Navigating SARS-CoV-2-related immunopathology in Crohn's disease: from molecular mechanisms to therapeutic challenges

Virol J. 2024 Nov 13;21(1):288. doi: 10.1186/s12985-024-02529-1.

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) not only posed major health and economic burdens to international societies but also threatens patients with comorbidities and underlying autoimmune disorders, including Crohn's disease (CD) patients. As the vaccinated population is gradually relieved from the stress of the latest omicron variant of SARS-CoV-2 due to competent immune responses, the anxiety of CD patients, especially those on immunosuppressive treatment, has not subsided. Whether the use of immunosuppressants for remission of CD outweighs the potential risk of severe coronavirus disease 2019 (COVID-19) has long been discussed. Thus, for the best benefit of CD patients, our primary goal in this study was to navigate the clinical management of CD during the COVID pandemic. Herein, we summarized COVID-19 outcomes of CD patients treated with immunosuppressive agents from multiple cohort studies and also investigated possible mechanisms of how SARS-CoV-2 impacts the host immunity with special consideration of CD patients. We first looked into the SARS-CoV-2-related immunopathology, including lymphocytopenia, T-cell exhaustion, cytokine storms, and their possible molecular interactions, and then focused on mechanistic actions of gastrointestinal systems, including interruption of tryptophan absorption, development of dysbiosis, and consequent local and systemic inflammation. Given challenges in managing CD, we summarized up-to-date clinical and molecular evidence to help physicians adjust therapeutic strategies to achieve the best clinical outcomes for CD patients.

Keywords: Crohn’s disease; Immunosuppressive treatment; SARS-CoV-2.

Publication types

  • Review

MeSH terms

  • COVID-19* / immunology
  • Crohn Disease* / drug therapy
  • Crohn Disease* / immunology
  • Cytokine Release Syndrome / drug therapy
  • Cytokine Release Syndrome / immunology
  • Humans
  • Immunosuppressive Agents* / therapeutic use
  • Lymphopenia / immunology
  • SARS-CoV-2* / immunology

Substances

  • Immunosuppressive Agents