Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Delphine Giusti"'
Autor:
Ailsa Robbins, Mathilde Bahuaud, Maxime Hentzien, Quentin Maestraggi, Coralie Barbe, Delphine Giusti, Richard Le Naour, Frederic Batteux, Amélie Servettaz
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundPatients with primary humoral immunodeficiency are more prone to invasive as well as recurrent pneumococcal infections. Therefore, anti-pneumococcal vaccination including the 13-valent conjugate vaccine is recommended. Nevertheless, to date
Externí odkaz:
https://doaj.org/article/baa2572665fc41eb852c465587bfc163
Autor:
Nellie Bourse Chalvon, Pauline Orquevaux, Delphine Giusti, Gregory Gatouillat, Thierry Tabary, Marcelle Tonye Libyh, Jan Chrusciel, Moustapha Drame, Grace Stockton-Bliard, Zahir Amoura, Laurent Arnaud, Hanns-Martin Lorenz, Gilles Blaison, Bernard Bonnotte, Nadine Magy-Bertrand, Sabine Revuz, Reinhard Edmund Voll, Oliver Hinschberger, Andreas Schwarting, Bach Nga Pham, Thierry Martin, Jean-Loup Pennaforte, Amelie Servettaz
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
IntroductionAnti-glomerular basement membrane (GBM) antibodies are pathogenic antibodies first detected in renal-limited anti-GBM disease and in Goodpasture disease, the latter characterized by rapidly progressive crescentic glomerulonephritis combin
Externí odkaz:
https://doaj.org/article/099b092abb9544c0b34f557d13543e1d
Autor:
Celine Konecki, Catherine Feliu, Yoann Cazaubon, Delphine Giusti, Marcelle Tonye-Libyh, Hedia Brixi, Guillaume Cadiot, Amélie Biron, Zoubir Djerada
Publikováno v:
Pharmaceutics, Vol 13, Iss 8, p 1191 (2021)
Despite the well-demonstrated efficacy of infliximab in inflammatory diseases, treatment failure remains frequent. Dose adjustment using Bayesian methods has shown in silico its interest in achieving target plasma concentrations. However, most of the
Externí odkaz:
https://doaj.org/article/76e1441d69c949259106efe961f75ad2
Autor:
Delphine Giusti, Gregory Gatouillat, Sébastien Le Jan, Julie Plée, Philippe Bernard, Frank Antonicelli, Bach Nga Pham
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract Bullous Pemphigoid (BP) is an inflammatory rare autoimmune bullous dermatosis, which outcome cannot be predicted through clinical investigations. Eosinophils are the main immune infiltrated cells in BP. However, the release of Major Basic Pr
Externí odkaz:
https://doaj.org/article/3412cd42f2764cabac2d7a9d47000b0d
Autor:
Delphine Giusti, Estela Bini, Christine Terryn, Kevin Didier, Sébastien Le Jan, Grégory Gatouillat, Anne Durlach, Stéphane Nesmond, Celine Muller, Philippe Bernard, Frank Antonicelli, Bach Nga Pham
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Background: DNA extracellular traps (ETs), released by neutrophils (NETs), or eosinophils (EETs), play a pathogenic role in several autoimmune disorders. However, to date, NETs have never been investigated in bullous pemphigoid (BP) with respect to c
Externí odkaz:
https://doaj.org/article/d245f1ce077f468a8fd0cf4fb5640f1e
Autor:
Ailsa Robbins, Maxime Hentzien, Segolene Toquet, Kevin Didier, Amelie Servettaz, Bach-Nga Pham, Delphine Giusti
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Anti-SS-A antibodies are often sought for in autoimmune diseases diagnosis. Two different target proteins have actually been identified: Ro52 and Ro60. Clinical and immunological associations seem different depending on anti-Ro52 or anti-Ro60 antibod
Externí odkaz:
https://doaj.org/article/ed0c3416dec74a9c87c11b53265c8e8d
Autor:
Kevin Didier, Delphine Giusti, Sebastien Le Jan, Christine Terryn, Celine Muller, Bach Nga Pham, Richard Le Naour, Frank D. Antonicelli, Amelie Servettaz
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 7, p 2136 (2020)
Systemic sclerosis (SSc) is a systemic disease characterized by a great clinical and immunological heterogeneity whose pathophysiology is still being unraveled. Recently, innate immunity has been proposed to participate to the pathogenesis of SSc. In
Externí odkaz:
https://doaj.org/article/d95a821f608347e2b5880456c3d99003
Autor:
Kevin Didier, Loïs Bolko, Delphine Giusti, Segolene Toquet, Ailsa Robbins, Frank Antonicelli, Amelie Servettaz
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Connective tissue diseases (CTDs) such as systemic lupus erythematosus, systemic sclerosis, myositis, Sjögren’s syndrome, and rheumatoid arthritis are systemic diseases which are often associated with a challenge in diagnosis. Autoantibodies (AAbs
Externí odkaz:
https://doaj.org/article/5238410b3f834d0a9706c3e4ca3aeb23
Autor:
Delphine Giusti, Grégory Gatouillat, Sébastien Le Jan, Julie Plée, Philippe Bernard, Frank Antonicelli, Bach-Nga Pham
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Bullous pemphigoid (BP) is an autoimmune bullous skin disease characterized by anti-BP180 and anti-BP230 autoantibodies (AAbs). Mucous membrane involvement is an uncommon clinical feature of BP which may evoke epidermolysis bullosa acquisita, another
Externí odkaz:
https://doaj.org/article/e58c99ed542e4f309f0c66bac54a43fc
Autor:
Soumaya Karaki, Marie Anson, Thi Tran, Delphine Giusti, Charlotte Blanc, Stephane Oudard, Eric Tartour
Publikováno v:
Vaccines, Vol 4, Iss 4, p 37 (2016)
Checkpoint inhibitor (CPI) blockade is considered to be a revolution in cancer therapy, although most patients (70%–80%) remain resistant to this therapy. It has been hypothesized that only tumors with high mutation rates generate a natural antitum
Externí odkaz:
https://doaj.org/article/cdb4a9b1eda944a0a0622066b2c0c13a