Quality of antibody responses by adults and young children to 13-valent pneumococcal conjugate vaccination and Streptococcus pneumoniae colonisation. Issue 50 (28th November 2022)
- Record Type:
- Journal Article
- Title:
- Quality of antibody responses by adults and young children to 13-valent pneumococcal conjugate vaccination and Streptococcus pneumoniae colonisation. Issue 50 (28th November 2022)
- Main Title:
- Quality of antibody responses by adults and young children to 13-valent pneumococcal conjugate vaccination and Streptococcus pneumoniae colonisation
- Authors:
- Wolf, Asia-Sophia
Mitsi, Elena
Jones, Scott
Jochems, Simon P.
Roalfe, Lucy
Thindwa, Deus
Meiring, James E.
Msefula, Jacquline
Bonomali, Farouck
Makhaza Jere, Tikhala
Mbewe, Maurice
Collins, Andrea M.
Gordon, Stephen B.
Gordon, Melita A.
Ferreira, Daniela M.
French, Neil
Goldblatt, David
Heyderman, Robert S.
Swarthout, Todd D. - Abstract:
- Abstract: Childhood pneumococcal conjugate vaccine (PCV) protects against invasive pneumococcal disease caused by vaccine-serotype (VT) Streptococcus pneumoniae by generating opsonophagocytic anti-capsular antibodies, but how vaccination protects against and reduces VT carriage is less well understood. Using serological samples from PCV-vaccinated Malawian individuals and a UK human challenge model, we explored whether antibody quality (IgG subclass, opsonophagocytic killing, and avidity) is associated with protection from carriage. Following experimental challenge of adults with S. pneumoniae serotype 6B, 3/21 PCV13-vaccinees were colonised with pneumococcus compared to 12/24 hepatitis A-vaccinated controls; PCV13-vaccination induced serotype-specific IgG, IgG1, and IgG2, and strong opsonophagocytic responses. However, there was no clear relationship between antibody quality and protection from carriage or carriage intensity after vaccination. Similarly, among PCV13-vaccinated Malawian infants there was no relationship between serotype-specific antibody titre or quality and carriage through exposure to circulating serotypes. Although opsonophagocytic responses were low in infants, antibody titre and avidity to circulating serotypes 19F and 6A were maintained or increased with age. These data suggest a complex relationship between antibody-mediated immunity and pneumococcal carriage, and that PCV13-driven antibody quality may mature with age and exposure. Highlights: PCV13Abstract: Childhood pneumococcal conjugate vaccine (PCV) protects against invasive pneumococcal disease caused by vaccine-serotype (VT) Streptococcus pneumoniae by generating opsonophagocytic anti-capsular antibodies, but how vaccination protects against and reduces VT carriage is less well understood. Using serological samples from PCV-vaccinated Malawian individuals and a UK human challenge model, we explored whether antibody quality (IgG subclass, opsonophagocytic killing, and avidity) is associated with protection from carriage. Following experimental challenge of adults with S. pneumoniae serotype 6B, 3/21 PCV13-vaccinees were colonised with pneumococcus compared to 12/24 hepatitis A-vaccinated controls; PCV13-vaccination induced serotype-specific IgG, IgG1, and IgG2, and strong opsonophagocytic responses. However, there was no clear relationship between antibody quality and protection from carriage or carriage intensity after vaccination. Similarly, among PCV13-vaccinated Malawian infants there was no relationship between serotype-specific antibody titre or quality and carriage through exposure to circulating serotypes. Although opsonophagocytic responses were low in infants, antibody titre and avidity to circulating serotypes 19F and 6A were maintained or increased with age. These data suggest a complex relationship between antibody-mediated immunity and pneumococcal carriage, and that PCV13-driven antibody quality may mature with age and exposure. Highlights: PCV13 reduces colonisation after experimental S. pneumoniae challenge in adults. Vaccinated adults had strong serotype-specific functional antibody responses. Unvaccinated adults with high avidity antibodies were less likely to be colonised. Residual carriage of vaccine serotypes maintains IgG titres in vaccinated children. Vaccinated children maintain serotype-specific avidity without antigen re-exposure. … (more)
- Is Part Of:
- Vaccine. Volume 40:Issue 50(2022)
- Journal:
- Vaccine
- Issue:
- Volume 40:Issue 50(2022)
- Issue Display:
- Volume 40, Issue 50 (2022)
- Year:
- 2022
- Volume:
- 40
- Issue:
- 50
- Issue Sort Value:
- 2022-0040-0050-0000
- Page Start:
- 7201
- Page End:
- 7210
- Publication Date:
- 2022-11-28
- Subjects:
- Pneumococcal conjugate vaccine -- Carriage -- Colonisation -- Pneumococcus -- Opsonophagocytosis -- Avidity -- PCV
PCV pneumococcal conjugate vaccine -- CPS capsular polysaccharide -- VT vaccine serotype -- IPD invasive pneumococcal disease -- OPK opsonophagocytic killing -- CoP correlate of protection -- HepA Hepatitis A -- EHPC Experimental Human Pneumococcal Challenge -- AUC area under the curve -- MOPA multiplex opsonophagocytosis assay -- OI opsonic index -- AI avidity index
Vaccines -- Periodicals
615.372 - Journal URLs:
- http://www.sciencedirect.com/science/journal/0264410X ↗
http://www.clinicalkey.com/dura/browse/journalIssue/0264410X ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/0264410X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.vaccine.2022.09.069 ↗
- Languages:
- English
- ISSNs:
- 0264-410X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9138.628000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24339.xml