Results 21 to 30 of about 1,437,318 (308)

Review of current and future therapeutics in ABPA

open access: yesTherapeutic Advances in Chronic Disease, 2021
Allergic bronchopulmonary aspergillosis is an allergic pulmonary condition caused by hypersensitivity to antigens of Aspergillus sp. found most commonly in patients with underlying asthma or cystic fibrosis.
Elisa Lewington-Gower   +2 more
doaj   +1 more source

Signalling C-Type Lectins in Antimicrobial Immunity [PDF]

open access: yes, 2013
Funding: This work was funded by the Wellcome Trust, Medical Research Council and the University of Aberdeen. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Peer ...
Brown, Gordon D., Drummond, Rebecca A.
core   +11 more sources

Functional Characterization of Hexacorallia Phagocytic Cells

open access: yesFrontiers in Immunology, 2021
Phagocytosis is the cellular defense mechanism used to eliminate antigens derived from dysregulated or damaged cells, and microbial pathogens. Phagocytosis is therefore a pillar of innate immunity, whereby foreign particles are engulfed and degraded in ...
Grace A. Snyder   +9 more
doaj   +1 more source

Discriminating antigen and non-antigen using proteome dissimilarity II: viral and fungal antigens [PDF]

open access: yesBioinformation, 2010
Immunogenicity arises via many synergistic mechanisms, yet the overall dissimilarity of pathogenic proteins versus the host proteome has been proposed as a key arbiter. We have previously explored this concept in relation to Bacterial antigens; here we extend our analysis to antigens of viral and fungal origin.
Ramakrishnan, Kamna, Flower, Darren R
openaire   +3 more sources

Germline IgM predicts T cell immunity to Pneumocystis

open access: yesJCI Insight, 2022
Pneumocystis is the most common fungal pulmonary infection in children under the age of 5 years. In children with primary immunodeficiency, Pneumocystis often presents at 3–6 months of age, a time period that coincides with the nadir of maternal IgG and ...
Kristin Noell   +6 more
doaj   +1 more source

Novel Pneumocystis Antigen Discovery Using Fungal Surface Proteomics [PDF]

open access: yesInfection and Immunity, 2014
ABSTRACT Pneumonia due to the fungus Pneumocystis jirovecii is a life-threatening infection that occurs in immunocompromised patients. The inability to culture the organism as well as the lack of an annotated genome has hindered antigen discovery that could be useful in developing novel vaccine- or ...
Mingquan, Zheng   +4 more
openaire   +3 more sources

Identification of Disease-Associated Cryptococcal Proteins Reactive With Serum IgG From Cryptococcal Meningitis Patients

open access: yesFrontiers in Immunology, 2021
Cryptococcus neoformans, an opportunistic fungal pathogen ubiquitously present in the environment, causes cryptococcal meningitis (CM) mainly in immunocompromised patients, such as AIDS patients.
A. Elisabeth Gressler   +11 more
doaj   +1 more source

Allergic bronchopulmonary aspergillosis: diagnostic and treatment challenges [PDF]

open access: yes, 2016
Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary disorder, occurring mostly in asthmatic and cystic fibrosis patients, caused by an abnormal T-helper 2 lymphocyte response of the host to Aspergillus fumigatus antigens.
CINICOLA, BIANCA LAURA   +3 more
core   +1 more source

Therapies and Vaccines Based on Nanoparticles for the Treatment of Systemic Fungal Infections

open access: yesFrontiers in Cellular and Infection Microbiology, 2020
Treatment modalities for systemic mycoses are still limited. Currently, the main antifungal 18 therapeutics include polyenes, azoles, and echinocandins. However, even in the setting of 19 appropriate administration of antifungals, mortality rates remain ...
Brenda Kischkel   +5 more
semanticscholar   +1 more source

Aspergillus fumigatus preexposure worsens pathology and improves control of Mycobacterium abscessus pulmonary infection in mice [PDF]

open access: yes, 2018
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. Mutations in this chloride channel lead to mucus accumulation, subsequent recurrent pulmonary infections, and ...
Elsegeiny, Waleed   +7 more
core   +2 more sources

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