- Open Access
Mutations in CECR1 associated with a neutrophil signature in peripheral blood
- Alexandre Belot1, 2, 3,
- Evangeline Wassmer4,
- Marinka Twilt5, 6,
- Jean-Christophe Lega1, 7,
- Leo AH Zeef8,
- Anthony Oojageer9,
- Paul R Kasher9,
- Anne-Laure Mathieu2,
- Christophe Malcus1, 10,
- Julie Demaret1, 10,
- Nicole Fabien1, 11,
- Sophie Collardeau-Frachon1, 12,
- Laura Mechtouff1, 13,
- Laurent Derex1, 13,
- Thierry Walzer2,
- Gillian I Rice9,
- Isabelle Durieu1, 7 and
- Yanick J Crow9, 14, 15, 16Email author
© Belot et al.; licensee BioMed Central Ltd. 2014
- Received: 25 July 2014
- Accepted: 19 September 2014
- Published: 24 September 2014
A reduction of ADA2 activity due to autosomal recessive loss of function mutations in CECR1 results in a newly described vasculopathic phenotype reminiscent of polyarteritis nodosa, with manifestations ranging from fatal systemic vasculitis with multiple strokes in children to limited cutaneous disease in middle-aged individuals. Evidence indicates that ADA2 is essential for the endothelial integrity of small vessels. However, CECR1 is not expressed, nor is the ADA2 protein detectable, in cultured human endothelial cells, thus implicating additional cell types or circulating factors in disease pathogenesis.
Considering the phenotypic overlap of ADA2 deficiency with the type I interferonopathy Aicardi-Goutières syndrome due to mutations in SAMHD1, we looked for the presence of an interferon signature in the peripheral blood of two newly ascertained ADA2-deficient patients.
We identified biallelic CECR1 mutations in two patients consistent with ADA2 deficiency. Both patients demonstrated an upregulation of interferon stimulated gene transcripts in peripheral blood. More strikingly however, genome-wide analysis revealed a marked overexpression of neutrophil-derived genes, suggesting that the vasculitis seen in ADA2 deficiency may be an indirect effect resulting from chronic and marked activity of neutrophils.
We hypothesise that ADA2 may act as a regulator of neutrophil activation, and that a reduction of ADA2 activity results in significant endothelial damage via a neutrophil-driven process.
- Adenosine deaminase
- Neutrophil signature
- Type I interferon
- Aicardi-Goutières syndrome
Autosomal recessive loss of function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), were recently described to cause a variable phenotype encompassing recurrent fevers, livedo reticularis, Raynaud’s phenomenon and digital necrosis, vascular aneurysms and stenoses, intestinal strictures, hepatosplenomegaly and hypogammaglobulinemia[1, 2]. Biopsies of affected tissues revealed an inflammatory vasculopathy showing overlap with polyarteritis nodosa as a major pathological feature, and signs of compromised endothelial integrity and endothelial cellular activation. The precise mechanism leading to disease remained undefined, but was suggested to relate to a function of ADA2 as an immune system molecule and/or as a growth factor.
Here we report two further patients with biallelic mutations in CECR1. In view of a clinical overlap with the Mendelian type I interferonopathy disease Aicardi-Goutières syndrome (AGS) due to mutations in SAMHD1, we searched for an interferon signature in peripheral blood[3, 4]. Both patients demonstrated an upregulation of interferon stimulated gene transcripts. However, more strikingly, we observed a marked overexpression of neutrophil-related genes on genome-wide microarray analysis, and circulating neutrophils demonstrated increased expression of myeloperoxidase compared to controls. Neutrophil counts were normal. These findings suggests that ADA2 deficiency may drive unregulated neutrophil activation, and thus play a role in the activation of endothelial cells and the pathogenesis of the vasculitis of this devastating disease.
For Sanger sequencing, primers were designed to amplify the coding exons of CECR1 (see Additional file1: Table S1). Purified PCR amplification products were sequenced using BigDye™ terminator chemistry and an ABI PRISM 3730 xL Genetic Analyzer (96-capillary system). Mutation description was based on the reference cDNA sequence NM_017424.2, with nucleotide numbering beginning from the first A in the initiating ATG codon.
Methods for the assessment of the expression of a panel of interferon stimulated genes (ISGs) have been described previously. Briefly, total RNA was extracted from blood (peripheral blood mononuclear cells) using a PAXgene (PreAnalytix) RNA isolation kit. Quantitative reverse transcription polymerase chain reaction (qPCR) analysis was performed using the TaqMan Universal PCR Master Mix (Applied Biosystems), and cDNA derived from 40 ng total RNA. Using TaqMan probes for IFI27 (Hs01086370_m1), IFI44L (Hs00199115_m1), IFIT1 (Hs00356631_g1), ISG15 (Hs00192713_m1), RSAD2 (Hs01057264_m1), and SIGLEC1 (Hs00988063_m1), the relative abundance of each target transcript was normalized to the expression level of HPRT1 (Hs03929096_g1) and 18S (Hs999999001_s1), and assessed with the Applied Biosystems StepOne Software v2.1 and DataAssist Software v.3.01. The median fold change of the six ISGs, when compared to the median of 29 healthy controls combined, was used to create an interferon score for each patient. RQ is equal to 2-ΔΔCt i.e. the normalized fold change relative to a control. When a patient was assayed on more than one occasion, the data for repeat measurements were combined to calculate a mean value. The mean interferon score of the controls plus two standard deviations above the mean (+2 SD) was calculated. Scores above this value (>2.466) were designated as positive. Neutrophil-expressed genes were assessed as above using Taqman probes for MMP8 (Hs01029057_m1), CEACAM6 (Hs03645554_m1), CRISP3 (Hs00195988_m1), LTF (Hs00914334_m1), DEFA4 (Hs01056651_g1) and LCN2 (Hs01008571_m1). Neutrophil-expressed gene expression in patients was normalized to expression in 4 healthy control samples.
RNA quality was checked using the RNA 6000 Nano Assay, and analyzed on an Agilent 2100 Bioanalyser (Agilent Technologies). RNA was quantified using a Nanodrop ultra-low-volume spectrophotometer (Nanodrop Technologies). Human Genome U133 Plus 2.0 Affymetrix GeneChips were run according to manufacturers instructions. RNA-Seq data was generated on a hiSeq 2500 using SENSE mRNA-seq library Prep kit (Lexogen).
For the microarray analysis, technical quality control and outlier analysis was performed with dChip (V2005) (http://www.hsph.harvard.edu/cli/complab/dchip/), using the default settings. Background correction, quantile normalization, and gene expression analysis were performed using RMA in Bioconductor.
For the RNA-Seq analysis, quality assessment was performed with FastQC software (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/). Mapping of reads to the human transcriptome was done with TopHat software and transcript assembly and differential expression will be performed with Cuffdiff of Cufflinks. Read counts were normalised with DESeq.
ADA2 activity in serum was assessed using a commercial kit (Diazyme Laboratories) based on the deamination of adenosine to inosine according to the manufacturer’s instructions.
The PerFix-no centrifuge assay Kit from Beckman Coulter (Hialeah, FL, USA) was used to measure myeloperoxidase (MPO) intracellular concentration. Staining of fresh whole blood was performed using Fluorescein IsoThioCyanate (FITC)-labeled anti-myeloperoxidase (clone CLB-MPO-1), Phycoerythrin (PE)-labeled anti-lactoferrin (clone CLB13.17), PE-Texas Red (ECD)-labeled anti-CD62L (clone DREG56), PE-Cyanine7 (PC7)-labeled anti-CD10 (clone ALB1), APC-Alexa fluor 750 (AA750)-labeled anti-CD11b (clone Bear1) and Pacific Blue (PB)-labeled anti-CD16 (clone 3G8). All reagents were purchased from Beckman Coulter. According to the manufacturer’s instructions, samples were first fixed with the Fixative Reagent and incubated for 15 min. Then, aliquots were simultaneously permeabilized and stained with fluorochrome-conjugated antibodies. After 35 min of incubation, samples were fixed using a solution containing formaldehyde. Cytometry analyses were performed on a NAVIOS flow cytometer using the NAVIOS software (Beckman Coulter).
The study was approved by a U.K. Multicentre Research Ethics Committee (reference number 04:MRE00/19) and the Comité de protection des personnes SUD-EST III (reference number 2013-011B).
Patient 1 (F785)
At the age of 15 years he experienced an acute abdominal crisis requiring surgery. This revealed stenosis of the ileo-caecum with evidence of a necrotizing vasculitis of the small and medium sized vessels evocative of polyarteritis nodosa (Additional file1: Figure S1). Soon thereafter he suffered an acute cerebrovascular accident resulting in a left-sided hemiparesis. Treatment with methotrexate and azathioprine was successfully introduced; but both were stopped because of side effects. Steroids were maintained. He developed a further motor deficit of the right arm with dysarthria a year later, at which point ischemic lesions of the left thalamus were noted on cranial magnetic resonance imaging. The introduction of rituximab did not prevent the occurrence of a further stroke-like episode. Subsequently, he developed a hemorrhagic lesion of the spleen whist on anticoagulant therapy. At the age of 21 years he presented with an intracerebral hemorrhage. Cutaneous peri-malleolar ulcerative lesions were noted at the age of 23 years. He was growth retarded with a height of 150 cm (−−2 SDs below the mean).
Patient 2 (F750)
This male child was born to consanguineous parents of Pakistani ancestry with no family history of note. Between the ages of 3 weeks and 2 years he experienced recurrent episodes of dactylitis of both hands mainly involving the metacarpophalangeal joints. From the age of 2 years he developed fevers lasting 4–5 days, associated with a raised CRP and ESR. Erythema nodosum was noted from the age of 2.5 years on all 4 limbs, but particularly affecting the legs. Biopsy demonstrated septal panniculitis.
He complained of intermittent headaches from the age of 4 years. Against a background of normal development, at age 6 years he suffered an intracranial hemorrhage treated with evacuation, leaving him with a right hemiplegia and speech impairment. Following the acute event he continued to have intermittent fever and raised ESR/CRP. He was also noted to have unexplained hypertension, requiring anti-hypertensive medication, and a vasculitic rash. Three months later he suffered 2 further acute neurological events, leaving him with a left and right third nerve palsy with optic neuritis. Cranial magnetic resonance imaging demonstrated multiple white matter abnormalities with linear enhancement and a left frontal porencephalic cyst. Over time, some of these lesions resolved and new lesions appeared. Angiography revealed multiple microaneurysms within the sub-segmental branches of multiple vessels in the liver, kidneys and superior mesenteric artery consistent with a vasculitis-type pattern. At age 6 years, cerebrospinal fluid (CSF) cells, oligoclonal bands and alpha interferon activity were normal. CSF pterins demonstrated a normal tetrahydrobiopterin and dihydrobiopterin, but an increased neopterin of >4 times the upper limit of normal (297 nmol/l: control 7 – 65).
Considering an inflammatory disorder, he was treated with intravenous steroids to which he made a positive response, with an improvement in his cranial neuropathy, and a settling of his fever and inflammatory markers. He was then started on steroids, mycophenolate mofetil and, as he remained steroid dependent, a course of cyclophosphamide.
In patient 1, Sanger sequencing revealed compound heterozygosity for two variants (c.506G > A, p.Arg169Gln; c.578C > T, p.Pro193Leu) in CECR1. The Arg169Gln mutation has been reported previously in the compound heterozygous state in 3 families. The Pro193Leu is novel but is considered likely pathogenic on the basis of conservation and prediction packages and its absence from publically available control sequence databases (Additional file1: Figure S2, Additional file1: Table S2). Each parent was heterozygous for one mutation.
Consistent with ADA2 deficiency, ADA2 activity was markedly decreased in serum (Additional file1: Figure S3).
In patient 2, Sanger sequencing, revealed a homozygous c.139G > C/p.Gly47Arg mutation in CECR1. This particular nucleotide variant has been reported in the compound heterozygous state in one Turkish patient, and results in the same amino acid substitution as a Georgian Jewish founder mutation (c.139G > A) described previously. This variant has not been seen in the EVS control database, is highly conserved and is predicted to be damaging (Additional file1: Figure S2, Additional file1: Table S2). Both parents were heterozygous for the variant. Interferon scores of 5.1, 7.0 and 3.3 were recorded at 6.73, 6.81 and 7.02 decimalised years of age respectively. Parental samples were not available for testing. A genome-wide expression array demonstrated marked upregulation of neutrophil-expressed genes (Figure 3), and these findings were confirmed on qPCR of a selection of 6 of the most upregulated genes identified in the array data (Figure 2).
Autosomal recessive loss of function mutations in CECR1, leading to a reduction of ADA2 activity in patient sera, result in a vasculopathic phenotype reminiscent of polyarteritis nodosa showing highly variable age at onset, severity and organ involvement, even within families and among patients with the same mutations. Manifestations range from fatal systemic vasculitis with multiple strokes in children, to limited cutaneous disease in middle-aged individuals. A tendency to aneurysmal and stenosis formation in the brain, heart, kidney and gut vasculature results in a substantial risk of both infarction and haemorrhage. Inflammation was noticed in most patients suggesting that the underlying mechanism is driven by immune cells[1, 2].
The clinical features observed in our patients conform to the phenotype of ADA2 deficiency already reported, and include recurrent fevers, livedo reticularis, ulcerative skin lesions/erythema nodosum, hypogammagobulinaemia, gastrointestinal strictures with microaneuryms and intracerebral vascular disease. We identified compound heterozygous CECR1 mutations in one patient, including a p.Arg169Gln substitution which has been previously seen in three families. Our second patient was homozygous for a c.139G > C/p.Gly47Arg mutation. This particular nucleotide variant has been reported in the compound heterozygous state in one Turkish patient, and results in the same amino acid substitution as a Georgian Jewish founder mutation, indicating the importance of the glycine at position 47 for enzyme activity (Additional file1: Figure S5).
In 2009, we identified mutations in SAMHD1 to cause a subtype of AGS, an inflammatory disease of the brain and skin associated with an upregulation of type I interferon signaling. Clinically, SAMHD1-related AGS differs from other AGS subtypes in that many patients, more than 20 described in the literature so far - ranging in age from neonate to adult, demonstrate a cerebral vasculopathy which can manifest both as stenotic, leading to a moyamoya appearance, and aneurysmal disease, which carry a high risk of intracerebral infarction and haemorrhage respectively[10–13]. In our experience, patients with SAMHD1-related intracerebral vascular disease invariably demonstrate marked peripheral skin involvement, reminiscent of the cutaneous lesions described in ADA2 deficiency, with features of a leucocytoclastic vasculitis on biopsy.
SAMHD1 acts as a deoxynucleoside triphosphate triphosphohydrolase which regulates the intracellular pool of dNTPs, and hence the production of DNA through reverse transcription in the cytosol. Patients with AGS consistently demonstrate an increased expression of ISGs, a so-called interferon signature, in peripheral blood. These observations are important in identifying AGS as an inflammatory disorder associated with the induction of a type I interferon mediated innate immune response, likely driven by endogenously-derived nucleic acids. It is of note that patients with AGS consistently demonstrate an upregulation of pterins, an inflammatory marker, in the cerebrospinal fluid, a feature also observed in our patient 2.
Considering the overlap between the ADA2 and SAMHD1 clinical and radiological phenotypes, we looked for the presence of an interferon signature in the peripheral blood of the two ADA2-deficient patients that we ascertained. Both demonstrated an upregulation of ISG transcripts, which was present on all three occasions in patient 1, and on two occasions in patient 2 when assayed. More strikingly however, genome-wide analysis revealed a marked overexpression of neutrophil-expressed genes. This finding was confirmed on qPCR of a selection of 6 of the most upregulated genes identified in the array data. In a previous report, extensive studies of serum cytokines, and of cytokines produced by cultured peripheral-blood mononuclear cells, did not demonstrate any convincing differences between ADA2 deficient patients and controls. Of note, an analysis of gene expression in peripheral blood was not reported. Here we show that ADA2 deficiency is associated with a marked upregulation of neutrophil expressed gene transcripts, which is distinct from the gene expression pattern seen in another monogenic inflammatory vasculitis due to mutations in SAMHD1.
Previous reports indicate that ADA2 is essential for the endothelial integrity of small vessels. However, CECR1 is not expressed, nor is the ADA2 protein detectable, in cultured human endothelial cells, thus implicating additional cell types, or circulating factors, in the disease pathogenesis. ADA2 is a secreted molecule which converts adenosine to inosine and 2′-deoxyadenosine to 2′-deoxyinosine[16, 17]. Neutrophils express receptors for adenosine which can have profound effects on their function. Our findings suggest that the vasculitis seen in ADA2 deficiency may be an indirect effect resulting from chronic and marked activity of neutrophils. As one possibility, MPO is a highly abundant neutrophil protein that has been recently reported as key disrupter of endothelial cell function. ADA2 may act as a plasmatic regulator of PMN cell activation and prevent MPO expression and subsequent endothelial damage.
Written informed consent was obtained from the patient and both parents (patient 1), and the family of patient 2 for the publication of this report and the accompanying images. The study was approved by the Leeds (East) Research Ethics Committee (reference number 10/H1307/132) and the Comité de protection des personnes SUD-EST III (reference number 2013-011B).
We sincerely thank the patients and their families included in this research.
European Union’s Seventh Framework Programme (FP7/2007-2013) under grant agreement 241779. European Research Council (GA 309449: Fellowship to Y.J.C), and a state subsidy managed by the National Research Agency (France) under the “Investments for the Future” program bearing the reference ANR-10-IAHU-01. Funding from Hospices Civils de Lyon and the Société Française de Rhumatologie (A.B.).
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