نتایج جستجو برای: cgd

تعداد نتایج: 685  

Journal: :Journal of immunology 2005
Julie A Lekstrom-Himes Douglas B Kuhns W Gregory Alvord John I Gallin

The innate immune response to bacterial infections includes neutrophil chemotaxis and activation, but regulation of inflammation is less well understood. Formyl peptides, byproducts of bacterial metabolism as well as mitochondrial protein biosynthesis, induce neutrophil chemotaxis, the generation of reactive oxygen intermediates (ROI), and the production of the neutrophil chemoattractant, IL-8....

Journal: :The European respiratory journal 2015
Hélène Salvator Nizar Mahlaoui Emilie Catherinot Elisabeth Rivaud Benoit Pilmis Raphael Borie Bruno Crestani Colas Tcherakian Felipe Suarez Bertrand Dunogue Marie-Anne Gougerot-Pocidalo Margarita Hurtado-Nedelec Jean-François Dreyfus Isabelle Durieu Fanny Fouyssac Olivier Hermine Olivier Lortholary Alain Fischer Louis-Jean Couderc

Chronic granulomatous disease (CGD) is a primary immunodeficiency caused by failure of superoxide production in phagocytic cells. The disease is characterised by recurrent infections and inflammatory events, frequently affecting the lungs. Improvement of life expectancy now allows most patients to reach adulthood. We aimed to describe the pattern of pulmonary manifestations occurring during adu...

2014
Sang-Mi Song Mi-Ran Park Do-Soo Kim Jihyun Kim Yae-Jean Kim Chang-Seok Ki Kangmo Ahn

Chronic granulomatous disease (CGD) is a rare immunodeficiency disease, which is characterized by the lack of a functional nicotinamide adenine dinucleotide phosphate (NADPH) oxidase in phagocytes. The disease presents leukocytosis, anemia, hypergammaglobulinemia, and granuloma formation of the skin, lung, or lymph nodes. The mutation of the CYBB gene encoding gp91phox, located on chromosome Xp...

Journal: :International immunopharmacology 2012
Fariba Naderi beni Fatemeh Fattahi Abbas Mirshafiey Mohammad Ansari Monireh Mohsenzadegan Masoud Movahedi Zahra Pourpak Mostafa Moin

Chronic granulomatous disease (CGD) is a rare immunodeficiency disorder in which phagocytic leukocytes fail to generate superoxide (O(2)(-)) and antimicrobial oxidants. The therapeutic validity of interferon-gamma (IFN-γ) has been well established in CGD patients but its underlying mechanisms remain poorly understood. One probable mechanism has been suggested to be modulation of nitric oxide (N...

Journal: :Infection and immunity 1971
J B Suzuki N Grecz D Windhorst

Leukocytes from two patients with chronic granulomatous disease of childhood (CGD) and from one female carrier were examined for their capacity to induce germination of Clostridium botulinum type A spores in vitro. Normal human leukocytes induced germination of C. botulinum spores to the same extent as guinea pig neutrophils. Germination was depressed by more than half when cells from CGD patie...

Journal: :Blood 2000
J Roesler J T Curnutte J Rae D Barrett P Patino S J Chanock A Goerlach

Chronic granulomatous disease (CGD) is an inherited disease caused by defects in the superoxide-generating nicotinamide adenine dinucleotide phosphate (NADPH) oxidase of phagocytes. Genetic lesions in any of 4 components of this antimicrobial enzyme have been detected. Family-specific mutations are found in 3 of 4 forms of CGD due to deficiencies of the gp91-phox, p22-phox, and p67-phox genes. ...

Journal: :PLoS ONE 2009
J. Merlijn van den Berg Elsbeth van Koppen Anders Åhlin Bernd H. Belohradsky Ewa Bernatowska Lucien Corbeel Teresa Español Alain Fischer Magdalena Kurenko-Deptuch Richard Mouy Theoni Petropoulou Joachim Roesler Reinhard Seger Marie-José Stasia Niels H. Valerius Ron S. Weening Baruch Wolach Dirk Roos Taco W. Kuijpers

CGD is an immunodeficiency caused by deletions or mutations in genes that encode subunits of the leukocyte NADPH oxidase complex. Normally, assembly of the NADPH oxidase complex in phagosomes of certain phagocytic cells leads to a "respiratory burst", essential for the clearance of phagocytosed micro-organisms. CGD patients lack this mechanism, which leads to life-threatening infections and gra...

ژورنال: :ابن سینا 0
پیام طبرسی p tabarsi shahid beheshti university of medical sciencesمتخصص عفونی، استادیار دانشگاه علوم پزشکی شهید بهشتی، بیمارستان مسیح دانشوری مهدی میرسعیدی m mirsaidi louisville university, united states of americaمتخصص عفونی، دانشگاه لوئیس ویل ایالات متحده امریکا شیرین کریمی sh karimi shahid beheshti university of medical sciencesمتخصص پاتولوژی، استادیار دانشگاه علوم پزشکی شهید بهشتی، بیمارستان مسیح دانشوری مجید امیری m amiri shahid beheshti university of medical sciencesمتخصص عفونی، استادیار دانشگ اه علوم پزشکی شهید بهشتی، بیمارستان مسیح دانشوری بهزاد بنی اقبال b banieghbal shahid beheshti university of medical sciencesفوق تخصص ریه، استادیار دانشگاه علوم پزشکی شهید بهشتی، بیمارستان مسیح دانشوری داوود منصوری d mansoori shahid beheshti university of medical sciencesفوق تخصص کلینیکال ایمونولوژی استاد دانشگاه علوم پزشکی شهید بهشتی، بیمارستان مسیح دانشوری

یک نقص ایمنی اولیه ی نادر است که ابتدا در کودکان شرح داده شد . این بیماری عمدتاً در cgd کودکان دیده می شود ولی مواردی از بیماری در بزرگسالان نیز گزارش شده است. در این گزارش که به همراه با برونشیولیت لنفوسیتیک در یک فرد بالغ بوده cgd به اولین مورد بررسی پرداخته شده است . بیماری 40 ساله که با سرفه و خلط چرکی و تنگی نفس و کاهش وزن مراجعه اسکن، بیوپسی باز ریه ct نموده است، دو دوره تحت درمان ضد سل قر...

Journal: :Japanese Journal of Clinical Immunology 2007

2013
J. F. Moreau John A. Ozolek P. Ling Lin Todd D. Green Elaine A. Cassidy Veena L. Venkat Andrew R. Buchert

Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency syndrome that results from abnormal nicotinamide adenine dinucleotide phosphate (NADPH) oxidase function. This defect leads to recurrent catalase-positive bacterial and fungal infections as well as associated granuloma formation. We review the case of a 2-year-old boy who presented with ascites and fever of an unknown orig...

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