HSV-2 gE2/gI2 are immune evasion molecules that bind IgG Fc to inhibit antibody-dependent cellular cytotoxicity

We conclude that antibodies to gC2/gD2/gE2 are targets of ADCC, that gE2/gI2 inhibits ADCC, and that an mAb that targets the gE2 IgG Fc binding domain can prevent this inhibition.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-03-03
DOI
https://doi.org/10.3389/fimmu.2026.1766722
Primary Topic
Herpesvirus Infections and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

HSV-2 gE2/gI2 are immune evasion molecules that bind IgG Fc to inhibit antibody-dependent cellular cytotoxicity

Giulia Tebaldi, Tina M. Cairns, Kevin P. Egan, Lauren M. Hook et al.
Frontiers in Immunology
Herpesvirus Infections and Treatments
article

HSV-2 gE2/gI2 are immune evasion molecules that bind IgG Fc to inhibit antibody-dependent cellular cytotoxicity

Giulia Tebaldi, Tina M. Cairns, Kevin P. Egan, Lauren M. Hook, Tomas Bergström, Kerry S. Campbell, Harvey M. Friedman, Gary H. Cohen
article en

Abstract

We conclude that antibodies to gC2/gD2/gE2 are targets of ADCC, that gE2/gI2 inhibits ADCC, and that an mAb that targets the gE2 IgG Fc binding domain can prevent this inhibition.

Frontiers in ImmunologyVol. 17
Fox Chase Cancer Center (US), Temple University Health System (US), University of Pennsylvania (US), University of Gothenburg (SE)
University of Pennsylvania, National Institutes of Health, National Cancer Institute, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 37%
Herpesvirus Infections and Treatments
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