Results 41 to 50 of about 5,467 (160)

Gut Microbiota-Dependent Trimethylamine N-Oxide Associates With Inflammation in Common Variable Immunodeficiency

Frontiers in Immunology, 2020
A substantial proportion of patients with common variable immunodeficiency (CVID) have inflammatory and autoimmune complications of unknown etiology.
Magnhild E. Macpherson, Magnhild E. Macpherson, Magnhild E. Macpherson, Johannes R. Hov, Johannes R. Hov, Johannes R. Hov, Johannes R. Hov, Thor Ueland, Thor Ueland, Thor Ueland, Tuva B. Dahl, Tuva B. Dahl, Tuva B. Dahl, Martin Kummen, Martin Kummen, Martin Kummen, Martin Kummen, Kari Otterdal, Kristian Holm, Kristian Holm, Kristian Holm, Rolf K. Berge, Tom E. Mollnes, Tom E. Mollnes, Tom E. Mollnes, Tom E. Mollnes, Marius Trøseid, Marius Trøseid, Marius Trøseid, Bente Halvorsen, Bente Halvorsen, Pål Aukrust, Pål Aukrust, Pål Aukrust, Børre Fevang, Børre Fevang, Silje F. Jørgensen, Silje F. Jørgensen, Silje F. Jørgensen   +38 more
doaj   +1 more source

IL-10-Producing Regulatory B Cells Are Decreased in Patients with Common Variable Immunodeficiency. [PDF]

PLoS ONE, 2016
Common variable immunodeficiency (CVID) is the most prevalent symptomatic primary immunodeficiency in adults. CVID patients often present changes in the frequency and function of B lymphocytes, reduced number of Treg cells, chronic immune activation ...
Nathalia Silveira Barsotti, Rafael Ribeiro Almeida, Priscilla Ramos Costa, Myrthes Toledo Barros, Jorge Kalil, Cristina Maria Kokron   +5 more
doaj   +1 more source

Association of serum copeptin levels with pulmonary complications and heart right ventricular functions in common variable immunodeficiency

BMC Immunology
Background and aims Common variable immunodeficiency (CVID) represents the most frequently diagnosed symptomatic primary immunodeficiency (PID), marked by a heterogeneous presentation involving infectious and non-infectious symptoms.
Mehmet Kılınç, Fatih Çölkesen, Filiz Sadi Aykan, Recep Evcen, Eray Yıldız, Bahadır Feyzioğlu, Metin Doğan, Yakup Alsancak, Sefa Tatar, Şevket Arslan   +9 more
doaj   +1 more source

Common variable immunodeficiency patients display elevated plasma levels of granulocyte activation markers elastase and myeloperoxidase

International Journal of Immunopathology and Pharmacology, 2019
Common variable immunodeficiency disorders (CVIDs) represent a group of primary immunodeficiency diseases characterized by hypogammaglobulinemia and dysfunctional immune response to invading pathogens.
Jiří Litzman, Zita Chovancová, Petr Bejdák, Marek Litzman, Zdeněk Hel, Marcela Vlková   +5 more
doaj   +1 more source

Common Variable Immunodeficiency (CVID)

Journal of Clinical Review & Case Reports, 2018
Common Variable Immunodeficiency (CVID) refers to a heterogeneous group of primary immune deficiency disorders (PIDD) presenting with recurrent sinopulmonary infections, hypogammagloblunemia, inadequate vaccination responses, and in a subset, co-existent autoimmune and inflammatory disease.
Suzahn Ebert, Sonali Bracken, John Woosley, Kevin G. Greene, Jonathan Hansen, Leonard Jason Lobo, Teresa Kathleen Tarrant   +6 more
openaire   +2 more sources

Characterizing Autoimmune and End-Organ Lympho-Infiltrative Disease Burden in Childhood-Onset Common Variable Immunodeficiency

Journal of Human Immunity
BackgroundCommon variable immunodeficiency (CVID) is the most prevalent inborn error of immunity. Although CVID is most commonly diagnosed in adulthood, a subset of patients is diagnosed in childhood.
Leon Reteig, Aditi Jogdand, Joseph Hong, Katherine Liu, Sara Barmettler, Jocelyn Farmer, Mei-Sing Ong   +6 more
doaj   +1 more source

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond

Frontiers in Immunology, 2018
Common variable immunodeficiency (CVID) is the most frequent symptomatic primary immunodeficiency characterized by recurrent infections, hypogammaglobulinemia and poor response to vaccines.
Guillem de Valles-Ibáñez, Ana Esteve-Solé, Ana Esteve-Solé, Mònica Piquer, Mònica Piquer, E. Azucena González-Navarro, E. Azucena González-Navarro, Jessica Hernandez-Rodriguez, Hafid Laayouni, Hafid Laayouni, Eva González-Roca, Eva González-Roca, Ana María Plaza-Martin, Ana María Plaza-Martin, Ángela Deyà-Martínez, Ángela Deyà-Martínez, Andrea Martín-Nalda, Andrea Martín-Nalda, Mónica Martínez-Gallo, Mónica Martínez-Gallo, Mónica Martínez-Gallo, Marina García-Prat, Marina García-Prat, Lucía del Pino-Molina, Ivón Cuscó, Ivón Cuscó, Marta Codina-Solà, Marta Codina-Solà, Laura Batlle-Masó, Laura Batlle-Masó, Manuel Solís-Moruno, Manuel Solís-Moruno, Tomàs Marquès-Bonet, Tomàs Marquès-Bonet, Tomàs Marquès-Bonet, Elena Bosch, Eduardo López-Granados, Juan Ignacio Aróstegui, Juan Ignacio Aróstegui, Pere Soler-Palacín, Pere Soler-Palacín, Roger Colobran, Roger Colobran, Roger Colobran, Jordi Yagüe, Jordi Yagüe, Laia Alsina, Laia Alsina, Manel Juan, Manel Juan, Ferran Casals   +50 more
doaj   +1 more source

Total and High Molecular Weight Adiponectin Expression Is Decreased in Patients with Common Variable Immunodeficiency: Correlation with Ig Replacement Therapy

Frontiers in Immunology, 2017
Adiponectin (Acrp30) is an adipokine widely studied for its beneficial metabolic properties. It circulates as low molecular weight (LMW), medium molecular weight (MMW), and high molecular weight (HMW) oligomers.
Antonio Pecoraro, Ersilia Nigro, Ersilia Nigro, Rita Polito, Rita Polito, Maria Ludovica Monaco, Olga Scudiero, Olga Scudiero, Ilaria Mormile, Azzurra Cesoni Marcelli, Mario Capasso, Mario Capasso, Francesco Habetswallner, Arturo Genovese, Aurora Daniele, Aurora Daniele, Giuseppe Spadaro   +16 more
doaj   +1 more source

Common variable immunodeficiency and autoimmune diseases: A 10-year single-center experience

The Turkish Journal of Gastroenterology
Objectives: This study aimed to determine the frequency of autoimmune diseases (ADs) accompanying common variable immunodeficiency (CVID) and evaluate clinical and immunological features, organ manifestation, and effects on malignancy and mortality ...
Filiz Sadi Aykan, Fatih Çölkesen, Recep Evcen, Mehmet Kılınç, Eray Yıldız, Şevket Arslan   +5 more
doaj  

Clinical and immunological differentiation of isolated IgG and combined IgG & IgM deficiencies from common variable immunodeficiency

Frontiers in Immunology
ObjectiveTo assess the clinical relevance of diagnosing and classifying isolated IgG deficiency and combined IgG/IgM deficiency separately from CVID.MethodsIn a retrospective cohort of patients with primary hypogammaglobulinemia, we evaluated and ...
Yagmur Dogru, Faranaz Atschekzei, Faranaz Atschekzei, Damla Dogru, Torsten Witte, Torsten Witte, Georgios Sogkas, Georgios Sogkas   +7 more
doaj   +1 more source