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Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome is an autoinflammatory syndrome recently described in children. We investigated the clinical phenotype, genetic cause and the immune dysregulation in nine CANDLE patients.
Genomic DNA from all patients was screened for PSMB8 (Proteasome subunit beta type-8) mutations. Serum cytokine levels were measured from four patients. Skin biopsies were evaluated immunohistochemically and blood microarray profile (n=4) and stat-1 phosphorylation (n=3) were assessed.
One patient was homozygous for a novel nonsense mutation in PSMB8 (c.405C>A) suggesting a protein truncation, four patients were homozygous and two were heterozygous for a previously reported missense mutation (c.224C>T), and one patient showed no mutation. None of these sequence changes was observed in chromosomes from 750 healthy controls. Of the four patients with the same mutation, only two share the same haplotype indicating a mutational hot spot. PSMB8 mutation-positive and -negative patients expressed high IP-10 (Interferon gamma-induced protein 10) levels. Levels of MCP-1, IL-6, and IL-1Ra were moderately elevated. Microarray profiles and monocyte stat-1 activation suggested a unique interferon (IFN) signaling signature, unlike in other autoinflammatory disorders.
CANDLE is caused by mutations in PSMB8, a gene recently reported to cause JMP syndrome (joint contractures, muscle atrophy and panniculitis induced lipodystrophy) in adults. We extend the clinical and pathogenic description of this novel autoinflammatory syndrome, thereby expanding the clinical and genetic disease spectrum of PSMB8-associated disorders. IFN may be a key mediator of the inflammatory response and may present a therapeutic target.
Auto-inflammatory diseases were first characterized more than 10 years ago by episodic, systemic and organ-specific inflammation (1, 2). These disorders differ from autoimmune diseases in that they primarily result from perturbations in the innate immune system, rather than in adaptive immunity, although overlapping features may occur (2, 3). During the past decade, the genetic basis for many autoinflammatory diseases has been revealed (1). Elucidating the underlying molecular basis for these monogenic disorders has increased the understanding of inflammation and has led to improved therapy, particularly interleukin-1 (IL-1) inhibition for patients with cryopyrin-associated periodic syndromes (CAPS) (4).
Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE syndrome) is a newly described autoinflammatory condition, now reported in five patients (5, 6). It is characterized by onset during the first year of life, recurrent fevers, purpuric skin lesions, violaceous swollen eyelids, arthralgias, progressive lipodystrophy, hypochromic or normocytic anemia, delayed physical development and increased acute phase reactants. Variable clinical features include hypertrichosis, acanthosis nigricans and alopecia areata (5, 6). The skin biopsy findings of a characteristic atypical, mixed mononuclear and neutrophilic infiltrate further confirm the diagnosis (5). A genetic etiology was suggested, possibly inherited in an autosomal recessive pattern. In order to elucidate the molecular basis of CANDLE syndrome, we performed genome-wide analysis and sequencing in eight families with nine affected patients.
The present study includes nine patients (3 Spanish, 3 Hispanic, 1 Ashkenazi Jew and 2 American/Caucasian) from eight families who were seen at five international centers (two in Spain, Israel and two in the US). The study was approved by the institutional review board at the respective sites and written informed consent was obtained from the subjects or their parents. Blood samples were collected from eight patients and their unaffected family members where available. All of the patients included in this study were discussed among the lead investigators of the five centers to ensure the diagnosis of CANDLE before they were included. All patients had to have episodic fevers, typical erythematous eruptions, arthralgia/arthritis and evidence of systemic inflammation (elevation of acute phase reactants). In addition, a skin biopsy showing an atypical mixed myeloid, neutrophilic, and histiocytic infiltrate positive for myeloperoxidase and CD68 had to be present. Patients 1–4 were previously described by Torrelo et al. (5), and patient 5 was reported by Ramot et al. (6); patient 3 died at 14 years of age, and blood samples were not available for analysis (5). Patients 6–9 have not been described before.
A genome-wide analysis of single-nucleotide polymorphisms was performed using the GeneChip Human Mapping 250K SNP Array of Affymetrix. For this analysis we used the blood samples of patients 1, 2, 4, 5 and 9. Genome-wide homozygosity analysis was performed by Homozygosity Mapper (7).
In parallel with the conventional Sanger sequencing, we also performed whole exome sequencing in patient 5. DNA captured with the Agilent SureSelect Human All Exon 50Mb kit was sequenced on an Illumina HiSeq 2000 platform. Sequence data were analyzed with a custom bioinformatics pipeline.
To identify additional mutations in PSMB8 (Proteasome subunit beta type-8) in the two patients who are heterozygous for the PSMB8 mutation T75M, and in the patient who did not have any mutation in PSMB8 on exonic sequencing, we sequenced the other five exons and all of the introns of the longest isoform of PSMB8 (Ensemble nomenclature, PSMB8.001). Alternative and cryptic splicing events were ruled out by sequencing the cDNA. We searched for genomic deletions by long range PCR with primers spanning the entire gene and ruled out the possibility of a heterozygous deletion at the primer binding site by sequencing the c.224C>T mutation using the long range PCR amplicon as template. In patients 6 and 7 both the maternal and paternal copies are present at PSMB8 locus, and the PSMB8 cDNA is of full-length (8). Assuming digenic inheritance in patient 7, we sequenced all the other beta subunits from PSMB1 to PSMB10 and two alpha subunits (PSMA6 and PSMA7). PSMB8 mRNA levels are similar to healthy controls by RT-qPCR from cDNA made from peripheral blood.
A structural model of both mutations identified was assembled. Structures are based on a previously published model (9). Figures were made with Pymol.
Serum was collected from patients 6, 7 and 8 and stored at −80°C. Cytokine concentrations were measured using the Bio-Plex system (Bio-Rad) in batches including patient control and healthy serum.
Total RNA was extracted from blood samples collected in Paxgene tubes (from patients 4, 6, 7, and 8) and processed as recommended by the manufacturer (Qiagen). RNA integrity was analyzed with an Agilent 2100 Bioanalyzer. cDNA synthesis and target amplification was done with the NuGene Ovation® Whole Blood Solution kit. Affimetrix HU-133 plus 2.0 gene chips were used for hybridization. Data analysis was done with Genespring 11.5 software and Partek software, after removal of non-annotated genes. Genes differentially expressed in comparison to the mean expression in healthy controls were at least 2 fold higher (FCH>2) with a p-value less than 0.05 adjusted for multiple hypotheses testing and controlling the false-discovery rate (FDR) (FDR<0.05). Groups were compared using the two-tailed Welch t-test. DEGs were then analyzed in Ingenuity pathway analysis (IPA) (Ingenuity Systems, Inc., http://www.ingenuity.com) to investigate dysregulated canonical pathways and gene ontology. Results for interferon induced genes were plotted as a heat map with upregulated genes in shades of red and downregulated genes in shades of blue.
Peripheral blood mononuclear cells (PBMC) were isolated by standard Ficoll density gradient centrifugation and frozen in liquid nitrogen. Cells were thawed, washed and resuspended in 0.1% BSA PBS at 2×106/ml and then aliquoted at 0.5ml per tube. For studies with the small molecule JAK kinase inhibitor tofacitinib[3-[(3R,4R)-4-methyl-3-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]piperidin-1-yl]-3-oxopropanenitrile, synthesized by Dr. Craig Thomas, NCGC/NIH], cells were treated with the inhibitor for 15 min before stimulation. Cells were stimulated with various concentrations of IFN-γ or control PBS buffer at 37°C for 15 min, fixed with 4% paraformaldehyde and then stained with CD14.PE and pSTAT1 Alexa 647 (BD Pharmingen) and analyzed with BD FACSCanto according to standard procedures. Data were analyzed with Flowjo software.
Punch biopsies of lesional skin were fixed in 10% neutral buffered formalin and routinely processed. Serial tissue sections of 5-μm thickness were made and spread on poly-L-lysine coated glass slides. Immunohistochemical staining was carried out using the Ventana Benchmark XT fully automatated slide preparation system (Ventana Medical Systems, Inc) using the following antibodies: MPO (DAKO; 1:1000 dilution), CD163 (Novacastra Laboratories: 1:100 dilution), and KP1/CD68 (DAKO: 1:400 dilution). Staining is developed with 3, 3′-diaminobenzidine tetrahydrochloride and counterstained with Meyer’s hematoxylin and mounted. Leder staining (Naphthol AS-D chloracetate esterase or specific esterase), which identifies cells of the granulocyte lineage, from the early promyelocyte stage to mature neutrophils, was carried out using the Sigma-Aldrich 91C-1KT following manufacturer’s protocol.
Table 1 summarizes the demographic characteristics and clinical presentation of the affected children. Most patients presented within the first 2–4 weeks of life (all by 6 months of age) with fever and repeated attacks of erythematous and violaceous, annular cutaneous plaques, lasting for a few days or weeks and leaving residual purpura. Later during infancy, patients developed persistent periorbital erythema and edema, finger or toe swelling and hepatomegaly with variable elevation of acute phase reactants. Other common clinical features that developed in the first years of life included progressive loss of peripheral fat (lipodystrophy), failure to thrive, lymphadenopathy and hypochromic or normocytic anemia. More variable findings included perioral swelling, parotitis, conjunctivitis/episcleritis, acanthosis nigricans and hypertrichosis, chondritis, aseptic meningitis, interstitial lung disease, nephritis, epididymitis, hypertriglyceridemia and intermittent positivity of ANA or ANCA autoantibodies (Table 1 and Figure 1). Our series includes 4 previously unreported patients from non-consanguineous families: two Caucasian males and a Hispanic female from the USA (patients 6–8), and one Caucasian male from Spain (patient 9) (Figures 1A–G). An MRI from the thigh showed irregular enhancement of fat, suggesting panniculitis, but no myositis (Figures 1H, I). Synovial enhancement, consistent with joint discomfort and arthralgia and/or arthritis was also seen (Figure 1J).
Responses to treatment have been variable (Table 1). Most clinical symptoms, including cutaneous eruption, joint pain and fever respond to high doses of steroids 1–2mg/kg/day, but rebound with tapering (around 0.5mg/kg/day). Responses to steroid sparing agents have been inconsistent. Methotrexate in combination with calcineurin inhibitors have permitted administration of lower doses of steroids, however skin and joint flares with fever in between led to the further addition of biologics. TNF-alpha inhibitors have provided temporary improvement in some cases, but flares in others. Anti-IL-1 therapy has not allowed a decrease in steroids, and IL-6 blocking agents have normalized acute phase reactants and anemia, but have had limited success in reducing the cutaneous eruption and improving fatigue (dose ranges of biologics see Table 1). The lipodystrophy has invariably progressed despite immunosuppressive therapy.
Skin biopsies stained with hematoxyilin and eosin (H&E) were reviewed from all patients. Characteristic features included a dense interstitial infiltrate of mononuclear cells with nuclear atypia and both mature and immature neutrophils, with areas of karyorrhexis (Figure 2A,B). Interstitial dermal collagen degeneration is seen. Immunohistochemical staining disclosed a mononuclear infiltrate composed of immature neutrophils/myeloid precursors (myeloperoxidase and Leder stains, Figure 2C), as well as atypical mononuclear cells that are most likely activated macrophages (positive for CD68-KP1 and CD163, negative for Leder stain) (Figure 2D–F).
A region of homozygosity shared by four patients (patients 1, 2, 4 and 5) was identified in chromosome 6p21 (haplotype cluster rs6924453- rs3763341) (Figure 3A), but not in patient 9. This region spans ~2.7Mb, and includes 164 genes, including 120 protein-coding genes, encompassing the major histocompatibility complex. Given that CANDLE is an immune-mediated disease, with prominent involvement of the skin and adipose tissues, we performed direct sequencing of the following candidate genes: AGPAT1 (gene ID 10554), TRIM27 (gene ID 5987), ITGB1 (gene ID 3688), SLC39A7 (gene ID 7922), NOTCH4 (gene ID 4855), SLC44A4 (gene ID 80736) and PSMB8 (gene ID 5969).
Sequencing of the six exons of the PSMB8 gene in patient 5 revealed a homozygous c.405C>A mutation in exon 3, changing cysteine at amino acid 135 to a stop codon (p.C135X; in accordance with ENST00000374882 transcript) (Figure 3B, supplementary Table 1). The cysteine at position 135 is highly conserved across species. A homozygous missense mutation, c.224C>T, which leads to the substitution of threonine with methionine at position 75 (p.T75M), was found in the patients 1, 2, 4 and 8. Interestingly, two patients were heterozygous for the mutation (patients 7 and 9) and, despite extensive analysis, no second mutation has been found; one patient (patient 6) shows no mutation in PSMB8. The genotype of the deceased pt 3 was deduced from her sister (pt 4) as both had the same disease. Mutations for the neighboring subunit PSMB2, and the other immunoproteasome (i-proteasome) specific subunits PSMB9 and PSMB10 were negative, but further analyses are ongoing (Figure 3C, supplementary Table 1). None of these sequence changes was observed in 750 healthy controls, including 100 Ashkenazi Jews.
Whole exome sequencing done in parallel generated 2.4 Gb of mappable sequence data and achieved 20-fold coverage of the targeted exome. On average, 57.74% of the bases originated from the targeted exome, with 81% of the targeted bases covered at least four times. Initial variant sites calling (>4x) resulted in the identification of 20,012 genetic variants, including 153 within the shared homozygous region on chromosome 6p21. Eight individual reads were mapped back to the genomic position of the c.405C>A PSMB8 mutation, confirming the homozygous nonsense mutation (Figure 3D).
We modeled mutations identified in PSMB8 in a ribbon diagram (Figure 4A). The β units of the i- proteasome are organized in 2 overlying rings containing 7 subunits each. Two of the mutations, one previously published in adults with severe lipodystrophy (p.T75M) (10) and the novel nonsense mutation, p.C135X, identified in the Jewish patient are shown (left image). The p.C135X mutation leads to a large deletion of the terminal 141 amino acids of the inducible β5i subunit. Intact residues are shown as red and deleted residues are shown as gray. The deleted residues would normally interact with the neighboring β4 subunit in the same ring, but also bind to the β4 unit of the adjacent ring (right image). The nonsense mutation therefore provided us with structural evidence that the i-proteasome, which requires the incorporation of the β5i subunit, cannot form. The T75 amino acid that is mutated in the other patients is represented by a purple ball.
To assess the dysregulated inflammatory response in CANDLE patients, we performed cytokine profiling in serum from peripheral blood of 3 patients: one patient with PSMB8 mutations on both alleles; one with only one identified PSMB8 mutation to date; and one without a detectable mutation in PSMB8. All showed very high, but variable levels of IP-10. Mean IP-10 levels in CANDLE patients were 77 fold higher than those observed in healthy controls and more than 30 fold higher than in untreated patients with an IL-1 mediated autoinflammatory syndrome neonatal-onset multisystem inflammatory disease (NOMID). Other cytokines that were significantly elevated in CANDLE patients compared to healthy controls and NOMID patients were MCP-1 and RANTES (Figure 4B). Notably, IL-6 and IL-1Ra were modestly elevated not only in CANDLE syndrome patients, but also in patients with NOMID.
The very high levels of IP-10 suggested excessive interferon responses in CANDLE patients (Supplementary figure 1). To probe for evidence of excessive IFN signaling in CANDLE patients in vivo, we assessed the transcriptome in whole blood microarray analysis in four CANDLE patients and four age and gender matched healthy controls. CANDLE patients had 507 genes (650 transcripts) that were more than two-fold differentially expressed compared to healthy controls (p<0.05) (Supplementary table 2). Differentially expressed genes (DEGs) were analyzed by the Ingenuity pathway analysis (IPA) program to identify dyregulated canonical pathways and the IFN pathway was the most differentially regulated in CANDLE patients (p=4.73E-06). Of the IFN induced gene list in IPA, most were IFN-γ induced (n=42) and 6 were also regulated by IFNα/β. The genes were plotted on a color-coded heat map and the pattern of increased (shades of red) and decreased DEGs (shades of blue) were strikingly similar among CANDLE patients, regardless of the presence or absence of detectable PSMB8 mutations (Figure 4C). IP-10 (CXCL10) which is highly expressed in the patients’ serum was among the IFN induced upregulated genes. We also compared our DEG list to interferon regulated genes published in www.interferome.org and 119 of the 507 DEGs were found to be interferon regulated.
Since Stat-1 is a downstream mediator of interferon-α/β and -γ signaling, we studied Stat-1 phosphorylation in the monocytes in response to IFN-γ stimulation. Compared with monocytes from healthy controls and a patient with NOMID, monocytes from CANDLE patients showed stronger Stat-1 phosphorylation in response to all IFN-γ concentrations used for stimulation (Figure 5A).
To assess the effect of various treatments the patients received on the IFN induced genes, blood samples from multiple visits were obtained in two patients, including one patient treated at different times with anti-TNF-alpha and anti-IL-6 therapy (supplementary figure 2). Although temporary clinical improvement was seen with anti-TNF-alpha and anti-IL-6 treatment (unpublished observation), the “IFN signature” did not improve. IL-6 blocking therapy normalized IL-6 inducible genes (data not shown) and CRP levels, however, skin lesions, fatigue or joint pain did not significantly improve and peripheral fat loss progressed, suggesting a possible association between the IFN signature and disease activity.
JAK kinases are critical signaling molecules mediating IFN signaling on the IFN receptors. To determine the effect of a JAK kinase inhibitor, tofacitinib, on the excessive interferon response in CANDLE patients, we assessed its inhibiting effect on stat-1 phosphorylation in patients’ monocytes stimulated with IFN-γ. Tofacitinib decreased stat-1 phosphorylation in a dose dependent manner in both CANDLE patients and healthy control monocytes (Figure 5B). Tofacitinib also inhibited IFN-γ induced IP-10 production in PBMC in a dose dependent manner and its inhibitory effect was more efficient than with the IL-1 receptor agonist anakinra or anti-IL-6 blockade with tocilizumab (data not shown). As tofacitinib and other agents blocking the IFN pathways are not available to use as a treatment in our patients, we could not assess the effect of blocking the IFN signaling pathway on the clinical and laboratory symptoms of CANDLE patients.
In the current study we identified mutations in the PSMB8 gene as the cause of CANDLE syndrome, extending the phenotypic spectrum of a novel recently described autoinflammatory syndrome caused by PSMB8 mutations (10). We also identified dysregulation of the IFN signaling pathway and suggest that the interferon pathway may be a target for treatment in these patients.
After the original report of CANDLE syndrome in four children, a syndrome diagnosed in three adult patients with joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced childhood-onset lipodystrophy was reported under the acronym “JMP” (10). Patients with JMP were recently demonstrated to carry a mutation in the PSMB8 gene (8). The patients described were homozygous for the same mutation, p.T75M, that we found in five of our patients (8, 10).
Although CANDLE patients have some overlapping features with JMP patients, including a cutaneous eruption and lipodystrophy (10), none of our patients has developed joint contractures and muscle atrophy was not a prominent disease feature, although two patients (1 and 7) developed an acute, self-healing attack of myositis. CANDLE patients, on the other hand, showed several key features that have not been described in the JMP patients, particularly recurrent febrile episodes, elevated acute phase reactants and a characteristic neutrophilic dermatosis with a mononuclear interstitial infiltrate including “immature” neutrophils in the dermis that seems pathognomonic for CANDLE syndrome. In fact two patients have been misdiagnosed as acute cutaneous myelogenous leukemia. Nevertheless, the detection of the same and additional mutations in PSMB8 unifies these disorders as a novel i-proteasome associated autoinflammatory syndrome. Clinical reports of children with disease manifestations that closely resemble CANDLE syndrome from families in Japan and Lebanon (11–13) might allow for the discovery of further molecular causes of this disease. While our data in young children illustrate manifestations of early severe, and potentially lethal disease and alert to the fact that muscle involvement and joint contractures may not present until later in life, the findings in the adult patients likely illustrate the natural course of the disease in untreated or partially treated patients (10, 11).
In one of our patients, no mutation in PSMB8 was discovered, and two patients showed a mutation in only 1 allele, despite sequencing the entire exonic and intronic sequence of the gene. In the boy without a mutation on either allele (patient 6), we similarly found no mutation in sequencing the two other i-proteasome specific subunits. These data indicate genetic heterogeneity underlying CANDLE syndrome and raises the prospect of other genes as the genetic cause for CANDLE syndrome.
The gene mutated in CANDLE, PSMB8, encodes the inducible β5i subunit of the proteasome, a protein complexe that consists of two α rings and two β rings, each ring is formed of 7 different globular α or β-subunits. Proteasomes are evolutionary conserved cylindrical structures that are critical for protein degradation (14). Upon IFN stimulation critical subunits of a constitutive proteasome, the β1, 2 and 5 subunits, are replaced with inducible i-subunits, β1i, β2i and β5i, to form i-proteasomes which are highly expressed in hemopoietic cells (15).
The functions of the i-proteasomes have been studied in vitro and in animal models. The i-proteasome can generate antigenic peptides for MHC class I presentation (16), but recent data in psmb8/lmp7 knockout mice (17) suggest an important additional role in maintaining cell homeostasis by removing accumulating proteins marked for degradation from the cells (18). Cellular stress such as infections or radiation lead to type I IFN induced production of reactive oxygen species and newly synthesized proteins that are particularly sensitive to oxidation (19–21). Failure to process/degrade protein will result in formation of ubiquitin-rich cytoplasmic aggregates or inclusions and consequently increase cellular sensitivity to apoptosis (18). It is thought that the excessive demand for protein processing/degradation is mainly met by cytokine-mediated upregulation of the ubiquitination machinery and increased assembly of the highly efficient i-proteasome (22, 23).
The persistent IFN signature in CANDLE patients on microarray and the increased Stat-1 phosphorylation in monocytes from CANDLE patients in response to IFN-γ stimulation could reflect ongoing “cellular stress” in CANDLE patients. In concordance with the current understanding of the i-proteasome function, we have suggested a disease model (supplementary figure 1) which proposes that defects in i-proteasome function may lead to accumulation of damaged proteins resulting in more cellular stress and a vicious cycle of increased IFN signaling. Interestingly, CANDLE flares are observed with infections and other stressful events. Some cells such as fat or muscle cells may be subject to cellular apoptosis due to accumulation of damaged proteins. In fact a Japanese patient with severe fat loss, muscle atrophy and suspected CANDLE syndrome died of cardiac failure at the age of 47. Histological examination of skeletal muscle on autopsy revealed intramitochondrial paracrystalline inclusions and cytoplasmic and myeloid bodies in muscle cells (24). Whether the inclusions seen constitute accumulation of oxidant damaged/aggregated proteins that cause cell death is an attractive hypothesis to account for muscle loss later in life, but studies on the cell specific effect of the i-proteasome deficiency are needed to explain the observed visceral effects of the mutations.
IP-10 is a type I or type II IFN induced protein, that functions as a C-X-C motif chemokine, also known as CXCL10 (supplementary figure 1). It is produced in a variety of cell types, including endothelial cells, keratinocytes, fibroblasts, mesangial cells, monocytes, dendritic cells, neutrophils and activated T cells (25). IP-10/CXCL10 is an important chemoattractant for effector T cells, its serum level has been shown to correlate with the extent of T cell infiltration in the tissue. IP-10 may contribute to the pathology in CANDLE patients by acting as a chemoattractant for T cells into tissues such as the skin with the described inflammatory infiltrate. Whether the inflammatory skin infiltrate of immature neutrophils and activated myeloperoxidase positive histiocytic cells is a consequence of IFN signaling needs further evaluation. However, the important role of IFN-γ in the recruitment of neutrophils through the induction of CCL3 (26) and the stimulation of myeloperoxidase production in monocyte/macrophages (27) are consistent with a possible pathogenic role of IFN in skin.
Given our own data and the clinical reports of devastating disease manifestations in adults, the outcome of untreated disease is expected to be poor. The partial responses and the continued need for steroids despite being on treatment with targeted therapies including IL-1 receptor antagonist, TNF-alpha blockage and IL-6 receptor inhibitors (see Table 1) urge the need for a better understanding of the disease pathogenesis and for identifying more effective targets for therapeutic intervention. Whether the persistence of the IFN signature on the treatment with targeted agents offers a clue to a more effective intervention is a testable hypothesis as agents blocking IFN signaling (including JAK inhibitors) are in clinical trials.
CANDLE and the other PSMB8-associated syndromes illustrate the profound effect of i-proteasome dysfunction on inflammation and organ function. In the current study we have established PSMB8 as the causative gene for CANDLE syndrome and describe clinical and histological features that can establish early diagnosis. The mutations in PSMB8, also found in JMP, illustrate the clinical and genetic spectrum of this novel i-proteasome associated autoinflammatory syndrome. Further studies to fully explore the role of the i-proteasome in autoinflammatory diseases and to identify other mutations in PSMB8 mutation negative CANDLE patients are needed and are ongoing.
Model of dysregulated IFN pathways in CANDLE. Mutant i-proteasome induced IFN signaling abnormality is depicted in this tentative model. In response to a trigger such as infections, IFNs are produced which upregulate the expression of the i-proteasome to process the accumulating polyubiquitinated proteins. Defects in i-proteasomes caused by PSMB8 mutations results in increase of polyubiquitinated proteins and cell stress, which then trigger more IFN production, leading to a vicious cycle.
IFN signature under treatment with biologics in one CANDLE patient. Various treatments with biologics [TNF-alpha inhibition (adalimumab), IL-6 inhibition (tocilizumab), inhibition of the CD28/CD86 interaction (abatacept), or a calcineurin inhibitor (tacrolimus)] led to persistence of the interferon signature on microarray analysis. In red are upregulated genes compared to healthy age matched children.
This research was supported by the Intramural Research Program of the National Institute of Arthritis and Musculoskeletal and Skin Diseases at the NIH, and by the Authority for Research and Development, Hebrew University of Jerusalem (AZ), the Hadassah Medical Center Young Clinician Award (YR).
The authors would like to thank Nikki Plass, RN., Deborah Stone M.D., Dawn Chapelle RN, Sapna Patel Vaghani, MD, and Rhina Castillo MD, for their help organizing patient visits and patient examinations. Adam Reinhardt MD, Elizabeth Brown MD, Paulina Navon-Elkan MD and Kristina Rother MD for their collaboration on patient treatment, Ivona Aksentijevich MD for her help with the interpretation of the genetic data, Hang Pham, MT for her help with the cytokine analysis, Max Gadina, PhD for his help with the initial cytokine analysis and the sharing of the synthetic CP-690550 (tofacitinib), and Isabel Colmenero MD, Luis Requena MD and Heinz Kutzner MD for their help in immunohistochemistry studies.
Conflict of interest: None.