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Sudan ebolavirus antigens (SUDV antigens)

Target
SUDV antigens
Molecular classification
Viral protein, Viral glycoprotein, Viral structural protein, Viral non-structural protein, Enveloped virus spike protein
01

Overview

Sudan ebolavirus (SUDV) antigens are the structural and functional proteins of the Sudan ebolavirus, the causative agent of Sudan virus disease (SVD), a severe hemorrhagic fever [1, 16]. The primary therapeutic target among these is the surface glycoprotein (GP), a trimeric spike responsible for viral attachment to host cells and membrane fusion through interactions with the Niemann-Pick C1 (NPC1) receptor [2, 10]. SUDV also encodes several other critical antigens, including the nucleoprotein (NP), which encapsulates the viral RNA, and viral proteins such as VP35 and VP24 that inhibit host innate immune signaling [5, 17]. A unique feature of ebolavirus pathogenesis is the production of a secreted glycoprotein (sGP), which acts as an immunological decoy by absorbing neutralizing antibodies intended for the surface GP [4, 9]. Therapeutic development focuses on neutralizing GP-mediated entry with monoclonal antibody cocktails, such as MBP134 or MBP431, and inhibiting viral replication using small-molecule antivirals like remdesivir or its oral prodrug obeldesivir [8, 11, 14]. These antigens also serve as the basis for various vaccine candidates, including the chimpanzee adenovirus vector vaccine cAd3-EBO S, which aims to elicit protective immune responses during outbreaks [12, 19].

Other names
Sudan virus (SUDV) proteinsSudan ebolavirus surface glycoproteinSUDV GPSudan virus antigensSUDV antigens
02

Mechanism of action

Viral entry inhibition, Neutralization of surface glycoprotein, Viral RNA-dependent RNA polymerase inhibition, Induction of protective adaptive immunity

03

Biological functions

Viral attachmentViral entryViral membrane fusionImmune evasionViral replicationViral assemblyInterferon antagonism
04

Disease associations

Sudan virus disease (SVD)Viral hemorrhagic fever (VHF)Infection
05

Safety considerations

Antigenic subversion by secreted glycoprotein (sGP) decoysAntibody-dependent enhancement (ADE) (theoretical risk)Rapid viral mutation leading to immune escapeCytokine storm induction during advanced infectionHigh biosafety level (BSL-4) requirements for drug development and testing
06

Interacting drugs

MBP134 (monoclonal antibody cocktail)

6 more in the full profile.

07

Biomarkers

Sudan ebolavirus RNA (RT-PCR)Sudan ebolavirus Glycoprotein (GP) antigen levelsAspartate aminotransferase (AST)D-dimerInterferon-gamma (IFN-gamma)Soluble Glycoprotein (sGP) serum levels

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