Target intelligence / Profile preview

HSV-2 glycoprotein D (gD2)

Target
gD2
Molecular classification
Viral glycoprotein (gD, gB, gC, gE, etc.), Capsid protein, Tegument protein, Non-glycosylated infected cell protein (e.g., ICP0, ICP8, RR-1), Other
01

Overview

HSV-2 antigens are a group of viral proteins from Herpes simplex virus type 2 that elicit host immune responses; the most clinically studied are the surface glycoproteins, especially glycoprotein D (gD), which is central to virus entry and a primary target of neutralizing antibodies and vaccine design[1][2]. Other important antigens include glycoprotein B (gB), critical for viral fusion and entry[5]; glycoprotein E (gE), involved in immune evasion by binding IgG Fc regions[3]; capsid and tegument proteins; and various non-glycosylated viral proteins present in infected cells. The breadth of antigens targeted by humoral and cellular immunity influences the effectiveness of vaccines and naturally acquired immunity. The precise selection and breadth of these antigens matters for vaccine efficacy and immune protection[1][2][5]. This entry should be split into specific antigen targets (e.g., "HSV-2 glycoprotein D" or "HSV-2 glycoprotein B") for structured databases, as "HSV-2 antigens" is too broad and imprecise for a canonical therapeutic target.

Other names
HSV-2 surface antigensHSV-2 viral antigensHSV2 gDHSV2 gBHSV2 gEHSV2 gC
02

Mechanism of action

Vaccine and antibody candidates: blockade of viral entry by neutralizing antibody binding to gD/gB, preventing viral attachment and fusion; some target gE to block immune evasion mechanisms.

03

Biological functions

Virus entry (especially gD, gB)Immune evasion (e.g., gE binds IgG Fc for immune evasion)Induction of adaptive immune responseViral replication (infected cell proteins)
04

Disease associations

InfectionImmune evasionPathogen-related inflammation
05

Safety considerations

Immune responses to subunit vaccines (e.g., gD alone) may not confer broad protection due to type-specific antigenic differences or immune evasion strategiesImmune enhancement or autoimmunity is a theoretical risk but not a significant safety concern in clinical HSV vaccines to date
06

Interacting drugs

Acyclovir, valacyclovir, famciclovir (antivirals; not direct antigen binding but inhibit viral replication)

1 more in the full profile.

07

Biomarkers

Serological detection of HSV-2-specific antibodies (anti-gD, anti-gB, or anti-ICP antibodies) for infection status and vaccine response

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