PspA Family Fusion Proteins Delivered by Attenuated Salmonella enterica Serovar Typhimurium Extend and Enhance Protection against Streptococcus pneumoniae
Pneumococcal surface protein A (PspA) is highly immunogenic and can induce a protective immune response against pneumococcal infection. PspA is divided into two major families based on serological variability: family 1 and family 2. To provide broad protection, PspA proteins from pneumococcal strain...
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description | Pneumococcal surface protein A (PspA) is highly immunogenic and can induce a protective immune response against pneumococcal infection. PspA is divided into two major families based on serological variability: family 1 and family 2. To provide broad protection, PspA proteins from pneumococcal strains Rx1 (family 1) and EF5668 (family 2) were combined to form two PspA fusion proteins, PspA/Rx1-EF5668 and PspA/EF5668-Rx1. Each protein was fused to a type II secretion signal and delivered by a recombinant attenuated Salmonella vaccine (RASV). Both PspA/Rx1-EF5668 and PspA/EF5668-Rx1 were synthesized in the RASV and secreted into the periplasm and supernatant. The fusion proteins reacted strongly with both anti-PspA/Rx1 and anti-PspA/EF5668 antisera. Oral immunization of BALB/c mice with RASV synthesizing either PspA fusion protein elicited serum immunoglobulin G (IgG) and mucosal IgA responses against both families of PspA. Analysis of IgG isotypes (IgG2a and IgG1) indicated a strong Th1 bias to the immune responses to both proteins. Sera from mice immunized with RASV synthesizing PspA/Rx1-EF5668 bound to the surface and directed C3 complement deposition on representative strains from all five PspA clades. Immunization with RASV synthesizing either protein protected mice against intraperitoneal challenge with Streptococcus pneumoniae WU2 strain (family 1), intravenous challenge with S. pneumoniae 3JYP2670 strain (family 2), and intranasal challenge with S. pneumoniae A66.1 (family 1). The PspA/Rx1-EF5668 protein elicited significantly greater protection than PspA/EF5668-Rx1, PspA/Rx1, or PspA/EF5668. These results indicate an RASV synthesizing a PspA fusion protein representing both PspA families constitutes an effective antipneumococcal vaccine, extending and enhancing protection against multiple strains of S. pneumoniae. |
doi_str_mv | 10.1128/IAI.00486-09 |
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PspA is divided into two major families based on serological variability: family 1 and family 2. To provide broad protection, PspA proteins from pneumococcal strains Rx1 (family 1) and EF5668 (family 2) were combined to form two PspA fusion proteins, PspA/Rx1-EF5668 and PspA/EF5668-Rx1. Each protein was fused to a type II secretion signal and delivered by a recombinant attenuated Salmonella vaccine (RASV). Both PspA/Rx1-EF5668 and PspA/EF5668-Rx1 were synthesized in the RASV and secreted into the periplasm and supernatant. The fusion proteins reacted strongly with both anti-PspA/Rx1 and anti-PspA/EF5668 antisera. Oral immunization of BALB/c mice with RASV synthesizing either PspA fusion protein elicited serum immunoglobulin G (IgG) and mucosal IgA responses against both families of PspA. Analysis of IgG isotypes (IgG2a and IgG1) indicated a strong Th1 bias to the immune responses to both proteins. Sera from mice immunized with RASV synthesizing PspA/Rx1-EF5668 bound to the surface and directed C3 complement deposition on representative strains from all five PspA clades. Immunization with RASV synthesizing either protein protected mice against intraperitoneal challenge with Streptococcus pneumoniae WU2 strain (family 1), intravenous challenge with S. pneumoniae 3JYP2670 strain (family 2), and intranasal challenge with S. pneumoniae A66.1 (family 1). The PspA/Rx1-EF5668 protein elicited significantly greater protection than PspA/EF5668-Rx1, PspA/Rx1, or PspA/EF5668. These results indicate an RASV synthesizing a PspA fusion protein representing both PspA families constitutes an effective antipneumococcal vaccine, extending and enhancing protection against multiple strains of S. pneumoniae.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.00486-09</identifier><identifier>PMID: 19687204</identifier><identifier>CODEN: INFIBR</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Administration, Oral ; Animals ; Antibodies, Bacterial - blood ; Antisera ; Bacterial Proteins - genetics ; Bacterial Proteins - immunology ; Bacteriology ; Biological and medical sciences ; Complement component C3 ; Enzyme-Linked Immunosorbent Assay ; Female ; Fundamental and applied biological sciences. Psychology ; Fusion protein ; Genetic Vectors ; Helper cells ; Humans ; Immune response ; Immunity, Mucosal ; Immunization ; Immunogenicity ; Immunoglobulin A ; Immunoglobulin A - analysis ; Immunoglobulin G ; Immunoglobulin G - blood ; Infection ; Intravenous administration ; Lymphocytes T ; Mice ; Mice, Inbred BALB C ; Microbial Immunity and Vaccines ; Microbiology ; Miscellaneous ; Mucosa ; periplasm ; Pneumococcal Infections - immunology ; Pneumococcal Infections - prevention & control ; Pneumococcal Vaccines - administration & dosage ; Pneumococcal Vaccines - genetics ; Pneumococcal Vaccines - immunology ; PspA protein ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - immunology ; Salmonella enterica ; Salmonella typhimurium - genetics ; secretion signals ; Streptococcus pneumoniae ; Streptococcus pneumoniae - genetics ; Streptococcus pneumoniae - immunology ; surface protein A ; Survival Analysis ; Vaccines</subject><ispartof>Infection and Immunity, 2009-10, Vol.77 (10), p.4518-4528</ispartof><rights>2009 INIST-CNRS</rights><rights>Copyright © 2009, American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-3967ae54c8f38b0e8d6a94a7c5010fc6b6dda61eb485e99156d301e25f23aa703</citedby><cites>FETCH-LOGICAL-c456t-3967ae54c8f38b0e8d6a94a7c5010fc6b6dda61eb485e99156d301e25f23aa703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2747926/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2747926/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21955425$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19687204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xin, Wei</creatorcontrib><creatorcontrib>Li, Yuhua</creatorcontrib><creatorcontrib>Mo, Hua</creatorcontrib><creatorcontrib>Roland, Kenneth L</creatorcontrib><creatorcontrib>Curtiss, Roy III</creatorcontrib><title>PspA Family Fusion Proteins Delivered by Attenuated Salmonella enterica Serovar Typhimurium Extend and Enhance Protection against Streptococcus pneumoniae</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>Pneumococcal surface protein A (PspA) is highly immunogenic and can induce a protective immune response against pneumococcal infection. PspA is divided into two major families based on serological variability: family 1 and family 2. To provide broad protection, PspA proteins from pneumococcal strains Rx1 (family 1) and EF5668 (family 2) were combined to form two PspA fusion proteins, PspA/Rx1-EF5668 and PspA/EF5668-Rx1. Each protein was fused to a type II secretion signal and delivered by a recombinant attenuated Salmonella vaccine (RASV). Both PspA/Rx1-EF5668 and PspA/EF5668-Rx1 were synthesized in the RASV and secreted into the periplasm and supernatant. The fusion proteins reacted strongly with both anti-PspA/Rx1 and anti-PspA/EF5668 antisera. Oral immunization of BALB/c mice with RASV synthesizing either PspA fusion protein elicited serum immunoglobulin G (IgG) and mucosal IgA responses against both families of PspA. Analysis of IgG isotypes (IgG2a and IgG1) indicated a strong Th1 bias to the immune responses to both proteins. Sera from mice immunized with RASV synthesizing PspA/Rx1-EF5668 bound to the surface and directed C3 complement deposition on representative strains from all five PspA clades. Immunization with RASV synthesizing either protein protected mice against intraperitoneal challenge with Streptococcus pneumoniae WU2 strain (family 1), intravenous challenge with S. pneumoniae 3JYP2670 strain (family 2), and intranasal challenge with S. pneumoniae A66.1 (family 1). The PspA/Rx1-EF5668 protein elicited significantly greater protection than PspA/EF5668-Rx1, PspA/Rx1, or PspA/EF5668. These results indicate an RASV synthesizing a PspA fusion protein representing both PspA families constitutes an effective antipneumococcal vaccine, extending and enhancing protection against multiple strains of S. pneumoniae.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antibodies, Bacterial - blood</subject><subject>Antisera</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - immunology</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Complement component C3</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fusion protein</subject><subject>Genetic Vectors</subject><subject>Helper cells</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunity, Mucosal</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin A - analysis</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin G - blood</subject><subject>Infection</subject><subject>Intravenous administration</subject><subject>Lymphocytes T</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbial Immunity and Vaccines</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Mucosa</subject><subject>periplasm</subject><subject>Pneumococcal Infections - immunology</subject><subject>Pneumococcal Infections - prevention & control</subject><subject>Pneumococcal Vaccines - administration & dosage</subject><subject>Pneumococcal Vaccines - genetics</subject><subject>Pneumococcal Vaccines - immunology</subject><subject>PspA protein</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>Recombinant Fusion Proteins - immunology</subject><subject>Salmonella enterica</subject><subject>Salmonella typhimurium - genetics</subject><subject>secretion signals</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - genetics</subject><subject>Streptococcus pneumoniae - immunology</subject><subject>surface protein A</subject><subject>Survival Analysis</subject><subject>Vaccines</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9vEzEQxVcIREvhxhksJDixxfbaXvuCFJUEIlWiUtqzNfHOJkb7r_ZuIF-FT4tDogInDpY18s_vzczLspeMXjLG9YflbHlJqdAqp-ZRds6o0bmUnD_OzillJjdSlWfZsxi_pVIIoZ9mZ8woXXIqzrOfN3GYkQW0vtmTxRR935Gb0I_ou0g-YeN3GLAi6z2ZjSN2E4ypWkHT9h02DRDsRgzeAVlh6HcQyO1-2Pp2Cn5qyfxH-lIRSGfebaFzeNR248EGNpBMRrIaAw5j73rnpkiGDqck7gGfZ09qaCK-ON0X2d1ifnv1Jb_--nl5NbvOnZBqzAujSkApnK4LvaaoKwVGQOkkZbR2aq2qChTDtdASjWFSVQVlyGXNC4CSFhfZx6PuMK1brFwaKUBjh-BbCHvbg7f_vnR-azf9zvJSlIarJPDuJBD6-wnjaFsf3WE9HfZTtKpUSigt_gtyJozRRZHA90fQhT7GgPVDN4zaQ-o2pW5_p26pSfirvyf4A59iTsDbEwDRQVOHlIWPDxxnRkrBZeLeHLmt32y_-4AWYmt92kBZHqyFZDpBr49QDb2FTUhCdytOWdpqGpLJovgF5ETNzQ</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Xin, Wei</creator><creator>Li, Yuhua</creator><creator>Mo, Hua</creator><creator>Roland, Kenneth L</creator><creator>Curtiss, Roy III</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091001</creationdate><title>PspA Family Fusion Proteins Delivered by Attenuated Salmonella enterica Serovar Typhimurium Extend and Enhance Protection against Streptococcus pneumoniae</title><author>Xin, Wei ; Li, Yuhua ; Mo, Hua ; Roland, Kenneth L ; Curtiss, Roy III</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-3967ae54c8f38b0e8d6a94a7c5010fc6b6dda61eb485e99156d301e25f23aa703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antibodies, Bacterial - blood</topic><topic>Antisera</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - immunology</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Complement component C3</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fusion protein</topic><topic>Genetic Vectors</topic><topic>Helper cells</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunity, Mucosal</topic><topic>Immunization</topic><topic>Immunogenicity</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulin A - analysis</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin G - blood</topic><topic>Infection</topic><topic>Intravenous administration</topic><topic>Lymphocytes T</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbial Immunity and Vaccines</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Mucosa</topic><topic>periplasm</topic><topic>Pneumococcal Infections - immunology</topic><topic>Pneumococcal Infections - prevention & control</topic><topic>Pneumococcal Vaccines - administration & dosage</topic><topic>Pneumococcal Vaccines - genetics</topic><topic>Pneumococcal Vaccines - immunology</topic><topic>PspA protein</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>Recombinant Fusion Proteins - immunology</topic><topic>Salmonella enterica</topic><topic>Salmonella typhimurium - genetics</topic><topic>secretion signals</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - genetics</topic><topic>Streptococcus pneumoniae - immunology</topic><topic>surface protein A</topic><topic>Survival Analysis</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xin, Wei</creatorcontrib><creatorcontrib>Li, Yuhua</creatorcontrib><creatorcontrib>Mo, Hua</creatorcontrib><creatorcontrib>Roland, Kenneth L</creatorcontrib><creatorcontrib>Curtiss, Roy III</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and Immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xin, Wei</au><au>Li, Yuhua</au><au>Mo, Hua</au><au>Roland, Kenneth L</au><au>Curtiss, Roy III</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PspA Family Fusion Proteins Delivered by Attenuated Salmonella enterica Serovar Typhimurium Extend and Enhance Protection against Streptococcus pneumoniae</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>77</volume><issue>10</issue><spage>4518</spage><epage>4528</epage><pages>4518-4528</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>Pneumococcal surface protein A (PspA) is highly immunogenic and can induce a protective immune response against pneumococcal infection. PspA is divided into two major families based on serological variability: family 1 and family 2. To provide broad protection, PspA proteins from pneumococcal strains Rx1 (family 1) and EF5668 (family 2) were combined to form two PspA fusion proteins, PspA/Rx1-EF5668 and PspA/EF5668-Rx1. Each protein was fused to a type II secretion signal and delivered by a recombinant attenuated Salmonella vaccine (RASV). Both PspA/Rx1-EF5668 and PspA/EF5668-Rx1 were synthesized in the RASV and secreted into the periplasm and supernatant. The fusion proteins reacted strongly with both anti-PspA/Rx1 and anti-PspA/EF5668 antisera. Oral immunization of BALB/c mice with RASV synthesizing either PspA fusion protein elicited serum immunoglobulin G (IgG) and mucosal IgA responses against both families of PspA. Analysis of IgG isotypes (IgG2a and IgG1) indicated a strong Th1 bias to the immune responses to both proteins. Sera from mice immunized with RASV synthesizing PspA/Rx1-EF5668 bound to the surface and directed C3 complement deposition on representative strains from all five PspA clades. Immunization with RASV synthesizing either protein protected mice against intraperitoneal challenge with Streptococcus pneumoniae WU2 strain (family 1), intravenous challenge with S. pneumoniae 3JYP2670 strain (family 2), and intranasal challenge with S. pneumoniae A66.1 (family 1). The PspA/Rx1-EF5668 protein elicited significantly greater protection than PspA/EF5668-Rx1, PspA/Rx1, or PspA/EF5668. These results indicate an RASV synthesizing a PspA fusion protein representing both PspA families constitutes an effective antipneumococcal vaccine, extending and enhancing protection against multiple strains of S. pneumoniae.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>19687204</pmid><doi>10.1128/IAI.00486-09</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Animals Antibodies, Bacterial - blood Antisera Bacterial Proteins - genetics Bacterial Proteins - immunology Bacteriology Biological and medical sciences Complement component C3 Enzyme-Linked Immunosorbent Assay Female Fundamental and applied biological sciences. Psychology Fusion protein Genetic Vectors Helper cells Humans Immune response Immunity, Mucosal Immunization Immunogenicity Immunoglobulin A Immunoglobulin A - analysis Immunoglobulin G Immunoglobulin G - blood Infection Intravenous administration Lymphocytes T Mice Mice, Inbred BALB C Microbial Immunity and Vaccines Microbiology Miscellaneous Mucosa periplasm Pneumococcal Infections - immunology Pneumococcal Infections - prevention & control Pneumococcal Vaccines - administration & dosage Pneumococcal Vaccines - genetics Pneumococcal Vaccines - immunology PspA protein Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - immunology Salmonella enterica Salmonella typhimurium - genetics secretion signals Streptococcus pneumoniae Streptococcus pneumoniae - genetics Streptococcus pneumoniae - immunology surface protein A Survival Analysis Vaccines |
title | PspA Family Fusion Proteins Delivered by Attenuated Salmonella enterica Serovar Typhimurium Extend and Enhance Protection against Streptococcus pneumoniae |
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