Frontiers in Immunology (Aug 2024)

Mucosal immunity in upper and lower respiratory tract to MERS-CoV

  • Khalid J. Shrwani,
  • Khalid J. Shrwani,
  • Waleed H. Mahallawi,
  • Abdulrhman I. Mohana,
  • Abdullah Algaissi,
  • Abdullah Algaissi,
  • Nabil Dhayhi,
  • Nouf J. Sharwani,
  • Eyad Gadour,
  • Eyad Gadour,
  • Saeed M. Aldossari,
  • Hasan Asiri,
  • Nader Kameli,
  • Ayad Y. Asiri,
  • Abdullah M. Asiri,
  • Alaa J. Sherwani,
  • Nigel Cunliffe,
  • Qibo Zhang

DOI
https://doi.org/10.3389/fimmu.2024.1358885
Journal volume & issue
Vol. 15

Abstract

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IntroductionMiddle East respiratory syndrome coronavirus (MERS-CoV) has emerged as a deadly pathogen with a mortality rate of up to 36.2%. MERS-CoV can cause severe respiratory tract disease and multiorgan failure. Therefore, therapeutic vaccines are urgently needed. This intensive review explores the human immune responses and their immunological mechanisms during MERS-CoV infection in the mucosa of the upper and lower respiratory tracts (URT and LRT, respectively).ObjectiveThe aim of this study is to provide a valuable, informative, and critical summary of the protective immune mechanisms against MERS-CoV infection in the URT/LRT for the purpose of preventing and controlling MERS-CoV disease and designing effective therapeutic vaccines.MethodsIn this review, we focus on the immune potential of the respiratory tract following MERS-CoV infection. We searched PubMed, Embase, Web of Science, Cochrane, Scopus, and Google Scholar using the following terms: “MERS-CoV”, “B cells”, “T cells”, “cytokines”, “chemokines”, “cytotoxic”, and “upper and lower respiratory tracts”.ResultsWe found and included 152 studies in this review. We report that the cellular innate immune response, including macrophages, dendritic cells, and natural killer cells, produces antiviral substances such as interferons and interleukins to prevent the virus from spreading. In the adaptive and humoral immune responses, CD4+ helper T cells, CD8+ cytotoxic T cells, B cells, and plasma cells protect against MERS-CoV infection in URT and LRT.ConclusionThe human nasopharynx-associated lymphoid tissue (NALT) and bronchus-associated lymphoid tissue (BALT) could successfully limit the spread of several respiratory pathogens. However, in the case of MERS-CoV infection, limited research has been conducted in humans with regard to immunopathogenesis and mucosal immune responses due to the lack of relevant tissues. A better understanding of the immune mechanisms of the URT and LRT is vital for the design and development of effective MERS-CoV vaccines.

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