Frontiers in Immunology (Oct 2022)

Long-term cellular immune response in immunocompromised unvaccinated COVID-19 patients undergoing monoclonal antibody treatment

  • Laura Thümmler,
  • Laura Thümmler,
  • Margarethe Konik,
  • Monika Lindemann,
  • Neslinur Fisenkci,
  • Michael Koldehoff,
  • Michael Koldehoff,
  • Anja Gäckler,
  • Peter A. Horn,
  • Fotis Theodoropoulos,
  • Christian Taube,
  • Markus Zettler,
  • Olympia Evdoxia Anastasiou,
  • Peer Braß,
  • Sarah Jansen,
  • Oliver Witzke,
  • Hana Rohn,
  • Adalbert Krawczyk,
  • Adalbert Krawczyk

DOI
https://doi.org/10.3389/fimmu.2022.980698
Journal volume & issue
Vol. 13

Abstract

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Immunocompromised patients are at increased risk for a severe course of COVID-19. Treatment of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection with anti-SARS-CoV-2 monoclonal antibodies (mAbs) has become widely accepted. However, the effects of mAb treatment on the long-term primary cellular response to SARS-CoV-2 are unknown. In the following study, we investigated the long-term cellular immune responses to SARS-CoV-2 Spike S1, Membrane (M) and Nucleocapsid (N) antigens using the ELISpot assay in unvaccinated, mAb-treated immunocompromised high-risk patients. Anti-SARS-CoV-2 mAb untreated though vaccinated COVID-19 immunocompromised patients, vaccinated SARS-CoV-2 immunocompromised patients without COVID-19 and vaccinated healthy control subjects served as control groups. The cellular immune response was determined at a median of 5 months after SARS-CoV-2 infection. Our data suggest that immunocompromised patients develop an endogenous long-term cellular immune response after COVID-19, although at low levels. A better understanding of the cellular immune response will help guide clinical decision making for these vulnerable patient cohorts.

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