{"title":"Tests in rufiventer and other marmosets of susceptibility to human hepatitis A virus.","authors":"P J Provost, V M Villarejos, M R Hilleman","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The rufiventer marmoset proved equally satisfactory to S. mystax for studies of human hepatitis A virus. C. jacchus, C. argentata, S. weddelli, and S. oedipomidas oedipus were not satisfactory. Livers of rufiventer marmosets produced satisfactory CR326 strain hepatitis A antigen for immune adherence tests both in amount and specificity. Rufiventer marmosets infected with human hepatitis A virus showed enzyme elevations and high titers of viral antigen in their livers as early as seven days after viral inoculation, indicating that a primary viral infection can cause hepatitis without need for a secondary autoimmune response to liver tissue.</p>","PeriodicalId":76345,"journal":{"name":"Primates in medicine","volume":"10 ","pages":"288-94"},"PeriodicalIF":0.0000,"publicationDate":"1978-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Primates in medicine","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The rufiventer marmoset proved equally satisfactory to S. mystax for studies of human hepatitis A virus. C. jacchus, C. argentata, S. weddelli, and S. oedipomidas oedipus were not satisfactory. Livers of rufiventer marmosets produced satisfactory CR326 strain hepatitis A antigen for immune adherence tests both in amount and specificity. Rufiventer marmosets infected with human hepatitis A virus showed enzyme elevations and high titers of viral antigen in their livers as early as seven days after viral inoculation, indicating that a primary viral infection can cause hepatitis without need for a secondary autoimmune response to liver tissue.