Blau Syndrome, the prototypic auto-inflammatory granulomatous disease
© Wouters et al.; licensee BioMed Central Ltd. 2014
Received: 9 May 2014
Accepted: 27 July 2014
Published: 6 August 2014
Blau syndrome is a monogenic disease resulting from mutations in the pattern recognition receptor NOD2, and is phenotypically characterized by the triad of granulomatous polyarthritis, dermatitis and uveitis. This paper reviews briefly the classical clinical features of the disease, as well as more recently described extra-triad symptoms. From an ongoing prospective multicenter study, we provide new data on the natural history of Blau syndrome, focusing on functional status and visual outcome. We also present an update of the range of different NOD2 mutations found in Blau syndrome as well as recent data on morphologic and immunohistochemical characteristics of the Blau granuloma. Finally, emerging insights into pathogenic mechanisms including activation of NOD2 signal transduction, and potential biomarkers of disease activity are discussed.
Introduction and nomenclature
In 1985, Blau syndrome (Blau) was described simultaneously by E Blau and D Jabs, as a familial granulomatous inflammatory disease with an autosomal dominant inheritance pattern[1, 2]. Once the causative mutations in NOD2 were discovered and later found to also be present in patients with Early Onset Sarcoidosis - a sporadic disease with the same phenotype[4, 5] - , it became clear that Blau and Early Onset Sarcoidosis are the familial and sporadic forms respectively, of the same disease. The authors originally suggested a unifying name for these two conditions, namely Pediatric Granulomatous Arthritis but this term did not gain traction, partly because it concealed the systemic and visceral manifestations of the disease. Further, arthritis although highly prevalent in this condition, is not a universal feature. In this paper we will utilize the term Blau syndrome to refer to both the sporadic and familial forms of the disease, recognizing that the presence or absence of a family history no longer has any relevance in terms of disease classification; of course the presence of an affected family member will be a valuable clinical feature for a diagnostician at the time of presentation.
Blau syndrome classically presents in early childhood as a triad of granulomatous dermatitis, arthritis and uveitis. Although there are exceptions, skin rash is the first symptom to appear, usually in the first year of life. Between the ages of 2–4 years, a boggy polyarthritis is observed. Finally, uveitis develops in 60–80% of patients at around 48 months of age. The majority of data presented in this review stem from two independent efforts. In 2005, the Blau syndrome International Registry (also referred to as the Pediatric Granulomatous Arthritis registry) was instituted. Thanks to the collaborative efforts of physicians taking care of Blau patients from around the world, genetic and clinical data based on retrospective review of medical records have been collected. This registry received support and is an integral part of the Eurofever project, since Blau syndrome is considered to be one of the monogenic auto-inflammatory diseases. Second, since 2009, a 5-year prospective multicenter study to investigate the natural history of the disease and its functional impact, to promote biomarker discovery, and to gain a better understanding of relevant pathogenic pathways, is being conducted by the authors. Some of the preliminary findings from this latter international effort will be discussed herein.
One of the most fascinating aspects of Blau syndrome is the presence of non-caseating epithelioid and giant cell granulomas in affected tissues. In fact, Blau syndrome is the only auto-inflammatory disease associated with a gain of function mutation to show granulomatous inflammation. The morphologic characteristics of the “Blau granuloma” are similar to those found in sarcoidosis, which is not associated with NOD2 mutations. Detailed morphological and immunohistochemistry studies on biopsy tissue from Blau patients have provided some insights as to the relevant pathogenic pathways involved in the disease process; however there is still a significant knowledge gap concerning a link between the canonical NOD2 signaling pathway and granuloma formation.
Classical clinical features
Uveitis presents as an insidious granulomatous iridocyclitis with posterior uveitis in many patients, and a potential evolution into a severe panuveitis with multifocal choroiditis. It is usually bilateral and associated with an increased risk of visual morbidity. About 80% of patients in both the retrospective international Blau registry and the prospective Blau cohort study developed ocular disease with a median age at onset of 4.4 years (unpublished data). Unlike the uveitis of JIA, which is almost always confined to the anterior uvea, involvement of the entire uveal tract with panuveitis was found in 75% of Blau patients in the prospective cohort study (unpublished data). Granulomatous uveitis may be suspected on slit lamp examination by the presence of nodular peripheral keratic precipitates noted on the limbus. The synechiae tend to be focal, and there can be nodules in the iris. Vitreous inflammation is common, and may remain persistently active for years. Posterior involvement is described as multifocal choroiditis.
The first systematic study to show the importance of extra-triad manifestations was published by Arostegui in 2007. Most notably fever and erythema nodosum were detected quite commonly in this Spanish cohort. As more patients were recruited in the Blau international registry we noticed expanded manifestations in about one third of the patients. Features included fever, sialadenitis, lymphadenopathy, erythema nodosum, leukocytoclastic vasculitis, transient neuropathies, granulomatous glomerular and interstitial nephritis, interstitial lung disease, arterial hypertension, pericarditis, pulmonary embolism, hepatic granulomas, splenic involvement and chronic renal failure.
Some of the extra-triad manifestations are of particular importance to be aware of when following Blau patients. The association between large vessel vasculitis and Blau syndrome was reported before the genetic mutation was discovered[18–21]. Other investigators reported silent aortitis in a patient with Blau syndrome. We recently described a case of Takayasu’s-like arteritis in a child from India with a novel NOD2 mutation.
Also of note, two young patients from the international registry developed severe systemic hypertension; although digital angiography could not demonstrate renovascular disease, the response to ACE inhibitors was manifest. A young patient with a typical triad phenotype without visceral manifestations for most of his life succumbed to acute onset intractable pulmonary hypertension at the age of 22 years, within a few months from the first symptoms of mild dyspnea (unpublished observation). Hence pulmonary and systemic hypertension may be seen in the course of Blau syndrome, requiring careful vigilance.
Cranial neuropathies, particularly facial palsy have also been documented in Blau[2, 21], but central nervous system involvement has not been reported. A patient with Blau syndrome and a new onset of a seizure disorder was recently published; yet the relationship with the disease process was not clearly demonstrated. Typical central nervous system manifestations seen in adult sarcoidosis, namely meningeal and white matter disease have not been described in Blau.
Interstitial lung disease, a major feature of adult sarcoidosis, was originally not considered part of the Blau phenotype. The first case with a documented NOD2 mutation was reported by our group. Pneumonitis in this child was characterized by ground glass infiltrates in the upper lobes easily controllable with a few weeks of corticosteroids, without sequelae and no recurrence while on anti-TNF therapy. Interstitial lung disease was observed in three additional patients of the prospective Blau study.
Erythema nodosum has been mentioned frequently; in fact it is the second most common cutaneous manifestation of Blau syndrome. Also leukocytoclastic vasculitis has been documented in a patient with Blau.
Renal involvement has been described as an interstitial nephritis in the context of Blau syndrome before the mutation was known. The first case of acute glomerular and interstitial nephritis with histological documentation of granulomatous inflammation both in the interstitium and the glomeruli was reported more recently.
Finally, involvement of the reticuloendotelial system is not uncommon. We found generalized lymphadenopathies and splenomegaly in more than one-fifth of patients in the Blau prospective study. Hepatomegaly can be seen, but liver enzymes and liver function are mostly normal. We have reported hepatic granulomas on a liver biopsy in a child with Blau syndrome without evidence of hepatic injury neither histologically nor by laboratory evaluation.
To date all studies on Blau have been either short case series or multicenter registries[6, 9] based on retrospectively collected data. The natural history of Blau and its functional consequences remain largely unknown. An ongoing prospective international study aiming at collecting data on disease course, and evolution of articular, ocular and visceral disease was established in 2009. At the time of writing this review, baseline visit data on the first 31 recruited Blau patients with a median disease course of 12.8 yrs were available (manuscript under review).
At the time of evaluation, more than fifty percent of Blau patients had articular deformities, with camptodactyly (flexion contracture at PIP joints) being most commonly observed. Radiographs of hands and wrist very rarely showed erosions, however some morphological changes of radial, ulnar and carpal bones were apparent. Functional capacity, assessed by CHAQ and HAQ, showed normal function in more than one-third of patients, mild impairment in one-third and moderate/severe in almost one-third. Almost half of Blau patients reported a moderate to severe impact of the disease on their global well-being, and moderate to severe pain.
At present, there is no evidence for an effective treatment for all patients with Blau. In the prospective Blau cohort study, more than two-thirds of Blau patients received medical therapy, often combining systemic steroids, immunosuppressive and/or biologic drugs to control both uveitis and arthritis. TNF-antagonists are the most commonly used biological therapy and seemingly useful in achieving partial control of articular disease. A few investigators however have reported a dramatic response both clinically and biologically to IL-1 inhibition[9, 29]. The observation of persistently active disease in a majority of Blau patients in this study underlines the need for development of effective targeted therapies.
The NOD2 genotypic spectrum
In the initial report in which NOD2 was identified as the causative gene in Blau syndrome, three different single base pair mutations were described in 4 families. Two of these families exhibited the same mutation, encoding an amino acid substitution of arginine to tryptophan at position 334 (R334Q), one family had an R334W, and one other a L469F substitution. The following year, Wang et al. published their study on the genetic analysis of NOD2 coding regions based on 10 families with Blau syndrome including members of the original family published by E. Blau. This paper mentioned a surprisingly low frequency of NOD2 mutations in patients with Blau; 5 of the 10 families did not show any mutations, yet the description of the phenotypes was not very detailed. A large series reported by investigators from Japan identified NOD2 mutations in 90% of their cases. In the international Blau registry, all patients with the classical clinical triad phenotype had a NOD2 mutation.
Over time the number of different NOD2 mutations associated with Blau has expanded greatly[31–36]. An update was published in 2011 by the authors, and new Blau-associated NOD2 mutations are being cataloged regularly in the Infevers registry.
It is unclear whether the type and/or location of the NOD2 mutation has an effect on the clinical features. In a study from Japan, an increased frequency and severity of ocular involvement was reported in association with R334W substitution, a finding we could not confirm in neither the international Blau registry nor the current prospective study.
Interestingly, although the penetrance of Blau-associated NOD2 mutations is very high, we reported a family with an E383K substitution, in which 2 members had the typical Blau phenotype and 4 additional members (including one adult) with the same substitutions, were asymptomatic.
Incomplete phenotypes are not uncommon; about 15-20% of patients with Blau syndrome do not develop eye disease. In addition, we recently described a young girl with a novel G464W substitution, who presented with an atypical phenotype comprising mild oligoarthritis, a Takayasu’s like large-vessel arteritis, but absence of rash and no uveitis.
Blau granuloma morphology and immunohistochemistry
Granulomas are organized inflammatory infiltrates characterized by a core of macrophages, epithelioid cells, multinucleated giant cells and a corona of lymphocytes and a variable presence of fibroblasts. Blau is the only auto-inflammatory disease with a gain-of-function mutation and granulomatous inflammation in affected tissues and organs. Interestingly, granulomas also commonly occur in the gastrointestinal tract in Crohn’s disease, and a subset of Crohn’s patients carry polymorphisms in NOD2, which are generally believed to confer loss of function.
We have performed an in-depth morphological and immunohistochemical study on granuloma-containing biopsies from Blau patients as well as from patients with Crohn’s disease and NOD2 polymorphisms. Our data show that Blau granulomas display a distinct morphology characterized by large polycyclic granulomas with dense lymphocytic coronas, reflecting an exuberant inflammatory response, and in line with a gain-of-function mutation in NOD2. In contrast, biopsies from Crohn’s patients show isolated granulomas with loose lymphocytic borders and sclerosis of surrounding tissue, which are also seen in immunodeficiency disorders, and therefore compatible with loss-of-function variants of NOD2.
In Blau granulomas, we also have documented widespread extensive emperipolesis (cell-in-cell phenomenon) of lymphocytes within multinucleated giant cells, which is associated with multinucleated giant cell death, a finding of interest in view of the recently reported role of NOD2 in autophagy (Figure 7).
Blau syndrome new insights into pathogenesis
A full account of the biology of the NOD2 protein is beyond the scope of this article, and has been extensively reviewed elsewhere[44, 45]. Briefly, NOD2 is a member of the NOD-like receptor (NLR) family of pattern recognition receptors, which are involved in inflammation and innate immune defense against invading pathogens. NOD2 has a tripartite structure with two N-terminal CARD domains, one centrally located NOD/NACHT domain and a C-terminal domain comprised of ten leucine-rich repeat (LRR) motifs (Figure 6). The LRR domain binds the NOD2 ligand muramyl dipeptide (MDP), a degradation product of ubiquitous bacterial cell wall peptidoglycan (Figure 6).
The hypothesis that NOD2 mutations in Blau syndrome act in a gain of function manner was initially suggested by the autosomal dominant inheritance pattern of the disease. Subsequently, studies by two groups demonstrated that over-expression of NOD2 carrying Blau mutations in transfected cells resulted in the hyper-activation of an NF-κB responsive reporter gene, whereas expression of NOD2 carrying loss of function Crohn’s disease mutations failed to activate the same reporter[30, 49]. These results are consistent with the observation that Blau NOD2 mutations occur in amino acid positions homologous to known gain of function mutations occurring in the related pattern recognitions receptor NLRP3 which lead to spontaneous IL-1β production in the auto-inflammatory Cryopyrin-associated periodic syndromes (CAPS).
Based on these studies, NF-κB activation and excess inflammatory cytokine production as a consequence of dominant gain of function mutations in NOD2 has become a widely accept concept in the field. However, we and other groups have observed that, in contrast to NLRP3-mutated CAPS, peripheral blood cells from Blau patients do not spontaneously produces inflammatory cytokines, and are in fact resistant to stimulation by the NOD2 ligand MDP[51, 52]. Although this may appear to be at odds with a gain of function model, it should be remembered that these peripheral cell populations may not reflect the activation state of immune cells present within granulomas in diseased tissue, where, as described above, we have seen evidence of constitutive inflammation. Indeed, we have also detected increased expression of S100A12 in Blau patient plasma, which is a marker of neutrophil-mediated inflammation. Reconciling all these observations will obviously require further work, particularly to understand the relationship between Blau gain of function mutations and the mechanism of granuloma formation.
The clinical spectrum of NOD2-associated granulomatous inflammatory diseases continues to expand. NOD2 mutations associated with Blau syndrome extend beyond the NACHT domain. The rarity of Blau syndrome has made it challenging to fully characterize the disease. However, the recent creation of an international registry and the ongoing natural history study are providing novel insights into the symptomology and etiology of this fascinating genetic disorder.
With more data available on the natural history of Blau syndrome, the need for more effective therapies in a substantial subset of patients is clear. Increased knowledge on NOD2 signaling and function remains essential to advance our understanding of NOD2-hyperactivation diseases.
We remain grateful to Tammy Martin PhD who was responsible for the initial genotyping work and her insights in disease pathogenesis have stimulated the author’s interest in the disease.
Currently the Blau repository is under the direction of Juan J Arostegui MD to whom the authors remain indebted for his work on genotyping and interpreting genetic data from participants and patients from around the world.
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