Lowrey Peyton

ORCID: 0009-0004-0933-758X
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About
Contact & Profiles
Research Areas
  • SARS-CoV-2 and COVID-19 Research
  • Immunotherapy and Immune Responses
  • vaccines and immunoinformatics approaches
  • Herpesvirus Infections and Treatments
  • Monoclonal and Polyclonal Antibodies Research
  • Galectins and Cancer Biology
  • Influenza Virus Research Studies
  • Immune responses and vaccinations
  • COVID-19 Clinical Research Studies

National Institutes of Health
2022-2024

Dartmouth Hospital
2024

Dartmouth College
2024

National Institute of Allergy and Infectious Diseases
2022-2023

An important consequence of infection with a SARS-CoV-2 variant is protective humoral immunity against other variants. However, the basis for such cross-protection at molecular level incompletely understood. Here, we characterized repertoire and epitope specificity antibodies elicited by Beta, Gamma WA1 ancestral variants assessed their cross-reactivity to these more recent Delta Omicron We developed method obtain immunoglobulin sequences concurrent rapid production functional assessment...

10.1038/s41467-022-35456-2 article EN cc-by Nature Communications 2022-12-14

Abstract As SARS-CoV-2 variants continue evolving, testing updated vaccines in non-human primates remains important for guiding human clinical practice. To date, such studies have focused on antibody titers and antigen-specific B T cell frequencies. Here, we extend our understanding by integrating innate adaptive immune responses to mRNA-1273 vaccination rhesus macaques. We sorted cells from a pre-vaccine time point, as well peripheral two weeks after each of vaccine doses used single-cell...

10.1038/s41467-023-43420-x article EN cc-by Nature Communications 2023-12-02

SUMMARY Broadly neutralizing antibodies (bNAbs) targeting the HIV-1 CD4-binding site (CD4bs) occur infrequently in macaques and humans have not been reproducibly elicited any outbred animal model. To address this challenge, we first isolated RHA10, an infection-induced rhesus bNAb with 51% breadth. The cryo-EM structure of RHA10 envelope (Env) resembled prototypic human CD4bs bNAbs CDR-H3-dominated binding. Env-antibody co-evolution revealed transient elimination two Env CD4bs-proximal...

10.1101/2024.12.30.630768 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-12-31

An important consequence of infection with a SARS-CoV-2 variant is protective humoral immunity against other variants. The basis for such cross-protection at the molecular level incompletely understood. Here we characterized repertoire and epitope specificity antibodies elicited by Beta, Gamma ancestral assessed their cross-reactivity to these more recent Delta Omicron We developed high-throughput approach obtain immunoglobulin sequences produce monoclonal functional assessment from single B...

10.1101/2022.03.28.486152 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-03-29
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