4.4 Article

Increased immunogenicity and induction of class switching by conjugation of complement C3d to pneumococcal serotype 14 capsular polysaccharide

期刊

INFECTION AND IMMUNITY
卷 69, 期 5, 页码 3031-3040

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AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.69.5.3031-3040.2001

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  1. NIAID NIH HHS [R37 AI025008, AI-25008, N01AI45250, R01 AI025008] Funding Source: Medline

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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 caps;lar 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 blv 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 prole useful as a component of vaccines against encapsulated bacteria.

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