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Neurological phenotypes in patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants



Neurological manifestations and the co-occurrence of multiple sclerosis (MS) have been reported in patients with autoinflammatory diseases (AID) and variants of the NLRP3-, MEFV-, or TNFRSF1A gene. However, type and frequency of neurological involvement are widely undetermined.


We assessed clinical characteristics of 151 (108 with MS) patients carrying NLRP3-, MEFV- and TNFRSF1A low-penetrance variants  from the Institute of Clinical Neuroimmunology. We evaluated demographic, genetic, and clinical features with a focus on central nervous system (CNS) involvement including magnetic resonance imaging (MRI) results and cerebrospinal fluid (CSF) data. The disease course of AID patients with MS was compared to a matched MS control group without mutations.


The genetic distribution comprised 36 patients (23%) with NLRP3- and 66 patients (43%) with TNFRSF1A low-penetrance variants as well as 53 (34%) patients carrying pathogenic mutations or low-penetrance variants in the MEFV gene. MS patients displayed most frequently the R92Q TNFRSF1A variant (n = 51; 46%) followed by the Q703K NLRP3 variant (n = 15; 14%) and the E148Q substitution (n = 9; 8%) in the MEFV gene. The disease course of MS was not influenced by the genetic variants and did not differ from MS patients (n = 51) without mutations. AID patients without MS most frequently harbored MEFV mutations (n = 19, 43%) followed by NLRP3- (n = 17, 39%) and TNFRSF1A (n = 8, 18%) low-penetrance variants. Sixteen (36%) of them suffered from severe CNS involvement predominantly recurrent aseptic meningoencephalitis and optic neuritis accompanied by abnormal MRI and CSF results. Severe CNS inflammation was associated with the Q703K allele. Headache was a highly prevalent neurological symptom (up to 74%), irrespective of the underlying genetic variation. The NLRP3 cohort without MS more frequently exhibited affections of the cranial nerves (CN) (p = 0.0228) and motor symptoms (p = 0.0455). Elevated acute-phase reactants were detected in all patients, and fever episodes were present in up to 50%. Arthralgias were the most frequently identified constitutional symptom among all subgroups.


Our data highlight the high prevalence of neurological manifestations, including concomitant MS, among NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants. In particular, patients carrying the Q703K NLRP3 variant are at risk for severe CNS inflammation and CN affection.


Cryopyrin-associated periodic syndromes (CAPS) including Muckle-Wells syndrome (MWS), familial cold autoinflammatory syndrome (FCAS) and neonatal-onset multisystem inflammatory disease (NOMID/CINCA), familial Mediterranean fever (FMF), and tumor necrosis factor receptor-associated periodic syndrome (TRAPS), all belong to a group of rare, monogenetic autoinflammatory diseases (AID) caused by a dysregulation of the innate immune system. While CAPS is mediated via gain-of-function mutations in the NLRP3 gene leading to a constitutively activated NLRP3 inflammasome, FMF is caused by sequence variants in the MEFV locus encoding the inflammasome complex pyrin [1, 2]. At the molecular level, NLRP3 serves as an intracellular danger signaling complex, while pyrin acts as a sensor detecting an imbalance in RhoGTPases activity [3]. Despite this diverging signaling pathway upstream of inflammasome activation exists, both CAPS and FMF result in a common overproduction of interleukin 1β (IL-1β) [4, 5]. On the contrary, TRAPS is caused by mutations in the TNFRSF1A gene, which encodes the tumor necrosis factor receptor (TNF) receptor, and has formerly been associated with an accumulation of mutated TNFR1 receptors in the endoplasmic reticulum due to inadequate shedding, thus triggering inflammatory response [6,7,8].

Clinically, AID are characterized by unexplained episodes of fever and systemic inflammation involving joints, skin, muscles, eyes, and serosal surfaces accompanied by elevated acute-phase reactants [9]. Neurological manifestations with the involvement of the central nervous system (CNS) including aseptic meningitis, headache, increased intracranial pressure, seizures, cerebral vasculitis, and inflammatory lesions in the brain have mainly been reported in CAPS, but are also present in FMF and TRAPS and may even dominate the clinical picture [10,11,12,13,14,15,16,17,18]. Furthermore, cases with multiple sclerosis (MS)-like presentations have been observed for all three of them [17, 19,20,21]. The importance of variants with unknown pathogenic significance (such as p.R92Q in TNFRSF1A or p.Q703K in NLRP3) is still under debate, and their clinical phenotypes are often challenging for clinicians [22, 23]. In recent studies, we could describe several patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants in association with inflammatory diseases of the CNS including MS [24,25,26,27,28,29].

The aim of this study was to evaluate genotype-phenotype correlations focusing on neurological manifestations in a monocentric cohort of 151 patients (with and without (w/o) MS) with predominantly low-penetrance mutations in the NLRP3-, MEFV-, or TNFRSF1 gene.


All patients were consecutively seen and examined by an experienced neurologist at our neuroimmunological outpatient clinic from 2006 to 2020, which is specialized on the diagnosis and treatment of adult patients with MS and other neuroimmunological diseases. Inclusion criteria encompassed clinical presentation suggestive of AID (≥ 2 symptoms compatible with AID) and the genetic proof of a variant in the NLRP3-, MEFV-, or TNFRSF1A genes. Genetic testing included sequencing of exons 3, 4, and 6 of the NLRP3 gene as well as exons 2, 3, and 10 of the MEFV gene and exons 2, 3, 4, and 6 of the TNFRSF1A gene. Patients were then grouped according to their AID and MS status into NLRP3-, MEFV-, and TNFRSF1A variants with and w/o MS. Patients harboring genetic mutations in two different genes were accordingly allocated to both subgroups. In addition, MS disease course of mutation carriers was compared to a matched MS control group (n = 51) lacking genetic variants in the NLRP3-, MEFV-, and TNFRSF1A genes.

Demographic data, family history, clinical characteristics, MRI, and laboratory findings (cerebrospinal fluid [CSF] and blood), as well as treatment information, were collected during standardized visits at our institute. In patients with MS, data on the disease course were evaluated using the Expanded Disability Status Scale (EDSS) and the Multiple Sclerosis Severity Scale (MSSS) was evaluated [30]. MRI and CSF data were analyzed in more detail in AID patients w/o MS, and CNS involvement was classified as mild (only clinical signs/symptoms, normal CSF, no MRI abnormalities) or severe (clinical signs/symptoms, abnormal CSF and/or MRI). In addition, neurological symptoms were specifically grouped into 5 categories: sensory and motor symptoms, cerebellar signs, cranial nerve (CN) affection, and headache. The term CN affection itself was defined as specific inflammation of the cranial nerves I-XII in patients with AID and CNS manifestation w/o MS. Clinical characteristics of constitutional symptoms were also assessed in all patients including disease course (chronic vs. episodic), fever, skin involvement, abdominal pain, arthralgias, myalgias, and ocular involvement (conjunctivitis/uveitis/retinitis/papillitis). All patients were classified according to the most recent classification criteria for AID [23]. Patients were followed over time whenever possible. Follow-up time of AID patients with MS (mean 10.5 ± 4.6) and of MS control group (mean 9.2 ± 2.8) ranged from 2 to 18 years. Mean follow-up time of AID patients w/o MS was 8.7 ± 3.1 (4–15) and exact follow-up time for each patient is shown in suppl. fig. 1.

Frequencies and percentages were used as descriptive statistics for categorical variables. Median and range were used to describe numerical variables. In order to analyze the clinical phenotype of the patients in relation to their gene variants and MS disease status, we divided the patients into six subgroups: NLRP3 variants without (w/o) or with MS, MEFV variants w/o or with MS, TNFRSF1A w/o or with MS. Intergroup comparisons of main clinical characteristics were assessed by Fisher’s exact test or chi2 test, as appropriate. All tests were two-sided. All analyses were performed with Prism Software (GraphPad©). The Benjamini-Hochberg procedure was used to correct for multiple comparisons, and the threshold for statistical significance was set to p < 0.05.


Demographic and general clinical characteristics

Altogether, 151 patients (40 males, 111 females mean age 44, range 20–75 years) with low-penetrance variants or pathogenic mutations in the NLRP3-, MEFV-, or TNFRSF1A gene and clinical presentation suggestive for AID were included in the study. One hundred and eight patients had a concomitant diagnosis of MS. Four of 151 patients carried a double mutation (1 patient w/o MS: NLRP3 and TNFRSF1A variants, 3 patients with MS: two with MEFV and TNFRSF1A variants, one with MEFV and NLRP3 variants) leading to 155 AID in total (AID w/o MS = 44; AID with MS = 111) (Table 1). The majority of patients were adults with a median age at AID-related symptom onset of 27.5 ± 6.8 years consistent with late-onset disease manifestation. None of the patients were diagnosed before the age of 6 months. The longest diagnostic latency for AID was observed in MS patients with MEFV variants with a mean of 12.3 ± 11.4 years. Only 38 (25%) patients were of Mediterranean origin, most of them carried MEFV variants (n = 22). Overall family history for AID was positive in 68 (44%) patients, with more affected family members in patients with NLRP3 variants w/o MS (65%, see Table 1). A total of 17 (11%) patients (4 with MS) were treated with anti-IL1 drugs (anakinra or canakinumab), while 20 (13%) patients (all with MEFV variants, 4 with MS) received colchicine. Detailed characteristics of all patient groups are presented in Table 1.

Table 1 Study population

Genetic data

In total, 4 different variants were found in the NLRP3 gene, 15 mutations were identified in the MEFV gene, and 6 genetic variants were found in the TNFRSF1A gene. The vast majority of patients carried low-penetrance mutations and was heterozygous for the respective mutation.

In detail, 36 patients (23%) showed a low-penetrance variant in the NLRP3 gene (78% carried a Q703K variant in exon 3), 53 patients (34%) exhibited pathogenic mutations or low-penetrance variants in the MEFV gene (26% with the E148Q variant in exon 2) and 66 patients (43%) showed variants in the TNFRSF1A gene (85% with the R92Q variant in exon 4). A complete overview of all genetic variants is given in Fig. 1a-c. In 13 (25%) FMF patients (10 w/o MS, three with MS), a compound mutation was identified. Severe disease-causing FMF mutations including M694V (+/–), M694V (+/+), K695R (+/-), and M680I (+/–) were found in 22 (42%) MEFV mutation carriers.

Fig. 1

Frequencies of NLRP3-, MEFV-, and TNFRSF1 low-penetrance variants. All patients had sequence variants in NLRP3 (exon 3, 4, 6), MEFV (exon 2, 3, 10), and/or TNFRSF1A (exon 2, 3, 4, 6) gene and were categorized due to their underlying mutation and their MS status (AID w/o or with MS). Pie charts demonstrate absolute numbers of mutations. a Red slices represent NLRP3 variants. b Green slices show different MEFV variants, while c TNFRSF1A variants are symbolized by blue charts. Homozygous variants are marked as +/+, heterozygous variants are labeled by +/− symbols

AID patients w/o MS (n = 40) most frequently harbored MEFV mutations (n = 19, 43%) followed by NLRP3- (n = 17, 39%) and TNFRSF1A (n = 8, 18%) low-penetrance variants (Fig. 1). AID patients with MS (n = 111) displayed most frequently the R92Q variant (n = 51; 46%) in the TNFRSF1A gene followed by the Q703K variant in the NLRP3- (n = 15; 14%) and the E148Q variant (n = 9; 8%) in the MEFV gene (Fig. 1). The MEFV low-penetrance variants K695R (n = 7) and R408Q (n = 8, in six cases as a compound heterozygous P369S-R408Q variant) were almost exclusively found in the MS cohort (Fig. 1b).

Neurological manifestation

Patients without MS

Taken together, 95% of AID patients w/o MS showed neurological manifestations, 16 (36%) of those suffered from severe CNS involvement. Genetically, significantly more patients with severe CNS involvement harbored a Q703K variant in the NLRP3 gene (n = 11; 69%) compared to MEFV- (n = 3, 19%) and TNFRSF1A (n = 2, 13%) low-penetrance variants (chi2 test: p = 0.0228). The clinical picture of severe CNS involvement was dominated by optic neuritis (n = 11; 69%) and aseptic meningitis/meningoencephalitis (n = 5; 31%) while one patient suffered from cerebral vasculitis (n = 1; 3%).

Headache syndromes were frequently observed among all AID subgroups w/o MS and most commonly found in patients with MEFV- (n = 14; 74%) followed by TNFRSF1A- (n = 5; 63%) and NLRP3 low-penetrance variants (n = 10, 59%). Patients with NLRP3 variants were also more commonly affected by motor symptoms (NLRP3 variants: n = 10, 59%; vs. MEFV variants: n = 3, 16%; p = 0.0455) compared to MEFV low-penetrance variants (Fig. 2a). In NLRP3 low variant carriers, CN affection was significantly more often identified compared to MEFV patients (NLRP3 variants: n = 14, 82%; vs. MEFV variants: n = 7, 37%; p = 0.0228). Distribution of NLRP3-, MEFV-, and TNFRSF1A low-penetrance variant carriers regarding CN affection are shown in Fig. 2b.

Fig. 2

Neurological symptoms of AID patients w/o MS. Neurological symptoms were distinguished as follows: a sensory and motor symptoms, cerebellar signs, cranial nerve (CN) affection and headache syndromes in NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants w/o MS. b Distribution of patients w/o MS and NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants and CN affection are shown as percentages

MRI data were available for 33 (75%) AID patients w/o MS (NLRP3 variants: n = 16; 94%, MEFV variants: n = 10; 53%, and TNFRSF1A variants: n = 7; 88%). Abnormal MRI findings were present in 11 (69%) patients with NLRP3 low-penetrance variants, in six (60%) patients with MEFV variants, and in three (43%) patients with TNFRSF1A variants. Unspecific white matter lesions were the most common neuroradiological feature. A disrupted blood-brain barrier indicated by an increased gadolinium uptake was only seen in patients with the Q703K NLRP3 variant. Further morphological MRI features are listed in Fig. 3.

Fig. 3

MRI data of AID patients w/o MS. MRI data of low-penetrance mutation carriers in the NLRP3-, MEFV-, or TNFRSF1A gene w/o MS are shown as percentages

CSF data were available in 31 (71%) AID patients w/o MS (NLRP3 variants: n = 15; 88%, MEFV variants: n = 10; 53%, and TNFRSF1A variants: n = 6; 75%). Pathological CSF findings were present in ten of NLRP3- (67%), two of MEFV- (20%), and two of TNFRSF1A (33%) low-penetrance variants (Fig. 4).

Fig. 4

CSF data of AID patients w/o MS. CSF data of low-penetrance mutation carriers in the NLRP3-, MEFV-, or TNFRSF1A gene w/o MS are shown as mean ± SD or as percentages (OCB)

MS patients

A total of 108 patients with AID had a concomitant MS. The majority of patients (n = 92) were classified as relapsing-remitting MS (RRMS), twelve had secondary progressive MS (SPMS), and seven patients were diagnosed with primary progressive MS (PPMS). Neurological presentations including headache, as well as MS-related disease course, disability, and severity, scores did not differ among AID groups (Fig. 5a, b) and were comparable to MS patients without mutations (Table 2). MS-related medications consisted of disease-modifying therapies (DMT) for mild disease course in 67 MS patients (60%) and for active disease course in 31 MS patients (28%). A slightly higher proportion of MS patients with AID was more often treated with DMT for active disease compared to the MS control group and also showed more often a positive family history for MS. Detailed clinical features of MS patients with AID and of MS control group are summarized in Table 2.

Fig. 5

Disability and severity scores of AID patients with MS. Expanded Disability Status Scale (EDSS) and the Multiple Sclerosis Severity Scale (MSSS) in NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants with MS are shown at initial presentation

Table 2 Clinical data of NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants with MS

Systemic symptoms

Overall 79% (n = 119) of patients fulfilled the most recent classification criteria for the respective AID [23]: 58% (n = 21) with NLRP3 variants, 60% (n = 32) with MEFV low-penetrance or pathogenic mutations, and 100% (n = 66) with TNFRSF1A variants. Most patients suffered from an episodic disease course (n = 137; 88%) with intermittent flares. Looking at all patients, arthralgias was the most common symptom followed by abdominal pain, myalgias, skin rash, fever and ocular involvement (Fig. 6a). Elevated acute-phase reactants (CRP 2.7 ± 1.6 [range 0.6–86] and SAA 31 ± 36.2 [range 5.2–3115]) were detected in all subgroups (Table 3). None of the patients so far showed evidence of amyloidosis or kidney disease. Twenty-two patients (14%) were also diagnosed with other autoimmune diseases including autoimmune thyroid disease, diabetes mellitus type I, Crohn’s disease and alopecia areata. Four patients had a concomitant diagnosis of a rheumatic disease (two patients with D12E and N116S variants in the TNFRSF1A gene had rheumatoid arthritis/polyarthritis, one patient with a M694V MEFV variant was diagnosed with systemic lupus erythematosus, and one patient with a compound P369/R408Q MEFV variant was diagnosed with ankylosing spondylitis).

Fig. 6

Systemic symptoms. Systemic symptoms were distinguished as follows: abdominal pain, skin rash, arthralgias, myalgias, ocular involvement, fever in all patients (a) of NLRP3-, MEFV-, and TNFRSF1 low-penetrance variants w/o (b) or with MS (c). Numbers represent percentages

Table 3 Laboratory data NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants

Patients without MS

Patients w/o MS and with TNFRSF1A variants showed significant more often myalgias (n = 7; 88%) compared to patients with MEFV variants (n = 7; 37%, p = 0.0169). Patients with TNFRSF1A variants (n = 8; 100%) also showed significant more often skin rashes compared to patients with MEFV variants (n = 4; 21%, p = 0.0074) (Fig. 6b).

Patients with MS

MS patients with NLRP3 low-penetrance variants (n = 4; 21%) suffered less frequently from gastrointestinal symptoms compared to MS patients with TNFRSF1A variants (n = 36; 62%, p = 0.0169). Ocular involvement specifically uveitis was most commonly identified in NLRP3 low-penetrance variants (n = 12; 63%) in comparison to TNFRSF1A- (n = 14; 24%, p = 0.0169) and MEFV variants (n = 6; 18%, p = 0.0141) (Fig. 6c). Neither treatment with colchicine nor with anti-IL-1 therapy (Table 1) had a negative impact on the disease course of MS.


This large, monocentric case series demonstrates a broad spectrum and high prevalence of neurological presentations in adult patients with AID predominantly caused by a variety of  low-penetrance mutations in the NLRP3-, MEFV-, or TNFRSF1A gene. Here, 95% of AID patients w/o MS suffered from neurological manifestations. This highlights the importance of neurological assessments in patients with AID and conversely, that neurologists may consider AID in patients with unexplained CNS as well as systemic symptoms caused by inflammation.

Low-penetrance variants occur at a high allelic frequency in the common population [26, 28, 31, 32]. Clinically, they usually present with a “late-onset” of AID and a more heterogeneous spectrum of symptoms, often accompanied by a milder disease course compared to classical pathogenic mutations in patients with AID [33,34,35,36]. Our results also show that the majority of patients had late onset of AID and a broad phenotype overlapping among the different subgroups. Nevertheless, one third of our patients had a severe phenotype involving the CNS. There is mounting evidence, based on both experimental and clinical studies, that also non-confirmatory genotypes can exert pro-inflammatory effects and may lead to severe organ involvement including CNS manifestations in a subset of those patients [24, 37, 38]. We observed severe CNS manifestations including recurrent aseptic meningitis/meningoencephalitis and optic neuritis as well as cerebral vasculitis in several patients w/o MS, most of them harboring the Q703K NLRP3 variant. This was underscored by a high number of abnormal MRI and CSF findings in those patients. CNS inflammation is often observed in patients with pathogenic NLRP3 mutations but has also been reported in patients with MEFV mutations [5, 12, 14, 15, 39, 40]. Regarding NLRP3, neurological involvement was so far reported for 40–95% of CAPS patients and has mainly been linked to the pathogenic R260W mutation of the NLRP3 gene, while the V198M variant was negatively associated with neurological involvement [12, 13, 35]. Thus, the high occurrence of severe CNS inflammation in patients with the low-penetrance Q703K variant compared to patients with other genotypes in our study is novel and unusual. In all our patients, a thorough and intensive diagnostic work-up was performed and other potential differential diagnoses such as neurosarcoidosis or rheumatological diseases such as lupus erythematodes with CNS involvement were ruled out. However, we cannot exclude other genetic factors contributing to the severe phenotype as we neither performed whole-exome sequencing and nor excluded somatic mosaicism in our patients [41].

Looking in more detail on neurological manifestations in patients w/o MS, headache was the most prevalent symptom among low-penetrance variant carriers irrespective of the underlying genotype. This finding demonstrates a similar result compared to AID patients carrying disease-causing variants, of whom headache syndromes were also reported at a high frequency such as 84% of CAPS and 72% of FMF patients [12, 39]. A greater proportion of patients with NLRP3 variants showed CN affection, which supports findings of our previous study and underscores the vulnerability of cranial nerves to inflammation caused by NLRP3-associated inflammasome activation [24]. Studies in animal models have shown that sensory neurons, including the trigeminal nucleus and ganglion, express NLRP3 which upon activation promotes IL-1 release and is blocked by MCC950, a specific NLRP3 inhibitor [42, 43]. Additional studies have also demonstrated that NLRP3 inflammasome activation within the cochlea and retina contributes to murine neuroinflammation [44, 45]. These observations may help explain the predominant affection of the vestibulocochlear nerve, the optic nerve, and the trigeminal nerves in patients with NLRP3 variants in our study.

The majority of patients in our cohort had concomitant MS. This and the fact that most patients were adults are readily explained by the fact that our outpatient clinic is specialized on the treatment of adult MS patients [13, 35]. Former studies already suggested that AID and MS are more likely to co-occur than expected by chance [21, 26, 46]. Previous studies have identified the R92Q variant in the TNFRSF1A gene as a risk factor for MS [47]. The high prevalence of this variant in our study supports these observations. In contrast, although the Q703K NLRP3- and the E148Q MEFV variants have been described in MS patients [24, 28], they have not been confirmed as a susceptibility factor for MS so far. Interestingly, we observed both the K695R and the R408Q (in six cases as a compound heterozygous P369S-R408Q mutation) variants almost exclusively in MS patients, which warrants further investigation in larger study populations. Overall, the disease course of MS in AID patients was similar to MS patients without mutations. This suggests that the underlying genetic variants serve more as a susceptibility factor rather than being a distinct disease modifier in MS [24, 26, 28]. In addition, treatment with colchicine and anti-IL-1 therapy had no major influence on the disease course of MS in our small patient cohort.

It can be difficult to distinguish between “MS with coexisting AID” and “AID with CNS involvement” since the clinical presentation may be similar. Both disorders manifest with variable and episodic symptoms, often affect the optic nerve, and show white matter lesions on MRI as well as abnormalities in the CSF. Thus, careful evaluation and follow-up investigations are of great importance. CAPS, FMF, and TRAPS usually occur with multisystemic inflammation and therefore require medical care and treatment by a collaborative, multidisciplinary team. If at all, adult patients with a presumed diagnosis of an AID are seen by rheumatologists first. As a consequence, neurological manifestations may be overlooked, as neurological examinations as well as MRI and CSF analysis are not routinely performed in such settings.

Although we observed some differences concerning systemic symptoms, overlapping systemic manifestation makes it difficult for the clinician to distinguish between NLRP3-, MEFV-, or TNFRSF1A variants. Thus, if an AID is suspected, we propose to perform a multipaneled genetic diagnostic test as it is offered now in many laboratories. In addition, it can be challenging to differentiate AID from other rheumatological diseases. This often results in delayed diagnosis of AID, in fact, a majority of our patients had a mean diagnosis latency of 10 years.

The strength of this study is its sample size and its monocentric character, thereby circumventing the bias of multiple study sites. Obvious limitations, on the other hand, involve the retrospective character, recruitment bias (as an outpatient clinic specialized in MS), and the lack of patients with clear disease-causing mutations in the NLRP3- and TNFRSF1A gene for comparison. In addition, although the disease course of MS with and without genetic variants did not differ in our patient cohort, we cannot exclude an influence of these variants on MS development and progression. Since we did not collect the respective biomaterial from all our patients, we were unable to investigate and compare cytokine profiles and immune cell subtypes in sera and CSF in MS patients with and without NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants. This is, however, of great interest since increased levels of IL-1ß have been reported in the CSF and in cerebral lesions of MS patients. Furthermore, IL-1β has recently been shown to correlate with cortical pathology load in MS at clinical onset [48, 49]. Additionally, a role of the NLRP3 inflammasome has been demonstrated in the development of experimental autoimmune encephalomyelitis (EAE) [50]. Taken together, a more comprehensive immunophenotyping in correlation to clinical phenotypes in MS patients with and without AID is warranted and may elucidate the impact of these genetic variants on MS disease course in future studies.


Taken together, a broad spectrum of neurological manifestations including coexisting MS may occur in patients with low-penetrance variants of the TNFRSF1A-, NLRP3-, and MEFV genes and both neurologists and rheumatologists should keep this in mind. Diagnosis of AID should be considered a potential differential diagnosis in patients with recurrent episodes of systemic inflammation with CNS involvement and unexplained CN affection.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.



Autoinflammatory diseases


Cryopyrin-associated periodic syndromes


Cranial nerve affection


Expanded Disability Status Scale


Autoimmune encephalomyelitis


Familial Mediterranean fever


Interleukin-1 beta


Multiple sclerosis


Multiple Sclerosis Severity Scale


Primary progressive MS


Secondary progressive MS


Tumor necrosis factor


Tumor necrosis factor receptor-associated periodic syndrome






  1. 1.

    Hoffman HM, Mueller JL, Broide DH, Wanderer AA, Kolodner RD. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nat Genet. 2001;29(3):301–5.

    CAS  PubMed  PubMed Central  Google Scholar 

  2. 2.

    Masters SL, Simon A, Aksentijevich I, Kastner DL. Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*). Annu Rev Immunol. 2009;27:621–68.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Xu H, Yang J, Gao W, Li L, Li P, Zhang L, et al. Innate immune sensing of bacterial modifications of Rho GTPases by the Pyrin inflammasome. Nature. 2014;513(7517):237–41.

    CAS  PubMed  Google Scholar 

  4. 4.

    de Torre-Minguela C, Mesa Del Castillo P, Pelegrin P. The NLRP3 and pyrin inflammasomes: implications in the pathophysiology of autoinflammatory diseases. Front Immunol. 2017;8:43.

    PubMed  PubMed Central  Google Scholar 

  5. 5.

    Abbara S, Grateau G, Ducharme-Benard S, Saadoun D, Georgin-Lavialle S. Association of vasculitis and familial Mediterranean fever. Front Immunol. 2019;10:763.

    CAS  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Rebelo SL, Bainbridge SE, Amel-Kashipaz MR, Radford PM, Powell RJ, Todd I, et al. Modeling of tumor necrosis factor receptor superfamily 1A mutants associated with tumor necrosis factor receptor-associated periodic syndrome indicates misfolding consistent with abnormal function. Arthritis Rheum. 2006;54(8):2674–87.

    CAS  PubMed  Google Scholar 

  7. 7.

    Probert L, Eugster HP, Akassoglou K, Bauer J, Frei K, Lassmann H, et al. TNFR1 signalling is critical for the development of demyelination and the limitation of T-cell responses during immune-mediated CNS disease. Brain. 2000;123(Pt 10):2005–19.

    PubMed  Google Scholar 

  8. 8.

    Caminero A, Comabella M, Montalban X. Tumor necrosis factor alpha (TNF-alpha), anti-TNF-alpha and demyelination revisited: an ongoing story. J Neuroimmunol. 2011;234(1-2):1–6.

    CAS  PubMed  Google Scholar 

  9. 9.

    Stojanov S, Kastner DL. Familial autoinflammatory diseases: genetics, pathogenesis and treatment. Curr Opin Rheumatol. 2005;17(5):586–99.

    CAS  PubMed  Google Scholar 

  10. 10.

    Schwarzbach CJ, Schmitt WH, Szabo K, Bazner H, Hennerici MG, Blahak C. Chorea in a patient with cryopyrin-associated periodic syndrome. Neurology. 2016;86(3):241–4.

    PubMed  Google Scholar 

  11. 11.

    Kitley JL, Lachmann HJ, Pinto A, Ginsberg L. Neurologic manifestations of the cryopyrin-associated periodic syndrome. Neurology. 2010;74(16):1267–70.

    CAS  PubMed  Google Scholar 

  12. 12.

    Parker T, Keddie S, Kidd D, Lane T, Maviki M, Hawkins PN, et al. Neurology of the cryopyrin-associated periodic fever syndrome. Eur J Neurol. 2016;23(7):1145–51.

    CAS  PubMed  Google Scholar 

  13. 13.

    Levy R, Gerard L, Kuemmerle-Deschner J, Lachmann HJ, Kone-Paut I, Cantarini L, et al. Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry. Ann Rheum Dis. 2015;74(11):2043–9.

    CAS  PubMed  Google Scholar 

  14. 14.

    Mamoudjy N, Maurey H, Marie I, Kone-Paut I, Deiva K. Neurological outcome of patients with cryopyrin-associated periodic syndrome (CAPS). Orphanet J Rare Dis. 2017;12(1):33.

    PubMed  PubMed Central  Google Scholar 

  15. 15.

    Kilic H, Sahin S, Duman C, Adrovic A, Barut K, Turanli ET, et al. Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndrome. Eur J Paediatr Neurol. 2019;23(3):466–72.

    PubMed  Google Scholar 

  16. 16.

    Schwabe AD, Monroe JB. Meningitis in familial Mediterranean fever. Am J Med. 1988;85(5):715–7.

    CAS  PubMed  Google Scholar 

  17. 17.

    Minden K, Aganna E, McDermott MF, Zink A. Tumour necrosis factor receptor associated periodic syndrome (TRAPS) with central nervous system involvement. Ann Rheum Dis. 2004;63(10):1356–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Wildemann B, Rudofsky G Jr, Kress B, Jarius S, Konig F, Schwenger V. The tumor-necrosis-factor-associated periodic syndrome, the brain, and tumor-necrosis-factor-alpha antagonists. Neurology. 2007;68(20):1742–4.

    CAS  PubMed  Google Scholar 

  19. 19.

    Compeyrot-Lacassagne S, Tran TA, Guillaume-Czitrom S, Marie I, Kone-Paut I. Brain multiple sclerosis-like lesions in a patient with Muckle-Wells syndrome. Rheumatology (Oxford). 2009;48(12):1618–9.

    Google Scholar 

  20. 20.

    Topcuoglu MA, Karabudak R. Familial Mediterranean fever and multiple sclerosis. J Neurol. 1997;244(8):510–4.

    CAS  PubMed  Google Scholar 

  21. 21.

    Akman-Demir G, Gul A, Gurol E, Ozdogan H, Bahar S, Oge AE, et al. Inflammatory/demyelinating central nervous system involvement in familial Mediterranean fever (FMF): coincidence or association? J Neurol. 2006;253(7):928–34.

    CAS  PubMed  Google Scholar 

  22. 22.

    Lidar M, Brantz Y, Shinar Y, Reznik-Wolf H, Livneh A, Ben Zvi I, et al. A high and equal prevalence of the Q703K variant in NLRP3 patients with autoinflammatory symptoms and ethnically matched controls. Clin Exp Rheumatol. 2017;35(Suppl 108(6)):82–5.

    PubMed  Google Scholar 

  23. 23.

    Gattorno M, Hofer M, Federici S, Vanoni F, Bovis F, Aksentijevich I, et al. Classification criteria for autoinflammatory recurrent fevers. Ann Rheum Dis. 2019;78(8):1025–32.

    CAS  PubMed  Google Scholar 

  24. 24.

    Schuh E, Lohse P, Ertl-Wagner B, Witt M, Krumbholz M, Frankenberger M, et al. Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations. J Neuroinflammation. 2015;2(4):e109.

    Google Scholar 

  25. 25.

    Havla J, Lohse P, Gerdes LA, Hohlfeld R, Kumpfel T. Symptoms related to tumor necrosis factor receptor 1-associated periodic syndrome, multiple sclerosis, and severe rheumatoid arthritis in patients carrying the TNF receptor superfamily 1A D12E/p.Asp41Glu mutation. J Rheumatol. 2013;40(3):261–4.

    CAS  PubMed  Google Scholar 

  26. 26.

    Kumpfel T, Hoffmann LA, Rubsamen H, Pollmann W, Feneberg W, Hohlfeld R, et al. Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation. Arthritis Rheum. 2007;56(8):2774–83.

    PubMed  Google Scholar 

  27. 27.

    Kumpfel T, Hoffmann LA, Pellkofer H, Pollmann W, Feneberg W, Hohlfeld R, et al. Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases. Neurology. 2008;71(22):1812–20.

    CAS  PubMed  Google Scholar 

  28. 28.

    Kumpfel T, Gerdes LA, Wacker T, Blaschek A, Havla J, Krumbholz M, et al. Familial Mediterranean fever-associated mutation pyrin E148Q as a potential risk factor for multiple sclerosis. Mult Scler. 2012;18(9):1229–38.

    CAS  PubMed  Google Scholar 

  29. 29.

    Hohne C, Schuh E, Kumpfel T, Straube A. Cryopyrin-associated periodic fever syndrome manifesting as Tolosa-Hunt syndrome. Cephalalgia. 2016;36(14):1392–6.

    CAS  PubMed  Google Scholar 

  30. 30.

    Roxburgh RH, Seaman SR, Masterman T, Hensiek AE, Sawcer SJ, Vukusic S, et al. Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity. Neurology. 2005;64(7):1144–51.

    CAS  PubMed  Google Scholar 

  31. 31.

    Aksentijevich I, Putnam CD, Remmers EF, Mueller JL, Le J, Kolodner RD, et al. The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model. Arthritis Rheum. 2007;56(4):1273–85.

    CAS  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Verma D, Lerm M, Blomgran Julinder R, Eriksson P, Soderkvist P, Sarndahl E. Gene polymorphisms in the NALP3 inflammasome are associated with interleukin-1 production and severe inflammation: relation to common inflammatory diseases? Arthritis Rheum. 2008;58(3):888–94.

    CAS  PubMed  Google Scholar 

  33. 33.

    Naselli A, Penco F, Cantarini L, Insalaco A, Alessio M, Tommasini A, et al. Clinical characteristics of patients carrying the Q703K variant of the NLRP3 gene: a 10-year multicentric national study. J Rheumatol. 2016;43(6):1093–100.

    CAS  PubMed  Google Scholar 

  34. 34.

    Vitale A, Lucherini OM, Galeazzi M, Frediani B, Cantarini L. Long-term clinical course of patients carrying the Q703K mutation in the NLRP3 gene: a case series. Clin Exp Rheumatol. 2012;30(6):943–6.

    PubMed  Google Scholar 

  35. 35.

    Lachmann HJ, Papa R, Gerhold K, Obici L, Touitou I, Cantarini L, et al. The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry. Ann Rheum Dis. 2014;73(12):2160–7.

    CAS  PubMed  Google Scholar 

  36. 36.

    Ben-Chetrit E, Lerer I, Malamud E, Domingo C, Abeliovich D. The E148Q mutation in the MEFV gene: is it a disease-causing mutation or a sequence variant? Hum Mutat. 2000;15(4):385–6.

    CAS  PubMed  Google Scholar 

  37. 37.

    Schuh E, Gross CJ, Wagner D, Schluter M, Gross O, Kumpfel T. MCC950 blocks enhanced interleukin-1beta production in patients with NLRP3 low penetrance variants. Clin Immunol. 2019;203:45–52.

    CAS  PubMed  Google Scholar 

  38. 38.

    Verma D, Sarndahl E, Andersson H, Eriksson P, Fredrikson M, Jonsson JI, et al. The Q705K polymorphism in NLRP3 is a gain-of-function alteration leading to excessive interleukin-1beta and IL-18 production. PLoS One. 2012;7(4):e34977.

    CAS  PubMed  PubMed Central  Google Scholar 

  39. 39.

    Canpolat M, Gumus H, Gunduz Z, Dusunsel R, Kumandas S, Bayram AK, et al. Neurological manifestations in familial Mediterranean fever: results of 22 children from a reference center in Kayseri, an urban area in Central Anatolia, Turkey. Neuropediatrics. 2017;48(2):79–85.

    PubMed  Google Scholar 

  40. 40.

    Gedalia A, Zamir S. Neurologic manifestations in familial Mediterranean fever. Pediatr Neurol. 1993;9(4):301–2.

    CAS  PubMed  Google Scholar 

  41. 41.

    Nishikomori R, Izawa K, Kambe N, Ohara O, Yasumi T. Low-frequency mosaicism in cryopyrin-associated periodic fever syndrome: mosaicism in systemic autoinflammatory diseases. Int Immunol. 2019;31(10):649–55.

    CAS  PubMed  Google Scholar 

  42. 42.

    Santoni G, Cardinali C, Morelli MB, Santoni M, Nabissi M, Amantini C. Danger- and pathogen-associated molecular patterns recognition by pattern-recognition receptors and ion channels of the transient receptor potential family triggers the inflammasome activation in immune cells and sensory neurons. J Neuroinflammation. 2015;12:21.

    PubMed  PubMed Central  Google Scholar 

  43. 43.

    He W, Long T, Pan Q, Zhang S, Zhang Y, Zhang D, et al. Microglial NLRP3 inflammasome activation mediates IL-1beta release and contributes to central sensitization in a recurrent nitroglycerin-induced migraine model. J Neuroinflammation. 2019;16(1):78.

    PubMed  PubMed Central  Google Scholar 

  44. 44.

    Puyang Z, Feng L, Chen H, Liang P, Troy JB, Liu X. Retinal ganglion cell loss is delayed following optic nerve crush in NLRP3 knockout mice. Sci Rep. 2016;6:20998.

    PubMed  PubMed Central  Google Scholar 

  45. 45.

    Nakanishi H, Kawashima Y, Kurima K, Chae JJ, Ross AM, Pinto-Patarroyo G, et al. NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy. Proc Natl Acad Sci U S A. 2017;114(37):E7766–E75.

    CAS  PubMed  PubMed Central  Google Scholar 

  46. 46.

    Blaschek A, Kries RV, Lohse P, Huss K, Vill K, Belohradsky BH, et al. TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis. Eur J Paediatr Neurol. 2018;22(1):72–81.

    PubMed  Google Scholar 

  47. 47.

    De Jager PL, Jia X, Wang J, de Bakker PI, Ottoboni L, Aggarwal NT, et al. Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. Nat Genet. 2009;41(7):776–82.

    PubMed  PubMed Central  Google Scholar 

  48. 48.

    Seppi D, Puthenparampil M, Federle L, Ruggero S, Toffanin E, Rinaldi F, et al. Cerebrospinal fluid IL-1beta correlates with cortical pathology load in multiple sclerosis at clinical onset. J Neuroimmunol. 2014;270(1-2):56–60.

    CAS  PubMed  Google Scholar 

  49. 49.

    Hauser SL, Doolittle TH, Lincoln R, Brown RH, Dinarello CA. Cytokine accumulations in CSF of multiple sclerosis patients: frequent detection of interleukin-1 and tumor necrosis factor but not interleukin-6. Neurology. 1990;40(11):1735–9.

    CAS  PubMed  Google Scholar 

  50. 50.

    Inoue M, Williams KL, Gunn MD, Shinohara ML. NLRP3 inflammasome induces chemotactic immune cell migration to the CNS in experimental autoimmune encephalomyelitis. Proc Natl Acad Sci U S A. 2012;109(26):10480–5.

    CAS  PubMed  PubMed Central  Google Scholar 

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We wish to thank H. Rodriguez and S. Mader for helpful comments on the manuscript and language editing; Sabine Pitter and Angelika Bamberger for patient care.


This work was supported by the Deutsche Forschungsgemeinschaft (German Research Foundation) within the framework of the Munich Cluster for Systems Neurology (EXC 1010 SyNergy) and the Clinical Competence Network for Multiple Sclerosis. JH is (partially) funded by the German Federal Ministry of Education and Research under 01ZZ1603[A-D] and 01ZZ1804[A-H] (DIFUTURE).

Author information




EM: acquisition, analysis, and interpretation of data; patient care and evaluation; and manuscript writing and editing. DW: acquisition, analysis, and interpretation of data and editing of the manuscript. JH, MS, IM, L.-A. G.: patient care and contribution to clinical data and editing of the manuscript. TK: development of study concept, study supervision, patient care and evaluation, analysis and interpretation of data, and writing, reviewing, and editing of the manuscript. All authors discussed the results and commented on the manuscript. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Tania Kümpfel.

Ethics declarations

The study was approved by the local ethics committee from the Ludwig-Maximilians University. All participants gave written informed consent (project 159-03, 163-16 and 600-15).

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Not applicable.

Competing interests

E. Mulazzani, D. Wagner, M. Schlüter, I. Meinl, and L.-A. Gerdes report no disclosures. J. Havla reports personal fees and non-financial support from Merck, Novartis, Roche, Santhera, Biogen, and Sanofi Genzyme and non-financial support of the Guthy-Jackson Charitable Foundation, all outside the submitted work.

T. Kümpfel has received speaker honoraria including advisory boards from Bayer Healthcare, Teva Pharma, Merck, Novartis Pharma, Sanofi-Aventis/Genzyme, Roche Pharma, and Biogen as well as grant support from Novartis and Chugai Pharma in the past.

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Mulazzani, E., Wagner, D., Havla, J. et al. Neurological phenotypes in patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants. J Neuroinflammation 17, 196 (2020).

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  • CAPS
  • FMF
  • Multiple sclerosis
  • Autoinflammation
  • Autoimmunity