Results 61 to 70 of about 4,530 (166)

Viral Immunity in Immunoglobulin Products: Global Immunity Debt and Autoimmunity in the Postpandemic Era

European Journal of Immunology, Volume 56, Issue 3, March 2026.
Immunoglobulin products derived from pooled global plasma reflect population‐level antiviral immunity. Analysis of batches from 2017 to 2023 reveals pandemic‐driven shifts in viral antibody profiles and a concurrent rise in autoantibodies, notably against TRIM21/Ro52, highlighting links between SARS‐CoV‐2, immunity debt, and autoimmunity.
Hannes Lindahl, Katy Shaw‐Saliba, H. Benjamin Larman, C. I. Edvard Smith, Peter Bergman   +4 more
wiley   +1 more source

A double dissociation between memory span and word processing among neurological patients attests to the functional independence of verbal short‐term memory

Journal of Neuropsychology, Volume 20, Issue 1, Page 101-114, March 2026.
Abstract Reports of patients with impaired verbal short‐term memory are central to the debate of whether there are independent short‐term stores or whether immediate repetition is supported by activated long‐term memory. Patients with selective impairments of verbal short‐term memory support models with independent buffers.
Tobias Bormann, Margret Seyboth, Dorothee Kümmerer, Volkmar Glauche, Michel Rijntjes, Cornelius Weiller   +5 more
wiley   +1 more source

Identification of microorganisms related to chronic rhinosinusitis in adult patients with variable common immunodeficiency

Revista Alergia México, 2016
Background: The prevalence of chronic rhinosinusitis in adult patients with common variable immunodeficiency (CVID) is 52%. The patients with CVID show higher incidence of chronic rhinosinusitis, which is an inflammatory disease that affects the lining ...
Gabriela Angulo-Pérez, Eulalio Vivar-Acevedo, Diana Andrea Herrera-Sánchez   +2 more
doaj   +1 more source

Allergic Diseases in Common Variable Immunodeficiency: A Prospective Cross‐Sectional Study on Prevalence and Allergy Biomarkers of Clinical Phenotypes [PDF]

Scand J Immunol
Allergy occurred in 27% of 60 CVID patients, while IgE deficiency was observed in 65% and was strongly correlated with serum IgA levels. Low serum IgE/IgA levels accurately identified lymphoproliferative and granulomatous phenotypes, thereby improving diagnostic and prognostic stratification in CVID.
Danieli M, Claudi I, Auria S, Martini M, Buti E, Brunetto S, Moroncini G, Minciullo P, Gangemi S, Bilò M.   +9 more
europepmc   +2 more sources

Managing Primary Immunodeficiency Immunoglobulin Replacement Therapy‐Related Adverse Events With Recombinant Human C1 Esterase Inhibitor Prophylaxis: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Immunoglobulin replacement therapy (IRT) for primary immunodeficiency reduces infection risk and subsequent complications and can be lifesaving. However, IRT can cause severe systemic adverse events (AEs) that may limit adequate dosing. These AEs may be caused, in part, by activation and/or consumption of complement proteins, thereby lowering ...
Douglas H. Jones, Heidi Memmott
wiley   +1 more source

Clinical Spectrum of Cutaneous, Ocular, and Hair Manifestations in Patients With Inborn Errors of Immunity: Insights From a Single Center in Turkey

Immunity, Inflammation and Disease, Volume 14, Issue 2, February 2026.
ABSTRACT Background Inborn errors of immunity (IEI), previously referred to as primary immunodeficiencies, are a heterogeneous group of genetic disorders affecting immune development and function. While once considered rare, IEIs are increasingly recognized, particularly in regions with high consanguinity rates.
Burcu Cil Yılmaz, Sibel Kaplan Sarikavak, Sezin Naiboglu, Gulsah Kalay, Erkan Cakmak, Ozge Turkyilmaz Ucar, Selami Ulas, Nermin Kapci, Pinar Gokmirza, Cigdem Aydogmus   +9 more
wiley   +1 more source

Primary immunodeficiency in adults: total variable immune deficiency clinical manifestations, immunological and genetic defects, treatment

Терапевтический архив, 2011
The most prevalent form of primary immunodeficiency with a total defect of antibody production in adults is common variable immunodeficiency (CVID). Compared to other forms of primary immunodeficiency, CVID is characterized by later onset of clinical ...
Aleksandr Viktorovich Karaulov, Irina Valentinovna Sidorenko, Vladimir Vladimirovich Androsov, Anna Sergeevna Kapustina, A V Karaulov, I V Sidorenko, V V Androsov, A S Kapustina   +7 more
doaj  

Castleman Disease in a Patient with Common Variable Immunodeficiency

Case Reports in Immunology, 2019
Common variable immunodeficiency (CVID) is a primary immunodeficiency due to a disorder of the adaptive immune system which causes hypogammaglobulinemia and therefore an increased susceptibility to infection; noninfectious, inflammatory conditions ...
Luisa Ricciardi, Fabiana Furci, Antonio Ieni, Antonio Macrì   +3 more
doaj   +1 more source

Improvement of common variable immunodeficiency using embryonic stem cell therapy in a patient with lyme disease: a clinical case report

Clinical Case Reports, 2018
Key Clinical Message Bone marrow transplantation and stem cell therapies have been used for the treatment of common variable immunodeficiency (CVID) and other life‐threatening medical disorders.
Richard Horowitz, Phyllis R. Freeman
doaj   +1 more source

Common variable immunodeficiency (CVID) with granulomatous interstitial lung disease (GLILD) and SARS COVID-19 infection: case report and review of literature. [PDF]

Allergy Asthma Clin Immunol, 2021
Pattanaik D, Ritter S, Fahhoum J.
europepmc   +2 more sources