45 results match your criteria: "University of Pierre et Marie Curie[Affiliation]"

The World Health Organization has estimated that air pollution is a major threat to health, causing approximately nine million premature deaths every year. Each individual has, over their lifetime, a unique exposure to air pollution through their habits, working and living conditions. Medical research requires dedicated tools to assess and understand individual exposure to air pollution in view of investigating its health effects.

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Fully automated detection, segmentation, and analysis of in vivo RPE single cells.

Eye (Lond)

May 2021

Laboratory of Applied Photonic Devices (LAPD), School of Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

Objective: To develop a fully automated method of retinal pigmented epithelium (RPE) cells detection, segmentation and analysis based on in vivo cellular resolution images obtained with the transscleral optical phase imaging method (TOPI).

Methods: Fourteen TOPI-RPE images from 11 healthy individuals were analysed. The developed image processing method encompassed image filtering and normalisation, detection and removal of blood vessels, cell detection and cell membrane segmentation.

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Nogo-A-targeting antibody promotes visual recovery and inhibits neuroinflammation after retinal injury.

Cell Death Dis

February 2020

CUO-Recherche, Centre de recherche du CHU de Québec-Université Laval and Département d'ophtalmologie, Faculté de médecine, Université Laval, Québec, Québec, Canada.

N-Methyl-D-aspartate (NMDA)-induced neuronal cell death is involved in a large spectrum of diseases affecting the brain and the retina such as Alzheimer's disease and diabetic retinopathy. Associated neurological impairments may result from the inhibition of neuronal plasticity by Nogo-A. The objective of the current study was to determine the contribution of Nogo-A to NMDA excitotoxicity in the mouse retina.

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Positive Impact of Expert Reference Center Validation on Performance of Next-Generation Sequencing for Genetic Diagnosis of Autoinflammatory Diseases.

J Clin Med

October 2019

Cellules souches, plasticité cellulaire, médecine régénératrice et immunothérapies, INSERM, University Montpellier, Department of Medical Genetics, Rare Diseases and Personalized Medicine, CEREMAIA, CHU Montpellier, 34295 Montpellier, France.

Monogenic autoinflammatory diseases (AIDs) are caused by variants in genes that regulate innate immunity. The current diagnostic performance of targeted next-generation sequencing (NGS) for AIDs is low. We assessed whether pre-analytic advice from expert clinicians could help improve NGS performance from our 4 years of experience with the sequencing of a panel of 55 AIDs genes.

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Ocular gene therapies in clinical practice: viral vectors and nonviral alternatives.

Drug Discov Today

August 2019

Inserm UMR_S 1138, Team 17, Centre de Recherche des Cordeliers, Paris, France; AP-HP Hôpitaux de Paris, Ophtalmopole Hôpital Cochin, Paris, France; Sorbonne University, University of Pierre et Marie Curie, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France; Paris Descartes University, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France. Electronic address:

Ocular gene therapy has entered into clinical practice. Although viral vectors are currently the best option to replace and/or correct genes, the optimal method to deliver these treatments to the retinal pigment epithelial (RPE) cells and/or photoreceptor cells remains to be improved to increase transduction efficacy and reduce iatrogenic risks. Beyond viral-mediated gene replacement therapies, nonviral gene delivery approaches offer the promise of sustained fine-tuned expression of secreted therapeutic proteins that can be adapted to the evolving stage of the disease course and can address more common nongenetic retinal diseases, such as age-related macular degeneration (AMD).

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Potential antiedematous effects of intravitreous anti-VEGF, unrelated to VEGF neutralization.

Drug Discov Today

August 2019

Inserm UMR_S 1138, Team 17, Centre de Recherche des Cordeliers, Paris, France; Sorbonne University, University of Pierre et Marie Curie, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France; Paris Descartes University, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.

The intravitreous injection of therapeutic proteins that neutralize vascular endothelial growth factor (VEGF) family members is efficient to reduce macular edema associated with wet age-related macular degeneration (AMD), retinal vein occlusion (RVO) and diabetic retinopathy (DR). It has revolutionized the visual prognosis of patients with macular edema. The antiedematous effect is dependent on an intravitreous dose of drug, which varies between patients and requires frequent and repeated injections to maintain its effects.

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Introduction: Striking recent advance has occurred in the field of medical retina, greatly because intraocular drugs have been developed, enhancing their clinical efficacy while avoiding systemic side-effects. However, the burden of repeated intraocular administration makes limits the optimal efficacy of treatments, prompting the development of new drugs with prolonged half-life or of sustained drug delivery systems.

Areas Covered: In this review, we describe the various drugs and drug delivery systems that have reached the clinical stage and those that are in clinical development and we discuss the limitations to clinical translation.

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Choroidal neovascularization (CNV) is a major cause of visual impairment in patients suffering from wet age-related macular degeneration (AMD), particularly when refractory to intraocular anti-VEGF injections. Here we report that treatment with the oral mineralocorticoid receptor (MR) antagonist spironolactone reduces signs of CNV in patients refractory to anti-VEGF treatment. In animal models of wet AMD, pharmacological inhibition of the MR pathway or endothelial-specific deletion of MR inhibits CNV through VEGF-independent mechanisms, in part through upregulation of the extracellular matrix protein decorin.

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Non-viral ocular gene therapy, pEYS606, for the treatment of non-infectious uveitis: Preclinical evaluation of the medicinal product.

J Control Release

September 2018

Eyevensys, SAS, 33 Avenue du Maine, 75015 Paris, France; Inserm UMR_S 1138, Team 17, Centre de Recherche des Cordeliers, Paris, France; AP-HP Hôpitaux de Paris, Ophtalmopole Hôpital Cochin, Paris, France; Sorbonne University, University of Pierre et Marie Curie, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France; Paris Descartes University, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France. Electronic address:

Non-infectious uveitis (NIU) is the first cause of blindness that can be cured if optimal anti-inflammatory therapy can be achieved. Systemic anti-TNF (Tumor Necrosis Factor) agents have been recently approved for NIU but no local delivery of anti-TNF is available. For sustained production of secreted therapeutic proteins into the eye, non-viral gene therapy using plasmid electrotransfer in the ciliary muscle has been proposed.

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Societal and technological changes have resulted in sitting being the dominant posture during most activities of daily living, such as learning, working, travelling and leisure time. Too much time spent in seated activities, referred to as sedentary behaviour, is a novel concern for public health as it is one of the key lifestyle causes of poor health. The European DEDIPAC (Determinants of Diet and Physical Activity) Knowledge Hub coordinated the work of 35 institutions across 12 European member states to investigate the determinants of sedentary behaviour.

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Author Correction: IMMP2L: a mitochondrial protease suppressing cellular senescence.

Cell Res

July 2018

Equipe 11 labelisée par la Ligue Nationale contre le Cancer, INSERM U1138, Centre de Recherche des Cordeliers, 75006, Paris, France.

We apologize for an error we just found in the paper published online on 29 May 2018. The protein SERPINB4 is mistakenly indicated as SERPIN4B for three times in the main text and once in Fig. 1.

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IMMP2L: a mitochondrial protease suppressing cellular senescence.

Cell Res

June 2018

Equipe 11 labelisée par la Ligue Nationale contre le Cancer, INSERM U1138, Centre de Recherche des Cordeliers, 75006, Paris, France.

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An accessory renal artery (ARA) represents an anatomic variation which can challenge endovascular aortic aneurysm repair (EVAR). The aim of this review was to summarize the current knowledge on postoperative outcomes following ARA coverage during EVAR. We performed a systematic literature review.

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Article Synopsis
  • DADA2 is a newly identified autoinflammatory disorder that requires genetic testing for diagnosis; a study analyzed 66 patients suspected of having DADA2.
  • Out of the patients tested, 19.6% had harmful mutations in the ADA2 gene, with seven mutations being newly discovered; symptoms included fever, vasculitis, and neurological issues.
  • The study developed a decision tree to guide genetic testing recommendations, suggesting key criteria like typical symptoms, inflammation markers, and attack patterns to improve diagnosis efficiency.
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Anti-CTLA-4 immunotherapy: uncoupling toxicity and efficacy.

Cell Res

May 2018

Equipe 11 labelisée par la Ligue Nationale contre le Cancer, INSERM U1138, Centre de Recherche des Cordeliers, Paris, 75006, France.

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Pelvi-ureteric junction obstruction corresponds to an impairment of urinary transport that can lead to renal dysfunction if not treated. Several mechanisms can cause the obstruction of the ureter including intrinsic factors or extrinsic factors such as the presence of crossing vessels. The treatment of the disease relies on surgical approaches, pyeloplasty being the standard reference.

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Revisiting Vision Rehabilitation.

Front Syst Neurosci

November 2017

Department of Ophthalmology, Limoges Hospital, Limoges, France.

Low vision is a condition caused by eye or brain disease, in which visual acuity is 20/70 (3/10 or 6/18) or poorer in the better-seeing eye and cannot be corrected or improved with regular eyeglasses. It impacts personal ability to perform vision-dependent tasks as activities of daily living, walking, reading or using a computer. Rehabilitation is a multidisciplinary training dedicated to improve patients' functional abilities and quality of life.

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Tolerance of high and low amounts of PLGA microspheres loaded with mineralocorticoid receptor antagonist in retinal target site.

J Control Release

November 2017

Inserm UMR_S 1138, Team 17: From Physiopathology of Retinal Diseases to Clinical Advances, Centre de Recherche des Cordeliers, Paris, France; Sorbonne University, University of Pierre et Marie Curie, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France; Paris Descartes University, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France; University of Lausanne, Switzerland.

Mineralocorticoid receptor (MR) contributes to retinal/choroidal homeostasis. Excess MR activation has been shown to be involved in pathogenesis of central serous chorioretinopathy (CSCR). Systemic administration of MR antagonist (MRA) reduces subretinal fluid and choroidal vasodilation, and improves the visual acuity in CSCR patients.

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In diabetic retinopathy, the exact mechanisms leading to retinal capillary closure and to retinal barriers breakdown remain imperfectly understood. Rho-associated kinase (ROCK), an effector of the small GTPase Rho, involved in cytoskeleton dynamic regulation and cell polarity is activated by hyperglycemia. In one year-old Goto Kakizaki (GK) type 2 diabetic rats retina, ROCK-1 activation was assessed by its cellular distribution and by phosphorylation of its substrates, MYPT1 and MLC.

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Imported Schistosomiasis in Children: Clinical, Diagnostic Aspects And Outcome in 5 Tertiary Hospitals in France.

Pediatr Infect Dis J

December 2017

From the *Department of Pediatrics, Paris 13 University, Jean Verdier Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Bondy, France; †Department of Microbiology, University Paris-Diderot, University Hospital Robert-Debré, ‡Department of Pediatric Emergency, University Paris-Diderot, Sorbonne Paris Cité, Hospital Robert Debré, §Department of Pediatric Surgery and Urology, University Paris-Diderot, University Hospital Robert Debré, and ¶Department of Parasitology-Mycology, University Pierre et Marie Curie, Universitary Hospitals Pitié-Salpétrière/Charles Foix, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France; ‖Department of General Pediatrics, Hospital Delafontaine, Saint-Denis, France; **Department of Surgery, University Paris Descartes, Necker-Enfants Malades Hospital, ††Department of General Pediatrics and Pediatric Infectious Diseases, University Paris Descartes, Necker-Enfants Malades Hospital, ‡‡Department of Parasitology-Mycology, University Paris Descartes, Cochin Hospital, and §§Department of Nephrology and Kidney Transplantation, University of Pierre et Marie Curie, Trousseau University Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France; ¶¶Department of Infectious and tropical diseases, Paris 13 University, Avicenne Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Bobigny, France; ‖‖Department of Parasitoloy, Paris 13 University, Jean Verdier Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Bondy, France; ***UMR 190, Unité des virus émergents, Université Aix-Marseille, Marseille, France; and †††Department of General Pediatrics, University Paris-Diderot, University Hospital Robert Debré, INSERM 1123 Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.

The objective of this retrospective study is to describe imported schistosomiasis in children in the Paris region between 2010 and 2015. Forty children with a diagnosis of schistosomiasis were included. Thirty-seven (93%) had a chronic urinary form with hematuria.

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The human gut microbiome modulates many host processes, including metabolism, inflammation, and immune and cellular responses. It is becoming increasingly apparent that the microbiome can also influence the development of cancer. In preclinical models, the host response to cancer treatment has been improved by modulating the gut microbiome; this is known to have an altered composition in many diseases, including cancer.

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Daily Practice Management of pT1a-b pN0 Breast Carcinoma: A Prospective French ODISSEE Cohort Study.

Clin Breast Cancer

April 2017

Assistance Publique Hôpitaux de Paris (AP-HP), Department of Radiation Oncology and Henri Mondor Breast Center, INSERM U955 E07, and University of Paris-Est Créteil (UPEC), France. Electronic address:

Article Synopsis
  • Most small breast cancer tumors (≤10 mm) have a good prognosis, but it's unclear which patients need additional systemic therapy according to current guidelines.
  • The ODISSEE study analyzed 616 patients with early-stage breast cancer (pT1a-b pN0) to assess treatment practices and outcomes, finding most tumors were detected during screening and almost all patients underwent conservative surgery.
  • After 5 years, survival rates were high, with overall survival at 98.4%, indicating that routine care in these cases aligns with international standards, primarily involving surgery, radiotherapy, and hormone therapy for ER-positive cancers.
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Mouse models in oncoimmunology.

Nat Rev Cancer

December 2016

Equipe 11 labelisée par la Ligue Nationale contre le Cancer, INSERM U1138, Centre de Recherche des Cordeliers, 75006 Paris, France.

Fundamental cancer research and the development of efficacious antineoplastic treatments both rely on experimental systems in which the relationship between malignant cells and immune cells can be studied. Mouse models of transplantable, carcinogen-induced or genetically engineered malignancies - each with their specific advantages and difficulties - have laid the foundations of oncoimmunology. These models have guided the immunosurveillance theory that postulates that evasion from immune control is an essential feature of cancer, the concept that the long-term effects of conventional cancer treatments mostly rely on the reinstatement of anticancer immune responses and the preclinical development of immunotherapies, including currently approved immune checkpoint blockers.

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Associations between disease activity, markers of HDL functionality and arterial stiffness in patients with rheumatoid arthritis.

Atherosclerosis

August 2016

Laboratory of Lipids and Lipoproteins, School of Pharmacy and Biochemistry, INFIBIOC, University of Buenos Aires, CONICET, Buenos Aires, Argentina.

Background And Aims: Rheumatoid arthritis (RA) is a chronic, inflammatory disease associated with increased risk of cardiovascular disease (CVD). Measures of HDL metabolism/function were shown to be altered in RA patients with high disease activity. We aimed at evaluating the effect of HDL characteristics on arterial stiffness in RA patients classified according to the inflammatory disease activity.

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Background: Periodontopathogens antibodies have been shown to be associated with primary myocardial events, but little is known regarding their impact on major adverse events after a prior acute myocardial infarction (AMI). The present prospective study evaluates the association between antibody levels of 4 periodontopathogens and the risk of all-cause death or non-fatal myocardial infarction (MI) at 1 year in 975 patients admitted for acute ST segment or non-ST segment elevation MI in French Registry of Acute ST-Elevation and Non-ST-Elevation Myocardial Infarction (FAST-MI), a nationwide French survey.

Methods: Multiserotype ELISAs were performed to assess levels of IgG and IgA against , , and .

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