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  • 1
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    German Medical Science GMS Publishing House; Düsseldorf
    In:  EbM zwischen Best Practice und inflationärem Gebrauch; 16. Jahrestagung des Deutschen Netzwerks Evidenzbasierte Medizin; 20150313-20150314; Berlin; DOC15ebmC1e /20150303/
    Publication Date: 2015-03-04
    Keywords: ddc: 610
    Language: German
    Type: conferenceObject
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  • 2
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    German Medical Science GMS Publishing House; Düsseldorf
    In:  51. Kongress für Allgemeinmedizin und Familienmedizin; 20170921-20170923; Düsseldorf; DOC17degam048 /20170905/
    Publication Date: 2017-09-05
    Keywords: Diabetes mellitus ; Patienteninitiierte Forschung ; Qualitative Methoden ; ddc: 610
    Language: German
    Type: conferenceObject
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  • 3
    Keywords: IN-VIVO ; PATHWAY ; THERAPY ; MICE ; PATTERNS ; HEMATOPOIETIC-CELLS ; MARROW-REPOPULATING CELLS ; GREEN FLUORESCENT PROTEIN ; insertional mutagenesis ; IN-VIVO SELECTION ; O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE ; retroviral vector integration ; CHRONIC GRANULOMATOUS-DISEASE ; LARGE-ANIMAL MODEL ; RESISTANCE GENE-THERAPY
    Abstract: Gene transfer of mutant O-6-methylguanine-DNA-methyltransferase (MGMT(P140K)) into hematopoietic stem cells (HSCs) protects hematopoiesis from alkylating agents and allows efficient in vivo selection of transduced HSCs. However, insertional mutagenesis, high regenerative stress associated with selection, and the genotoxic potential of alkylating drugs represent considerable risk factors for clinical applications of this approach. Therefore, we investigated the long-term effect of MGMT(P140K) gene transfer followed by repetitive, dose-intensive treatment with alkylating agents in a murine serial bone marrow transplant model and assessed clonality of hematopoiesis up to tertiary recipients. The substantial selection pressure resulted in almost completely transduced hematopoiesis in all cohorts. Ligation-mediated PCR and next-generation sequencing identified several repopulating clones carrying vector insertions in distinct genomic regions that were similar to 9 kb of size (common integration sites). Beside polyclonal reconstitution in the majority of the mice, we also detected monoclonal or oligoclonal re-population patterns with HSC clones showing vector insertions in the Usp10 or Tubb3 gene. Interestingly, neither Usp10, Tubb3, nor any of the genes located in common integration sites have been linked to clonal expansion in previous preclinical or clinical gene therapy trials. However, a considerable number of these genes are involved in DNA damage response and cell fate decision pathways following cytostatic drug application. Thus, in summary, our study advocates ligation-mediated PCR and next generation sequencing as an effective and reliable method to identify gene products associated with clonal survival in specific experimental settings such as chemoselection using alkylating agents
    Type of Publication: Journal article published
    PubMed ID: 21319998
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  • 4
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    German Medical Science GMS Publishing House; Düsseldorf
    In:  16. Deutscher Kongress für Versorgungsforschung (DKVF); 20171004-20171006; Berlin; DOCP156a /20170926/
    Publication Date: 2017-09-26
    Keywords: ddc: 610
    Language: German
    Type: conferenceObject
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  • 5
    ISSN: 1468-2494
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Sunlight is essential for human life but we need to avoid overexposure to the sun. Chronic exposure of the skin to UV radiation leads to photoageing (sunburn, wrinkles, spots, freckles, skin texture changes, and dilated blood vessels), immunosuppression, and sometime more serious lesions. UV radiation also causes DNA damage, which is a critical event in skin photoageing and photocarcinogenesis [1]. Exposure to UV light induces wide range of DNA lesions on skin cells by direct absorption (UVB), or via oxidative stress (UVA and UVB). We choose to work on healthy Chinese women skin because it is demonstrated that Asian people developed less skin cancer than Caucasian, and few studies have been done on DNA damage in the skin of Asian subjects [2, 3].The formation of 8-hydroxy-2'deoxyguanosine (8-oxo-dG) is a major type of DNA lesion resulting from oxidative stress. It is a biological marker of oxidative stress on DNA. It causes the transversion of G : C to T : A during DNA replication, which occurs frequently in some genes in human skin lesions on areas exposed to sunlight [4]. Skin cells have evolved several DNA repair mechanisms to counteract immediately the deleterious effects of such lesions that can lead to genomic instability. These repair pathways are present in all living cells and are extremely well conserved. P53 is a phosphoprotein that is activated by stress, up-regulates DNA repair enzymes, participates directly in DNA repair, blocks cell cycles during DNA repair, and induces apoptosis in critically damaged cells. After exposure to UV, basal keratinocytes repair damaged DNA whereas differentiating keratinocytes undergo cell death, both processes are regulated by p53 [5].Repeated exposure of the skin to UV light induces pigmentation and thickening of the epidermis, both of which help to increase tolerance of sunlight. Some studies have shown that this photo-adaptation can help preserve epidermal DNA from UV injury [2, 6–8]. However, as most of these studies were performed by exposing the skin to a single or several acute bursts of radiation, they do not necessarily reflect the effect of chronic exposure to sunlight. The first aim of this study on 15 healthy Chinese women was to determine the effects of chronic exposure to sunlight on DNA damage in the skin. We compared, on sun-protected and sun-exposed skin of the same patient, the amounts of p53 protein and 8-oxo-dG determined by immunohistochemistry method. Blood samples from these women were used to measure their anti-oxidant stress status and hence their intrinsic defence capacities.We also evaluated how changes in the skin induced by chronic exposure to sunlight helped preserve DNA from an acute radiation. The two areas (chronically exposed to and protected from sunlight) were exposed to a relatively low dose of 1 minimal erythema dose (MED). The amounts of the markers (p53 protein and 8-oxo-dG) and the responses of the two areas were compared 24 h after exposure.〈section xml:id="abs1-2"〉〈title type="main"〉Methods〈section xml:id="abs1-3"〉〈title type="main"〉VolunteersVolunteers were recruited and biopsies removed at the Laboratoires Dermexpert (Paris, France), in accordance with international ethical procedures.Volunteers completed a questionnaire that allowed us to estimate their skin sensitivity, phototype, life styles and eating habits. The skin of patients was clinically evaluated by a dermatologist. Blood and urine were taken and analysed. Skin punch biopsies (3 mm) were taken from the anterior surface of the upper arm (protected area) and the posterior surface of the forearm (exposed area). MED was determined. Two zones (one exposed and one protected) on the other arm were irradiated at 1 MED. Punch biopsies (3 mm) were taken from the two irradiated zones 24 h after irradiation.〈section xml:id="abs1-4"〉〈title type="main"〉MED determinationThe MED values were determined using a multiport solar light (601 model). The anterior forearm test site was exposed to six increasing doses (13.44; 16.8; 21.0; 26.46; 32.76 and 40.95 mJ cm–²). The skin reaction was evaluated visually 24 h later. The lowest dose of UV energy that caused a perceptible demarcated erythema was considered to be 1 MED. Those subjects that had a very mild erythema after the maximum dose (40.95 mJ cm–²) were to be irradiated at 51.24 mJ cm–².〈section xml:id="abs1-5"〉〈title type="main"〉Oxidative stress statusSamples of blood and morning urine were carried out from fasting subjects. The blood samples were used to measure the following parameters: antioxidants (vitamin C, vitamin E, carotenoids, glutathione, thiol proteins, uric acid, total antioxidant capacity), trace metals (selenium, copper, zinc), markers of oxidative stress (lipid peroxidation), and iron status (free iron, ferritin, transferrin). The urine samples were used to assay 8-oxo-dG. Assays were performed by Probiox SA (Liege, Belgium) [9, 10].〈section xml:id="abs1-6"〉〈title type="main"〉ImmunohistochemistryThe punch biopsies were immediately placed in 10% neutral buffered formalin (4% formaldehyde) and fixed for 24 h at ambient temperature. They were then embedded in fresh wax and p53 and 8-oxo-dG detected immunohistochemically using BP53-12-1 and N45.1 monoclonal antibodies respectively [11]. Two hundred epidermal cells were counted per sample and the numbers of p53 or 8-oxo-dG positive and negative cells were determined.The statistical methods used were analysis of variance (anova) and linear regression, and all data were assessed for statistical significance (P 〈 0.05).〈section xml:id="abs1-7"〉〈title type="main"〉ResultsThe 15 healthy Chinese women living in France with a age range of 31--43 years (mean: 36 years). The clinical evaluation of the skin performed by a dermatologist and based on wrinkles, heliodermy and pigmentation disorders, showed that all 15 women had similar degree of cutaneous photoageing. Similarly, analysis of global anti-oxidant stress status showed that all 15 women had the same antioxidant potential, providing same intrinsic defence capacities.The amounts of 8-oxo-dG in protected (six to 64 positive cells per 200 epidermal cells; mean: 18.8) and exposed areas (two to 40 positive cells per 200 epidermal cells; mean: 17.1) varied greatly from one individual to another. No difference in the 8-oxo-dG contents was observed between the two areas (〈link href="#f1-16"〉Fig. 1). And there was no statistical correlation between the 8-oxo-dG in the skin and in the urine. The large differences in 8-oxo-dG in the skin between individuals were not correlated with any of the life style parameters in the questionnaire or with any of the blood antioxidant parameters.〈figure xml:id="f1-16"〉1〈mediaResource alt="image" href="urn:x-wiley:01425463:ICS254_16_16:ICS_254_f1-16"/〉Epidermal detection of p53 protein and 8-oxo-dG in sun-protected and chronically sun-exposed skin. Data are the mean of 15 biopsies. These was no statistical difference in the p53 or 8-oxo-dG in the protected and exposed areas.Immunochemical staining for p53 in biopsies of protected skin from all individuals showed one to seven (mean 1.8) stained cells per 200 cells in the epidermis. The skin chronically exposed to sunlight had the same number of p53-stained cells (mean: 1.7) for all women (〈link href="#f1-16"〉Fig. 1). P53-positive nuclei were found in the basal and suprabasal cells of the epidermis. Thus, the sun-protected and sun-exposed areas of skin contained the same amounts of both 8-oxodG and p53.The second part of the study compared the responses of protected and chronically exposed samples of skin from the same patient to a single acute UV radiation. The skin areas of all 15 subjects were exposed to 1 MED and the removal of DNA lesions (8-oxo-dG) and p53 were quantified 24 h later. The MED were similar for 15 volunteers (40.95 or 51.24 mJ cm–²), suggesting that they were all similarly sensitive to sunlight. There was erythema in both areas 24 h after radiation, but it was more
    Type of Medium: Electronic Resource
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  • 6
    Publication Date: 2018-02-03
    Description: Mendelian susceptibility to mycobacterial disease is a rare primary immunodeficiency characterized by severe infections caused by weakly virulent mycobacteria. Biallelic null mutations in genes encoding interferon gamma receptor 1 or 2 ( IFNGR1 or IFNGR2 ) result in a life-threatening disease phenotype in early childhood. Recombinant interferon (IFN-) therapy is inefficient, and hematopoietic stem cell transplantation has a poor prognosis. Thus, we developed a hematopoietic stem cell (HSC) gene therapy approach using lentiviral vectors that express Ifnr1 either constitutively or myeloid specifically. Transduction of mouse Ifnr1 –/– HSCs led to stable IFNR1 expression on macrophages, which rescued their cellular responses to IFN-. As a consequence, genetically corrected HSC-derived macrophages were able to suppress T-cell activation and showed restored antimycobacterial activity against Mycobacterium avium and Mycobacterium bovis Bacille Calmette-Guérin (BCG) in vitro. Transplantation of genetically corrected HSCs into Ifnr1 –/– mice before BCG infection prevented manifestations of severe BCG disease and maintained lung and spleen organ integrity, which was accompanied by a reduced mycobacterial burden in lung and spleen and a prolonged overall survival in animals that received a transplant. In summary, we demonstrate an HSC-based gene therapy approach for IFNR1 deficiency, which protects mice from severe mycobacterial infections, thereby laying the foundation for a new therapeutic intervention in corresponding human patients.
    Keywords: Hematopoiesis and Stem Cells, Immunobiology and Immunotherapy, Gene Therapy
    Print ISSN: 0006-4971
    Electronic ISSN: 1528-0020
    Topics: Biology , Medicine
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