SARS‐CoV‐2 memory B and T cell profiles in mild COVID‐19 convalescent patients. (February 2022)
- Record Type:
- Journal Article
- Title:
- SARS‐CoV‐2 memory B and T cell profiles in mild COVID‐19 convalescent patients. (February 2022)
- Main Title:
- SARS‐CoV‐2 memory B and T cell profiles in mild COVID‐19 convalescent patients
- Authors:
- Gurevich, Michael
Zilkha-Falb, Rina
Sonis, Polina
Magalashvili, David
Menascu, Shay
Flechter, Shlomo
Dolev, Mark
Mandel, Mathilda
Achiron, Anat - Abstract:
- Highlights: COVID-19 convalescents displayed an adaptive immune response for up to 7 months. The T cell response is characterized by IFN-γ-, IL2-, and IFN-γ+IL2-secreting memory T cells. Waning anti-SARS-CoV-2 IgG is associated with robust memory B cell and memory T cell responses. The SNMO peptide pools elicited the strongest memory T cell response. Abstract: Objectives: Antiviral adaptive immunity involves memory B cells (MBC) and memory T cells (MTC). The dynamics of MBC and MTC in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) convalescents warrant further investigation. Methods: In this cross-sectional and longitudinal study, blood-derived MBC and MTC responses were evaluated in 68 anti-spike IgG-positive mild coronavirus disease 2019 (COVID-19) convalescents at visit 1, between 1 and 7 months (median 4.1 months) after disease onset. SARS-CoV-2 anti-spike IgG was determined by ELISA, MBC by SARS-CoV-2-specific receptor binding domain (RBD) ELISpot, and interferon gamma (IFN-γ)-, interleukin 2 (IL2)-, and IFN-γ+IL2-secreting MTC by IFN-γ and IL2 SARS-CoV-2 FluoroSpot. For 24 patients sampled at the first visit, the IgG, MBC, and MTC analyses were also performed 3 months later at the second visit. Results: Seventy-two percent of convalescents were both MBC- and MTC-positive, 18% were MBC-positive and MTC-negative, and 10% were MTC-positive and MBC-negative. The peak MBC response level was detected at 3 months after COVID-19 onset and persisted up to 7 monthsHighlights: COVID-19 convalescents displayed an adaptive immune response for up to 7 months. The T cell response is characterized by IFN-γ-, IL2-, and IFN-γ+IL2-secreting memory T cells. Waning anti-SARS-CoV-2 IgG is associated with robust memory B cell and memory T cell responses. The SNMO peptide pools elicited the strongest memory T cell response. Abstract: Objectives: Antiviral adaptive immunity involves memory B cells (MBC) and memory T cells (MTC). The dynamics of MBC and MTC in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) convalescents warrant further investigation. Methods: In this cross-sectional and longitudinal study, blood-derived MBC and MTC responses were evaluated in 68 anti-spike IgG-positive mild coronavirus disease 2019 (COVID-19) convalescents at visit 1, between 1 and 7 months (median 4.1 months) after disease onset. SARS-CoV-2 anti-spike IgG was determined by ELISA, MBC by SARS-CoV-2-specific receptor binding domain (RBD) ELISpot, and interferon gamma (IFN-γ)-, interleukin 2 (IL2)-, and IFN-γ+IL2-secreting MTC by IFN-γ and IL2 SARS-CoV-2 FluoroSpot. For 24 patients sampled at the first visit, the IgG, MBC, and MTC analyses were also performed 3 months later at the second visit. Results: Seventy-two percent of convalescents were both MBC- and MTC-positive, 18% were MBC-positive and MTC-negative, and 10% were MTC-positive and MBC-negative. The peak MBC response level was detected at 3 months after COVID-19 onset and persisted up to 7 months post infection. Significant MTC levels were detected 1 month after onset in response to S1, S2_N, and SNMO peptide pools. The frequency and magnitude of the MTC response to SNMO was higher than those to S1 and S2_N. Longitudinal analysis demonstrated that even when specific humoral immunity declined, the cellular immunity persisted. Conclusions: The study findings demonstrate the durability of adaptive cellular immunity at least for 7 months after SARS-CoV-2 infection, suggesting long-lasting protection. … (more)
- Is Part Of:
- International journal of infectious diseases. Volume 115(2022)
- Journal:
- International journal of infectious diseases
- Issue:
- Volume 115(2022)
- Issue Display:
- Volume 115, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 115
- Issue:
- 2022
- Issue Sort Value:
- 2022-0115-2022-0000
- Page Start:
- 208
- Page End:
- 214
- Publication Date:
- 2022-02
- Subjects:
- SARS-CoV-2 -- Convalescents -- Memory B cells -- Memory T cells -- IgG
SARS-CoV-2 severe acute respiratory syndrome coronavirus 2 -- MBC memory B cells -- MTC memory T cells -- COVID-19 coronavirus disease 2019 -- IgG immunoglobulin G -- RBD receptor binding domain -- SFU spot-forming units -- IFN-γ interferon gamma -- IL2 interleukin 2
Communicable diseases -- Periodicals
Communicable Diseases -- Periodicals
Communicable diseases
Periodicals
Electronic journals
616.9 - Journal URLs:
- http://bibpurl.oclc.org/web/73769 ↗
http://www.journals.elsevier.com/international-journal-of-infectious-diseases/ ↗
http://www.sciencedirect.com/science/journal/12019712 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/12019712 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/12019712 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ijid.2021.12.309 ↗
- Languages:
- English
- ISSNs:
- 1201-9712
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.304750
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20348.xml