https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 Distinguishing erosive lichen planus from differentiated vulvar intraepithelial neoplasia https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:24429 Wed 24 Nov 2021 15:52:25 AEDT ]]> What do postdocs need to succeed? A survey of current standing and future directions for Australian researchers https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:50040 Wed 07 Feb 2024 18:02:20 AEDT ]]> Repurposing existing therapeutics, its importance in oncology drug development: Kinases as a potential target https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:45654 Wed 02 Nov 2022 15:37:57 AEDT ]]> Cancer therapies inducing DNA damage https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:49650 Thu 25 May 2023 14:37:48 AEST ]]> Progesterone activates multiple innate immune pathways in <i>Chlamydia trachomatis</i>-infected endocervical cells https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:21378 Chlamydia trachomatis infection is increased by oral contraceptives and modulated by sex hormones. We therefore sought to determine the effects of female sex hormones on the innate immune response to C. trachomatis infection. Method of study: ECC-1 endometrial cells, pre-treated with oestradiol or progesterone, were infected with C. trachomatis and the host transcriptome analysed by Illumina Sentrix HumanRef-8 microarray. Primary endocervical epithelial cells, prepared at either the proliferative or secretory phase of the menstrual cycle, were infected with C. trachomatis and cytokine gene expression determined by quantitative RT-PCR analysis. Results: Chlamydia trachomatis yield from progesterone-primed ECC-1 cells was significantly reduced compared with oestradiol-treated cells. Genes upregulated in progesterone-treated and Chlamydia-infected cells only included multiple CC and CXC chemokines, IL-17C, IL-29, IL-32, TNF-α, DEFB4B, LCN2, S100A7-9, ITGAM, NOD2, JAK1, IL-6ST, type I and II interferon receptors, numerous interferon-stimulated genes and STAT6. CXCL10, CXCL11, CX₃CL1 and IL-17C, which were also upregulated in infected secretory-stage primary cells, and there was a trend towards higher levels of immune mediators in infected secretory-phase compared with proliferative-phase cells. Conclusion: Progesterone treatment primes multiple innate immune pathways in hormone-responsive epithelial cells that could potentially increase resistance to chlamydial infection.]]> Sat 24 Mar 2018 08:04:59 AEDT ]]>