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AuthorLima, Suelen Cristina
AuthorGomes da Silva, Isaura Isabelle Fonseca
AuthorNascimento, Denise de Queiroga
Authorde Moura, Ronald Rodrigues
AuthorMesquita, Matheus da Silva
AuthorAsano, Nadja Maria Jorge
AuthorFernandes, Gisele Vagjel
AuthorValente, Lucila Maria
AuthorRushansky, Eliezer
AuthorMariano, Maria Helena Queiroz de Araújo
AuthorXavier, Ricardo Machado
AuthorChies, José Artur Bogo
AuthorCrovella, Sergio
AuthorSandrin-Garcia, Paula
Available date2022-01-25T07:10:21Z
Publication Date2021-10-01
Publication NameInternational Journal of Immunogenetics
Identifierhttp://dx.doi.org/10.1111/iji.12548
CitationLima, S. C., Gomes da Silva, I. I. F., Nascimento, D. D. Q., de Moura, R. R., Mesquita, M. D. S., Asano, N. M. J., Fernandes, G. V., Valente, L. M., Rushansky, E., Mariano, M. H. Q. D. A., Xavier, R. M., Chies, J. A. B., Crovella, S., & Sandrin-Garcia, P. (2021). CIITA gene polymorphism (rs3087456) in systemic lupus erythematosus and rheumatoid arthritis: A population-based cohort study. International Journal of Immunogenetics, 48, 429– 434. https://doi.org/10.1111/iji.12548
ISSN17443121
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85115172117&origin=inward
URIhttp://hdl.handle.net/10576/25916
AbstractSystemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) are influenced by genetic variants in immune system HLA genes. The Class II Major Histocompatibility Complex Transactivator (CIITA) is an important co-activator of the HLA transcriptional complex; the single nucleotide variant (SNV) rs3087456 localized in the gene promoter region (−168 A/G) has been reported as able to modify its transcription level. In our study, we assessed CIITA rs3087456 SNV in 1,044 Brazilians from two Brazilian regions (Northeast and South) to verify the association with susceptibility and clinical manifestations of (SLE) and (RA) using TaqMan SNP Genotyping Assays System. We observed a protection for a recessive model (GG x AA+AG) for RA susceptibility and increased risk for erosion development in AG genotype patients. No significant association was observed for SLE susceptibility; however, we observed significant increased risk for Class IV and V nephritis development in G allele and GG genotype patients. In conclusion, we showed the contribution of CIITA rs3087456 to SLE or RA clinical features and RA susceptibility in the studied populations.
Languageen
PublisherWiley
Subjecthuman leukocyte antigen (HLA)
MHC2TA
rheumatoid arthritis
single nucleotide variation
systemic lupus erythematosus
TitleCIITA gene polymorphism (rs3087456) in systemic lupus erythematosus and rheumatoid arthritis: A population-based cohort study
TypeArticle
Pagination429-434
Issue Number5
Volume Number48
ESSN1744-313X
dc.accessType Full Text


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