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Gamma-irradiation of <Emphasis Type="Italic">Streptococcus pneumoniae</Emphasis> for the use as an immunogenic whole cell vaccine
Authors:Min Yong Jwa  Soyoung Jeong  Eun Byeol Ko  A Reum Kim  Hyun Young Kim  Sun Kyung Kim  Ho Seong Seo  Cheol-Heui Yun  Seung Hyun Han
Institution:1.Department of Oral Microbiology and Immunology, DRI, and BK21 Plus Program, School of Dentistry,Seoul National University,Seoul,Republic of Korea;2.Research Division for Biotechnology,Korea Atomic Energy Research Institute,Jeongeup,Republic of Korea;3.Department of Agricultural Biotechnology and Research Institute for Agriculture and Life Sciences,Seoul National University,Seoul,Republic of Korea
Abstract:Streptococcus pneumoniae is a major respiratory pathogen that causes millions of deaths worldwide. Although subunit vaccines formulated with the capsular polysaccharides or their protein conjugates are currently-available, low-cost vaccines with wide serotype coverage still remain to be developed, especially for developing countries. Recently, gamma- irradiation has been considered as an effective inactivation method to prepare S. pneumoniae vaccine candidate. In this study, we investigated the immunogenicity and protective immunity of gamma-irradiated S. pneumoniae (r-SP), by comparing with heat-inactivated S. pneumoniae (h-SP) and formalin-inactivated S. pneumoniae (f-SP), both of which were made by traditional inactivation methods. Intranasal immunization of C57BL/6 mice with r-SP in combination with cholera toxin as an adjuvant enhanced S. pneumoniaespecific antibodies on the airway mucosal surface and in sera more potently than that with h-SP or f-SP under the same conditions. In addition, sera from mice immunized with r-SP potently induced opsonophagocytic killing activity more effectively than those of h-SP or f-SP, implying that r-SP could induce protective antibodies. Above all, immunization with r-SP effectively protected mice against S. pneumoniae infection. Collectively, these results suggest that gamma- irradiation is an effective method for the development of a killed whole cell pneumococcal vaccine that elicits robust mucosal and systemic immune responses.
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