Background: In rheumatoid arthritis (RA), the CD40-CD40L axis plays a key role in immune cell activation and the production of inflammatory mediators. Although the soluble form of CD40 (sCD40) has been identified and investigated in various autoimmune disorders, its significance in RA and its relationship with inflammatory and humoral markers remain to be fully elucidated. Methods: Sixty-two patients with RA, classified according to the 2010 ACR/EULAR criteria, and 31 age- and sex-matched healthy controls were included. Clinical characteristics, disease activity (DAS28-ESR), and acute-phase reactant levels (CRP and ESR) were evaluated in patients with RA. Autoantibodies (RF, ACPA, anti-MCV, and anti-PAD4), serum cytokines, and sCD40 levels were quantified using ELISA and multiplex bead-based assays. Group differences and associations were assessed using nonparametric tests. Multiple linear regression analysis was performed to account for potential confounding variables. Results: Serum sCD40 levels did not differ significantly between patients with RA and healthy controls or among patient subgroups stratified by disease activity or sex. No associations were observed between sCD40 levels and autoantibody seropositivity or titers. sCD40 levels were positively correlated with age (rs = 0.293, p = 0.02). Notably, after adjustment for age, sCD40 showed a significant negative correlation with IL-2 (rs = −0.317, p = 0.01). Conclusions: Serum sCD40 does not reflect disease activity or the humoral immune response in RA. Nevertheless, further studies are needed to evaluate its relevance during early stages of the disease and to further characterize its role in cytokine production.
Valeria Miroslava Limón-López, J. Muñóz-Valle, Zyanya Reyes-Castillo et al.· Journal of Clinical Medicine· 0 citations
Influenza A(H3N2) remains a significant public health threat due to its rapid antigenic drift, which often compromises vaccine effectiveness. This study characterized the molecular and epidemiological profile of hemagglutinin (HA) variants circulating in Western Mexico throughout 2022. Among 476 positive cases, A(H3N2) was the predominant subtype (88%), with infection peaks during epidemiological weeks (EW) 1, 45, and 46. Sanger sequencing of the HA gene identified 64 amino acid substitutions, with 85.9% of the substitutions located in the HA1 subunit, primarily within the receptor-binding domain (RBD). Homology modeling and molecular docking were performed on five representative variants: C156S, D158N, Y159N, C136S, and L227P. All variants exhibited a slight decrease in binding affinity for sialic acid compared to the 1HGE reference. Notably, while mutations such as D158N and Y159N remodeled the interaction network, Glu190 and His183 remained critical for stabilizing the HA-ligand complex through hydrogen bonds and non-covalent interactions in the structural models. These structural findings suggest that contemporary mutations in the RBD may contribute to changes in receptor-binding interactions while preserving key structural features associated with host cell attachment.
Karen M Hernandez-Gonzalez, A. S. Carranza-Aranda, J. Muñóz-Valle et al.· International Journal of Mol...· 0 citations