Your browser doesn't support javascript.
Functional SARS-CoV-2-specific immune memory persists after mild COVID-19.
Rodda, Lauren B; Netland, Jason; Shehata, Laila; Pruner, Kurt B; Morawski, Peter A; Thouvenel, Chris; Takehara, Kennidy K; Eggenberger, Julie; Hemann, Emily; Waterman, Hayley R; Fahning, Mitchell L; Chen, Yu; Rathe, Jennifer; Stokes, Caleb; Wrenn, Samuel; Fiala, Brooke; Carter, Lauren; Hamerman, Jessica A; King, Neil P; Gale, Michael; Campbell, Daniel J; Rawlings, David; Pepper, Marion.
  • Rodda LB; Department of Immunology, University of Washington School of Medicine, Seattle, WA, USA.
  • Netland J; These authors contributed equally.
  • Shehata L; Department of Immunology, University of Washington School of Medicine, Seattle, WA, USA.
  • Pruner KB; These authors contributed equally.
  • Morawski PA; Department of Immunology, University of Washington School of Medicine, Seattle, WA, USA.
  • Thouvenel C; These authors contributed equally.
  • Takehara KK; Department of Immunology, University of Washington School of Medicine, Seattle, WA, USA.
  • Eggenberger J; These authors contributed equally.
  • Hemann E; Center for Fundamental Immunology, Benaroya Research Institute, Seattle, WA, USA.
  • Waterman HR; These authors contributed equally.
  • Fahning ML; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA and Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.
  • Chen Y; Department of Immunology, University of Washington School of Medicine, Seattle, WA, USA.
  • Rathe J; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA, USA.
  • Stokes C; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA, USA.
  • Wrenn S; Center for Fundamental Immunology, Benaroya Research Institute, Seattle, WA, USA.
  • Fiala B; Center for Fundamental Immunology, Benaroya Research Institute, Seattle, WA, USA.
  • Carter L; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA and Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, USA.
  • Hamerman JA; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA, USA.
  • King NP; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA, USA.
  • Gale M; Department of Biochemistry, University of Washington, Seattle, WA, USA and Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Campbell DJ; Department of Biochemistry, University of Washington, Seattle, WA, USA and Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Rawlings D; Department of Biochemistry, University of Washington, Seattle, WA, USA and Institute for Protein Design, University of Washington, Seattle, WA, USA.
  • Pepper M; Department of Immunology, University of Washington School of Medicine, Seattle, WA, USA.
Res Sq ; 2020 Aug 13.
Article in English | MEDLINE | ID: covidwho-725304
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
See preprint
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.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Long Covid Language: English Year: 2020 Document Type: Article Affiliation country: Rs.3.rs-57112

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Long Covid Language: English Year: 2020 Document Type: Article Affiliation country: Rs.3.rs-57112