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High-throughput Quantitative Real-time RT-PCR Assay for Determining Expression Profiles of Types I and III Interferon Subtypes
Published on: March 24, 2015
Type III Interferons in Systemic Lupus Erythematosus: Association Between Interferon λ3, Disease Activity, and
Luis M Amezcua-Guerra1, Ricardo Márquez-Velasco, Adriana K Chávez-Rueda
1From the *Doctoral-Degree Program in Health and Biological Sciences (Programa del Doctorado en Ciencias Biológicas y de la Salud), Universidad Autónoma Metropolitana; †Department of Health Care, Universidad Autónoma Metropolitana-Xochimilco; ‡Department of Immunology, Instituto Nacional de Cardiología Ignacio Chávez; §Immunology Unit, Hospital de Pediatría, CMN Siglo XXI, Instituto Mexicano del Seguro Social; ∥Department of Dermatology, Hospital General de Zona 32, Instituto Mexicano del Seguro Social; ¶Department of Physiology, Instituto Nacional de Cardiología Ignacio Chávez; and #Department of Dermatology, Hospital General de Zona 1-A, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Objective:
The aim of this study was to assess associations between serum type III (λ) interferons (IFN-λ) and disease activity in systemic lupus erythematosus (SLE).
Methods:
Serum levels of IFN-λ1, IFN-λ2, and IFN-λ3 were measured in 93 SLE patients and 67 healthy individuals. The associations with overall disease activity, organ-specific damage, and SLE-related antibodies were assessed.
Results:
Median IFN-λ1 levels were 0 pg/mL (range, 0-510 pg/mL) and 0 pg/mL (0-171 pg/mL; P = 0.814) in SLE patients and control subjects, respectively. These figures were 0 pg/mL (0-28 pg/mL) and 0 pg/mL (0-43 pg/mL; P = 0.659) for IFN-λ2, as well as 83 pg/mL (0-965 pg/mL) and 42 pg/mL (0-520 pg/mL; P = 0.002) for IFN-λ3, respectively. According to the Systemic Lupus Erythematosus Disease Activity Index categories, IFN-λ3 levels were 44 pg/mL (0-158 pg/mL) in quiescent, 117 pg/mL (0-344 pg/mL) in mild, 79 pg/mL (0-965 pg/mL) in moderate, and 78 pg/mL (0-329 pg/mL) in severe disease, with the highest levels found in patients with serosal or cutaneous involvement. In line with this, IFN-λ3 levels were inversely correlated with C3 (ρ = -0.44; 95% confidence interval, -0.62 to -0.20; P = 0.0003) and C4 (ρ = -0.40; 95% confidence interval, -0.59 to -0.15; P = 0.0001) complement proteins. In addition, higher IFN-λ3 levels were found in patients positive for anti-Ro/SSA antibodies than in those negative for that antibody (122 pg/mL [0-965 pg/mL] vs. 0 pg/mL [0-165 pg/mL]; P = 0.001). The concentration of IFN-λ3 also was higher in patients receiving glucocorticoids (104 pg/mL [0-965 pg/mL] vs. 30 pg/mL [0-165 pg/mL]; P = 0.009), and a dose-related effect was observed.
Conclusions:
Interferon λ3, a subtype of type III IFNs, is associated with the extent of lupus activity, in particular with active serosal and cutaneous disease. This association could be mechanistically related to anti-Ro/SSA antibodies.
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