Publications by authors named "Art Marzok"

Neutralizing antibodies are known to have a crucial role in protecting against SARS-CoV-2 infection and have been suggested to be a useful correlate of protection for vaccine clinical trials and for population-level surveys. In addition to neutralizing virus directly, antibodies can also engage immune effectors through their Fc domains, including Fc receptor-expressing immune cells and complement. The outcome of these interactions depends on a range of factors, including antibody isotype-Fc receptor combinations, Fc receptor-bearing cell types and antibody post-translational modifications.

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Vaccination route dictates the quality and localization of immune responses within tissues. Intranasal vaccination seeds tissue-resident adaptive immunity, alongside trained innate responses within the lung/airways, critical for superior protection against SARS-CoV-2. This protocol encompasses intranasal vaccination in mice, step-by-step bronchoalveolar lavage for both cellular and acellular airway components, lung mononuclear cell isolation, and detailed flow cytometric characterization of lung tissue-resident memory T cell responses, and airway macrophage-trained innate immunity.

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Article Synopsis
  • - The study reveals that type I interferons (IFNs) are crucial for controlling viral infections and preventing excessive tissue damage, known as immunopathology, which can worsen disease outcomes.
  • - Researchers found that when the type I IFN receptor is absent, severe immunopathology occurs after viral infections due to macrophages and IL-6, and inhibiting these can reduce tissue damage.
  • - The research highlights that macrophage-derived matrix metalloproteinases (MMPs) are involved in tissue destruction during viral infections, suggesting that targeting MMPs could be a potential treatment strategy.
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The compounding challenges of low signal, high background, and uncertain targets plague many metagenomic sequencing efforts. One solution has been DNA capture, wherein probes are designed to hybridize with target sequences, enriching them in relation to their background. However, balancing probe depth with breadth of capture is challenging for diverse targets.

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Article Synopsis
  • - The current COVID-19 vaccines may be less effective against emerging SARS-CoV-2 variants, highlighting the need for new vaccine approaches.
  • - Research using adenoviral vectors has shown that an intranasal vaccine, especially one based on chimpanzee adenoviruses, produces stronger immunity compared to traditional intramuscular shots.
  • - This intranasal method effectively triggers broad immune responses and offers protection against both the original virus and new variants, suggesting it could be a promising strategy for future COVID-19 vaccines.
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Background: Although influenza vaccines provide protection against influenza viruses, concern has been raised that they may increase susceptibility to non-influenza respiratory viruses. As pandemic lockdowns end, temporal overlap of circulation of seasonal influenza viruses and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is expected. Understanding the impact of influenza vaccination on risk of coronavirus infection is therefore of considerable public health importance.

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