Literature DB >> 32676618

D614G Spike Variant Does Not Alter IgG, IgM, or IgA Spike Seroassay Performance.

Carleen Klumpp-Thomas, Heather Kalish, Jennifer Hicks, Jennifer Mehalko, Matthew Drew, Matthew J Memoli, Matthew D Hall, Dominic Esposito, Kaitlyn Sadtler.   

Abstract

Emergence of a new variant of spike protein (D614G) with increased infectivity and transmissibility has prompted many to analyze the potential role of this variant in the SARS-CoV-2 pandemic. When a new variant emerges, there is a concern regarding whether an individual exposed to one variant of a virus will have cross-reactive immune memory to the second variant. Accordingly, we analyzed the serologic reactivity of D614 (original) and G614 variant spike proteins. We found that antibodies from a high-incidence population in New York City reacted both toward the original D614 spike and the G614 spike variant. These data suggest that patients who have been exposed to either SARS-CoV-2 variant have humoral immunity that can respond against both variants. This is an important finding both for SARS-CoV-2 disease biology and for potential antibody-based therapeutics.

Entities:  

Year:  2020        PMID: 32676618      PMCID: PMC7359543          DOI: 10.1101/2020.07.08.20147371

Source DB:  PubMed          Journal:  medRxiv


  2 in total

Review 1.  Polyclonal hyper immunoglobulin: A proven treatment and prophylaxis platform for passive immunization to address existing and emerging diseases.

Authors:  Tharmala Tharmalingam; Xiaobing Han; Ashley Wozniak; Laura Saward
Journal:  Hum Vaccin Immunother       Date:  2021-05-19       Impact factor: 4.526

2.  Rapid, inexpensive methods for exploring SARS CoV-2 D614G mutation.

Authors:  Sirwan M A Al-Jaf; Sherko S Niranji; Zana H Mahmood
Journal:  Meta Gene       Date:  2021-07-18
  2 in total

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