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      Longitudinal Imaging Using PET/CT with Collagen-I PET-Tracer and MRI for Assessment of Fibrotic and Inflammatory Lesions in a Rat Lung Injury Model

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          Abstract

          Non-invasive imaging biomarkers (IBs) are warranted to enable improved diagnostics and follow-up monitoring of interstitial lung disease (ILD) including drug-induced ILD (DIILD). Of special interest are IB, which can characterize and differentiate acute inflammation from fibrosis. The aim of the present study was to evaluate a PET-tracer specific for Collagen-I, combined with multi-echo MRI, in a rat model of DIILD. Rats were challenged intratracheally with bleomycin, and subsequently followed by MRI and PET/CT for four weeks. PET imaging demonstrated a significantly increased uptake of the collagen tracer in the lungs of challenged rats compared to controls. This was confirmed by MRI characterization of the lesions as edema or fibrotic tissue. The uptake of tracer did not show complete spatial overlap with the lesions identified by MRI. Instead, the tracer signal appeared at the borderline between lesion and healthy tissue. Histological tissue staining, fibrosis scoring, lysyl oxidase activity measurements, and gene expression markers all confirmed establishing fibrosis over time. In conclusion, the novel PET tracer for Collagen-I combined with multi-echo MRI, were successfully able to monitor fibrotic changes in bleomycin-induced lung injury. The translational approach of using non-invasive imaging techniques show potential also from a clinical perspective.

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            Mechanisms of fibrosis: therapeutic translation for fibrotic disease.

            Fibrosis is a pathological feature of most chronic inflammatory diseases. Fibrosis, or scarring, is defined by the accumulation of excess extracellular matrix components. If highly progressive, the fibrotic process eventually leads to organ malfunction and death. Fibrosis affects nearly every tissue in the body. Here we discuss how key components of the innate and adaptive immune response contribute to the pathogenesis of fibrosis. We also describe how cell-intrinsic changes in important structural cells can perpetuate the fibrotic response by regulating the differentiation, recruitment, proliferation and activation of extracellular matrix-producing myofibroblasts. Finally, we highlight some of the key mechanisms and pathways of fibrosis that are being targeted as potential therapies for a variety of important human diseases.
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              Animal research: reporting in vivo experiments: the ARRIVE guidelines.

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                Author and article information

                Contributors
                On behalf of : on behalf of the TRISTAN Consortium
                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                18 November 2020
                November 2020
                : 9
                : 11
                : 3706
                Affiliations
                [1 ]Department of Medical Radiation Physics, Institution of Translational Medicine, Faculty of Medicine, Lund University, 20502 Malmö, Sweden; lars_e.olsson@ 123456med.lu.se
                [2 ]Truly Labs, Medicon Village, 223 63 Lund, Sweden; nina@ 123456trulylabs.com (N.F.P.); Jian@ 123456trulylabs.com (J.L.); hanna@ 123456trulylabs.com (H.F.H.); karin@ 123456trulylabs.com (K.v.W.)
                [3 ]Department of Oncology and Pathology, Clinical Sciences, Lund University, 22184 84 Lund, Sweden; anders.orbom@ 123456med.lu.se
                [4 ]Lund University BioImaging Centre, Faculty of Medicine, Lund University, 221 42 Lund, Sweden; rene.in_t_zandt@ 123456med.lu.se (R.I.Z.); ritha.gidlof@ 123456med.lu.se (R.G.); marie.sydoff@ 123456med.lu.se (M.S.)
                Author notes
                [* ]Correspondence: irma.mahmutovic_persson@ 123456med.lu.se ; Tel.: +46-73-683-9562
                [†]

                Shared last authorship.

                [‡]

                TRISTAN-IMI Consortium (Translational Imaging in Drug Safety Assessment—Innovative Medicines Initiative) (#IB4SD-116106).

                Author information
                https://orcid.org/0000-0001-5959-3777
                https://orcid.org/0000-0002-5049-1544
                https://orcid.org/0000-0001-6895-0414
                https://orcid.org/0000-0003-0579-2484
                https://orcid.org/0000-0001-6090-6697
                Article
                jcm-09-03706
                10.3390/jcm9113706
                7699272
                33218212
                adb8468f-b3f2-4b95-8ba4-94e4f5af1cde
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 25 September 2020
                : 16 November 2020
                Categories
                Article

                lung imaging,interstitial lung disease (ild),drug toxicity,collagen-i,fibrosis,drug-induced interstitial lung disease (diild),magnetic resonance imaging (mri),positron emission tomography (pet),animal model,bleomycin

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