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Primary immunodeficiency [PDF]

open access: yesAllergy, Asthma & Clinical Immunology, 2018
Primary immunodeficiency disorder (PID) refers to a large heterogeneous group of disorders that result from defects in immune system development and/or function.
C. Mccusker, J. Upton, R. Warrington
semanticscholar   +5 more sources

Primary immunodeficiency: common variable immunodeficiency [PDF]

open access: yesĶazaķstannyṇ Klinikalyķ Medicinasy, 2016
By definition, primary immunodeficiencies are genetically determined diseases, which are fundamental molecular or organic defects associated with impaired immune responses, in this case there is the clinic of infectious and autoimmune diseases, with an ...
Oksana Ussenova   +3 more
doaj   +2 more sources

Research on Rare Diseases in Germany – The GAIN Registry: a registry for individuals with congenital multi-organ autoimmune diseases [PDF]

open access: yesJournal of Health Monitoring, 2023
Background: Patient registries are an important tool for networking medical caregivers and research, especially in the field of rare diseases. Individuals afflicted by multi-organ autoimmune diseases typically suffer from inflammation of multiple organs.
Cynthia Stapornwongkul   +10 more
doaj   +1 more source

Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study

open access: yesFrontiers in Immunology, 2021
Predominantly antibody deficiencies (PAD) are a heterogeneous group of disorders characterized by dysfunctional antibody production, low immunoglobulin levels in serum and impaired vaccine responses.
Jessica Rojas-Restrepo   +31 more
doaj   +1 more source

From Flies to Men: ROS and the NADPH Oxidase in Phagocytes

open access: yesFrontiers in Cell and Developmental Biology, 2021
The cellular formation of reactive oxygen species (ROS) represents an evolutionary ancient antimicrobial defense system against microorganisms. The NADPH oxidases (NOX), which are predominantly localized to endosomes, and the electron transport chain in ...
Zohreh Mansoori Moghadam   +4 more
doaj   +1 more source

Monocyte progenitors give rise to multinucleated giant cells

open access: yesNature Communications, 2021
Multinucleated giant cells characterize granuloma formation in mycobacterial infections. Here the authors identify monocyte precursors with distinct immunological and metabolic properties as a source of the granuloma multinucleated giant cell compartment.
Anne Kathrin Lösslein   +18 more
doaj   +1 more source

Impact of IL-15 and latency reversing agent combinations in the reactivation and NK cell-mediated suppression of the HIV reservoir

open access: yesScientific Reports, 2022
Inhibitors of histone deacetylases (HDACis) are major latency reversing agent (LRA) candidates in ‘shock and kill’ strategies to eradicate the HIV reservoir in infected patients.
Daniela Angela Covino   +2 more
doaj   +1 more source

Intra-Household and Close-Contact SARS-CoV-2 Transmission Among Children – a Systematic Review

open access: yesFrontiers in Pediatrics, 2021
Introduction: The outbreak of the novel coronavirus disease (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to a range of emergency measures worldwide. Early in the pandemic, children were suspected to act as
Benedikt D. Spielberger   +7 more
doaj   +1 more source

Combined immunodeficiencies

open access: yesJornal de Pediatria, 2021
Inborn Errors of Immunity (IEI), also known as primary immunodeficiencies, correspond to a heterogeneous group of congenital diseases that primarily affect immune response components. The main clinical manifestations comprise increased susceptibility to infections, autoimmunity, inflammation, allergies and malignancies.
Carolina Sanchez Aranda   +2 more
openaire   +5 more sources

Adoptive T cell therapy cures mice from active hemophagocytic lymphohistiocytosis (HLH)

open access: yesEMBO Molecular Medicine, 2022
Primary hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome caused by impaired lymphocyte cytotoxicity. First‐line therapeutic regimens directed against activated immune cells or secreted cytokines show limited efficacy since they do
Kristoffer Weißert   +7 more
doaj   +1 more source

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