biosystems, Richmond, IL) for 24 h, and then these were embedded in paraffin and sectioned at 50–100 μm deep at a thickness of 5 μm. Paraffin-embedded sections were deparaffinized by immersing in xylene, followed by dehydration in ethanol, and tissue sections were stained with hematoxylin and eosin (H&E) dye (UF College of Veterinary Medicine Histology Tech Services, Gainesville, FL). To measure the extent of leukocyte infiltration into the salivary glands, a single histological section per gland per mouse was scanned using an Aperio ScanScope (Aperio, San Diego, CA) slide digitizer at 20× magnification as previously described40. Sections containing leukocyte-infiltrated regions were identified and calculated using the Aperio ImageScope software. The extent of the infiltrate varied between 1 and in 4 mm2, and samples from each mouse for each treatment group were calculated.
Serum antinuclear antibody (ANA) determinations
To measure the presence of ANA levels, individual serum from mice treated with PBS or LL 301 was examined using the HEp-2 ANA kit (Inova Diagnostics, Inc., San Diego, CA, USA) by following manufacturer’s instructions14,15,16,69. Serum samples, each diluted 1:40, were incubated on HEp-2-fixed substrate slides for one hr at room temperature in a humidified chamber. After three 5-min washes with PBS, the slides were treated with a 1:100 dilution of Alexa 488 goat anti-mouse IgG (H + L) (Life Technologies) for 45 min at room temperature. After three washes, Vectashield DAPI mounting medium (Vector Laboratories, Burlingame, CA, USA) was applied, and overlaid with a glass coverslip. Fluorescence was detected by fluorescence Nikon microscopy at 400× magnification, and all images were obtained with exposure of 200 ms.
Lymphocyte cell culture
Head and neck lymph node (HNLNs), mesenteric LNs (MLNs), and spleens were aseptically removed, and single cell suspensions were prepared as previously described70. Briefly, tissues were homogenized using a single sterile, stainless steel bead (McMaster-Carr, Elmhurst, IL) in sterile 2.0 ml locking microfuge tube (Qiagen) shaken in a Tissue Lyser (QIAGEN), then filtered through 80 μm nylon mesh (Component Supply Company, Sparta TN), and washed for 5 min at 4 °C in incomplete media (ICM): RPMI 1640 with L-glutamine (Genesee Scientific, El Cajon, CA); 10 mM HEPES buffer (Caisson Labs); and 10 mM penicillin/streptomycin (Caisson Labs). Splenic red blood cells were lysed using 5 ml of ammonium-chloride-potassium (ACK) buffer (0.15 M NH4Cl, 10 mM KHCO3, 0.1 mM Na2EDTA) for 5 min. Lymphocytes were cultured in a complete medium (CM): ICM plus 10% fetal bovine serum (Atlanta Biologicals, Oakwood, Georgia) and supplemented with 1 mM sodium pyruvate, and 0.1 mM nonessential amino acids (Invitrogen, Carlsbad, CA. For restimulation assays, lymphocytes were cultured in triplicate using 106 cells/well for 2–4 days at 37 °C in 96-well, round-bottomed tissue culture plates (Millipore, Billerica, MA) coated with 5 µg/ml anti-CD3 mAb (clone 17A2; Invitrogen, Carlsbad, CA, USA) plus 2.5 µg/ml of soluble anti-CD28 mAb (clone 37.51; Invitrogen). Cell culture supernatants were collected and then stored at −20 °C until assayed by cytokine-specific ELISAs.
Flow cytometry
For flow cytometry analysis, restimulated lymphocytes were treated with 5 µg/mL brefeldin A (Biovision, San Francisco, CA, USA) for 3–4 h to block cytokine release. Splenic and LN lymphocytes were subjected to a viability stain using a LIVE/DEAD Fixable Blue Dead Cell Stain Kit, for UV excitation (ThermoFisher). Cells were then washed with Dulbecco’s PBS (Gibco, ThermoFisher) plus 10% fetal bovine serum (Atlanta Biologicals), and labeled with mAbs specific for TCR-β, CD4, CD8α, CD19, CD25, CXCR5 (clone L138D7), PD-1 (clone 29F.1A12), TGF-β (BioLegend, San Diego, CA), and CD39 (eBioscience, San Diego, CA). The mAb clones were the same as those previously described39 unless indicated. Cells were then fixed and permeabilized using the True-Nuclear Transcription Factor Buffer Set (BioLegend) and labeled with mAbs specific for IFN-γ (clone XMG1.2), IL-10 (clone JES5-16F3), IL-17 (clone TC11-18H10.1), Bcl-6 (clone 7D1; BioLegend); IL-6 (clone MP5-20F3; BD Pharmingen, San Jose, CA); IL-21 (clone mhalx21), GM-CSF (clone MP1-22E9), and Foxp3 (clone FJK-16a; eBioscience). Fluorescence was acquired on a Fortessa flow cytometer (Becton Dickinson Franklin Lakes, NJ), using FACSDiva software (Becton Dickinson). All samples were analyzed using FlowJo software (BD Biosciences, Ashland, OR).
Cytokine ELISA
At termination of the studies, harvested HNLN, MLN, and splenic lymphocytes were restimulated and cultured as described above. Cytokine capture ELISAs were used to quantify levels of IFN-γ, GM-CSF, IL-6, IL-10, IL-17, and TGF-β present in culture supernatants. Identical mAb pairs and methods were used as previously described40. For IL-21, a goat anti-mouse IL-21 and biotinylated goat anti-mouse IL-21 (R&D Systems) were used. A horseradish peroxidase conjugated goat anti-biotin Ab (Vector Laboratories) was used for the tertiary Ab. The color reaction was developed using and ABTS peroxidase substrate (Moss, Inc., Pasadena, ME), and absorbances were measured using an Epoch Microplate Spectrophotometer (BioTek Instruments, Winooski, VT). Cytokine concentrations were extrapolated from standard curves generated by recombinant murine cytokines IFN-γ and IL-21 (Peprotech, Cranbury, NJ), IL-6 (BD Pharmingen), IL-10, IL-17, GM-CSF (eBioscience, San Diego, CA), and TGF-β (R&D Systems, Minneapolis, MN, USA).
Statistics
A power analysis was conducted, and found that 5 mice per group were needed to show a significant difference for at least a 20% change in SFR. All presented data are the mean ± standard error of the mean (SEM). Statistical significance was tested using GraphPad Prism 8 (Prism, Irvine, CA). One-way ANOVA with Tukey’s multiple comparisons test were used to compare FACS data, cell counts, cytokine production, and salivary flow rates. All results are discerned to the 95% confidence interval.
Data availability
The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author.
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Acknowledgements
This work is supported by NIH NIDCR grants, DE026379 (GF), DE030833 (GF), and DE026450 (DP). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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A.A., C.F., M.M., N.F., G.F., and D.P. conceived and designed the experiments. A.A. and C.H. completed experiments for Figs. 1, 2, 3, 4, 5, 6 and 7; AV completed experiments for Fig. 1F. A.A., C.F., M.M., N.F., G.F., A.V., C.N., and D.P. analyzed data for Figs. 1, 2, 3, 4, 5, 6 and 7. A.A., C.F., G.F., C.N., and D.P. prepared the manuscript. All authors reviewed the manuscript.
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Akgul, A., Freguia, C.F., Maddaloni, M. et al. Treatment with a Lactococcus lactis that chromosomally express E. coli cfaI mitigates salivary flow loss in a Sjögren’s syndrome-like disease. Sci Rep 13, 19489 (2023). https://doi.org/10.1038/s41598-023-46557-3
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DOI: https://doi.org/10.1038/s41598-023-46557-3
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