Immune dysregulation associated with co-occurring germline CBL and SH2B3 variants

Abstract

Background

CBL syndrome is a RASopathy caused by heterozygous germline mutations of the Casitas B-lineage lymphoma (CBL) gene. It is characterized by heterogeneous clinical phenotype, including developmental delay, facial dysmorphisms, cardiovascular malformations and an increased risk of cancer development, particularly juvenile myelomonocytic leukemia (JMML). Although the clinical phenotype has been progressively defined in recent years, immunological manifestations have not been well elucidated to date.

Methods

We studied the genetic, immunological, coagulative, and clinical profile of a family with CBL syndrome that came to our observation after the diagnosis of JMML, with homozygous CBL mutation, in one of the members.

Results

Variant analysis revealed the co-occurrence of CBL heterozygous mutation (c.1141 T > C) and SH2B3 mutation (c.1697G > A) in two other members. Patients carrying both mutations showed an ALPS-like phenotype characterized by lymphoproliferation, cytopenia, increased double-negative T-cells, impaired Fas-mediated lymphocyte apoptosis, altered cell death in PBMC and low TRECs expression. A coagulative work-up was also performed and showed the presence of subclinical coagulative alterations in patients carrying both mutations.

Conclusion

In the reported family, we described immune dysregulation, as part of the clinical spectrum of CBL mutation with the co-occurrence of SH2B3.

Introduction

CBL syndrome [MIM 613563] is a RASopathy caused by heterozygous germline variants of the Casitas B-lineage lymphoma (CBL) gene [MIM 165360] [1]. CBL encodes an E3 ubiquitin-protein ligase that negatively regulates intracellular signaling, including the RAS-MAPK pathway [2]. Pathogenic CBL variants are predominantly missense or splice site changes affecting the RING finger domain and linker region and resulting in defective ubiquitin ligase activity. The clinical phenotype of CBL syndrome is highly variable and overlaps with Noonan syndrome (NS) [OMIM 163,950, PS163950] [3, 4], the most common disorder among the RASopathies [5]. Although the clinical manifestations have progressively been defined in recent years [3], the complete clinical spectrum seems far to be entirely described. Impaired growth, cognitive deficits, cryptorchidism, distinctive facial features, cardiovascular malformations and vasculitis have been reported [6]. Patients with RASopathies are known to be at increased risk of cancer development, CBL syndrome is associated with an increased risk of JMML and CBL mutations occurs in of a variety of myeloid neoplasms [7, 8]. Leukemogenesis in germ-line mutations is mainly related to the loss of wild-type CBL allele in somatic hematopoietic stem cells (HSCs) by acquired uniparental isodisomy of the 11q23 chromosomal region encompassing the mutated allele [7, 9]. Higher incidence of vasculitis and other autoimmune phenomena (e.g., cytopenia, uveitis) have also been described in patients with CBL syndrome [6, 10,11,12]. The pathogenesis of these autoimmune manifestations may be related to an acquired resistance to death signals in T-cell maturation process due to the inactivation of E3 ubiquitin ligase activity of CBL [13]. It has been shown that mice lacking CBL in T and B cells develop severe vascular lesions with massive infiltration of T cells and a lupus-like syndrome associated with perivascular infiltration and hyperactivation of B-cell receptor (BCR) signaling [14, 15]. While the biological role of CBL in immune homeostasis has been partially elucidated [16], specific immunological features of patients with CBL syndrome have not accurately been characterized so far. Lymphocyte adaptor protein (LNK), also called SH2B3 [MIM 605093], as referred hereafter, is a member of the Src homology 2 (SH2) domain-containing family of adaptor proteins, involved in modulating cytokines and growth hormone signaling by JAK/STAT pathway modulation. It has been described as a regulator of hematopoiesis and lymphocyte differentiation [17]. SH2B3 negatively regulates intracellular signaling elicited by different cell-surface receptors, such as c-kit, thrombopoietin receptor and erythropoietin receptor, all converging towards the activation of the JAK-STAT cascade [18]. Somatic mutations in SH2B3 gene have been described in myeloproliferative neoplasms [19], while germline SH2B3 pathogenic variants have been reported in myelodysplastic syndromes and acute lymphoblastic leukemia [20, 21]. Variants in SH2B3 were also described in autoimmune diseases, particularly autoimmune type 1 diabetes [22]. CBL and SH2B3 are functionally related, contributing to the modulation of signal strength promoted by JAK proteins [23]. We herein report a family segregating pathogenic variants in CBL and SH2B3 presenting novel clinical features, particularly related to immune dysregulation.

Material and methods

Genetic analysis

DNA from peripheral venous blood was available from subjects: I.2, II.1, II.2, III.1, and III.2. In addition, DNA specimens from peripheral blood mononuclear cell (PBMC) before transplantation and buccal mucosa after transplantation were available for subject III: 3 (Fig. 1). Following purification (QIAamp DNA Mini kit, Qiagen), genomic DNA was used to assess the mutational profile of the affected individuals by capture-based parallel sequencing using a NextSeq550 platform (Illumina). A total of 554 genes were included in the designed gene panel (list available on request) using custom-designed NimbleGen SeqCap probe hybridization (Roche NimbleGen).Read alignment to the reference genome (UCSC-GRCh37/hg19) and variant calling, filtering and prioritization analyses were performed using an in-house implemented pipeline mainly based on the GATK Best Practices (GATKv3.7, http://www.broadinstitute.org/gatk/). Variants of possible clinical interest were extracted by setting filtering criteria on population frequency, as well as disease associations and in silico prediction of impact.

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Segregation analyses were performed by Sanger sequencing. PCR primers on the CBL and SH2B3 sequence have been drawn with the Primer Express software in the regions flanking CBL exon 8 (F: 5’-GGACCCAGACTAGATGCTTTCT-3’ and R: 5’-TCGCTGTTTAGATCCGTACCTG-3’) and SH2B3 exon 7 (F: 5’-AGGTCTGACCCTACTGCCC-3’ and R: 5’-GCCAGGTGGATAGATGAAACCT-3’).

PCR was performed using the FastStart Taq DNA Polymerase kit (Roche) according to the manufacturer instruction with the following program: 95 °C for 5 min, (95 °C for 30 s, 60 °C for 30 s, 72 °C for 30 s) for 35 cycles, 72 °C for 7 min. Samples were sequenced using the BigDye Terminator v1.1 Cycle Sequencing kit (Applied Biosystems) and loaded on the 96-capillary ABI 3730 DNA Analyzer (Applied Biosystems), and sequences were read using the Sequencher 4.1 software (Gene Codes Corporation).

Immunological analysis

Immunophenotype by flow cytometric analysis

On peripheral blood, after red blood cell lysis with ammonium chloride, the following antibodies were employed: CD3 PerCP (clone BW264/56, MiltenyiBiotec, BergischGladbach, Germany), CD4 APC (clone OKT4, Becton Dickinson, Franklin Lakes, NJ, USA), CD8 PE-Cy7 (clone RPA-T8, Becton Dickinson, USA), TCR alpha–beta APC (clone T10B9, Becton Dickinson), TCR gamma-delta FITC (11F3, MiltenyiBiotec, DE), CD45RA APC-H7 (clone T6D11, MiltenyiBiotec, DE), CCR7 PE (clone 3D12, Ebioscience, San Diego, CA, USA), CD127 PE-CY7 (clone eBioRDR5, eBiosciences), CD16 PE (clone 3G8), CD56 PE (clone NCAM16.2), CD19 PE-CY7 (clone SJ25C1, Becton Dickinson), CD27 FITC (clone M-T271, Becton Dickinson), CXCR5 (clone J252D4 Biolegend), CD31 (cloneWM59, Miltenyi Biotec, DE).

ELISA Immunoassay for IgM, IgA, and IgG

Plasma and secreted Igs were quantified with ELISA immunoassay after stimulation with CpG. 96-well plates (Corning) were coated with purified anti-human IgA, IgG, and IgM (Jackson ImmunoResearch Laboratories, PA, USA), washed with PBS/0.1% Tween and blocked with PBS/1% gelatine. Subsequently, two incubation steps for 1 h at 37 °C, first with culture supernatants and second with peroxidase-conjugated goat anti-human IgA, IgG, or IgM Abs (JacksonImmunoResearch Laboratories, PA, USA) were performed. Chromogenic substrate was o-phenylene-diamine solution (Sigma-Aldrich, St. Louis, MO, USA).

Lymphocyte proliferation assay

PBMC were labeled with 5 µM of carboxyfluorescein diacetate succinimidyl ester (CFDA-SE) [8 min at room temperature]. Plates of CFSE-stained cells were stimulated for 72 h with antiCD3/CD28 beads (Dynabeads Human T-activator CD3/CD28, Life Technologies, 50 beads/1 CD3) or PHA (10 μg/mL, Roche). Proliferating T cells were stained with anti-CD4 PeCy7, 7-Amino-actinomycin D (7-AAD) and anti-CD8 APC. Final analysis was performed with FlowJo software 2.2 (TreeStar Inc, Ashland, Ore).

Fas-mediated apoptosis test

Fas-mediated apoptosis was tested on T-cells. PBMCs were activated with phytohemagglutinin (PHA) at days 0 (1 mg/mL) and 15 (0.2 mg/mL) and cultured in RPMI 1640 plus 10% fetal calf serum plus recombinant interleukin-2 (IL-2; 5 U/mL; Biogen, Geneva, Switzerland). On day 21, cells were incubated with anti-Fas MoAb (IgM isotype; 1 mg/mL; UBI, Lake Placid, NY) or anti-Fas MoAb plus anti-IgM rabbit antimouse serum (1 mg/mL; Serotec, Oxford, UK). IL-2 (5 U/mL) was added to minimize spontaneous cell death. Cell survival was evaluated after 18 and 48 h. Surviving cells were counted by trypan blue exclusion test. The results were expressed as percentage of specific cell survival.

TRECs expression

Real-time quantitative PCR for TRECs was performed by a ViiA7 real-time PCR system (Applied Biosystems, Foster City, Calif) and optimized based on custom reagents provided by Affymetrix (Santa Clara, Calif). TREC levels were normalized per microliter of blood, considering that single 3.2-mm punch contains approximately 3 μL of whole blood. Abnormal TREC results were defined as less than 8 TRECs/μL of dried blood.

Phospho-S6 protein assay

Ex vivo assessment of S6 Ser235/236 phosphorylation was performed on whole blood using an antibody against phosphorylated S6 Ser235/236 (clone D57.2.2E, catalog 8520S, Cell Signaling Technology) and the PerFix EXPOSE kit, according to the manufacturer’s recommendations (Beckman Coulter). Briefly, 100 μl of fresh blood was incubated in the presence of surface antibody for 10 min at 37 °C in a water bath. B- and T-cell surface markers were: CD19 (clone HIB19, catalog 2,111,030, Sony), CD3 (clone UCHT1, catalog 25-0038-42, BD), CD4 (clone VIT4, catalog 130-092- 373, MiltenyiBiotec), CD8 (clone BW135/80, catalog 130-096-902, MiltenyiBiotec). The reaction was stopped using buffer 1 and red blood cells were lysed with buffer 2 for 5 min at 37 °C. The samples were centrifuged, and the pellets underwent intracellular staining with buffer 3 for 1 h. The cells were then washed with the dedicated buffer, re-suspended, and analyzed with a FacsAriaIII flow cytometer (Becton–Dickinson).

Patient consent and ethical approval

The patients gave written informed consent for the clinical evaluations and genetic analyses prior to inclusion in the study, in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. All the analyses were performed within the common clinical practice of the treating hospital, the IRCCS Azienda Ospedaliero-Universitaria di Bologna, and thus no specific research protocol was approved in accordance with the Area Vasta Emilia Centro Ethic Committee requirements. The clinical data for the patients were obtained from questionnaires completed by the attending physician, as well as from medical records. Informed consent was obtained from the patient to publish the images in an online open access publication.

Results

III.3 presented CBL syndrome and developed JMML due to a second somatically acquired hit.

Figure 1 summarizes selected clinical, pathologic, and molecular findings of the analyzed family. The proband (III.3) came to our attention in 2000 for the presentation of severe anemia and thrombocytopenia associated with marked splenomegaly during infancy. Diagnosis of Juvenile Myelomonocytic Leukemia (JMML) was made according to clinical features, laboratory criteria and hypersensitivity to GM-CSF [24]. For the subsequent worsening of the clinical conditions and severe transfusion dependency, the patient received allogeneic HSCT from a fully HLA matched sibling donor (III.1). Conditioning regimen with Busulfan, Thiotepa and Cyclophosphamide and standard cyclosporine-based graft-vs-host disease (GvHD) prophylaxis were used, and 8.73 × 108 total nucleated bone marrow cells/kg were infused. He did not present major early post-HSCT complications, and currently shows complete donor chimerism. Three years after HSCT, he developed hypothyroidism. During the 21 years of follow-up, he never showed recurrence of the primary disease. During his late adolescence, he developed pericardial effusion that resolved spontaneously. He presented with typical features of CBL syndrome, including facial dysmorphisms (Additional file 1: Fig. S1), and mild cognitive impairment. He also showed dental agenesis, tracheomalacia, multiple lipomas and cerebellar tonsils herniation. Considering this clinical phenotype alongside with the previous diagnosis of JMML, we suspected CBL syndrome. Genetic analysis performed on DNA from buccal mucosa and hair follicles showed a heterozygous variant at chromosomal position chr11:119,148,921 (GRCh37/hg19) in CBL (c.1141 T > C; GenBank: NM_005188.4). The nucleotide change affected exon 8 of the gene, and predicted the substitution of a cysteine residue at codon 381 by arginine [p.Cys381Arg]. Cys381 is a highly conserved residue located in the RING finger domain, whose proper function is required for the ubiquitin ligase activity of CBL. In silico predictive algorithms consistently indicated a deleterious effect on protein structure/function. This variant has been annotated in the dbSNP database (rs757874631), but it was not reported in gnomAD (Version: 2.1). The variant was classified as pathogenic according to the recommendation of American College of Medical Genetics and Genomics (ACMG), and was reported as pathogenic in the COSMIC database (COSM34056); however, conflict interpretations of pathogenicity (i.e., likely pathogenic vs variant of uncertain significance [VUS])were reported in the ClinVAr database. Following analyses on stored bone marrow samples collected after JMML diagnosis and before HSCT documented homozygosity for the CBL variant. The somatically acquired LOH resulted from isodisomy.

III.2 and II.2 showed CBL syndrome with ALPS-like features and harbored a concurrent missense variant in the SH2B3 gene

This finding prompted us to extend genetic testing in family members, revealing the occurrence of the same CBL variant in individuals III.2 and II.2 (Fig. 1). The variant was absent in DNA samples extracted from peripheral blood and buccal swab of the paternal grandfather (I.1). The lack of paternal grandmother’s samples did not allow us to conclude whether it was a de novo or an inherited event. Like his younger brother, subject III.2 presented with mild facial dysmorphism and mild cognitive impairment. Additional findings include mixed bilateral hearing loss, dermatofibroma, brachydactyly, inguinal hernia and horseshoe kidney. In the first years of life, the subject suffered from recurrent petechiae and easy bruising. During his early childhood, he was referred to our tertiary center for splenomegaly, micro-hematuria, and mild thrombocytopenia (platelet count, 87.000/microliter) in presence of anti-platelet antibodies. In the suspicion of autoimmune lymphoproliferative syndrome (ALPS), Fas-mediated lymphocyte apoptosis assay was performed and resulted altered (95% of surviving lymphocytes, normal values [n. v.] < 82%). Increased double negative T (DNT) cells CD3 + CD4-CD8-TCR α/β + (3.10% of CD3 + , n. v. < 2.5%), leading to the diagnosis of ALPS according to the revised criteria from the 2009 NIH International Group [25]. Genetic analysis excluded pathogenic variants in FAS, FASL or CASP10 and the disease was classified as ALPS-U (unknown genetic cause) [25]. During his middle childhood, he showed mild anemia (Hb, 12.1 g/dL), leukopenia (white blood cells, 580/microliter), thrombocytopenia (platelet count, 103.000/microliter) and persistent splenomegaly. Morphological evaluation of bone marrow (BM) smear revealed hypercellularity with mild-to-moderate left shift in myeloid maturation, pelgeroid granulocytes and absence of dysmorphic features (Additional file 1: Fig. S2). Mild dysmorphism was also noticed in subject II.2. ALPS was diagnosed due to the presence of chronic splenomegaly, together with defective Fas-mediated lymphocyte apoptosis (83% of surviving lymphocytes) and increased DNT (2.9% of CD3 +), while complete blood count resulted normal. Of note, vitamin B12 levels were within normal limits both in patient II.2 and in patient III.2. Targeted sequencing allowed to identify a missense variant in the SH2B3 gene (c.1697G > A; GenBank: NM_005475.3) in both individuals (Fig. 1; Additional file 1: Fig. S3). The variant was absent in individuals I.2, II.1, III.1, and III.3. We cannot conclude whether it was a de novo or an inherited event in II.2. The missense change is predicted to replace an arginine residue at codon 566 by glutamine (p.Arg566Gln). This variant was classified as a VUS according to the ACMG guidelines and had previously been reported in the dbSNP database (rs148791142), but not in ClinVar database, and has an extremely low frequency in gnomAD (ƒ = 0.0000878; Version:2.1). It was reported as pathogenic in COSMIC (COSM6947187). Consistent with the molecular findings, subjects I.2, II.1 and III.1 did not show any constitutional characteristics and pathological features resembling CBL syndrome. Of note, subject I.2 was affected by a Philadelphia positive chronic myeloid leukemia in treatment with Imatinib. Subject II.3 presented type 4 spastic paraplegia with an intragenic heterozygous deletion of the SPAST gene (2p22.3), anti-phospholipid syndrome with suspected neurological involvement, bilateral retinal detachment, endometriosis, recurrent oral ulceration, alopecia, and splenomegaly. Laboratory findings included positive antinuclear antibody, Lupus anticoagulant (LAC) and anti-platelets antibodies in the absence of thrombocytopenia, together with non-specific alterations at the capillaroscopy. However, diagnostic criteria for systemic lupus erythematosus (SLE) were not matched. Spastic tetraparesis involving the I and II motoneurons was also diagnosed in subject I.1, during the adult age, without a genetic characterization. Splenomegaly was also present in this subject. While the clinical features were suggestive of CBL syndrome in subjects II.3 and I.1, CBL genetic status is not available.

Affected subjects show impaired cell death in PBMC and low TRECs expression in absence of PI3K-AKT pathway upregulation

To identify occurrence of immunological alterations associated with the CBL and SH2B3 variants, extensive immunological characterization was carried out (Table 1, Additional file 1: Table S1).

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Peripheral blood immunophenotyping by flow-cytometry analysis showed increased DNT in patients with CBL syndrome. Of note, subject III.1 presented increased DNT levels, not presenting any genetic or pathological findings of CBL syndrome. The role of DNTs remains a matter of debate since they represent a shared feature for other non-ALPS autoimmune diseases, such as celiac disease, and thus cannot be considered a specific CBL syndrome feature [26,27,28]. Extensive immunophenotyping in patients with CBL syndrome highlighted other modest alterations in T-cell subsets, showing γδ + T-cell and effector CD8 + T memory cell expansion, suggesting that the immune CBL-mediated dysregulation may primarily affect T lymphocytes. No major alteration was noted in the B-cell population, presenting with normal immunoglobulin (Ig) levels and antibody responses in all tested members, with the exception of partial memory deficiency detected in subject II.2. Resistance to apoptosis via Fas/Fas ligand was analyzed, resulting defective in subjects II.2 and III.2 (data not shown), similar to what is typically described in ALPS [25]. Further studies were performed on peripheral blood mononuclear cells (PBMC) to investigate spontaneous or PHA-stimulated cell death, showing an increment of death in unstimulated patients’ cells, with any relevant differences with respect to healthy donors (HDs) in stimulated cells (Fig. 2A). Notably, evaluation of the surviving fraction of PHA-stimulated CD4 and CD8 subsets documented a mild resistance to cell death in CD8 cells from all three investigated patients (II.2, III.2 and III.3) and in CD4 cells from patient III.2 but revealed that CD4 cells from patients II.2 and III.3 have a cell death resistance comparable to that of HDs (Fig. 2B). These findings revealed an impaired cell death mechanism in patients’ cells. Subjects II.2, III.2, and III.3 showed low T-cell receptor excision circles (TRECs) expression compared to the other adult healthy family members (Table 1). Thymic output generally decreases with age, but an adequate output is still maintained into late adulthood. We noticed a significant difference between the patients and adult healthy controls. Considering the role of CBL in regulating phosphatidylinositol 3-kinase (PI3K)/AKT/mTOR pathway in mouse models [2, 13], we tested phosphoS6 basal levels on both T- and B-cell subsets, and AKT phosphorylation on PHA-stimulated T cells, as markers of PI3K activity. No significant differences were identified. Equivalent modulation of phospho-AAK by IC87114, an inhibitor of the pathway, was also observed, suggesting that CBL mutation does not alter the PI3K-AKT/mTOR signaling cascade (Fig. 2C).

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Mild coagulative alterations in patients affected by CBL syndrome

We then performed systematic revision of the clinical records to search for possible clinical signs of vasculopathies. We found that subject III.3 experienced an episode of pericarditis, occurred about 20 years after transplantation. The attribution of this pericarditis to CBL syndrome is controversial, since this clinical manifestation has not previously been reported in the disorder [23]. Moreover, subject III.3 received HSCT from the sister carrying wild-type CBL gene and a healthy immune system. We further performed a complete diagnostic work-up to reveal potential signs of endothelial alterations in the patient and other members of the family. Laboratory analysis revealed a pattern of hereditary coagulative alterations (Table 2).

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Subject III.3 presented with positive LAC before HSCT and no alteration in the levels of von Willebrand factor (vWF) and D-dimer. However, prolongation of international normalized ratio (INR) and activated partial thromboplastin time (aPTT) was observed. Five years after HSCT from III.1, INR and aPTT of III.3 were normal, and LAC resulted negative. Slight reduction in the levels of vWF was observed in subject III.2, using both vWF antigen (0.56 UI/ml; n.v. 0.65–1.20) and vWF ristocetin cofactor (0.46 UI/ml; n.v. 0.70–1.50) alongside with a reduction in fVIII activity (0.55 UI/ml; n.v. 0.70–1.50). The patient’s blood group type was A negative. Prolongation of INR and aPTT was observed, with negative LAC. aPTT resulted normal after correction with normal plasma. Further coagulation work-up revealed slight reduction in the activity of fII, fV, fX, fXI, fXII, but no alteration in the levels of D-dimer was found. Subject II.2 received a diagnosis of a mild form of vW disease without clinical manifestations, and LAC was found to be negative. His sister, patient II.3, has asymptomatic vW disease, slight reduction in fXI and positive LAC. Finally, subject I.1 and her sister, identified as I.3, were both reported to be diagnosed with vW disease and to have positive LAC.

Discussion

Here, we reported on a three-generation family transmitting a pathogenic CBL missense variant, which co-occurred with a likely pathogenic SH2B3 variant in two subjects. Besides the constitutional features fitting CBL syndrome, peculiar immunological alterations were documented in the two subjects heterozygous for the concomitant CBL and SH2B3 variants.

Immune dysregulation has not extensively been described in patients with germline CBL mutations so far. However, CBL proteins (particularly CCBL and CBLB) have been demonstrated to regulate lymphocyte stimulation and the engagement of death-promoting signals by actively interacting with T-Cell receptor (TCR) signaling [2, 13]. Autoimmune and lymphoproliferative features observed in the present patients were initially diagnosed as manifestations of ALPS, but are likely to be related to CBL syndrome, particularly in the presence of a concomitant pathogenic variant in SH2B3. A comparable phenomenon has been associated with upregulated RAS function [29, 30]. Activating variants in genes coding for protein with role in RAS signaling are known to play a significant role in human diseases, including malignancies, and developmental and lymphoproliferative disorders [5, 31]. Activating mutations of NRAS and KRAS were also noted in a recently described pathological entity called RAS-associated autoimmune leukoproliferative disorder (RALD), which shares overlapping features with JMML and ALPS [32,33,34].

Germline mutations in SH2B3 have been reported in different diseases, particularly myelodysplastic syndrome and JMML [19, 20, 35, 36]. Notably, SH2B3 was not mutated in our patient affected by JMML. Biallelic germline SH2B3 mutations have been reported in two siblings with autoimmune manifestations [21]. While one of them developed a B-cell precursor ALL, the other presented a non-malignant clinical phenotype similar to II.2 and III.2 (immune cytopenia, developmental delay) [21]. Interestingly, association between type 1 diabetes and variants in the chromosome region 12q24 that contains SH2B3 has been demonstrated [37]. Occurrence of the SH2B3 missense change was associated with higher T-cell proliferation on PMBCs, stimulated with CD28 and CD3, suggesting a role of altered SH2B3 function in the pathogenesis of autoimmune disorders [22].

Based on previous data indicating a role of c-CBL in TCR-induced thymocyte apoptosis in mouse models [13, 38], we investigated residual thymic output by measuring TRECs by real time quantitative PCR. In subject III.3, the reduced thymic function could be attributed at least in part to the toxic effect of HSCT. In addition, we hypothesize that thymic dysfunction could mainly be ascribed to the CBL deficiency, thus potentially contributing to the immunological alterations observed in the patients. We also speculate that even if HSCT effectively reconstituted a healthy immune system, germ-line CBL mutation in thymocytes could directly produce progressive thymus loss [38]. It should be noted that SH2B3 is expressed in hematopoietic progenitors, and his overexpression in lymphoid precursors impairs the expansion of T cells in thymus [39]. LNK/SH2B3 also negatively regulates IL-7-induced JAK/STAT signaling in B-cell progenitors [40]. Hematopoietic stem cells of Lnk deficient mice (Lnk -/-) presented with a high proliferative capacity resulting in splenomegaly and multi-lineage hyperplasia in BM together with an augmented ability to reconstitute the hematopoietic system in transplantation models [41,42,43].

Immune dysregulation could help to explain the vascular alteration and endothelial complications reported in CBL syndrome [6]. Some patients with JMML due to germline CBL mutations experiencing spontaneous resolution of the myeloproliferative/myelodysplastic disorder have been reported to develop different types of cardiovascular manifestations, including hypertension, cardiomyopathy, Moyamoya disease and Takayasu arteritis [6, 44]. Moyamoya disease has also been described in patients harboring de novo CBL mutations [10], and in CBL syndrome without JMML [45]. On the contrary, individuals with JMML and homozygous CBL mutations who undergo HSCT seem not to develop vasculitis, suggesting that a normal immune/hematopoietic system could be pivotal in preventing these manifestations [6]. Moreover, mice lacking CBL in peripheral immune cells present vascular infiltration of lymphocytes hypersensitive to TCR/BCR signaling, leading to endothelial damage [14, 15], highlighting the determinant role of immune dysregulation in vascular complications [6]. Recent emerging evidence also suggests a critical role of CBL in angiogenesis and endothelial cells signaling [16]. Defective CBL function seems to promote myofibroblast migration into the endothelium and subsequent proliferation via signaling elicited by the PDGF receptor, potentially contributing to the vascular disorders [46]. It is therefore reasonable that CBL mutations contribute to endothelial damage even if the underpinning of the biological mechanisms needs to be fully uncovered.

These findings collectively show the presence of a subclinical coagulative alteration with intrafamilial recurrence in the family members with CBL syndrome. Decreased vWF and coagulation factors consumption in these subjects could be attributable to diffuse activation of the coagulation system. We believe that these alterations are consistent with CBL syndrome, because they could be possibly related to endothelial damage due to CBL syndrome-associated vasculitis [6]. These features could be explained by increased platelet responses to GpVI agonists and thrombin linked with CBL loss of function, leading to increased platelet activation [47]. Interestingly, coagulative alterations have been reported in two patients with germline CBL mutations and Moyamoya disease [10]. The contribution of the co-occurring SH2B3 variant to the coagulative alterations observed in subject II.2 and III.2 still needs to be fully characterized. SH2B3 has been shown to be a key negative regulator of signaling in endothelial cells, reducing activation and inflammation [48]. The normalization of the coagulation anomalies after allo-HSCT from his sister in subjects III.3 suggests a critical role of the hematopoietic and immune system in these alterations, rather than a direct effect of CBL and SH2B3 mutations on the endothelial cells. However, further studies are needed to understand the exact contribution of the immune system, endothelium, and coagulation system in the biology of vascular damage in CBL syndrome.

This report presents some limitations. Experimental data are needed to define the exact biological mechanisms underpinning the relationship between CBL and immunological and coagulative disorders. Possible perturbations in PI3K/AKT/mTOR pathway need to be investigated in CBL syndrome [49,50,51]. Moreover, the role of adaptor proteins, like SH2B3, in the pathogenesis of immunological manifestations, necessarily requires further investigations.

Our data support the requirement of an extensive immunological characterization and monitoring of patients with CBL syndrome. Following confirmation of these findings, guidelines for surveillance and treatment of immune-related complications should be implemented. The present report also highlights the need for further investigation on coagulative and vascular alterations associated with CBL syndrome. Our findings suggest a cooperative role of pathogenic SH2B3 and CBL variants in the development of immune dysregulation, also corroborated by the experimental evidence of the role of both these proteins in hematopoietic stem and immune system cells [40, 52]. In conclusion, this report contributes to expand the clinical spectrum of CBL syndrome, uncovering previously undescribed immunological and coagulative features to be taken into account for a more effective management, follow-up and treatment of this disorder.

Availability of data and materials

The datasets used and analyzed during the current study available from the corresponding author on reasonable request.

References

Martinelli S, De Luca A, Stellacci E, Rossi C, Checquolo S, Lepri F, et al. Heterozygous germline mutations in the CBL tumor-suppressor gene cause a noonan syndrome-like phenotype. Am J Hum Genet. 2010;87:250–7. https://doi.org/10.1016/j.ajhg.2010.06.015.

Schmidt MHH, Dikic I. The Cbl interactome and its functions. Nat Rev Mol Cell Biol. 2005;6:907–18.

Martinelli S, Stellacci E, Pannone L, D’Agostino D, Consoli F, Lissewski C, et al. Molecular diversity and associated phenotypic spectrum of germline CBL mutations. Hum Mutat. 2015;36:787–96.

Pérez B, Mechinaud F, Galambrun C, Ben Romdhane N, Isidor B, Philip N, et al. Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia. J Med Genet. 2010;47:686–91.

Tartaglia M, Gelb BD. Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms. Ann NY Acad Sci. 2010;1214:99–121.

Niemeyer CM, Kang MW, Shin DH, Furlan I, Erlacher M, Bunin NJ, Bunda S, Finklestein JZ, Sakamoto KM, Gorr TA, Mehta P. Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic Leukemia. Nat Genet. 2010;42(9):794–800.

Loh ML, Sakai DS, Flotho C, Kang M, Fliegauf M, Archambeault S, et al. Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. Blood. 2009;114:1859–63.

Masetti R, Vendemini F, Zama D, Biagi C, Pession A, Locatelli F. Acute myeloid leukemia in infants: biology and treatment. Front Pediatr. https://doi.org/10.3389/fped.2015.00037

Strullu M, Caye A, Cassinat B, Fenneteau O, Touzot F, Blauwblomme T, et al. In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia. Leukemia. 2013;27(12):2404–7. https://doi.org/10.1038/leu.2013.203.

Guey S, Grangeon L, Brunelle F, Bergametti F, Amiel J, Lyonnet S, et al. De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy. J Med Genet. 2017;54:550–7.

Cortellazzo Wiel L, Pastore S, Taddio A, Tommasini A. A case of uveitis in a patient with juvenile myelomonocytic leukemia successfully treated with adalimumab. J Pediatr Hematol Oncol. 2020;42:e373–6.

Ali AM, Cooper J, Walker A, Jones D, Saad A. Adult‐onset acute myeloid leukaemia in a patient with germline mutation of CBL. Br J Haematol. 2021;192(3):665–7. https://doi.org/10.1111/bjh.17234.

Thien CBF, Dagger SA, Steer JH, Koentgen F, Jansen ES, Scott CL, et al. c-Cbl promotes T cell receptor-induced thymocyte apoptosis by activating the phosphatidylinositol 3-kinase/Akt pathway. J Biol Chem. 2010;285(14):10969–81. https://doi.org/10.1074/jbc.M109.094920.

Kitaura Y, Jang IK, Wang Y, Han YC, Inazu T, Cadera EJ, et al. Control of the B cell-intrinsic tolerance programs by ubiquitin ligases Cbl and Cbl-b. Immunity. 2007;26:567–78.

Naramura M, Jang I-K, Kole H, Huang F, Haines D, Gu H. c-Cbl and Cbl-b regulate T cell responsiveness by promoting ligand-induced TCR down-modulation. Nat Immunol. 2002;3:1192–9.

Lyle CL, Belghasem M, Chitalia VC. c-Cbl: an important regulator and a target in angiogenesis and tumorigenesis. Cells. 2019;8:498.

Morris R, Butler L, Perkins A, Kershaw NJ, Babon JJ. The role of LNK (SH2B3) in the regulation of JAK-STAT signalling in haematopoiesis. Pharmaceuticals (Basel). 2021;15(1):24.

Devallire J, Charreau B. The adaptor Lnk (SH2B3): an emerging regulator in vascular cells and a link between immune and inflammatory signaling. Biochem Pharmacol. 2011;82:1391–402.

Maslah N, Cassinat B, Verger E, Kiladjian JJ, Velazquez L. The role of LNK/SH2B3 genetic alterations in myeloproliferative neoplasms and other hematological disorders. Leukemia Nat Publish Group. 2017;31:1661–70.

Coltro G, Lasho TL, Finke CM, Gangat N, Pardanani A, Tefferi A, et al. Germline SH2B3 pathogenic variant associated with myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis. Am J Hematol. 2019;94:E231–4.

Perez-Garcia A, Ambesi-Impiombato A, Hadler M, Rigo I, LeDuc CA, Kelly K, et al. Genetic loss of SH2B3 in acute lymphoblastic leukemia. Blood. 2013;122:2425–32.

Lavrikova EY, Nikitin AG, Kuraeva TL, Peterkova VA, Tsitlidze NM, Chistiakov DA, et al. The carriage of the type 1 diabetes-associated R262W variant of human LNK correlates with increased proliferation of peripheral blood monocytes in diabetic patients. Pediatr Diabetes. 2011;12:127–32.

Leardini D, Messelodi D, Muratore E, Baccelli F, Bertuccio SN, Anselmi L, et al. Role of CBL mutations in cancer and non-malignant phenotype. Cancers. 2022;14(3):839. https://doi.org/10.3390/cancers14030839.

Niemeyer CM, Aricó M, Basso G, Biondi A, Cantú Rajnoldi A, Creutzig U, et al. Chronic myelomonocytic leukemia in childhood: a retrospective analysis of 110 cases. Blood. 1997;89:3534–43.

Oliveira JB, Bleesing JJ, Dianzani U, Fleisher TA, Jaffe ES, Lenardo MJ, et al. Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop. Blood. 2010;116:35–40.

Li H, Tsokos GC. Double-negative T cells in autoimmune diseases. Curr Opin Rheumatol. 2021;33:163–72.

Russell TB, Kurre P. Double-negative T cells are non-ALPS-specific markers of immune dysregulation found in patients with aplastic anemia. Blood. 2010;116:5072–3.

Steenholt JV, Nielsen C, Baudewijn L, Staal A, Rasmussen KS, Sabir HJ, et al. The composition of T cell subtypes in duodenal biopsies are altered in coeliac disease patients. PLoS One. 2017;12:e0170270.

Oliveira JB, Bidère N, Niemela JE, Zheng L, Sakai K, Nix CP, et al. NRAS mutation causes a human autoimmune lymphoproliferative syndrome. Proc Natl Acad Sci USA. 2007;104:8953–8.

Takagi MM, Shinoda K, Piao J, Mitsuiki N, Takagi MM, Matsuda K, et al. Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation. Blood Am Soc Hematol. 2011;117:2887–90. https://doi.org/10.1182/blood-2010-08-301515.

Simanshu DK, Nissley DV, McCormick F. RAS proteins and their regulators in human disease. Cell Elsevier. 2017;170:17–33.

Calvo KR, Price S, Braylan RC, Oliveira JB, Lenardo M, Fleisher TA, et al. JMML and RALD (Ras-associated autoimmune leukoproliferative disorder): common genetic etiology yet clinically distinct entities. Blood. 2015;125:2753–8.

Neven Q, Boulanger C, Bruwier A, de Ville M, de Goyet I, Meyts LM, et al. Clinical spectrum of ras-associated autoimmune leukoproliferative disorder (RALD). J Clin Immunol. 2020;41(1):51–8. https://doi.org/10.1007/s10875-020-00883-7.

Li P, Huang P, Yang Y, Hao M, Peng H, Li F. Updated understanding of autoimmune lymphoproliferative syndrome (ALPS). Clin Rev Allergy Immunol. 2016;50:55–63.

Koren-Michowitz M, Gery S, Tabayashi T, Lin D, Alvarez R, Nagler A, et al. SH2B3 (LNK) mutations from myeloproliferative neoplasms patients have mild loss of function against wild type JAK2 and JAK2 V617F. Br J Haematol. 2013;161:811–20.

Morales CE, Stieglitz E, Kogan SC, Loh ML, Braun BS. Nf1 and Sh2b3 mutations cooperate in vivo in a mouse model of juvenile myelomonocytic leukemia. Blood Adv. 2021;5:3587–91.

Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, et al. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nat Genet. 2007;39:857–64.

Thien CBF, Scaife RM, Papadimitriou JM, Murphy MA, Bowtell DDL, Langdon WY. A mouse with a loss-of-function mutation in the c-Cbl TKB domain shows perturbed thymocyte signaling without enhancing the activity of the ZAP-70 tyrosine kinase. J Exp Med. 2003;197:503–13.

Takaki S, Tezuka Y, Sauer K, Kubo C, Kwon S-M, Armstead E, et al. Impaired lymphopoiesis and altered B cell subpopulations in mice overexpressing lnk adaptor protein. J Immunol. 2003;170:703–10.

Cheng Y, Chikwava K, Wu C, Zhang H, Bhagat A, Pei D, et al. LNK/SH2B3 regulates IL-7 receptor signaling in normal and malignant B-progenitors. J Clin Invest. 2016;126:1267–81.

Ema H, Sudo K, Seita J, Matsubara A, Morita Y, Osawa M, et al. Quantification of self-renewal capacity in single hematopoietic stem cells from normal and Lnk-deficient mice. Dev Cell. 2005;8:907–14.

Velazquez L, Cheng AM, Fleming HE, Furlonger C, Vesely S, Bernstein A, et al. Cytokine signaling and hematopoietic homeostasis are disrupted in Lnk-deficient mice. J Exp Med. 2002;195:1599–611.

Tong W, Zhang J, Lodish HF. Lnk inhibits erythropoiesis and Epo-dependent JAK2 activation and downstream signaling pathways. Blood. 2005;105:4604–12.

Hyakuna N, Muramatsu H, Higa T, Chinen Y, Wang X, Kojima S. Germline mutation of CBL is associated with moyamoya disease in a child with juvenile myelomonocytic leukemia and Noonan syndrome-like disorder. Pediatr Blood Cancer. 2015;62:542–4.

Seaby EG, Gilbert RD, Andreoletti G, Pengelly RJ, Mercer C, Hunt D, et al. Unexpected findings in a child with atypical hemolytic uremic syndrome: an example of how genomics is changing the clinical diagnostic paradigm. Front Pediatr. 2017;5:1–6.

Hong Y, Keylock A, Jensen B, Jacques TS, Ogunbiyi O, Omoyinmi E, et al. Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene. Neurology Genetics. 2020;6(4):e448. https://doi.org/10.1212/NXG.0000000000000448.

Auger JM, Best D, Snell DC, Wilde JI, Watson SP. c-Cbl negatively regulates platelet activation by glycoprotein VI. J Thromb Haemost J Thromb Haemost. 2003;1:2419–26.

Devalliè J, Atrice Charreau B. The adaptor Lnk (SH2B3): An emerging regulator in vascular cells and a link between immune and inflammatory signaling.

Thien CBF, Langdon WY. c-Cbl and Cbl-b ubiquitin ligases: Substrate diversity and the negative regulation of signalling responses. Biochem J. 2005;391:153–66.

Sanada M, Suzuki T, Shih LY, Otsu M, Kato M, Yamazaki S, et al. Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms. Nat Publish Group. 2009;460:904–8.

Chiang YJ, Kole HK, Brown K, Naramura M, Fukuhara S, Hu RJ, et al. Cbl-b regulates the CD28 dependence of T-cell activation. Nature. 2000;403:216–20.

Lv K, Jiang J, Donaghy R, Riling CR, Cheng Y, Chandra V, et al. CBL family E3 ubiquitin ligases control JAK2 ubiquitination and stability in hematopoietic stem cells and myeloid malignancies. Genes Dev. 2017;31:1007–23.