Inflammatory cutaneous lesions and pulmonary manifestations in a new patient with autosomal recessive ISG15 deficiency case report

Interferon-stimulated gene 15 (ISG15) was the first ubiquitin-like modifier protein identified that acts by protein conjugation (ISGylation) [1]. It is one of the most upregulated genes upon Type I interferon treatment or pathogen infections, and its secreted form stimulates the production of cytokines and proliferation of NK cells in humans [2]. ISG15 is present in the gelatinase and secretory granules (but not in the azurophilic or specific granules) of steady-state neutrophils, which release it upon bacterial challenge [3]. ISG15 is also secreted by many other cell types, including myeloid cells, acting as a very potent interferon gamma (IFN-γ) inducing cytokine in lymphocytes (particular NK cells), and in synergy with IL-12. In humans, biallelic mutations in ISG15 were reported to result in an impaired IFN-γ mediated immunity, leading to an increase predisposition to mycobacterial infections in most cases, as also observed in patients with Mendelian Susceptibility to Mycobacterial Diseases (MSMD) [4]; [5]; [6] (see Additional file 1: Table S2). Interestingly, ISG15-deficient patients usually present features of type 1 interferonopathy with cerebral calcifications; attributed to the role of ISG15 in controlling IFN-alpha/beta responses [8].

In the present work, we report a new patient with autosomal recessive (AR) complete ISG15 deficiency, followed for ulcerative skin lesions and lung disease. The patient was born in 2013 from a non-consanguineous Argentinean family. The brotherhood is completed with a healthy younger brother, and a healthy paternal stepbrother (Fig. 1a). She received BCG (Bacillus Calmette–Guérin) vaccination at birth. At 6 months of age, she presented with neck and axillary papulo-ulcerated lesions. At that time she was admitted at the hospital and received antibiotic treatment without clinical response, followed by spontaneous resolution 2 months later. Between 6 and 15 months of age, and due to recurrent skin ulcers, she was initially suspected of presenting BCG-itis. At 1 year old she showed novel similar lesions in the inguinal region and external genitalia, with bilateral and asymmetrical location and without response to either local or systemic treatments. The lesions showed slow healing (3 months) and the biopsy reported ulceration of dermis and epidermis, with necrosis of underlying hypodermis and without inflammatory reaction. Periodic acid–Schiff, acid-fast bacilli and Ziehl–Neelsen reactions were negative. Cultures for pyogenic bacteria, mycobacteria and fungi were also negative. Immunofluorescence of skin samples were negative for immunoglobulins (Ig) IgA, IgG, IgM and C3.

Starting at 2 years and 8 months of age, the patient began having respiratory manifestations including recurrent wheeze and lobar pneumonias (seven isolated and unrelated episodes over the span of 4 years). Three of them required hospitalization, antibiotics and oxygen therapy (for a period of 5 days on average); while one presented with images resembling necrotizing pneumonia with negative microbiological tests. She was kept asymptomatic between episodes. Lung and chest computed tomography (CT) scanning (Fig. 2a) showed some non specific and residual lesions, while brain CT evidenced basal ganglia calcifications (Fig. 2b). Due to the pulmonary manifestations, mycobacterial infection was suspected again. However, clinical inspection by the attending physician discarded BCG-itis, since: (i) no mycobacteria species (or other microorganisms) were isolated from either skin biopsies, or from multiple bronchoalveolar lavages (BAL); (ii) the skin lesions healed without the use of any antimycobacterial treatment, and (iii) the pulmonary manifestations, although seemed progressive, were presented in multiple episodes affecting different sections of the lung parenchyma.

Laboratory tests showed elevated acute-phase reactants, mainly the erythrocyte sedimentation rate. Number and percentages of T, B and NK cells showed to be in adequate range for the age, as well as Igs, C3 and C4. In addition, inadequate antibody response to some protein antigens and polysaccharides was found (Additional file 3: Table S3). The dihydrorhodamine (DHR) assay on neutrophils was normal. Autoimmune workup revealed transient positive lupus anticoagulant and non specific ASMA auto-Ab. Due to the patient multisystemic picture affecting predominantly the skin (chronic and recurrent ulcers) and the lower respiratory tract (lung disease associated with hypoxia and persistent lesions despite adequate treatment), the patient was initially suspected to carry an autoinflammatory disease. Currently, the patient is 7 years old and presents height and weight appropriate for her age. Healing lesions are still present in retroauricular regions, cervical, bilateral axillary, bilateral inguinal and in labia majora, with associated lipoatrophy. She shows delayed and peculiar dentition with the absence of canines and no other abnormalities. Additionally, she displays chronic lung disease with hypoxemic chronic respiratory failure and is being treated with oxygen therapy at home (0.5 L/min in sleep and 1 L/min during the day).

Whole Exome Sequencing (WES) was performed and a total of 100,341 variants were obtained. The first analysis was focused on 55 autoinflammatory genes (Additional file 1: Table S1), but no clinical significant variants were found. However, two clinical relevant heterozygous variants in the ISG15 gene (see Additional file 1: Fig. S1), which codifies for an Ubiquitin-like protein (termed Ubiquitin like modifier ISG15), were identified. The first heterozygous variant c.285del (NM_005101.4, GRCh37(hg19)), also known as c.284del, corresponds to a single nucleotide deletion that is predicted to cause a frameshift in exon 2 (p.Tyr96Thrfs*5) and produces the gain of a stop codon 5 residues downstream from the variant. The second heterozygous variant, c.299_312del (NM_005101.4, GRCh37(hg19)), also known as c.297_313del, corresponds to a 14 nucleotide deletion in exon 2 which is also predicted to produce a frameshift below residue Leu100; p.Leu100Argfs (Fig. 1b). Sanger sequencing and familial segregation were performed confirming that the patient is a compound heterozygous for the above described mutations in ISG15 gene (Fig. 1d). The parents were each heterozygous for one of the reported variants, and the younger brother does not present any of them. All data is consistent with an AR mode of inheritance of ISG15 deficiency (Fig. 1a). According to ACMG criteria [7], both variants follow the pathogenic criterion: pathogenic very strong (PVS1), since they are both null variants, pathogenic moderate 2 (PM2) due to their low frequencies (with no reports or very low allele frequency in population databases such as GnomAD); and pathogenic moderate 3 (PM3), since we confirmed by Sanger Sequencing that the patient inherited both variants in trans, each from one parent. Moreover, it was reported that both variants result in loss of expression and LOF (PS3). To accomplish that, Dusan and col. used an in vitro overexpression system in which both variant carrying alleles were compared with the wild type form of ISG15 [8] .

The ISG15 protein is composed of two tandem repeats of ubiquitin-like domains, the N-terminal domain is required for the efficient E3 ligase-mediated transfer of ISG15 from the E2 enzyme UbCH8 to its substrates, although it is dispensable in the activation and transthiolation steps [9]. The two ubiquitin domains of ISG15 play different critical roles in ISGylation, which is unique among ubiquitin and ubiquitin-like modifiers. Both frameshifts variants clearly disrupt the second domain, causing the loss of the C-terminus ending that contains a very conserved amino acid sequence Leu Arg Leu Arg Gly Gly (LRLRGG), corresponding to the ISGylation site and thus triggering the loss of function of the entire protein [10] (Fig. 1b, c). Compared with ubiquitin, which has very high (close to 100% identity) cross-species conservation, ISG15 protein has relatively low cross-species conservation. Its absence in many eukaryotic species suggests that it is not an essential housekeeping gene, leaving more room for its diversification during evolution. Pathogenic variants in ISG15 gene are a recently defined cause of type I human interferonopathy [11]. Biallelic loss-of‐function variants in ISG15 were initially described in the context of patients with Immunodeficiency 38 (OMIM: 616126), an AR disorder which confers syndromic Mendelian susceptibility to Mycobacterial diseases (MSMD) and affects about 1 in 50,000 individuals exposed to environmental mycobacteria or BCG vaccine strains [4]. Surprisingly, and despite the antiviral functions of ISG15 described in mice, patients described to date do not present viral susceptibility phenotype. The ISG15-IFN-γ circuit operates principally between granulocytes and NK cells [4, 12]. Elevated ISG expression and cerebral calcification are consistent features in patients with biallelic pathogenic variants in ISG15, with a strong neuroradiological overlap with patients with Aicardi–Goutières syndrome (AGS) [13.]

STING-associated vasculopathy with onset in infancy (known as SAVI syndrome) is an early-onset systemic inflammatory phenotype characterized by severe cutaneous vasculopathy and major interstitial lung disease, caused by enhanced sensitivity or ligand-independent (constitutive) activation of a non-nucleic acid receptor component (for example, an adaptor molecule) of the IFN-induced signalling pathway, such as in the case of de novo and inherited pathogenic variants in TMEM173 gene, which encodes the protein STING (stimulator of interferon genes) [14, 15].