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Natural immunity against capsular group X N. meningitidis following an outbreak in Togo, 2007
- Source :
- Vaccine, Vaccine, Elsevier, 2018, 36 (10), pp.1297-1303. ⟨10.1016/j.vaccine.2018.01.031⟩, Vaccine, 2018, 36 (10), pp.1297-1303. ⟨10.1016/j.vaccine.2018.01.031⟩
- Publication Year :
- 2018
- Publisher :
- Elsevier, 2018.
-
Abstract
- Background Capsular group X N. meningitidis (MenX) has emerged as a cause of localized disease outbreaks in sub-Saharan Africa, but the human immune response following exposure to MenX antigens is poorly described. We therefore assessed the natural immunity against MenX in individuals who were living in an area affected by a MenX outbreak during 2007 in Togo, West Africa. During 2009, 300 healthy individuals (100 aged 3–5 years, 100 aged 13–19 years and 100 aged 20–25 years) were included in the study, and serum responses were compared with sera from age-matched controls from the U.K. and Burkina Faso. Methods MenX serum bactericidal antibody (SBA) was measured using rabbit complement, and antibodies against MenX polysaccharide (XPS) and outer membrane vesicles (XOMVs) were quantified by ELISA. Results The proportion of Togolese individuals with an SBA titer of ≥8 against the MenX strain was 29% (95% confidence interval (CI) 18–41) among those aged 3–5 years, 34% (95% CI 9–60) among those aged 13–19 years and 32% (95% CI 24–40) among those aged 20–25 years. These were significantly higher than observed in the control populations from the U.K (range 13–16%) and Burkina Faso (range 2–6%). Conclusion In Togolese individuals, the concentration of serum IgG against XPS was higher among the two older age groups as compared to the youngest age group. Antibody concentrations against MenX PS correlated significantly with SBA titers. This supports further development of a MenX PS based conjugate vaccine. Further studies are needed to verify the ability of MenX PS to induce SBA in humans.
- Subjects :
- Male
[SDV]Life Sciences [q-bio]
Physiology
Neisseria meningitidis
medicine.disease_cause
MESH: Meningococcal Vaccines
Disease Outbreaks
0302 clinical medicine
Seroepidemiologic Studies
MESH: Child
MESH: Antibodies, Bacterial
030212 general & internal medicine
MESH: Disease Outbreaks
Child
Polysaccharide
MESH: Immunoglobulin G
Meningococcal
biology
MESH: Meningitis, Meningococcal
Age Factors
11 Medical And Health Sciences
Antibodies, Bacterial
3. Good health
Titer
Infectious Diseases
MESH: Young Adult
Child, Preschool
Population Surveillance
Togo
Molecular Medicine
MESH: Immunity, Innate
Female
Antibody
Adult
Adolescent
030231 tropical medicine
Meningococcal Vaccines
Meningitis, Meningococcal
MESH: Neisseria meningitidis
Antibodies
MESH: Population Surveillance
Capsular group X
Young Adult
03 medical and health sciences
Immune system
Antigen
Conjugate vaccine
Virology
medicine
Humans
MESH: Adolescent
MESH: Age Factors
Antigens, Bacterial
MESH: Humans
MESH: Seroepidemiologic Studies
Innate immune system
General Veterinary
General Immunology and Microbiology
business.industry
MESH: Child, Preschool
Public Health, Environmental and Occupational Health
Outbreak
MESH: Adult
06 Biological Sciences
MESH: Male
Immunity, Innate
MESH: Togo
Immunoglobulin G
biology.protein
Bactericidal
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
07 Agricultural And Veterinary Sciences
business
MESH: Female
MESH: Antigens, Bacterial
Subjects
Details
- Language :
- English
- ISSN :
- 0264410X
- Database :
- OpenAIRE
- Journal :
- Vaccine, Vaccine, Elsevier, 2018, 36 (10), pp.1297-1303. ⟨10.1016/j.vaccine.2018.01.031⟩, Vaccine, 2018, 36 (10), pp.1297-1303. ⟨10.1016/j.vaccine.2018.01.031⟩
- Accession number :
- edsair.doi.dedup.....a5e9c6db108195dd0f4810f73d251bad