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Chromosome 2q33genetic polymorphisms in Tunisian endemic pemphigus foliaceus.
Abida, Olfa; Bahloul, Emna; Ben Jmaa, Mariem; Sellami, Khadija; Zouidi, Ferjani; Fakhfakh, Raouia; Mahfoudh, Nadia; Turki, Hamida; Masmoudi, Hatem.
Afiliación
  • Abida O; "Autoimmunity, Cancer And Immunogenetics" research laboratory (LR18SP12), Immunology Department, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
  • Bahloul E; Dermatology Department, Hedi Chaker Hospital, University of Sfax, Sfax, Tunisia.
  • Ben Jmaa M; "Autoimmunity, Cancer And Immunogenetics" research laboratory (LR18SP12), Immunology Department, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
  • Sellami K; Dermatology Department, Hedi Chaker Hospital, University of Sfax, Sfax, Tunisia.
  • Zouidi F; "Autoimmunity, Cancer And Immunogenetics" research laboratory (LR18SP12), Immunology Department, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
  • Fakhfakh R; "Autoimmunity, Cancer And Immunogenetics" research laboratory (LR18SP12), Immunology Department, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
  • Mahfoudh N; Immunology Department, HediChaker Hospital, University of Sfax, Sfax, Tunisia.
  • Turki H; Dermatology Department, Hedi Chaker Hospital, University of Sfax, Sfax, Tunisia.
  • Masmoudi H; "Autoimmunity, Cancer And Immunogenetics" research laboratory (LR18SP12), Immunology Department, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
Mol Genet Genomic Med ; 8(11): e1476, 2020 11.
Article en En | MEDLINE | ID: mdl-32875738
ABSTRACT

BACKGROUND:

Several studies have suggested that polymorphisms within genes encoding T-lymphocyte immune regulating molecules CD28, CTLA-4, and ICOS, may alter the signaling process and subsequently could be involved in susceptibility to a broad spectrum of autoimmune diseases.

METHODS:

This study aimed to replicate associations between common polymorphisms in the 2q33.2 cluster and susceptibility to pemphigus foliaceus (PF) in the Tunisian population. We investigated seven polymorphisms rs3116496 and rs1879877 (CD28), rs231775, rs3087243, and (AT)n repeat (CTLA4); rs11889031 and rs10932029 (ICOS) in a case-control study which enrolled 106 Tunisian PF patients and 205 matched healthy controls.

RESULTS:

We confirmed the associations with CTLA4((AT)13 , p = 0.00137, OR = 3.96 and (AT)20 , p = 0.008, OR = 5.22; respectively) and ICOS genes (rs10932029>CT, p = 0.034, OR = 2.12 and rs10932029>TT, p = 0.04 and OR = 0.41).

CONCLUSION:

Our results indicate that susceptibility to PF is located in the proximal and the distal 3' flanking region of the CTLA4/ICOS promoter. These findings may open avenues to the treatment of patients with biological drugs targeting CTLA4/ICOS molecules, in a personalized manner to achieve more effective treatment.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pénfigo / Polimorfismo de Nucleótido Simple / Antígeno CTLA-4 / Proteína Coestimuladora de Linfocitos T Inducibles Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article País de afiliación: Túnez

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pénfigo / Polimorfismo de Nucleótido Simple / Antígeno CTLA-4 / Proteína Coestimuladora de Linfocitos T Inducibles Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article País de afiliación: Túnez