scholarly journals Induction of a protective capsular polysaccharide antibody response to a multiepitope DNA vaccine encoding a peptide mimic of meningococcal serogroup C capsular polysaccharide

Immunology ◽  
2003 ◽  
Vol 110 (2) ◽  
pp. 242-249 ◽  
Author(s):  
Deborah M. Prinz ◽  
S. Louise Smithson ◽  
Thomas Kieber-Emmons ◽  
M. A. Julie Westerink
Vaccine ◽  
2001 ◽  
Vol 19 (13-14) ◽  
pp. 1717-1726 ◽  
Author(s):  
Gregory B Lesinski ◽  
S.Louise Smithson ◽  
Neeti Srivastava ◽  
Dexiang Chen ◽  
Georg Widera ◽  
...  

2003 ◽  
Vol 16 (2) ◽  
pp. 308-318 ◽  
Author(s):  
Andrew S. Artz ◽  
William B. Ershler ◽  
Dan L. Longo

SUMMARY As individuals advance in age, the risk of infection, bacteremia, and mortality caused by Streptococcus pneumoniae rises. Retrospective data demonstrate that the licensed penumococcal polysaccharide vaccine (PPV) is effective in older persons in reducing serotype-specific invasive disease. PPV demonstrates good immunogenicity in older adults, generally comparable to that in younger subjects, although certain cohorts respond less well. The response to PPV is T cell independent, however, and does not elicit immunologic memory. The duration of the anti-capsular polysaccharide antibody response appears to wane as early as 3 years after vaccination. In older persons, revaccination induces an antibody response, although it may not be as strong as that from the initial vaccine. While revaccination of older adults has been recommended, clinical efficacy has not yet been proven. Measures of antibody function may be at least as important in determining protection as are quantitative antibody levels. Additional studies of immunogenicity, particularly regarding revaccination, will facilitate the design of an optimal pneumococcal vaccination policy. Research into conjugate- and protein-based pneumococcal vaccines, which elicit T-cell-dependent responses and induce immunologic memory, is needed in older persons. In the meantime, administering to PPV to recommended groups should be a public health priority.


2015 ◽  
Vol 83 (7) ◽  
pp. 2889-2896 ◽  
Author(s):  
Leen Moens ◽  
Bert Verbinnen ◽  
Kris Covens ◽  
Greet Wuyts ◽  
Marina Johnson ◽  
...  

The role of CD19+CD5+and CD19+CD5−B cell subpopulations in the antibody response to pneumococcal capsular polysaccharides (caps-PSs) is controversial. In the present study, we evaluated the role of human CD19+CD5+and CD19+CD5−cell populations in the serotype-specific antibody response to caps-PS. After vaccination of 5 healthy human adults with Pneumovax (23-valent pneumococcal polysaccharide vaccine [PPV23]), IgG anti-caps-PS serotype 4 antibody-producing cells resided mainly in the CD19+CD5−B cell subset, as assessed by enzyme-linked immunosorbent spot (ELISpot) analysis. Moreover, in a humanized SCID mouse model, CD19+CD5−B cells were more effective than CD19+CD5+cells in producing IgG anti-cap-PS antibodies. Finally, an association was found between the level of IgG anti-caps-PS antibodies and the number of CD19+CD5−B cells in 33 humans vaccinated with PPV23. Taken together, our data suggest that CD5 defines a functionally distinct population of B cells in humans in the anti-caps-PS immune response.


2006 ◽  
Vol 39 (12) ◽  
pp. 1587-1592 ◽  
Author(s):  
B.T. Costa-Carvalho ◽  
R.M.A. Martinez ◽  
A.T.N. Dias ◽  
C.A. Kubo ◽  
P. Barros-Nunes ◽  
...  

2001 ◽  
Vol 69 (5) ◽  
pp. 3031-3040 ◽  
Author(s):  
Samuel T. Test ◽  
Joyce Mitsuyoshi ◽  
Charles C. Connolly ◽  
Alexander H. Lucas

ABSTRACT Previous studies have demonstrated an adjuvant effect for the C3d fragment of complement C3 when coupled to T-dependent protein antigens. In this study, we examined the antibody response to covalent conjugates of C3d and a T-independent antigen, the capsular polysaccharide of serotype 14 Streptococcus pneumoniae (PPS14). We prepared a conjugate of mouse C3d and PPS14 and compared its immunogenicity with that of a conjugate of PPS14 and ovalbumin (OVA). When BALB/c mice were immunized with PPS14-C3d, there was a significant increase in serum anti-PPS14 concentrations compared with either native PPS14 or control PPS14-glycine conjugates. This was accompanied by a switch in anti-PPS14 from predominantly immunoglobulin M (IgM) to IgG1 by day 25 following primary immunization. Following secondary immunization with PPS14-C3d, there was a marked booster response and a further increase in the ratio of IgG1 to IgM anti-PPS14. Although the primary antibody response to the PPS14-OVA conjugate exceeded that induced by immunization with PPS14-C3d, serum anti-PPS14 concentrations after a second injection of PPS14-C3d were nearly identical to those induced by secondary immunization with PPS14-OVA. Experiments with athymic nude mice suggested that T cells were not required for the adjuvant effect of C3d on the primary immune response to PPS14 but were necessary for enhancement of the memory response after a second injection of PPS14-C3d. These studies show that the adjuvant effects of C3d extend to T-independent antigens as well as T-dependent antigens. As a means of harnessing the adjuvant potential of the innate immune system, C3d conjugates may prove useful as a component of vaccines against encapsulated bacteria.


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