Background: Abnormalities of the immune system are rarely reported in patients affected by RASopathies. Aim of the current study was to investigate the prevalence of immune system dysfunction in a cohort of patients affected by RASopathies. Study design: A group of 69 patients was enrolled: 60 at the Federico II University, Naples, 7 at University Magna Graecia of Catanzaro, 2 at "Scuola Medica Salernitana", Salerno. An age- and sex-matched control group was also enrolled. Autoimmune disorders were investigated according to international consensus criteria. Immune framework was also evaluated by immunoglobulin levels, CD3, CD4, CD8, CD19, CD56 lymphocyte subpopulations, autoantibodies levels and panel of inflammatory molecules, in both patients and controls. Results: Frequent upper respiratory tract infections were recorded in 2 patients; pneumonia, psoriasis and alopecia in single patients. Low IgA levels were detected in 8/44 patients (18.18%), low CD8 T cells in 13/35 patients (37.14%). Anti-tg and anti-TPO antibodies were detected in 3/24 patients (12.5%), anti r-TSH in 2 cases (8.33%), all in euthyroidism. Serum IgA and CD8 levels were significantly lower in patients than in controls (p 0.00685; p 0.000656 respectively). All tested patients showed increased inflammatory molecules compared to controls. These findings may anticipate the detection of overt autoimmune disease. Conclusions: Patients affected by RASopathies are at risk to develop autoimmune disorders. Routine screening for autoimmunity is recommended in patients with RASopathy.

Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity / Siano, M A; Marchetti, V; Pagano, S; Di Candia, F; Alessio, M; De Brasi, D; De Luca, A; Pinna, V; Sestito, S; Concolino, D; Tartaglia, M; Strisciuglio, P; D'Esposito, V; Cabaro, S; Perruolo, G; Formisano, P; Melis, D. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 16:1(2021), p. 410. [10.1186/s13023-021-02050-6]

Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity

Di Candia, F;Alessio, M;Strisciuglio, P;D'Esposito, V;Cabaro, S;Perruolo, G;Formisano, P;Melis, D
2021

Abstract

Background: Abnormalities of the immune system are rarely reported in patients affected by RASopathies. Aim of the current study was to investigate the prevalence of immune system dysfunction in a cohort of patients affected by RASopathies. Study design: A group of 69 patients was enrolled: 60 at the Federico II University, Naples, 7 at University Magna Graecia of Catanzaro, 2 at "Scuola Medica Salernitana", Salerno. An age- and sex-matched control group was also enrolled. Autoimmune disorders were investigated according to international consensus criteria. Immune framework was also evaluated by immunoglobulin levels, CD3, CD4, CD8, CD19, CD56 lymphocyte subpopulations, autoantibodies levels and panel of inflammatory molecules, in both patients and controls. Results: Frequent upper respiratory tract infections were recorded in 2 patients; pneumonia, psoriasis and alopecia in single patients. Low IgA levels were detected in 8/44 patients (18.18%), low CD8 T cells in 13/35 patients (37.14%). Anti-tg and anti-TPO antibodies were detected in 3/24 patients (12.5%), anti r-TSH in 2 cases (8.33%), all in euthyroidism. Serum IgA and CD8 levels were significantly lower in patients than in controls (p 0.00685; p 0.000656 respectively). All tested patients showed increased inflammatory molecules compared to controls. These findings may anticipate the detection of overt autoimmune disease. Conclusions: Patients affected by RASopathies are at risk to develop autoimmune disorders. Routine screening for autoimmunity is recommended in patients with RASopathy.
2021
Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity / Siano, M A; Marchetti, V; Pagano, S; Di Candia, F; Alessio, M; De Brasi, D; De Luca, A; Pinna, V; Sestito, S; Concolino, D; Tartaglia, M; Strisciuglio, P; D'Esposito, V; Cabaro, S; Perruolo, G; Formisano, P; Melis, D. - In: ORPHANET JOURNAL OF RARE DISEASES. - ISSN 1750-1172. - 16:1(2021), p. 410. [10.1186/s13023-021-02050-6]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/866047
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