tetano
Editor, Senior Moderator
Front Immunol
. 2022 Oct 13;13:980698.
doi: 10.3389/fimmu.2022.980698. eCollection 2022.
Long-term cellular immune response in immunocompromised unvaccinated COVID-19 patients undergoing monoclonal antibody treatment
Laura Thümmler[SUP] 1 2 [/SUP], Margarethe Konik[SUP] 1 [/SUP], Monika Lindemann[SUP] 2 [/SUP], Neslinur Fisenkci[SUP] 2 [/SUP], Michael Koldehoff[SUP] 3 4 [/SUP], Anja Gäckler[SUP] 5 [/SUP], Peter A Horn[SUP] 2 [/SUP], Fotis Theodoropoulos[SUP] 6 [/SUP], Christian Taube[SUP] 6 [/SUP], Markus Zettler[SUP] 1 [/SUP], Olympia Evdoxia Anastasiou[SUP] 7 [/SUP], Peer Braß[SUP] 1 [/SUP], Sarah Jansen[SUP] 1 [/SUP], Oliver Witzke[SUP] 1 [/SUP], Hana Rohn[SUP] 1 [/SUP], Adalbert Krawczyk[SUP] 1 7 [/SUP]
Affiliations
Abstract
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.
Keywords: COVID-19; SARS-CoV-2; cellular immune response; immunosuppression; monoclonal antibody treatment.
. 2022 Oct 13;13:980698.
doi: 10.3389/fimmu.2022.980698. eCollection 2022.
Long-term cellular immune response in immunocompromised unvaccinated COVID-19 patients undergoing monoclonal antibody treatment
Laura Thümmler[SUP] 1 2 [/SUP], Margarethe Konik[SUP] 1 [/SUP], Monika Lindemann[SUP] 2 [/SUP], Neslinur Fisenkci[SUP] 2 [/SUP], Michael Koldehoff[SUP] 3 4 [/SUP], Anja Gäckler[SUP] 5 [/SUP], Peter A Horn[SUP] 2 [/SUP], Fotis Theodoropoulos[SUP] 6 [/SUP], Christian Taube[SUP] 6 [/SUP], Markus Zettler[SUP] 1 [/SUP], Olympia Evdoxia Anastasiou[SUP] 7 [/SUP], Peer Braß[SUP] 1 [/SUP], Sarah Jansen[SUP] 1 [/SUP], Oliver Witzke[SUP] 1 [/SUP], Hana Rohn[SUP] 1 [/SUP], Adalbert Krawczyk[SUP] 1 7 [/SUP]
Affiliations
- PMID: 36311723
- PMCID: PMC9606643
- DOI: 10.3389/fimmu.2022.980698
Abstract
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.
Keywords: COVID-19; SARS-CoV-2; cellular immune response; immunosuppression; monoclonal antibody treatment.