Case Report: A Peculiar Case of Inflammatory Colitis After SARS-CoV-2 Infection

Front Immunol. 2022 Feb 9:13:849140. doi: 10.3389/fimmu.2022.849140. eCollection 2022.

Abstract

We report a case of inflammatory colitis after SARS-CoV-2 infection in a patient with no additional co-morbidity who died within three weeks of hospitalization. As it is becoming increasingly clear that SARS-CoV-2 infection can cause immunological alterations, we investigated the expression of the inhibitory checkpoint PD-1 and its ligand PD-L1 to explore the potential role of this axis in the break of self-tolerance. The presence of the SARS-CoV-2 virus in colon tissue was demonstrated by qRT-PCR and immunohistochemical localization of the nucleocapsid protein. Expression of lymphocyte markers, PD-1, and PD-L1 in colon tissue was investigated by IHC. SARS-CoV-2-immunoreactive cells were detected both in the ulcerated and non-ulcerated mucosal areas. Compared to healthy tissue, where PD-1 is weakly expressed and PD-L1 is absent, PD-1 and PD-L1 expression appears in the inflamed mucosal tissue, as expected, but was mainly confined to non-ulcerative areas. At the same time, these markers were virtually undetectable in areas of mucosal ulceration. Our data show an alteration of the PD-1/PD-L1 axis and suggest a link between SARS-CoV-2 infection and an aberrant autoinflammatory response due to concomitant breakdown of the PD-1/PD-L1 interaction leading to early death of the patient.

Keywords: COVID-19; PD-1/PD-L1 axis; SARS-CoV-2; cytotoxic immune cells; necrotizing ulcerative colitis.

Publication types

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

MeSH terms

  • Aged
  • B7-H1 Antigen / metabolism
  • COVID-19 / immunology*
  • Colitis / immunology*
  • Colon / metabolism*
  • Colon / pathology
  • Cytokine Release Syndrome / immunology*
  • Fatal Outcome
  • Female
  • Humans
  • Inflammation / immunology*
  • Programmed Cell Death 1 Receptor / metabolism
  • SARS-CoV-2 / physiology*
  • Self Tolerance
  • Signal Transduction

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor