The binding of Streptococcus pneumoniae 14C-9N and 14C-9V polysaccharides (PSs) to lymphocytes and polymorphonuclear leukocytes of human blood were studied. The quantity of 14C-9N and 14C-9V PSs bound to leukocytes was proportional to the number of leukocytes and the incubation time; the binding was temperature-dependent. The binding activity appeared to be specific, since the binding was inhibited by prior treatment with homologous group 9 PSs. The binding was also inhibited by prior treatment with cross-reactive group 9 PSs. The binding of 14C-9V PS to leukocytes was greater than that of 14C-9N PS. Reciprocal plot analysis revealed 6.4 X 10(4) binding sites for 9N PS on each lymphocyte and 9.5 X 10(4) binding sites for 9V PS on each lymphocyte, while the affinity constant for 9N PS was 3.7 X 10(9) M-1 and that for 9V PS was 9.4 X 10(8) M-1. Furthermore, there were 7.8 X 10(4) binding sites for 9N PS on each polymorphonuclear leukocyte and 1.2 X 10(5) binding sites for 9 V PS on each polymorphonuclear leukocyte, while the affinity constant for 9N PS was 1.6 X 10(9) M-1 and that for 9V PS was 8.5 X 10(8) M-1. There was a high degree of inhibition of the binding of 14C-9N PS to leukocytes by prior treatment with 9V PS, and a low degree of inhibition of the binding of 14C-9V PS to leukocytes by prior treatment with 9N PS. The high degree of inhibition of binding of 9V PS to leukocytes was not directly related to the production of cross-reactive antibodies to 9N PS. The serum antibody and the plaque-forming cell responses in mice immunized with 9V PS were significantly greater than responses in mice immunized with 9N PS.
Characterization of the binding of and the immune response to pneumococcal group 9 capsular polysaccharides
[Category] 폐렴구균 감염증,
[Article Type] article
[Source] pubmed
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