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Homogeneous Glycoconjugate Produced by Combined Unnatural Amino Acid Incorporation and Click-Chemistry for Vaccine Purposes
Published on: December 19, 2020
[Conjugated vaccines]
1International Scientific & Clinical Affairs, Wyeth Vaccines, La Défense, Paris, France. fritzeb@wyeth.com
Insights
Conjugate vaccines protect infants from encapsulated bacterial pathogens like Hib and pneumococcus by converting T-independent antigens into T-dependent ones, significantly reducing invasive diseases and providing herd protection.
Area of Science:
- Immunology
- Vaccinology
- Microbiology
Context:
- Infants and young children are vulnerable to encapsulated bacterial pathogens due to waning maternal antibodies and immature immune systems.
- Polysaccharide capsules of bacteria like Haemophilus influenzae type b (Hib), Neisseria meningitidis, and Streptococcus pneumoniae are T-independent antigens, poorly immunogenic in young children.
Purpose:
- To explain the mechanism of polysaccharide-protein conjugate vaccines in overcoming the immunodeficiency in infants against encapsulated bacteria.
- To highlight the public health impact of conjugate vaccines in reducing invasive bacterial diseases.
Summary:
- Conjugate vaccines convert bacterial polysaccharide antigens into T-dependent antigens by linking them to carrier proteins.
- This conversion enables infants to mount a robust T-cell dependent immune response, leading to protective immunity.
- Vaccination with conjugate vaccines has dramatically reduced the incidence of invasive diseases caused by Hib, meningococcus, and pneumococcus.
Impact:
- Conjugate vaccines have led to an over 80% reduction in invasive diseases caused by targeted pathogens, representing a major public health achievement.
- These vaccines confer 'herd protection' by reducing nasopharyngeal colonization in vaccinated children, thereby protecting unvaccinated individuals.
- Future research focuses on expanding the serogroups targeted by meningococcal and pneumococcal conjugate vaccines to broaden protection.
Abstract:
Encapsulated bacterial pathogens (e.g. Haemophilus influenzae type b [Hib], Neisseria meningitidis, or Streptococcus pneumoniae) target infants and young children who have lost any protective anti-capsular antibodies supplied maternally and whose immune systems are ineffective against T-independent antigens such as the polysaccharides of the capsule. The polysaccharide-protein conjugate vaccines overcome this limitation by converting the polysaccharide to a T-dependent antigen, which allows a vaccinated infant to mount a protective immune response. Where conjugated vaccines have been introduced into paediatric vaccination schedules, the incidence of invasive diseases caused by Hib, the group C meningococcus, or the pneumococcus has plummeted by at least 80%, a major public health success. Furthermore, surveillance has demonstrated that the conjugate vaccines provide 'herd protection' through their beneficial impact on nasopharyngeal colonisation among vaccinated children. Promising future approaches include enhancement of the number of capsular serogroups targeted by the meningococcal or pneumococcal conjugate vaccines.
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