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dc.contributor.authorCarmelo, Emma 
dc.contributor.authorGómez, Inmaculada
dc.contributor.authorThomas, M. Carmen
dc.contributor.authorPalacios, Génesis
dc.contributor.authorEgui, Adriana
dc.contributor.authorCarrilero, Bartolomé
dc.contributor.authorSimón, Marina
dc.contributor.authorValladares Hernández, Basilio 
dc.contributor.authorSegovia, Manuel
dc.contributor.authorLópez, Manuel Carlos
dc.contributor.otherObstetricia y Ginecología, Pediatría, Medicina Preventiva y Salud Pública, Toxicología y Medicina Legal y Forense y Parasitología
dc.contributor.otherInvestigación en Parasitología
dc.date.accessioned2024-04-25T20:05:58Z
dc.date.available2024-04-25T20:05:58Z
dc.date.issued2021
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/37288
dc.description.abstractInfection by the Trypanosoma cruzi parasite causes Chagas disease and triggers multiple immune mechanisms in the host to combat the pathogen. Chagas disease has a variable clinical presentation and progression, producing in the chronic phase a fragile balance between the host immune response and parasite replication that keeps patients in a clinically silent asymptomatic stage for years. Since the parasite is intracellular and replicates within cells, the cell-mediated response of the host adaptive immunity plays a critical role. This function is mainly orchestrated by T lymphocytes, which recognize parasite antigens and promote specific functions to control the infection. However, little is known about the immunological markers associated with this asymptomatic stage of the disease. In this large-scale analysis, the differential expression of 106 immune systemrelated genes has been analyzed using high-throughput qPCR in T. cruzi antigenstimulated PBMC from chronic Chagas disease patients with indeterminate form (IND) and healthy donors (HD) from endemic and non-endemic areas of Chagas disease. This analysis revealed that there were no differences in the expression level of most genes under study between healthy donors from endemic and non-endemic areas determined by PCA and differential gene expression analysis. Instead, PCA revealed the existence of different expression profiles between IND patients and HD (p < 0.0001), dependent on the 32 genes included in PC1. Differential gene expression analysis also revealed 23 upregulated genes (expression fold change > 2) and 11 downregulated genes (expression fold change < 0.5) in IND patients versus HD. Enrichment analysis showed that several upregulated genes in IND patients participate in relevant immunological pathways suchasantigen-dependent B cell activation, stress induction of HSP regulation, NO2-dependent IL12 pathway in NK cells, and cytokine-inflammatory response. The antigen-specific differential gene expression profile detected in these patients and the relevant immunological pathways that seem to be activated could represent potential biomarkers of the asymptomatic form of Chagas disease, helpful to diagnosis and infection controlen
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesFrontiers in Cellular and Infection Microbiology, 11:722984
dc.rightsLicencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES
dc.titleDifferential Expression of Immune Response Genes in Asymptomatic Chronic Chagas Disease Patients Versus Healthy Subjectsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3389/fcimb.2021.722984
dc.subject.keywordchronic Chagas diseaseen
dc.subject.keywordTrypanosoma cruzien
dc.subject.keywordtranscriptional profilingen
dc.subject.keywordhigh-throughput RT-qPCRen
dc.subject.keywordimmunological pathwayen
dc.subject.keywordbiomarkersen
dc.subject.keywordindeterminate formen


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