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

Authors :
Zehner M
Alt M
Ashurov A
Goldsmith JA
Spies R
Weiler N
Lerma J
Gieselmann L
Stöhr D
Gruell H
Schultz EP
Kreer C
Schlachter L
Janicki H
Laib Sampaio K
Stegmann C
Nemetchek MD
Dähling S
Ullrich L
Dittmer U
Witzke O
Koch M
Ryckman BJ
Lotfi R
McLellan JS
Krawczyk A
Sinzger C
Klein F
Source :
Immunity [Immunity] 2023 Nov 14; Vol. 56 (11), pp. 2602-2620.e10.
Publication Year :
2023

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 UL <subscript>128/130/131A</subscript> 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.<br />Competing Interests: Declaration of interests A patent application encompassing aspects of this work has been filed by the University of Cologne, the University of Ulm, and the University of Duisburg-Essen, listing F.K., C. Sinzger, A.K., M.Z., and M.A. as inventors.<br /> (Copyright © 2023 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4180
Volume :
56
Issue :
11
Database :
MEDLINE
Journal :
Immunity
Publication Type :
Academic Journal
Accession number :
37967532
Full Text :
https://doi.org/10.1016/j.immuni.2023.10.009