Single-cell analysis of memory B cells from top neutralizers reveals multiple sites of vulnerability within HCMV Trimer and Pentamer. Academic Article uri icon

Overview

abstract

  • Human cytomegalovirus (HCMV) can cause severe diseases in fetuses, newborns, and immunocompromised individuals. Currently, no vaccines are approved, and treatment options are limited. Here, we analyzed the human B cell response of four HCMV top neutralizers from a cohort of 9,000 individuals. By single-cell analyses of memory B cells targeting the pentameric and trimeric HCMV surface complexes, we identified vulnerable sites on the shared gH/gL subunits as well as complex-specific subunits UL128/130/131A and gO. Using high-resolution cryogenic electron microscopy, we revealed the structural basis of the neutralization mechanisms of antibodies targeting various binding sites. Moreover, we identified highly potent antibodies that neutralized a broad spectrum of HCMV strains, including primary clinical isolates, that outperform known antibodies used in clinical trials. Our study provides a deep understanding of the mechanisms of HCMV neutralization and identifies promising antibody candidates to prevent and treat HCMV infection.

authors

  • Zehner, Matthias
  • Alt, Mira
  • Ashurov, Artem
  • Goldsmith, Jory A
  • Spies, Rebecca
  • Weiler, Nina
  • Lerma, Justin
  • Gieselmann, Lutz
  • Stöhr, Dagmar
  • Gruell, Henning
  • Schultz, Eric P
  • Kreer, Christoph
  • Schlachter, Linda
  • Janicki, Hanna
  • Laib Sampaio, Kerstin
  • Stegmann, Cora
  • Nemetchek, Michelle D
  • Dähling, Sabrina
  • Ullrich, Leon
  • Dittmer, Ulf
  • Witzke, Oliver
  • Koch, Manuel
  • Ryckman, Brent J
  • Lotfi, Ramin
  • McLellan, Jason S
  • Krawczyk, Adalbert
  • Sinzger, Christian
  • Klein, Florian

publication date

  • November 14, 2023

Research

keywords

  • Cytomegalovirus
  • Viral Envelope Proteins

Identity

Scopus Document Identifier

  • 85176143061

Digital Object Identifier (DOI)

  • 10.1016/j.immuni.2023.10.009

PubMed ID

  • 37967532

Additional Document Info

volume

  • 56

issue

  • 11