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An integrative genomics approach identifies KDM4 as a modulator of trained immunity

Title: An integrative genomics approach identifies KDM4 as a modulator of trained immunity
Authors: Moorlag, SJCFM; Matzaraki, V; van Puffelen, JH; van der Heijden, C; Keating, S; Groh, L; Röring, RJ; Bakker, OB; Mourits, VP; Koeken, VACM; de Bree, LCJ; Smeekens, SP; Oosting, M; Gamboa, RA; Riksen, NP; Xavier, RJ; Wijmenga, C; Kumar, V; van Crevel, R; Novakovic, B; Joosten, LAB; Li, Y; Netea, MG
Publisher Information: WILEY
Publication Year: 2022
Collection: The University of Melbourne: Digital Repository
Description: Innate immune cells are able to build memory characteristics via a process termed "trained immunity." Host factors that influence the magnitude of the individual trained immunity response remain largely unknown. Using an integrative genomics approach, our study aimed to prioritize and understand the role of specific genes in trained immunity responses. In vitro-induced trained immunity responses were assessed in two independent population-based cohorts of healthy individuals, the 300 Bacillus Calmette-Guérin (300BCG; n = 267) and 200 Functional Genomics (200FG; n = 110) cohorts from the Human Functional Genomics Project. Genetic loci that influence cytokine responses upon trained immunity were identified by conducting a meta-analysis of QTLs identified in the 300BCG and 200FG cohorts. From the identified QTL loci, we functionally validated the role of PI3K-Akt signaling pathway and two genes that belong to the family of Siglec receptors (Siglec-5 and Siglec-14). Furthermore, we identified the H3K9 histone demethylases of the KDM4 family as major regulators of trained immunity responses. These data pinpoint an important role of metabolic and epigenetic processes in the regulation of trained immunity responses, and these findings may open new avenues for vaccine design and therapeutic interventions.
Document Type: article in journal/newspaper
Language: English
ISSN: 0014-2980
Relation: https://hdl.handle.net/11343/301762
Availability: https://hdl.handle.net/11343/301762
Rights: https://creativecommons.org/licenses/by-nc-nd/4.0 ; CC BY-NC-ND
Accession Number: edsbas.A09B63A6
Database: BASE