Eosinophils as potential biomarkers in respiratory viral infections

Front Immunol. 2023 Jul 6:14:1170035. doi: 10.3389/fimmu.2023.1170035. eCollection 2023.

Abstract

Eosinophils are bone marrow-derived granulocytes that, under homeostatic conditions, account for as much as 1-3% of peripheral blood leukocytes. During inflammation, eosinophils can rapidly expand and infiltrate inflamed tissues, guided by cytokines and alarmins (such as IL-33), adhesion molecules and chemokines. Eosinophils play a prominent role in allergic asthma and parasitic infections. Nonetheless, they participate in the immune response against respiratory viruses such as respiratory syncytial virus and influenza. Notably, respiratory viruses are associated with asthma exacerbation. Eosinophils release several molecules endowed with antiviral activity, including cationic proteins, RNases and reactive oxygen and nitrogen species. On the other hand, eosinophils release several cytokines involved in homeostasis maintenance and Th2-related inflammation. In the context of SARS-CoV-2 infection, emerging evidence indicates that eosinophils can represent possible blood-based biomarkers for diagnosis, prognosis, and severity prediction of disease. In particular, eosinopenia seems to be an indicator of severity among patients with COVID-19, whereas an increased eosinophil count is associated with a better prognosis, including a lower incidence of complications and mortality. In the present review, we provide an overview of the role and plasticity of eosinophils focusing on various respiratory viral infections and in the context of viral and allergic disease comorbidities. We will discuss the potential utility of eosinophils as prognostic/predictive immune biomarkers in emerging respiratory viral diseases, particularly COVID-19. Finally, we will revisit some of the relevant methods and tools that have contributed to the advances in the dissection of various eosinophil subsets in different pathological settings for future biomarker definition.

Keywords: COVID-19; IL-33; allergic asthma; biomarkers; eosinophils; respiratory virus infection.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma*
  • Biomarkers
  • COVID-19*
  • Cytokines / metabolism
  • Eosinophils
  • Humans
  • Inflammation
  • SARS-CoV-2 / metabolism
  • Viruses* / metabolism

Substances

  • Cytokines
  • Biomarkers

Grants and funding

This work was supported in part by AIRC (IG 21366) to GS, and by “Rome Technopole Foundation” (2022-2025, funded under the PNRR rules, project no. 3277, “Ecosistemi dell’Innovazione”, Mission 4 “Istruzione e Ricerca”, Component 2, Investment 1.5).