The presence of IFL3/4 rs12979860 C allele influences the in vitro IP-10 production by mononuclear cells from patients with systemic lupus erythematosus

Author:

Juárez-Vicuña Y12,Pérez-Ramos J3,Adalid-Peralta L4,Sánchez F5,Springall R2,Villaseñor-Jasso J6,Sixtos-Alonso M S7,Ballinas-Verdugo M A2,Márquez-Velasco R2,Bojalil R28,Amezcua-Guerra L M28ORCID,Sánchez-Muñoz F2ORCID

Affiliation:

1. Doctorate Program in Health and Biological Sciences (Programa del Doctorado en Ciencias Biológicas y de la Salud), Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico

2. Department of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico

3. Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico

4. Unit for the Study of Neuroinflammation in Neurological Pathologies, Instituto de Investigaciones Biomédicas, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico

5. Department of Agricultural and Animal Production, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico

6. Department of Nephrology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico

7. Gastroenterology Laboratory, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

8. Department of Health Care, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico

Abstract

Objective To explore whether the IFNL3/4 rs12979860 genotype may influence serum levels or production of interferon-inducible protein-10 (IP-10) by peripheral blood mononuclear cells from patients with systemic lupus erythematosus (SLE). Methods Sixty-six patients with SLE and 22 healthy blood donors (controls) were included. The IFNL3/4 rs12979860 polymorphism was genotyped by real-time polymerase chain reaction. IP-10 levels in sera supernatants of IFNα stimulated peripheral blood mononuclear cells were measured by enzime-linked immunosorbent assay. Results Allelic frequencies were CC (29%), CT (52%) and TT (20%) in SLE, and CC (32%), CT (41%) and TT (27%) in healthy controls. Median serum IP-10 levels were higher in SLE patients than in controls (190.8 versus 118.1 pg/ml; p < 0.001), particularly in those with high disease activity (278.5 versus 177.2 pg/ml; p = 0.037). However, serum IP-10 levels were not influenced by IFNL3/4 genotypes. Higher IP-10 production by peripheral blood mononuclear cells was found in both SLE patients (median 519.3 versus 207.6 pg/ml; p = 0.012) and controls (median 454.0 versus 201.7 pg/ml; p = 0.034) carrying the IFNL3/4 C allele compared with carriers of the T allele. Conclusions Although IFNL3/4 rs12979860 allele C does not appear to influence serum IP-10 levels in SLE, it plays an important role in the production of IP-10 by peripheral blood mononuclear cells after IFNα stimulation.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

SAGE Publications

Subject

Rheumatology

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