HIV-1-exposed seronegative individuals show alteration in TLR expression and pro-inflammatory cytokine production ex vivo: An innate immune quiescence status?

Pattern recognition receptors (PRRs) are involved in direct recognition of viruses, promoting cellular activation and the production of pro-inflammatory cytokines. However, despite the reduced systemic immune activation described in HIV-1-exposed seronegatives (HESNs), few studies have focused on determining the relationship between PRR expression and cytokine production. We have aimed here to evaluate the expression level of PRRs and cytokines in HESNs, HIV-1 patients and healthy donors. Basal PRR expression levels in PBMCs, dendritic cells (DCs) and monocytes, and plasma cytokine levels as well as the PRR ligand-induced cytokine productions were determined by flow cytometry, qPCR and ELISA. Higher TLR2/4 expression in DCs and monocytes from HESNs was observed. Nevertheless, TLR4/8, NOD2 and RIG-I mRNA levels were lower in PBMCs from HESNs than HIV-1-infected patients. Comparable IL-1ß, IL-18 and TNF-a mRNA levels were observed among the groups examined; however, at the protein level, production of IL-1ß, IL-6 and IL-10 was significantly lower in plasma from HESNs than from HIV-1-infected patients. Our results suggest that exposure to HIV-1 without infection could be associated with reduced basal pro-inflammatory responses. Further studies are required to define the cell subsets responsible for these differences and the role of PRRs on protection against HIV-1 infection. © 2015, Springer Science+Business Media New York.

• Autores: Hernández López, Juan Carlos; St Laurent G.; Urcuqui-Inchima S.
• Tipo de recurso: Article of journal
• Fecha de publicación: 2023
• Institución: Universidad Cooperativa de Colombia
• Repositorio: Repositorio UCC
• OAI Identifier: oai:repository.ucc.edu.co:20.500.12494/49577
• Acceso en línea: https://doi.org/10.1007/s12026-015-8748-8; https://www.scopus.com/inward/record.uri?eid=2-s2.0-84955626129&doi=10.1007%2fs12026-015-8748-8&partnerID=40&md5=0a80b2e9a102fdfa633e5c45cf8e385f; https://hdl.handle.net/20.500.12494/49577
• Palabra clave: ADULT; ARTICLE; AUTACOID; BLOOD; CASPASE RECRUITMENT DOMAIN PROTEIN 15; CELL CULTURE; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; CYTOKINE; CYTOKINE PRODUCTION; DDX58 PROTEIN, HUMAN; DEAD BOX PROTEIN; DENDRITIC CELL; EX VIVO STUDY; FEMALE; GENETICS; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS 1; HUMAN IMMUNODEFICIENCY VIRUS 1 INFECTION; HUMAN IMMUNODEFICIENCY VIRUS ANTIBODY; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; IMMUNOLOGY; IMMUNOMODULATION; INNATE IMMUNITY; INTERLEUKIN 10; INTERLEUKIN 18; INTERLEUKIN 1BETA; INTERLEUKIN 6; MALE; MESSENGER RNA; METABO; MONOCYTE; NOD2 PROTEIN, HUMAN; NONHUMAN; PATHOGENESIS; PATTERN RECOGNITION RECEPTOR; PERIPHERAL BLOOD MONONUCLEAR CELL; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; PROTEIN FUNCTION; RETINOIC ACID INDUCIBLE PROTEIN I; TOLL LIKE RECEPTOR; TOLL LIKE RECEPTOR 2; TOLL LIKE RECEPTOR 4; TOLL LIKE RECEPTOR 8; TUMOR NECROSIS FACTOR ALPHA
• Rights: openAccess
• License: http://purl.org/coar/access_right/c_abf2