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Presentation_1_Whole blood RNA signatures in tuberculosis patients receiving H56:IC31 vaccine as adjunctive therapy.pdf

Title: Presentation_1_Whole blood RNA signatures in tuberculosis patients receiving H56:IC31 vaccine as adjunctive therapy.pdf
Authors: Noelia Alonso-Rodríguez; Eleonora Vianello; Suzanne van Veen; Synne Jenum; Kristian Tonby; Rosalie van Riessen; Xiaoran Lai; Rasmus Mortensen; Tom H. M. Ottenhoff; Anne Ma Dyrhol-Riise
Publication Year: 2024
Collection: Frontiers: Figshare
Subject Terms: Immunology; Applied Immunology (incl. Antibody Engineering; Xenotransplantation and T-cell Therapies); Autoimmunity; Cellular Immunology; Humoural Immunology and Immunochemistry; Immunogenetics (incl. Genetic Immunology); Innate Immunity; Transplantation Immunology; Tumour Immunology; Immunology not elsewhere classified; Genetic Immunology; Animal Immunology; Veterinary Immunology; tuberculosis; H56:IC31 vaccine; host directed therapy; transcriptomics; RNA signature
Description: Introduction Therapeutic vaccination in tuberculosis (TB) represents a Host Directed Therapy strategy which enhances immune responses in order to improve clinical outcomes and shorten TB treatment. Previously, we have shown that the subunit H56:IC31 vaccine induced both humoral and cellular immune responses when administered to TB patients adjunctive to standard TB treatment (TBCOX2 study, NCT02503839). Here we present the longitudinal whole blood gene expression patterns in H56:IC31 vaccinated TB patients compared to controls receiving standard TB treatment only. Methods The H56:IC31 group (N=11) and Control group (N=7) underwent first-line TB treatment for 182 days. The H56:IC31 group received 5 micrograms of the H56:IC31 vaccine (Statens Serum Institut; SSI, Valneva Austria GmbH) intramuscularly at day 84 and day 140. Total RNA was extracted from whole blood samples collected in PAXgene tubes on days 0, 84, 98, 140, 154, 182 and 238. The expression level of 183 immune-related genes was measured by high-throughput microfluidic qPCR (Biomark HD system, Standard BioTools). Results The targeted gene expression profiling unveiled the upregulation of modules such as interferon (IFN) signalling genes, pattern recognition receptors and small nucleotide guanosine triphosphate (GTP)-ases in the vaccinated group compared to controls two weeks after administration of the first H56:IC31 vaccine. Additionally, the longitudinal analysis of the Adolescent Cohort Study-Correlation of Risk (ACS-COR) signature showed a progressive downregulation in both study arms towards the end of TB treatment, in congruence with reported treatment responses and clinical improvements. Still, two months after the end of TB treatment, vaccinated patients, and especially those developing both cellular and humoral vaccine responses, showed a lower expression of the ACS-COR genes compared to controls. Discussion Our data report gene expression patterns following H56:IC31 vaccination which might be interpreted as a lower risk of relapse in ...
Document Type: conference object
Language: unknown
Relation: https://figshare.com/articles/presentation/Presentation_1_Whole_blood_RNA_signatures_in_tuberculosis_patients_receiving_H56_IC31_vaccine_as_adjunctive_therapy_pdf/25230590
DOI: 10.3389/fimmu.2024.1350593.s001
Availability: https://doi.org/10.3389/fimmu.2024.1350593.s001; https://figshare.com/articles/presentation/Presentation_1_Whole_blood_RNA_signatures_in_tuberculosis_patients_receiving_H56_IC31_vaccine_as_adjunctive_therapy_pdf/25230590
Rights: CC BY 4.0
Accession Number: edsbas.F76C97A9
Database: BASE