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For Research Use Only. Not For Clinical Use.


Background

Group B N. meningitidis (MenB), which is responsible for up to 80% of the total cases of disease in industrialized countries, has been resistant to any attempt to develop a capsulebased vaccine due to the poor immunogenicity of the CP even after protein conjugation. This is probably due to the similarity between the MenB CP and a polymer expressed on the neuronal cell adhesion molecule of mammalian tissues. Both polysaccharides are homolinear polymers of N-acetylneuraminic acid (polysialic acid), although the bacterial CP is longer than human polysialic acid (200 vs 50 residues, respectively). Therefore, the MenB CP is a self-Ag unable to stimulate an immune response and with the potential to induce autoimmunity if used as a vaccine.
Protein class

Cancer-related genes, Candidate cardiovascular disease genes, Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets, Transporters

Predicted location

Intracellular, Secreted (different isoforms)

Single cell type specificity

Cell type enhanced (Hepatocytes, Muller glia cells, Club cells, Glandular and luminal cells, Respiratory ciliated cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enriched (EFO-21)

Molecular function

Oxidoreductase

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