scholarly journals Memory B-Cell Pools Predict the Immune Response to Pneumococcal Conjugate Vaccine in Immunocompromised Children

2015 ◽  
Vol 213 (5) ◽  
pp. 848-855 ◽  
Author(s):  
Takayuki Hoshina ◽  
Shouichi Ohga ◽  
Junko Fujiyoshi ◽  
Etsuro Nanishi ◽  
Tomoko Takimoto ◽  
...  
2007 ◽  
Vol 15 (2) ◽  
pp. 182-193 ◽  
Author(s):  
Elizabeth A. Clutterbuck ◽  
Sarah Oh ◽  
Mainga Hamaluba ◽  
Sharon Westcar ◽  
Peter C. L. Beverley ◽  
...  

ABSTRACT Glycoconjugate vaccines have dramatically reduced the incidence of encapsulated bacterial diseases in toddlers under 2 years of age, but vaccine-induced antibody levels in this age group wane rapidly. We immunized adults and 12-month-old toddlers with heptavalent pneumococcal conjugate vaccine to determine differences in B-cell and antibody responses. The adults and 12-month-old toddlers received a pneumococcal conjugate vaccine. The toddlers received a second dose at 14 months of age. The frequencies of diphtheria toxoid and serotype 4, 14, and 23F polysaccharide-specific plasma cells and memory B cells were determined by enzyme-linked immunospot assay. The toddlers had no preexisting polysaccharide-specific memory B cells or serum immunoglobulin G (IgG) antibody but had good diphtheria toxoid-specific memory responses. The frequencies of plasma cells and memory B cells increased by day 7 (P < 0.0001) in the adults and the toddlers following a single dose of conjugate, but the polysaccharide responses were significantly lower in the toddlers than in the adults (P = 0.009 to <0.001). IgM dominated the toddler antibody responses, and class switching to the IgG was serotype dependent. A second dose of vaccine enhanced the antibody and memory B-cell responses in the toddlers but not the ex vivo plasma cell responses. Two doses of pneumococcal conjugate vaccine are required in toddlers to generate memory B-cell frequencies and antibody class switching for each pneumococcal polysaccharide equivalent to that seen in adults.


2017 ◽  
Vol 36 (5) ◽  
pp. e130-e135 ◽  
Author(s):  
Johannes Trück ◽  
Ruth Mitchell ◽  
Sena Jawad ◽  
Elizabeth A. Clutterbuck ◽  
Matthew D. Snape ◽  
...  

Vaccine ◽  
2015 ◽  
Vol 33 (14) ◽  
pp. 1688-1694 ◽  
Author(s):  
Per Nived ◽  
Charlotte Sværke Jørgensen ◽  
Bo Settergren

Vaccine ◽  
2017 ◽  
Vol 35 (29) ◽  
pp. 3639-3646 ◽  
Author(s):  
Per Nived ◽  
Johanna Nagel ◽  
Tore Saxne ◽  
Pierre Geborek ◽  
Göran Jönsson ◽  
...  

Vaccine ◽  
2013 ◽  
Vol 31 (42) ◽  
pp. 4765-4774 ◽  
Author(s):  
Gail L. Rodgers ◽  
Susanna Esposito ◽  
Nicola Principi ◽  
Maricruz Gutierrez-Brito ◽  
Javier Diez-Domingo ◽  
...  

Author(s):  
Aklima Akter ◽  
Meagan Kelly ◽  
Richelle C. Charles ◽  
Jason B. Harris ◽  
Stephen B. Calderwood ◽  
...  

Oral cholera vaccination protects against cholera; however, responses in young children are low and of short duration. The best current correlates of protection against cholera target Vibrio cholerae O-specific polysaccharide (anti-OSP), including vibriocidal responses. A cholera conjugate vaccine has been developed that induces anti-OSP immune responses, including memory B-cell responses. To address whether cholera conjugate vaccine would boost immune responses following oral cholera vaccination, we immunized mice with oral cholera vaccine Inaba CVD 103-HgR or buffer only (placebo) on day 0, followed by parenteral boosting immunizations on days 14, 42, and 70 with cholera conjugate vaccine Inaba OSP: recombinant tetanus toxoid heavy chain fragment or PBS/placebo. Compared with responses in mice immunized with oral vaccine alone or intramuscular cholera conjugate vaccine alone, mice receiving combination vaccination developed significantly higher vibriocidal, IgM OSP-specific serum responses and OSP-specific IgM memory B-cell responses. A combined vaccination approach, which includes oral cholera vaccination followed by parenteral cholera conjugate vaccine boosting, results in increased immune responses that have been associated with protection against cholera. These results suggest that such an approach should be evaluated in humans.


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