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Correlation analysis between auto-immunological and mutational profiles in myelodysplastic syndromes.
Cristiano, Antonio; Belardi, Riccardo; Hajrullaj, Hajro; Fabiani, Emiliano; Falconi, Giulia; Galossi, Elisa; Bernardini, Sergio; Voso, Maria Teresa; Nuccetelli, Marzia.
Afiliación
  • Cristiano A; Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Via Montpellier 1, 00133, Rome, Italy. cristianoantonio93@hotmail.it.
  • Belardi R; Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.
  • Hajrullaj H; Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Via Montpellier 1, 00133, Rome, Italy.
  • Fabiani E; Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Via Montpellier 1, 00133, Rome, Italy.
  • Falconi G; UniCamillus-Saint Camillus International University of Health Sciences, Rome, Italy.
  • Galossi E; Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Via Montpellier 1, 00133, Rome, Italy.
  • Bernardini S; Department of Biomedicine and Prevention, University of Rome "Tor Vergata", Via Montpellier 1, 00133, Rome, Italy.
  • Voso MT; Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.
  • Nuccetelli M; Tor Vergata University Hospital, Rome, Italy.
Inflamm Res ; 72(8): 1695-1707, 2023 Aug.
Article en En | MEDLINE | ID: mdl-37507570
ABSTRACT
OBJECTIVE AND

DESIGN:

Systemic-Inflammatory-Autoimmune-Diseases (SIAD) is increasingly considered in Myelodysplastic-Syndromes (MDS). In this line, we evaluated the MDS auto-immunological profile, correlating it to the mutational landscape, trying to identify a molecular-genetic trigger agent related to SIAD. METHODS AND MATERIALS Eighty-one MDS were enrolled and t-NGS was performed. Anti-Nuclear-Antibodies (ANA) were tested, and ANA-antigenic-specificity was characterized by ANA-profile, ENA-screen, anti-dsDNA. Non-Hematological-Patients (NHP) and Healthy-Donors (HD) were used as controls.

RESULTS:

At clinically relevant cut-off (≥ 1160), ANA was significantly more frequent in MDS, while ANA-antigenic-specificity showed a low association rate. ANA ≥ 1160-positive MDS showed a mutational landscape similar to ANA-negative/ANA < 1160 MDS. No significant correlations between mutational and immunological profiles were found and UBA1 mutations, related to VEXAS, were absent.

CONCLUSIONS:

Although ANA-positivity was found to be increased in MDS, the low ANA-antigenic-specificity suggests that autoantibodies didn't recognize autoimmune-pathognomonic antigens. The lack of relationship between genetic profile and ANA-positivity, suggests that MDS genetic variants may not be the direct cause of SIAD.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Autoanticuerpos / Síndromes Mielodisplásicos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Inflamm Res Asunto de la revista: ALERGIA E IMUNOLOGIA / PATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Autoanticuerpos / Síndromes Mielodisplásicos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Inflamm Res Asunto de la revista: ALERGIA E IMUNOLOGIA / PATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Italia