{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,19]],"date-time":"2026-10-19T16:40:46Z","timestamp":1792428046224,"version":"4.5.0"},"reference-count":29,"publisher":"American Society for Microbiology","issue":"12","license":[{"start":{"date-parts":[[2011,12,1]],"date-time":"2011-12-01T00:00:00Z","timestamp":1322697600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Clin Vaccine Immunol"],"published-print":{"date-parts":[[2011,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            Leptospirosis is the most widespread zoonosis in the world. Current vaccines are based on whole-cell preparations that cause severe side effects and do not induce satisfactory immunity. In light of the leptospiral genome sequences recently made available, several studies aimed at identification of protective recombinant immunogens have been performed; however, few such immunogens have been identified. The aim of this study was to evaluate 27 recombinant antigens to determine their potential to induce an immune response protective against leptospirosis in the hamster model. Experiments were conducted with groups of female hamsters immunized with individual antigen preparations. Hamsters were then challenged with a lethal dose of\n            <jats:named-content content-type=\"genus-species\">Leptospira interrogans<\/jats:named-content>\n            . Thirteen antigens induced protective immune responses; however, only recombinant proteins LIC10325 and LIC13059 induced significant protection against mortality. These results have important implications for the development of an efficacious recombinant subunit vaccine against leptospirosis.\n          <\/jats:p>","DOI":"10.1128\/cvi.05297-11","type":"journal-article","created":{"date-parts":[[2011,10,27]],"date-time":"2011-10-27T00:47:05Z","timestamp":1319676425000},"page":"2026-2030","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":24,"title":["Subunit Approach to Evaluation of the Immune Protective Potential of Leptospiral Antigens"],"prefix":"10.1128","volume":"18","author":[{"given":"Samuel R.","family":"F\u00e9lix","sequence":"first","affiliation":[{"name":"N\u00facleo de Biotecnologia\u2014CDTec, Universidade Federal de Pelotas, Pelotas, RS, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daiane D.","family":"Hartwig","sequence":"additional","affiliation":[{"name":"N\u00facleo de Biotecnologia\u2014CDTec, Universidade Federal de Pelotas, Pelotas, RS, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ana Paula C.","family":"Argondizzo","sequence":"additional","affiliation":[{"name":"Instituto de Tecnologia em Imunobiol\u00f3gicos (Bio-Manguinhos), Funda\u00e7\u00e3o Oswaldo Cruz, Rio de Janeiro, RJ, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"\u00c9verton F.","family":"Silva","sequence":"additional","affiliation":[{"name":"N\u00facleo de Biotecnologia\u2014CDTec, Universidade Federal de Pelotas, Pelotas, RS, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fabiana K.","family":"Seixas","sequence":"additional","affiliation":[{"name":"N\u00facleo de Biotecnologia\u2014CDTec, Universidade Federal de Pelotas, Pelotas, RS, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amilton C. 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