Publications by authors named "J P Dessaint"

Article Synopsis
  • Recent research has advanced our understanding of SARS-CoV-2 and antibody responses, but the detailed composition of circulating antibodies remains largely unexplored.
  • A study using Ig-Seq analyzed the antibody profiles specific to SARS-CoV-2's spike protein and its receptor binding domain in four subjects over six months after infection, revealing that about 50% of RBD-specific IgG did not recognize the spike protein in its stabilized form.
  • The study also evaluated monoclonal antibodies from infected individuals, finding that while some neutralized the virus, others showed limited binding to different variants, highlighting the complexities of the immune response to SARS-CoV-2.
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Data on adverse events from research bronchoscopy with bronchoalveolar lavage (BAL) in patients with cystic fibrosis (CF) is lacking. As research bronchoscopy with BAL is useful for isolation of immune cells and investigation of CF lung microbiome, we sought to investigate the safety of bronchoscopy in adult patients with CF. Between November 2016 and September 2019, we performed research bronchoscopies on CF subjects (32) and control subjects (82).

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Various pathogens use differing strategies to evade host immune response including modulating the host's epigenome. Here, we investigate if EVs secreted from alter DNA methylation in human lung macrophages, thereby potentially contributing to a dysfunctional innate immune response. Using a genome-wide DNA methylation approach, we demonstrate that EVs alter certain host cell DNA methylation patterns.

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, a Gram-negative bacterium, is one of the most common pathogens colonizing the lungs of cystic fibrosis patients. secrete extracellular vesicles (EVs) that contain LPS and other virulence factors that modulate the host's innate immune response, leading to an increased local proinflammatory response and reduced pathogen clearance, resulting in chronic infection and ultimately poor patient outcomes. Lung macrophages are the first line of defense in the airway innate immune response to pathogens.

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Cystic fibrosis (CF) is a genetic disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, resulting in chronic bacterial lung infections and tissue damage. CF macrophages exhibit reduced bacterial killing and increased inflammatory signaling. Iron is elevated in the CF lung and is a critical nutrient for bacteria, including the common CF pathogen Pseudomonas aeruginosa (Pa).

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