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The Haemophilus influenzae type b (Hib) capsular polysaccharide antigen, specifically polyribosylribitol phosphate (PRP), when conjugated to a carrier protein like tetanus toxoid, diphtheria toxoid, CRM197, or Neisseria meningitidis OMP, forms the active component of Hib conjugate vaccines. These vaccines stimulate a T-dependent immune response, leading to long-lasting immunity against invasive Hib diseases in infants and young children.
Conjugation of PRP to a carrier protein (Tetanus toxoid, Diphtheria toxoid, CRM197, or Neisseria meningitidis OMP) enhances immunogenicity by converting a T-independent antigen into a T-dependent antigen, leading to robust B and T cell activation, class switching to IgG, affinity maturation, memory B cell formation, and long-lasting immunity.
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