H. Noto , Y. Fujii , K. Takahashi , S. Kishimoto , S. Mishiro
{"title":"含pres2疫苗对乙型肝炎病毒疫苗逃逸变体(Thr127)感染婴儿的治疗效果","authors":"H. Noto , Y. Fujii , K. Takahashi , S. Kishimoto , S. Mishiro","doi":"10.1016/S0928-4346(96)00343-X","DOIUrl":null,"url":null,"abstract":"<div><p>A male baby born to HBV-infected mother received HBIG and vaccine (S-gene recombinant) according to the conventional protocol for prevention of vertical HBV transmission, but did not show active production of anti-HBs. Additional two shots of S-gene recombinant vaccines at months 9 and 12 also failed to induce antibody despite increased doses. Then, at months 14, 15, and 19, a preS2-containing vaccine was injected, followed by a prompt seroconversion to anti-HBs. Retrospective analyses of the baby's sera revealed that HBV DNA was repeatedly positive in this baby's sera throughout the period of time when anti-HBs antibody remained negative (months 6–15). Genetic analyses of HBV DNA from the mother and her baby showed that: (i) mother's HBV DNA was a mixture of <em>adw</em> and <em>adr</em> subtypes, whereas baby's HBV DNA consisted solely of <em>adr</em> subtype; and (ii) baby's HBV was a S-gene variant with its 127th codon coding for threonine instead of proline that is typical to wild type HBV/<em>adr</em> (Thr<sup>127</sup>). Thus, it seems in this case that the Thr<sup>127</sup> mutant did escape conventional vaccines but could not escape preS2-induced immune response, and that eventually the preS2-containing vaccine worked as a therapeutic vaccine.</p></div>","PeriodicalId":13746,"journal":{"name":"International Hepatology Communications","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0928-4346(96)00343-X","citationCount":"4","resultStr":"{\"title\":\"Therapeutic effect of preS2-containing vaccine in an infant infected with a vaccine-escape variant (Thr127) of hepatitis B virus\",\"authors\":\"H. Noto , Y. Fujii , K. Takahashi , S. Kishimoto , S. Mishiro\",\"doi\":\"10.1016/S0928-4346(96)00343-X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A male baby born to HBV-infected mother received HBIG and vaccine (S-gene recombinant) according to the conventional protocol for prevention of vertical HBV transmission, but did not show active production of anti-HBs. Additional two shots of S-gene recombinant vaccines at months 9 and 12 also failed to induce antibody despite increased doses. Then, at months 14, 15, and 19, a preS2-containing vaccine was injected, followed by a prompt seroconversion to anti-HBs. Retrospective analyses of the baby's sera revealed that HBV DNA was repeatedly positive in this baby's sera throughout the period of time when anti-HBs antibody remained negative (months 6–15). Genetic analyses of HBV DNA from the mother and her baby showed that: (i) mother's HBV DNA was a mixture of <em>adw</em> and <em>adr</em> subtypes, whereas baby's HBV DNA consisted solely of <em>adr</em> subtype; and (ii) baby's HBV was a S-gene variant with its 127th codon coding for threonine instead of proline that is typical to wild type HBV/<em>adr</em> (Thr<sup>127</sup>). Thus, it seems in this case that the Thr<sup>127</sup> mutant did escape conventional vaccines but could not escape preS2-induced immune response, and that eventually the preS2-containing vaccine worked as a therapeutic vaccine.</p></div>\",\"PeriodicalId\":13746,\"journal\":{\"name\":\"International Hepatology Communications\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0928-4346(96)00343-X\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Hepatology Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S092843469600343X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Hepatology Communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S092843469600343X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Therapeutic effect of preS2-containing vaccine in an infant infected with a vaccine-escape variant (Thr127) of hepatitis B virus
A male baby born to HBV-infected mother received HBIG and vaccine (S-gene recombinant) according to the conventional protocol for prevention of vertical HBV transmission, but did not show active production of anti-HBs. Additional two shots of S-gene recombinant vaccines at months 9 and 12 also failed to induce antibody despite increased doses. Then, at months 14, 15, and 19, a preS2-containing vaccine was injected, followed by a prompt seroconversion to anti-HBs. Retrospective analyses of the baby's sera revealed that HBV DNA was repeatedly positive in this baby's sera throughout the period of time when anti-HBs antibody remained negative (months 6–15). Genetic analyses of HBV DNA from the mother and her baby showed that: (i) mother's HBV DNA was a mixture of adw and adr subtypes, whereas baby's HBV DNA consisted solely of adr subtype; and (ii) baby's HBV was a S-gene variant with its 127th codon coding for threonine instead of proline that is typical to wild type HBV/adr (Thr127). Thus, it seems in this case that the Thr127 mutant did escape conventional vaccines but could not escape preS2-induced immune response, and that eventually the preS2-containing vaccine worked as a therapeutic vaccine.