Gulnara P. Borja-Cabrera , Flavia B. Santos , Dirlei Nico , A.E. Gravino , Laura Manna , Marcos Palatnik , Clarisa B. Palatnik-de-Sousa
{"title":"The Leishmune®́s Nucleoside hydrolase DNA vaccine as an aid in immunotherapy of canine visceral leishmaniasis","authors":"Gulnara P. Borja-Cabrera , Flavia B. Santos , Dirlei Nico , A.E. Gravino , Laura Manna , Marcos Palatnik , Clarisa B. Palatnik-de-Sousa","doi":"10.1016/j.provac.2012.04.009","DOIUrl":null,"url":null,"abstract":"<div><p>The Nucleoside hydrolase of <em>Leishmania donovani</em> (NH36) is the main antigen of Leishmune®, the first licensed prophylactic vaccine against canine visceral leishmaniasis (CVL). Compared to untreated controls, mongrel dogs infected with 7 x 108 <em>Leishmania chagasi</em> amastigotes and treated with the NH36-DNA vaccine developed significant increases in the size and proportions of DTH reactions and NH36-specific CD4+ T cell proportions which recognized the C-terminal moiety of NH36. Increases in IgG2/IgG1 anti-NH36 antibody ratios and in CD8+ T cell counts were directed to the NH36 N-terminal. The immunotherapy treatment reduced the parasite load and loss of weight and increased dog survival time.</p></div>","PeriodicalId":89221,"journal":{"name":"Procedia in vaccinology","volume":"6 ","pages":"Pages 64-73"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.provac.2012.04.009","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Procedia in vaccinology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1877282X12000112","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13
Abstract
The Nucleoside hydrolase of Leishmania donovani (NH36) is the main antigen of Leishmune®, the first licensed prophylactic vaccine against canine visceral leishmaniasis (CVL). Compared to untreated controls, mongrel dogs infected with 7 x 108 Leishmania chagasi amastigotes and treated with the NH36-DNA vaccine developed significant increases in the size and proportions of DTH reactions and NH36-specific CD4+ T cell proportions which recognized the C-terminal moiety of NH36. Increases in IgG2/IgG1 anti-NH36 antibody ratios and in CD8+ T cell counts were directed to the NH36 N-terminal. The immunotherapy treatment reduced the parasite load and loss of weight and increased dog survival time.