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41.
Moinard-Butot Fabien Poprawa Elodie Schohn Anna Pietro Addeo Benabdelghani Meher 《World Journal of Clinical Cases》2023,11(6):1372-1378
BACKGROUND Gemcitabine is an antimetabolite used in the treatment of pancreatic cancer. One of the side effects of gemcitabine is vascular toxicity. Here, we report the case of a patient treated with gemcitabine who had peripheral vascular disease concomitant with a prolonged antitumor response.CASE SUMMARY A 75-year-old man was diagnosed with locally recurrent pancreatic cancer. Partial response was achieved after 9 mo of gemcitabine. At the same time, the patient reported peripheral vascular d... 相似文献
42.
Laetitia Dard Christophe Hubert Pauline Esteves Wendy Blanchard Ghina Bou About Lyla Baldasseroni Elodie Dumon Chloe Angelini Mgane Delourme Vronique Guyonnet-Duprat Stphane Claverol Laura Fontenille Karima Kissa Pierre-Emmanuel Sgula Jean-Benoît Thambo Lvy Nicolas Yann Herault Nadge Bellance Nivea Dias Amoedo Frdrique Magdinier Tania Sorg Didier Lacombe Rodrigue Rossignol 《The Journal of clinical investigation》2022,132(8)
Germline mutations that activate genes in the canonical RAS/MAPK signaling pathway are responsible for rare human developmental disorders known as RASopathies. Here, we analyzed the molecular determinants of Costello syndrome (CS) using a mouse model expressing HRAS p.G12S, patient skin fibroblasts, hiPSC-derived human cardiomyocytes, a HRAS p.G12V zebrafish model, and human fibroblasts expressing lentiviral constructs carrying HRAS p.G12S or HRAS p.G12A mutations. The findings revealed alteration of mitochondrial proteostasis and defective oxidative phosphorylation in the heart and skeletal muscle of CS mice that were also found in the cell models of the disease. The underpinning mechanisms involved the inhibition of the AMPK signaling pathway by mutant forms of HRAS, leading to alteration of mitochondrial proteostasis and bioenergetics. Pharmacological activation of mitochondrial bioenergetics and quality control restored organelle function in HRAS p.G12A and p.G12S cell models, reduced left ventricle hypertrophy in CS mice, and diminished the occurrence of developmental defects in the CS zebrafish model. Collectively, these findings highlight the importance of mitochondrial proteostasis and bioenergetics in the pathophysiology of RASopathies and suggest that patients with CS may benefit from treatment with mitochondrial modulators. 相似文献
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44.
Théo Willeman Julia Tonini Cécile Garnaud Sébastien Bailly Peggy Gandia Françoise Stanke-Labesque Danièle Maubon Elodie Gautier-Veyret 《Fundamental & clinical pharmacology》2020,34(2):279-287
Therapeutic drug monitoring (TDM) of antifungal triazole was recommended, except for isavuconazole (ISA) whose target trough concentrations (Cmin) need to be specified. Concerning posaconazole (POS), tablet formulation results in higher exposure but no upper Cmin threshold has been yet proposed. We aimed to investigate the pharmacokinetic–pharmacodynamic relationship of POS and ISA, using a bioassay approach as surrogate marker of antifungal activity, in order to refine the therapeutic Cmin of both antifungals. A bioassay using a cellulose disk diffusion method was performed to determine the growth inhibition zone (GIZ) of POS and ISA on Aspergillus fumigatus and Candida parapsilosis (ISA only). GIZs of plasma from patients undergoing TDM for POS (n = 136) or ISA (n = 40) were determined. GIZs of plasma patients and antifungal Cmin were highly correlated for ISA (A. fumigatus: ρ = 0.942, P < 0.0001; C. parapsilosis: ρ = 0.949, P < 0.0001) and POS (ρ = 0.922, P < 0.0001), and these relationships were represented with a Michaelis–Menten model. Based on this modeling, the recommended thresholds of 0.7, 1, and 1.25 mg/L for the POS Cmin corresponded to 50.1, 55.2, and 59.1% of the maximal GIZ, respectively. We propose an upper threshold of 4.8 mg/L for the POS Cmin and a lower threshold of 2.0 mg/L for the Cmin of ISA, as they respectively corresponded to concentrations leading to 90% and 50% of the maximal GIZ on A. fumigatus. The determination of antifungal activity using this bioassay allowed refining target Cmin of POS and ISA, especially the upper threshold of POS (4.8 mg/L) and the lower threshold of ISA (2.0 mg/L). 相似文献
45.
Stéphanie Lejeune Muriel Pichavant Ilka Engelmann Laurent Béghin Elodie Drumez Olivier Le Rouzic Rodrigue Dessein Stéphanie Rogeau Timothée Beke Gwenola Kervoaze Céline Delvart Héloïse Ducoin Guillaume Pouessel Armelle Le Mée Sophie Boileau Juliette Roussel Cécile Bonnel Clémence Mordacq Caroline Thumerelle Philippe Gosset Antoine Deschildre 《Pediatric allergy and immunology》2020,31(6):651-661
46.
Bellil Hela Herve Bérenice Herzog Elodie Ayoubi Jean-Marc Vialard François Poulain Marine 《Journal of assisted reproduction and genetics》2020,37(3):573-577
Journal of Assisted Reproduction and Genetics - Tetrasomy 9p (ORPHA: 3310) (i(9p)) is a rare chromosomal imbalance. It is characterized by the presence of a supernumerary chromosome incorporating... 相似文献
47.
48.
Sabrina Gaudin Elodie Chaillou Marie‐Anne Wycke Fabien Cornilleau Chantal Moussu Ludovic Calandreau Anne‐Lyse Lainé Raymond Nowak 《Developmental psychobiology》2018,60(1):90-103
Characteristics of attachment were assessed in peer‐ and object‐reared lambs, and compared to mothered subjects by taking into consideration distress, proximity seeking, and exploration during two separation‐reunion tests in both the familiar and a novel environment. Plasma cortisol and oxytocin were assayed as physiological indicators of stress and being comforted during the separation‐reunion test. Rewarding properties of the familiar figures were also determined in a conditioned place preference‐like paradigm. Between‐group analysis revealed the existence of secure attachment with the mother, alteration of secure attachment with the peer and weaker attachment with the object. Weaker attachment was expressed by a lack of distress during separation in the home pen and no preference for the place conditioned with the familiar object. Elevated basal plasma oxytocin levels, but not cortisol, observed in maternally deprived lambs were more likely linked to the absence of a maternal figure rather than social comfort during reunion. 相似文献
49.
Daniela A Bermejo Mar��a C Amezcua Vesely Mahmood Khan Eva V Acosta Rodr��guez Carolina L Montes Maria C Merino Kai Michael Toellner Elodie Mohr Dale Taylor Adam F Cunningham Adriana Gruppi 《Immunology》2011,132(1):123-133
Acute infection with Trypanosoma cruzi, the aetiological agent of Chagas’ disease, results in parasitaemia and polyclonal lymphocyte activation. It has been reported that polyclonal B‐cell activation is associated with hypergammaglobulinaemia and delayed parasite‐specific antibody response. In the present study we analysed the development of a B‐cell response within the different microenvironments of the spleen during acute T. cruzi infection. We observed massive germinal centre (GC) and extrafollicular (EF) responses at the peak of infection. However, the EF foci were evident since day 3 post‐infection (p.i.), and, early in the infection, they mainly provided IgM. The EF foci response reached its peak at 11 days p.i. and extended from the red pulp into the periarteriolar lymphatic sheath. The GCs were detected from day 8 p.i. At the peak of parasitaemia, CD138+ B220+ plasma cells in EF foci, red pulp and T‐cell zone expressed IgM and all the IgG isotypes. Instead of the substantial B‐cell response, most of the antibodies produced by splenic cells did not target the parasite, and parasite‐specific IgG isotypes could be detected in sera only after 18 days p.i. We also observed that the bone marrow of infected mice presented a strong reduction in CD138+ B220+ cells compared with that of normal mice. Hence, in acute infection with T. cruzi, the spleen appears to be the most important lymphoid organ that lodges plasma cells and the main producer of antibodies. The development of a B‐cell response during T. cruzi infection shows features that are particular to T. cruzi and other protozoan infection but different to other infections or immunization with model antigens. 相似文献
50.
Elodie Elkaim Christophe Picard Claire Galambrun Vincent Barlogis Anderson Loundou Catherine Curtillet Claire Oudin Isabelle Thuret Hervé Chambost Gérard Michel 《British journal of haematology》2014,166(4):557-565
This study aimed to describe kinetics of complete donor chimerism occurrence (cDC, >99·9% donor) after unrelated cord blood transplantation (UCBT), to identify its predictive factors and its impact on post‐transplant outcome. Ninety‐four children who received single UCBT after a myeloablative conditioning regimen had blood chimerism evaluation at predefined post‐transplant dates, using a real‐time polymerase chain reaction method with 0·1% sensitivity. Cumulative incidence of cDC at 1 year post‐transplantation was 61·8%. Three predictive factors were identified in multivariate analysis: history of malignant disease (P = 0·03), older age (above 2·16 years, the first quartile of age, P = 0·0055) and higher level of cord/recipient human leucocyte antigen mismatch (4/6 vs. 5‐6/6, P < 0·001) increased the probability of post‐transplant cDC. Although graft cell dose had a strong impact on haematological recovery, it did not apparently influence cDC occurrence. Early cDC (i.e. more than 99·9% donor chimerism on days 15–30 post‐transplant) appeared useful to predict engraftment (P = 0·003) as well as acute and chronic graft‐versus‐host disease (GvHD). Severe acute or chronic GvHD never occurred in patients with DC ≤99·9%, suggesting than even minimal residual host haematopoiesis is associated with a very low risk of GvHD after UCBT. 相似文献