Staphylococcus aureus infection and persistence in chronic rhinosinusitis: Focus on leukocidin ED

Dimitri Poddighe, Luca Vangelista

Research output: Contribution to journalReview articlepeer-review

29 Citations (Scopus)

Abstract

Chronic rhinosinusitis (CRS) is thought to be a multifactorial disease that includes a direct involvement of bacteria that trigger inflammation and contribute to CRS pathogenesis. Staphylococcus aureus infection and persistence is associated with chronic rhinosinusitis (CRS), and it may be particularly relevant in the form with nasal polyps (CRSwNP). The large array of exotoxins deployed by S. aureus is instrumental for the bacterium to warrant its infection and dissemination in different human body districts. Here, we analyze the common Th2 environment in CRSwNP and prospect a possible dynamic role played by S. aureus leukocidins in promoting this chronic inflammation, considering leukocidin ED (LukED) as a strong prototype candidate worth of therapeutic investigation. CCR5 is an essential target for LukED to exert its cytotoxicity towards T cells, macrophages and dendritic cells. Therefore, CCR5 blockade might be an interesting therapeutic option for CRS and, more specifically, persistent and relapsing CRSwNP. In this perspective, the arsenal of CCR5 antagonists being developed to inhibit HIV-1 entry (CCR5 being the major HIV-1 co-receptor) could be easily repurposed for CRS therapeutic investigation. Finally, direct targeting of LukED by neutralizing antibodies could represent an important additional solution to S. aureus infection.

Original languageEnglish
Article number678
JournalToxins
Volume12
Issue number11
DOIs
Publication statusPublished - Oct 28 2020

Funding

Funding: This research was funded by the Ministry of Education and Science of the Republic of Kazakhstan (AP05134810).

Keywords

  • CCR5
  • Chronic rhinosinusitis (CRS)
  • LukED
  • Nasal polyps
  • Persistent infection
  • Staphylococcus aureus

ASJC Scopus subject areas

  • Toxicology
  • Health, Toxicology and Mutagenesis

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