Immunological and senescence biomarker profiles in patients after spontaneous clearance of hepatitis C virus: gender implications for long-term health risk

Author:

Martín-Escolano Rubén,Vidal-Alcántara Erick Joan,Crespo Javier,Ryan Pablo,Real Luis Miguel,Lazo-Álvarez Juan Ignacio,Cabezas-González Joaquín,Macías Juan,Arias-Loste María Teresa,Cuevas Guillermo,Virseda-Berdices Ana,Briz Veronica,Resino Salvador,Jiménez-Sousa María Ángeles,Fernández-Rodríguez Amanda

Abstract

Abstract Background About 25% of patients with acute hepatitis C virus (HCV) infection show spontaneous clearance within the first six months of infection but may remain at risk of inflammaging, aging, and liver and non-liver disease complications. This study evaluated the differences in the plasma levels of immune checkpoints (ICs) and senescence-associated secretory phenotype (SASP) biomarkers between patients who had spontaneously eliminated HCV infection (SC group) and individuals without evidence of HCV infection (C group). Methods We performed a multicenter retrospective study of 56 individuals: 32 in the SC and 24 in the C groups. ICs and SASP proteins were analyzed using a Luminex 200TM analyzer. The statistical analysis used Generalized Linear Models with gamma distribution (log-link) adjusted by significant variables and sex. Results 13 ICs (BTLA, CD137(4-1BB), CD27, CD28, CD80, GITR, HVEM, IDO, LAG-3, PD-1, PD-L1, PD-L2, and TIM-3) and 13 SASP proteins (EGF, Eotaxin, IL-1alpha, IL-1RA, IL-8, IL-13, IL-18, IP-10, SDF-1alpha, HGF, beta-NGF, PLGF-1, and SCF) were significantly higher in SC group after approximately more than two years of HCV clearance. After stratifying by sex, differences remained significant for males, which showed higher levels for 13 ICs and 4 SASP proteins in SC. While only PD-L2 was significantly higher in SC women, and no differences in SASP were found. Conclusions Higher plasma levels of different IC and SASP proteins were found in individuals after more than two years of HCV clearance, mainly in men. Alterations in these molecules might be associated with an increased risk of developing liver and non-hepatic diseases.

Funder

Ministerio de Ciencia e Innovación

Consorcio Centro de Investigación Biomédica en Red

Instituto de Salud Carlos III

Fundación Universidad Alfonso X el Sabio

Publisher

Springer Science and Business Media LLC

Subject

Aging,Immunology

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