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Click here for Nimenrix® (meningococcal groups A, C, W-135 and Y conjugate vaccine) Prescribing Information for Great Britain (GB) and Northern Ireland (NI). Click here for Trumenba®▼ (meningococcal group B vaccine (recombinant, adsorbed)) Prescribing Information for GB and NI.
Adverse event reporting information can be found at the bottom of the page.

Meningococcal Disease - mechanism of diseaseMeningococcal Disease - mechanism of disease

Meningococcal disease refers to any illness caused by the bacterium Neisseria meningitidis.1
N. meningitidis is only pathogenic (disease-causing) in humans.2​​​​​​​

Ordinarily, antigens on the surface of bacteria are the target of immunological activity from the host immune system.3 In order to cause disease, N.meningitidis must survive in the bloodstream and avoid being killed by the innate immune mechanisms of the host, particularly the complement system.​​​​​​​3 

It is the structure of N. meningitidis that helps the bacterium to resist phagocytosis and complement-mediated lysis.4 The bacterium contains an outer membrane which is surrounded by a polysaccharide capsule.4

​​​​​​​The polysaccharide capsule partly acts as a protective shell to prevent binding of the complement system and resulting cleavage of C3 to C3b.2 This cleavage would usually result in the effector functions of complement such as opsonisation which leads to phagocytosis.2 Evasion can also be enhanced by other methods such as mimicry of host molecules and recruiting factor H.​​​​​​​2

Figure 1: Polysaccharide capsule mechanism. Adapted from Tan LKK, Carlone GM, Borrow R. Advances in the development of vaccines against Neisseria meningitidis. N Engl J Med. 2010; 362:1511-20.5​​​​​​​

PfizerPro Learn more about Nimenrix

Nimenrix (meningococcal groups A, C, W-135 and Y conjugate vaccine) is indicated for active immunisation of individuals from the age of 6 weeks against invasive meningococcal disease caused by Neiserria meningitidis serogroups A, C, W-135 and Y​​​​​​​10

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Disease progression & SymptomsDisease Progression & Symptoms

Meningococcal disease most commonly presents as meningitis and septicaemia.6

The incubation period of meningococcal disease is two to seven days.6 The rate at which the disease develops varies between patients.7 

  • The early symptoms (prodrome) could include fever, malaise, and lethargy.7
  • The common symptoms of meningitis then could include neck stiffness, severe headache, and photophobia.7
  • Comparatively, the common symptoms of sepsis could include limb/joint pain, pale/mottled blueish skin and tachycardia.7
  • Both meningitis and sepsis may result in confusion, drowsiness, and impaired consciousness.​​​​​​​7
Burden of Disease

Currently invasive meningococcal disease (IMD) incidence is below 1 per 100,000 in England.8

​​​​​​​The UK Health Security Agency Meningococcal Reference Unit confimed 205 cases in England between July 2021 and June 2022 (epidemiological year).​​​​​​​8

Immunisation & Treatment - History & Advances

In 1906, scientists began to recommend anti-meningococcal serum therapy to protect humans against meningococcal disease.9 This therapy was initially based on antibodies derived from the blood of horses. Later, the antibodies were derived from patients, or individuals recovering from meningococcal disease.9

​​​​​​​Antibiotics revolutionised treatment for meningitis however they do not always act fast enough to prevent damage that the bacteria can cause.9 The UK later introduced a conjugate vaccine against meningococcal disease with the MenC vaccine introduced in 1999.​​​​​​​9

PfizerProFind out more about Trumenba

Trumenba (meningococcal group B vaccine (recombinant, adsorbed)) is indicated for active immunisation of individuals 10 years and older to prevent invasive meningococcal disease caused by Neisseria meningitidis serogroup B.11

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References: 
Rosenstein NE, Perkins BA, Stephens DS, Popovic T, Hughes JM. Meningococcal disease. N Engl J Med. 2001; 344(18):1378-1388.Panatto D, Amicizia D, Lai PL, Gasparini R. Neisseria meningitidis B vaccines. Exp Rev Vacc. 2011; 10(9):1337-1351.Schneider MC, Exley RM, Chan H, et al. Functional significance of factor H binding to Neisseria meningitidis. J Immunol. 2006; 176:7566-7575.United States Centers for Disease Control and Prevention (CDC). Meningococcal Disease. Epidemiology and Prevention of Vaccine-Preventable Diseases. Available at: https://www.cdc.gov/vaccines/pubs/pinkbook/mening.html#print. Last accessed July 2023Tan LKK, Carlone GM, Borrow R. Advances in the development of vaccines against Neisseria meningitidis. N Engl J Med. 2010; 362:1511-20.UKHSA. The Green Book, Chapter 22: Meningococcal Disease. Available at: https://www.gov.uk/government/publications/meningococcal-the-green-book-chapter-22 . Last accessed July 2023Meningitis Research Foundation. Meningococcal Meningitis and Septicaemia Guidance Notes: Diagnosis and Treatment in General Practice. United Kingdom: Meningitis Research Foundation; 2018. Available at: https://www.meningitis.org/getmedia/cf777153-9427-4464-89e2-fb58199174b6/gp_booklet-UK-sept-16. Last accessed July 2023.UKHSA. Invasive meningococcal disease in England: annual laboratory confirmed reports for epidemiological year 2021 to 2022. Available at https://www.gov.uk/government/publications/meningococcal-disease-laboratory-confirmed-cases-in-england-in-2021-to-2022/invasive-meningococcal-disease-in-england-annual-laboratory-confirmed-reports-for-epidemiological-year-2021-to-2022. Last accessed July 2023Meningitis Research Foundation. 2020. The history of meningitis. Available at: https://www.meningitis.org/blogs/the-history-of-meningitis. Last accessed July 2023. Nimenrix. Summary of Product Characteristics, Great Britain.Trumenba. Summary of Product Characteristics, Great Britain.
PP-NIM-GBR-0399 July 2023

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