| Literature DB >> 32817957 |
Lauren B Rodda, Jason Netland, Laila Shehata, Kurt B Pruner, Peter M Morawski, Christopher Thouvenel, Kennidy K Takehara, Julie Eggenberger, Emily A Hemann, Hayley R Waterman, Mitchell L Fahning, Yu Chen, Jennifer Rathe, Caleb Stokes, Samuel Wrenn, Brooke Fiala, Lauren P Carter, Jessica A Hamerman, Neil P King, Michael Gale, Daniel J Campbell, David Rawlings, Marion Pepper.
Abstract
The recently emerged SARS-CoV-2 virus is currently causing a global pandemic and cases continue to rise. The majority of infected individuals experience mildly symptomatic coronavirus disease 2019 (COVID-19), but it is unknown whether this can induce persistent immune memory that might contribute to herd immunity. Thus, we performed a longitudinal assessment of individuals recovered from mildly symptomatic COVID-19 to determine if they develop and sustain immunological memory against the virus. We found that recovered individuals developed SARS-CoV-2-specific IgG antibody and neutralizing plasma, as well as virus-specific memory B and T cells that not only persisted, but in some cases increased numerically over three months following symptom onset. Furthermore, the SARS-CoV-2-specific memory lymphocytes exhibited characteristics associated with potent antiviral immunity: memory T cells secreted IFN-γ and expanded upon antigen re-encounter, while memory B cells expressed receptors capable of neutralizing virus when expressed as antibodies. These findings demonstrate that mild COVID-19 elicits memory lymphocytes that persist and display functional hallmarks associated with antiviral protective immunity.Entities:
Year: 2020 PMID: 32817957 PMCID: PMC7430599 DOI: 10.1101/2020.08.11.20171843
Source DB: PubMed Journal: medRxiv