Target intelligence / Profile preview

Neisseria meningitidis serogroup B capsular polysialic acid (NmB polysialic acid)

Target
NmB polysialic acid
Molecular classification
Other (Bacterial capsular polysaccharide), Virulence factor
01

Overview

Neisseria meningitidis serogroup B capsular polysialic acid is a homopolymeric, (α2→8)-linked polymer of N-acetylneuraminic acid (sialic acid) that forms a capsule enveloping the bacterium. This capsule enables the bacteria to evade innate and adaptive immune responses by resisting complement-mediated lysis and phagocytosis; it interferes with antibody access to other surface antigens and modulates complement deposition. The capsule is a critical virulence determinant in group B meningococci and is, therefore, a major target for vaccine design. However, vaccines based directly on this polysaccharide have proven challenging because the epitope is poorly immunogenic and mimics human neural cell polysialic acid, raising difficulties in generating effective and safe immune responses. For this reason, vaccines against group B meningococcus typically exploit protein antigens rather than targeting the capsule directly, unlike vaccines for serogroups A, C, Y, and W-135.

Other names
Meningococcal group B polysaccharideGroup B capsular polysialic acidNmB polysialic acidSerogroup B polysaccharide(α2→8)-linked polysialic acid capsule
02

Mechanism of action

Vaccine-induced antibodies bind to the capsular polysialic acid and promote complement-mediated bactericidal activity. Some experimental monoclonal antibodies may promote opsonization or neutralize the capsule’s immune evasion properties.

03

Biological functions

Immune evasion (resistance to complement-mediated killing and phagocytosis)Inhibition of antibody binding to other surface antigensModulation of complement activation and deposition
04

Disease associations

Infection (principal virulence factor in invasive meningococcal disease, including sepsis and meningitis)
05

Safety considerations

The capsule is structurally identical to human neural cell adhesion molecule (NCAM) polysialic acid, making it *poorly immunogenic* and raising concerns about potential autoimmunity if robust immunity is inducedPoor immunogenicity in infants and children, limiting the success of polysaccharide vaccines
06

Interacting drugs

No widely used, direct, small-molecule drugs.

1 more in the full profile.

07

Biomarkers

Expression of the (α2→8)-linked polysialic acid capsule on N. meningitidis, as detectable by immunochemical or molecular tests, is a biomarker for serogroup B meningococcus

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