The STING inhibitor (ISD-017) reduces glomerulonephritis in 129.B6.Fcgr2b-deficient mice

The absence of stimulator of interferon genes (STING) in 129.B6.Fcgr2b-deficient mice rescue lupus phenotypes. The administration of a STING inhibitor (ISD017) into the young 129.B6.Fcgr2b-deficient mice prevents lupus nephritis development. This study mainly aimed to evaluate the effects of STING inhibition (ISD107) on established SLE in mice to prove that ISD017 could be a good therapeutic drug to reverse the already set-up autoimmunity and kidney impairment. Twenty-four-week-old Fcgr2b-deficient mice were treated with cyclophosphamide (25 mg/kg, intraperitoneal, once per week), ISD017 (10 mg/kg, intraperitoneal, three times per week), or control vehicle for 8 weeks, and were analyzed for phenotypes. Both ISD017 and cyclophosphamide treatment increased long-term survival and reduced the severity of glomerulonephritis in Fcgr2b-deficient mice. While cyclophosphamide reduced activated B cells (B220+GL-7+), ISD017 decreased activated T cells (CD4+CD69+) and neutrophils (Ly6c+Ly6g+) in Fcgr2b-deficient mice. In addition, ISD017 reduced IL-1β and interferon-inducible genes. In summary, ISD017 treatment in symptomatic 129.B6.Fcgr2b-deficient mice reduced the severity of glomerulonephritis and increased long-term survival. ISD017 worked comparably to cyclophosphamide for treating lupus nephritis in 129.B6.Fcgr2b-deficient mice. ISD017 reduced activated T cells and neutrophils, while cyclophosphamide targeted activated B cells. These results suggested that STING inhibitors can potentially be a new therapeutic drug for treating lupus.


Scientific Reports
| (2024) 14:11020 | https://doi.org/10.1038/s41598-024-61597-zwww.nature.com/scientificreports/maintain the original 129.Fcgr2b-deficient mice.The littermates of 129.B6.Fcgr2b-deficient mice, both male and female mice, were followed up to the age of 6 months and screened for anti-dsDNA to confirm the development of the lupus phenotype before randomly enrolling into three groups.The three treatments were cyclophosphamide (CYC) (25 mg/kg, intraperitoneal, once per week) 36 , ISD-017 (10 mg/kg, intraperitoneal, three times per week) 34 , or control vehicle (PBS), and the treatment period lasted for 8 weeks.We assessed the anti-double-stranded DNA (anti-dsDNA) in all groups of mice before initiating treatment and after treatment for 8 weeks.The survival of the mice was observed during the treatment period.The number of laboratory mouse cohorts at the initial treatment of the ISD-017, CYC, and PBS groups was 15, 9, and 20 mice, respectively.Mice were monitored throughout treatment, and those that expired prematurely were excluded from analysis.After 8 weeks of treatment, the surviving mice were humanely euthanized, and blood, kidney, spleen, and urine were collected for further analysis.Mice were bred and housed at the Faculty of Medicine, Chulalongkorn University.All experiments were performed with the approval of the Animal Experimentation Ethics Committee of Chulalongkorn University Medical School with all relevant institutional guidelines (research no.003/2563).All methods were performed following the ARRIVE guidelines.

ISD017 (STING antagonist)
ISD 017 was derived from the conserved hemagglutinin fusion peptide (FP) that antagonizes type I interferon production induced by membrane fusion or influenza A virus 37 .ISD017 is specific to cGAS and impacts dsDNA sensing without impacting other nucleic acids 34 .In addition, ISD017 inhibited dsDNA activation of both type I IFN and TNF production 34 .To dissolve ISD017, a panel of solvents was tested, namely, H 2 O, 0.9% NaCl, TBS (pH 7.3), PBS (pH 7.4), HEPES, and PBS (pH 7.4) + 1 M NaOH.For the latter, which was most successful, 194 µL of PBS mixed with 6 µL of 1 M NaOH was added to 1 mg of ISD017.

Detection of anti-nuclear antibodies (ANA)
The sera (1:400) of Fcgr2b-deficient mice were diluted at 8 months, and wild-type mice were tested for ANA as described 11 .In short, diluted serum (30 µL) was added to the Hep-2 cell-coated slide, and phosphate-buffered saline (PBS) was used as a negative control, followed by incubation for 30 min.Then, the cells were washed with PBS 2 times and incubated with 30 µL of goat anti-mouse IgG-Alexa (1:500) (Abcam, Cambridge, MA, USA; cat.FA 1512-1010-1) for 30 min and washed with PBS.Finally, the slides were fixed and analyzed under a fluorescence microscope.The researcher will be blinded and grade the intensity as 4 = maximal fluorescence (brilliant yellow-green), 3 = less brilliant (yellow-green fluorescence), 2 = definite (dull yellow-green), and 1 = very dim (subdued fluorescence).

Detection of anti-dsDNA antibodies
The quantitative ELISA for anti-dsDNA was performed from the sera collected two months after treatment using the previous protocol 11 .In short, ds-DNA in carbonate coating buffer (10 µL/mL) was coated on a 96-well plate at 4 °C overnight.Then, the plate was washed with 0.05% Tween-20/PBS (washing buffer) 5 times, and 100 µL of blocking solution (10% BSA/Tween-20/PBS) was added and incubated at room temperature for 90 min.Afterward, the cells were washed with washing buffer 5 times, 100 µL of serum (1:100) was added, and the cells were incubated at 37 °C for 60 min and washed 5 times.The anti-dsDNA antibody was detected using goat antimouse IgG conjugated with HRP and ABTS peroxidase substrate; then, the absorption value was measured at a wavelength of 450 nm.

Flow cytometry analysis
The spleens were dissected and passed through a 70-µm filter.Splenocytes were placed in PBS solution and centrifuged at 1500 rpm for 5 min to precipitate the cells.The pellet was treated with ACK buffer (NH4Cl, KHCO3, and EDTA) to eliminate erythrocytes.The staining protocol was previously described 11 using the following antibodies: anti-CD4 (clone: GK1.The analysis of serum cytokines was performed using the LEGENDplex™ Mouse Inflammation Panel kit (Biolegend, San Diego, CA, USA; Cat.No. 740446) following the manufacturer's instructions.Flow cytometry was performed using an LSR II flow cytometer (BD Biosciences, USA) and analyzed using FlowJo software (USA).LEGENDplexTM Data Analysis Software was used to analyze the cytokine data.

Measurement of creatinine
The evaluation of creatinine in blood and urine was performed using a QuantiChrom™ Creatinine Assay Kit (DICT-500) following the manufacturer's description.The serum was extracted from the blood, and the urine was diluted (1:50).Next, 30 µL of the serum and the diluted urine in PBS were dripped into a 96-well plate.Then, 200 µL of the working reagent, a 1:1 ratio of reagents A and B, was added to each well and gently mixed.The light absorption of each sample was measured at 1 min and 5 min using a spectrophotometer at a wavelength range of 490-530 nm (with peak absorbance at 510 nm).The result is calculated using a specific formula (as below: n = dilution factor) to evaluate the creatinine levels in the blood and urine samples.

Histopathology
Kidney tissues were fixed in 10% neutral buffered formalin for 24 h.Five-micrometer-thick paraffin-embedded (FFPE) sections were stained with hematoxylin and eosin.The pathology grading from kidney sections was blinded by an experienced researcher.As previously described, the histology scores were reported as glomerular and interstitial scores [38][39] .In brief, glomerular scores were defined as 0 = normal;

Immunofluorescence
The frozen renal sections were first fixed in acetone and then blocked with 1% BSA in PBS.Next, the sections were stained using FITC-conjugated goat anti-mouse IgG (cat.4408) or anti-C3c FITC (cat.Ab4212) (Abcam, Cambridge, MA, USA).Afterward, the samples were stained with DAPI (4ʹ,6-Diamidino-2-Phenylindole, Dihydrochloride) (Thermo Fisher Scientific, MA, USA) for 5 min in the dark at room temperature.Following staining, the slides underwent three washes and were subsequently mounted with ProLongTM Diamond Antifade Mountant (Invitrogen, CA, USA).The fluorescent signals were then visualized using ZEISS LSM 800 with Airyscan (Carl Zeiss, Germany).The fluorescence intensity was quantified using ZEISS ZEN Microscope Software (Carl Zeiss, Germany).

Measurement of Total IgG
The 96-well plates were coated with 100 µL of Goat Anti-Rabbit IgG (H + L) (AffiniPure™) and incubated at 4 °C overnight.The supernatant was removed and washed with 1X PBST three times.Subsequently, the samples were diluted 1:30,000 in 1X PBST.A volume of 100 µL of each diluted sample was then added to the wells and incubated at 37 °C for 1 h.Afterward, the clear supernatant was removed, and the wells were washed three times with 1X PBST.Subsequently, 100 µL of the secondary antibody (Peroxidase AffiniPure™ Goat Anti-Rabbit IgG (H + L)), diluted 1:8000 in 1X PBST, was added to each well.The samples were then incubated at 37 °C for 1 h.After the supernatant was removed, 100 µL of the substrate was added to each well and then incubated at room temperature for 20 min in the dark.Finally, add 2N H 2 SO 4 to stop the reaction and measure the absorbance value at 492 nm using a Cytation™ 5 machine.

Statistical analysis
For multiple comparisons, two-tailed ANOVA was used, and p-values were calculated to determine the statistical significance of differences among groups using GraphPad Prism software (version 7, San Diego, CA, USA).Data will be expressed for all experiments as the mean ± s.e.m., and p values < 0.05 were considered statistically significant: *p ≤ 0.05 and **p ≤ 0.01.

ISD017 significantly increased the survival of symptomatic Fcgr2b −/− mice
We intraperitoneally injected symptomatic Fcgr2b −/− mice (5-6 months old) with ISD017 or cyclophosphamide to determine whether ISD017 can be used as a treatment for overt lupus phenotypes compared to the standard treatment, cyclophosphamide (Fig. 1A).We screened the level of anti-dsDNA in the experimental mice and randomly assigned the treatment groups.The level of anti-dsDNA between the Fcgr2b −/− and treatment groups did not differ (Fig. 1B).The survival of the mice was observed during the treatment period.Upon evaluating the viability of laboratory mouse cohorts, all of the mice in the ISD017 treatment (N = 15) and CYC treatment (N = 9) groups survived.However, only 11 out of 20 mice in the PBS treatment group survived.We observed that Fcgr2b −/− mice survived significantly longer in the ISD017-and CYC-treated mice than the non-treated Fcgr2b −/− mice (p = 0.004).All ISD017-and CYC-treated Fcgr2b −/− mice survived throughout the treatment, while 55% of the non-treated Fcgr2b −/− mice died (Fig. 1C).

ISD017 reduced the severity of glomerulonephritis in Fcgr2b −/− mice
The Fcgr2b −/− mice showed serum creatinine levels higher than WT mice at the same age (Fig. 2A).The mice treated with ISD017 and CYC showed comparable serum creatinine levels with non-treated mice (Fig. 2A); however, only CYC reduced the urine protein/creatinine ratio (Fig. 2B).Next, the histological findings of the kidneys by H&E staining showed that Fcgr2b −/− mice developed fibrocellular crescent, glomerulosclerosis, and interstitial infiltration, while the treated Fcgr2b −/− mice with ISD017 and CYC had less severe disease (Fig. 2C, top row).The kidney glomerular scores (Fig. 2D) and interstitial scores (Fig. 2E) in both treatment groups were significantly decreased compared to those in non-treated Fcgr2b −/− mice.The immunofluorescence staining of IgG (Fig. 3C, middle row, and 3F) in the ISD017-and CYC-treated Fcgr2b −/− mice were reduced.However, the C3c staining in the kidney was significantly reduced in the ISD017-treated mice (Fig. 3C, bottom row, and 3G).

CYC decreased spontaneously activated B cells
The immunofluorescence staining using Hep-2 cells identified the anti-nuclear antibody (ANA) (Fig. 3A).The ANA patterns of serum from the Fcgr2b −/− mice showed homogenous and fine-speckled patterns, which did not change by the treatment (Fig. 3A).However, the intensity of ANA staining was reduced in ISD017 and CYCtreated Fcgr2b −/− mice.The analysis of ANA levels revealed that the untreated Fcgr2b −/− group had significantly higher values than WT mice and the two treatment groups (Fig. 3B).However, no statistically significant difference was observed in the anti-dsDNA level after the treatment among the Fcgr2b −/− groups (Fig. 3C).After the normalization of anti-dsDNA, the ratio of anti-dsDNA (before/after) did not show a difference between treated groups and non-treated Fcgr2b −/− mice (Fig. 3D).Next, we tested the total IgG to see the treatment effect.The CYC-treated Fcgr2b −/− mice tend to have lower IgG levels but did not reach the statistical significance (Fig. 3E).The expansion of spontaneous germinal center B cells has been shown in Fcgr2b −/− mice 40 , and germinal center formation is required to exclude autoreactive B cells 41 .Then, we identified germinal center B cells using GL-7 hi FAS hi staining (Supplementary Fig. 1A) and did not detect the reduction of this subset by the ISD017 and CYC treatment (Fig. 3F,G).Next, we looked at the activating state of B cells by using the GL-7 + and IAb + .However, GL-7 + B cells significantly decreased in percentages (Fig. 3H) and absolute cell numbers (Fig. 3I) in CYC-treated Fcgr2b −/− mice.Similarly, the percentage (Fig. 3J) and total cell numbers (Fig. 3K) of B220 + IAb + cells were significantly lower in the CYC-treated mice.However, no significant difference was found between the non-treated and ISD-017-treated Fcgr2b −/− mice.The B220 + cells showed a comparable mean fluorescence   www.nature.com/scientificreports/intensity (MFI) of IAb among all groups (Supplementary Fig. 1B).Notably, the expression of plasma cells showed no difference among the three Fcgr2b −/− groups in percentage (Fig. 3L) and absolute cell numbers (Fig. 3M).

ISD017 diminished the expansion of neutrophils and the production of IL-1β
Innate immunity is critical for lupus development 43 .The expansion of myeloid dendritic cells and neutrophils in Fcgr2b −/− mice have been previously described 11,40 .Then, we analyzed the treatment effect on myeloid dendritic cells (CD11b + CD11c + ) (Fig. 5A,B) and did not detect the difference in the absolute number of this population (Fig. 5B).To better identify more specific mature dendritic cells, we analyzed the CD11b + CD11c + IAb + cells (Fig. 5C,D) and did not identify the difference in the number of CD11b + CD11c + IAb + cells among the Fcgr2b −/− mice (Fig. 5D).Next, we identified the effect of treatment on neutrophils (Ly6c + Ly6g + ) (Fig. 5E,F).Although ISD017 and CYC did not change the percentage of neutrophils (Fig. 5E), ISD017 significantly reduced the total number of neutrophils (Fig. 5F).Furthermore, ISD017 reduced serum IL-1β in the treated Fcgr2b −/− mice (Fig. 5G) but did not change the IL-6 level (Fig. 5H).

Discussion
The increased levels of type I IFN and the upregulation of IFN-stimulated genes (ISGs) have been consistently observed in the blood and tissues of SLE patients and suggested severe disease activity 44 .This dysregulated production of type I IFN is thought to arise from the activation of plasmacytoid dendritic cells (pDCs) and the aberrant recognition of self-nucleic acids, leading to the induction of IFN-responsive genes and the subsequent promotion of autoimmune responses 45 .STING is an intracellular sensor that recognizes cytosolic DNA and triggers the production of type I IFN and proinflammatory cytokines 46 .Mice with enhanced type I IFN signaling or overexpression of STING exhibit lupus-like features.Conversely, suppressing STING signaling ameliorates  www.nature.com/scientificreports/lupus-like manifestations in several mouse models 11,47,48 .Inhibition of type I IFN using monoclonal antibodies or small molecules has shown promising results in reducing disease activity in SLE patients 7 .Similarly, STING inhibitors are being developed as potential therapeutic agents to modulate aberrant immune responses in SLE.ISD017, a STING inhibitor, blocks the trafficking of STING from the ER to the Golgi, reducing inflammatory cytokines and type I interferon production 34 .ISD017 is specific to dsDNA-activated Sting but not MAVS or TRIF 34 .A previous study showed that ISD017 administration at a young age in Fcgr2b-deficient mice can reduce anti-dsDNA, inflammatory cytokines, and glomerulonephritis 34 .However, ISD017-treated preclinical lupusprone mice might not represent the actual clinical situation of SLE patients with overt active lupus phenotypes.Thus, we treated symptomatic lupus mice that presented with autoantibodies and proteinuria with ISD017 or the standard treatment (cyclophosphamide) and compared the efficacy and targeted effector cells of these 2 reagents.
Treatment with ISD017 and CYC reduced the mortality of Fcgr2b-deficient lupus mice with a comparable survival rate, suggesting that ISD017 could be a therapeutic drug for SLE.Although the mice did not show a difference in serum creatinine among the groups, only CYC reduced the urine protein creatinine ratio during the treatment period of 2 months.CYC is an alkylating agent that is cycle-cell nonspecific.It exerts a marked action against cells in the dividing phase and may also alkylate quiescent cells, which could reduce proteinuria in glomerular diseases 49 .Based on the treatment in human SLE, the duration of induction therapy for lupus nephritis is 6 months.Although the effect of ISD017 treatment did not change proteinuria (urine albumin/ urine creatinine ratio), the reason could be derived from the short treatment interval in this study (2 months).If ISD017 treatment is extended longer than 2 months, the proteinuria may reduce.One limitation of our study is the omission of the total proteinuria score, recognized as a valuable indicator of lupus nephritis activity.
Some studies show that proteinuria did not correlate with renal activity because persistent protein could occur from active nephritis or inactive fibrosis.The follow-up studies of kidney biopsy in SLE patients after treatment of lupus nephritis showed that proteinuria did not predict the activity of glomerulonephritis [50][51][52] .Thus, we assessed the efficacy of ISD017 by measuring the histopathology of the kidney representing lupus nephritis.ISD017 and CYC significantly reduced glomerular and interstitial scores, confirming the ability of ISD017 to decrease the severity of lupus nephritis, similar to standard CYC treatment.In addition, ISD017 showed a significant reduction of IgG and C3c deposition in the glomeruli.We believe that the effect of ISD017 treatment is significant in changing renal pathology and increasing the survival of treated mice compared to untreated mice.These data suggested that the efficacy of ISD017 is at least comparable to that of CYC.
Autoantibodies in systemic lupus erythematosus (SLE) indicate impaired B cell function.This impairment can stem from intrinsic dysfunctions within B cells or indirect stimulation caused by SLE.The presence of antinuclear antibody (ANA) serves as an essential marker for autoimmune diseases.Detection of ANA is a screening for autoantibodies against self-antigens, which contains polyclonal specificity of autoantibodies 53 .ANA can occur after polyclonal B cell activation 54 .The ANA patterns of serum from the Fcgr2b −/− mice showed homogenous and fine-speckled patterns, which did not change by the treatment.The observed homogenous patterns in the ANA staining are indicative of anti-dsDNA specificity.The presence of multiple ANA staining patterns in the Fcgr2b −/− mice suggests the existence of various autoantibodies.
We opted to focus on anti-dsDNA antibodies due to their noted association with the lupus nephritis phenotype and anti-dsDNA change in a previous paper on the double deficiency of Fcgr2b and Sting mice 11 .Anti-dsDNA is a pathogenic autoantibody in lupus nephritis 55 .However, anti-dsDNA partly correlates with SLE disease activity 56 .The sensitivity of the anti-dsDNA level might not represent the lupus nephritis activity in our experiment.This result may be explained by the short duration of treatment (2 months), and the treatment did not reduce the number of plasma cells.The reduction in ANA but not anti-dsDNA and total IgG after ISD017 and CYC treatment suggested that these drugs may target specific activated B cells but not plasma cells.The observation that treatment reduced ANA levels without a corresponding decrease in anti-dsDNA suggests that the therapeutic intervention may preferentially impact autoantibodies other than anti-dsDNA.These potentially affected autoantibodies were not identified within the scope of this study, representing a limitation of our research.
The germinal center serves as the site where B cells encounter antigens presented by APCs, leading to their differentiation.Germinal center B cells actively proliferate, causing somatic hypermutation 57 .Fully differentiated plasma cells are dormant and show less proliferation 58 .Both CYC and ISD017 did not reduce the germinal center B cells (B220 + GL7 + FAS + ) and plasma cells (B220 + CD138 + ).However, only CYC reduced activated B cells (B220 + GL7 + ).While the MFI of IAb on B cells represents the activation of B cells, we did not detect the difference in MFI between the non-treated and treated Fcgr2b −/− groups.However, the number and percentage of B220 + IAb + cells were decreased by CYC treatment.The discrepancy in the IAb data could be that some B220 + cells showed a mixed response to the treatment, creating the IAb hi and IAb low cells, which may cause high variability and make MFI at an insignificant level.However, the number of IAb + B220 + cells represented B cells with IAb hi , which may suggest the readiness of B cells for presenting antigens to activate CD4 + T cells.CYC is an alkylating agent that preferentially attacks proliferating cells and has less influence on quiescent cells.The data suggested different targeted mechanisms between ISD017 and CYC.Additionally, previous research has provided evidence highlighting the crucial role of CYC, a specific substance, in regulating the expression and function of critical cells involved in B cell immunity 59 .
Effector memory T cells are the major producers of inflammatory cytokines and provide help for B cell proliferation.Moreover, T cell activation also contributes to B cell activation, leading to autoantibody secretion and causing damage to various tissues 60 .While ISD017 and CYC effectively reduced the expansion of effector memory T cells, the number of activated naïve T cells increased during CYC treatment.ISD017 decreased the expansion of CD69 + CD4 + T cells but did not decrease the MFI of CD69 on CD4 + T cells.This data suggested that ISD017 may inhibit the differentiation of mature T cells but did not directly act on T cell activation.Given CD69 is an early-activated marker, and its expression on T cells leads to cytokine production and cell proliferation 61 .The interaction between these cells and dendritic cells, facilitated by the MHC molecule, triggers the activation of CD69 + T cells.As a result, significant changes occur in cell function, leading to the differentiation of Th1 or Th17 cells and a notable increase in the production of various cytokines 62 .While ISD017 did not decrease anti-dsDNA levels, an earlier study reported a strong correlation between the expression levels of CD69 and the SLE disease activity index (SLEDAI) score 63 .Therefore, CD69 + T cells may be pathogenic, causing active disease activity.The fact that we did not test the T-follicular cells or T-regulatory cells, we could not know whether ISD017 affects these cells or not.
Granulocytes can disrupt the normal functioning of B-cell or T-cell immune cells, leading to the production of type-I interferons, tumor necrosis factor-alpha (TNFα), B-cell activating factor (BAFF), and a proliferationinducing ligand (APRIL).The complex interaction among these factors is crucial for driving the proliferation pathways involved in SLE and regulating epigenetic expression, which can negatively affect SLE development and progression 64 .These granulocytes form neutrophil extracellular traps (NETs) when activated by autoantibodies, releasing large DNA complexes-this immune complex triggers the activation of plasmacytoid dendritic cells, the primary source of type-I interferons.Imbalances in NET production and elimination may be pivotal in advancing disease 65 .
Notably, experimental studies utilizing lupus models have provided compelling evidence supporting the link between increased expression of IL-1β and the severity and accelerated progression of the disease 66,67 .IL-1β knockout in lupus-prone NZM2328 mice still leads to the development of lupus phenotypes 68 .This finding suggested that the other signaling pathway is required for lupus development in NZM2328 mice.STINGmediated lysosomal damage activates NLRP3 inflammasome-dependent pyroptosis 69 .The reduction in IL-1β in the ISD017-treated mice should be an effect of STING inhibition in this model.Activation of the STING pathway induces type I IFN and proinflammatory cytokines, including IL-6 and TNF-α 70 .Here, we detected a reduction in interferon-inducible genes but not IL-6.IL-6 in Fcgr2b-deficient mice may be produced via a STING-independent pathway.
ISD-017 effectively reduced the expansion of granulocytes (Ly6c + Ly6g + ) and the production of IL-1β, an inflammasome-mediated cytokine, but CYC did not.However, the kidney pathology of Fcgr2b-deficient mice showed NETs 40 .Netosis of neutrophils can activate complement cascade 71 .The immunofluorescence staining of C3c was significantly reduced with ISD017 but not CYC.The effect of ISD017 in rescued lupus nephritis may be derived from the reduction in neutrophils, NETs formation, and complement activation.STING can activate IRF3 and IRF7 to induce type I IFN production 72 .The absence of Sting in Fcgr2b-deficient mice decreased the expression of both Irf3 and Irf7 in the kidney 11 .Treatment with ISD017 and CYC targeted different interferon-inducible genes in the kidney of Fcgr2b −/− mice.Both ISD017 and CYC reduced Isg15 expression, with CYC showing more effect than ISD017.CYC suppressed Irf3 expression better than ISD017.However, ISD017 suppressed Irf7 and Mx1 in the kidneys of Fcgr2b-deficient mice.The data suggested that ISD017 and CYC preferentially inhibited interferon-inducible genes in the kidney, which lessened glomerulonephritis in Fcgr2b −/− mice.
It should be noted that this study does not provide information on long-term survival and potential longterm side effects.Further research is necessary to explore these aspects comprehensively.It would be interesting to see the effect of ISD017 in other lupus mouse models, which is beyond the scope of this study.Due to some controversies regarding STING function in mouse models and the heterogeneity of lupus disease, further study of STING function in other mouse models or human SLE is needed to clarify the beneficial role of targeting STING-mediated signaling in a specific subgroup of SLE.
In summary, ISD017 rescued lupus nephritis in symptomatic129.B6.Fcgr2b-deficient mice.While CYC targeted activated B cells, ISD017 targeted activated T cells and neutrophils.Since ISD017 impacts different parameters compared to cyclophosphamide, it presents a unique opportunity to be used in conjunction with cyclophosphamide in treatment protocols.This dual approach could reduce the required dosage of cyclophosphamide, thereby minimizing its side effects while maintaining therapeutic efficacy. https://doi.org/10.1038/s41598-024-61597-zwww.nature.com/scientificreports/

Figure 3 .
Figure 3. CYC decreased spontaneously activated B cells.Serum from the treated and control Fcgr2b −/− mice showed (A) the anti-nuclear antibody (ANA) by immunofluorescence staining of Hep-2 cells and (B) a semiquantitative level of the anti-nuclear antibody (ANA) graded by fluorescence intensity, (C) anti-dsDNA (Before and after treatment), and (D) The OD ratio of anti-dsDNA (before/after treatment) from the serum of the treated Fcgr2b −/− mice and control Fcgr2b −/− mice.(E) total IgG detected by ELISA (N = 9-15 per group).(F-M) Isolated splenocytes from Fcgr2b −/− mice (8 months old) from ISD017-or CYC-treated and control Fcgr2b −/− mice were analyzed by flow cytometry.(F) The percentage of GC B cells and (G) cell numbers of GC B cells are shown.(H) The percentage of B220 + GL-7 + and (I) cell numbers of B220 + GL-7 + are shown.(J) The percentage of B220 + IAb + and (K) cell numbers of B220 + IAb + are shown.(L) The percentage of B220 + CD138 + (plasma cells) and (M) cell numbers of B220 + CD138 + are shown (N = 9-15 per group).Data are shown as the mean ± SEM; *p < 0.05, **p < 0.01 and ***p < 0.001.