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A potent and protective human neutralizing antibody targeting a novel vulnerable site of Epstein-Barr virus.
- Source :
-
Nature communications [Nat Commun] 2021 Nov 16; Vol. 12 (1), pp. 6624. Date of Electronic Publication: 2021 Nov 16. - Publication Year :
- 2021
-
Abstract
- Epstein-Barr virus (EBV) is associated with a range of epithelial and B cell malignancies as well as autoimmune disorders, for which there are still no specific treatments or effective vaccines. Here, we isolate EBV gH/gL-specific antibodies from an EBV-infected individual. One antibody, 1D8, efficiently neutralizes EBV infection of two major target cell types, B cells and epithelial cells. In humanized mice, 1D8 provides protection against a high-dose EBV challenge by substantially reducing viral loads and associated tumor burden. Crystal structure analysis reveals that 1D8 binds to a key vulnerable interface between the D-I/D-II domains of the viral gH/gL protein, especially the D-II of the gH, thereby interfering with the gH/gL-mediated membrane fusion and binding to target cells. Overall, we identify a potent and protective neutralizing antibody capable of reducing the EBV load. The novel vulnerable site represents an attractive target that is potentially important for antibody and vaccine intervention against EBV infection.<br /> (© 2021. The Author(s).)
- Subjects :
- Animals
Antibodies, Neutralizing chemistry
B-Lymphocytes immunology
Crystallography, X-Ray
Epithelial Cells immunology
Epitopes
Epstein-Barr Virus Infections virology
Glycoproteins chemistry
Humans
Membrane Fusion
Mice
Nerve Tissue Proteins chemistry
Viral Proteins metabolism
Virus Replication
Antibodies, Neutralizing immunology
Antibodies, Viral immunology
Epstein-Barr Virus Infections immunology
Herpesvirus 4, Human immunology
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 34785638
- Full Text :
- https://doi.org/10.1038/s41467-021-26912-6