The Effect of the Hepatitis B Vaccine Derived from Genotype C on Infants Born to Mothers Infected with Genotype D
Objective There is a paucity of information on whether the hepatitis B virus (HBV) vaccine, derived from HBV genotype C, can prevent mother-to-child transmission of HBV genotype D. The aim of this study was to clarify this issue. Methods The subjects consisted of 25 children (8.5±4.1 years old, 7 ma...
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| Published in | Internal Medicine Vol. 59; no. 22; pp. 2825 - 2830 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Japan
The Japanese Society of Internal Medicine
15.11.2020
Japan Science and Technology Agency |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0918-2918 1349-7235 1349-7235 |
| DOI | 10.2169/internalmedicine.5090-20 |
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| Abstract | Objective There is a paucity of information on whether the hepatitis B virus (HBV) vaccine, derived from HBV genotype C, can prevent mother-to-child transmission of HBV genotype D. The aim of this study was to clarify this issue. Methods The subjects consisted of 25 children (8.5±4.1 years old, 7 males, 18 females), born to 17 mothers who were chronically infected with HBV genotype D. Of these, 20 children were inoculated with the genotype C-derived vaccine, one was inoculated with the genotype A-derived vaccine, and one was inoculated with both the A- and C-derived vaccines. Information on the type of vaccine given to the remaining three children was not available. The serum levels of HB surface antigen (HBsAg), antibody to HBsAg (anti-HBs), and antibody to HB core (anti-HBc) of the children, as well as HBV markers of the mothers, were examined. Results All mothers were positive for HBsAg (6,563±11,005 IU/mL), negative for HBeAg, and positive for anti-HBe. HBV-DNA levels (log IU/mL) were <3.3 in 7 mothers, 3.3-4.3 in 9 mothers, and >4.3 in one mother. HBsAg and anti-HBc were negative in all children, regardless of the type of vaccine used. Anti-HBs were positive in 13 children and negative in 12. Conclusion All children born to mothers infected with genotype D, including 20 who were inoculated with the genotype C-derived vaccine, were negative for both HBsAg and anti-HBc. These results suggest that the genotype C-derived HB vaccine is effective in preventing mother-to-child transmission from mothers infected with HBV genotype D. |
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| AbstractList | Objective There is a paucity of information on whether the hepatitis B virus (HBV) vaccine, derived from HBV genotype C, can prevent mother-to-child transmission of HBV genotype D. The aim of this study was to clarify this issue. Methods The subjects consisted of 25 children (8.5±4.1 years old, 7 males, 18 females), born to 17 mothers who were chronically infected with HBV genotype D. Of these, 20 children were inoculated with the genotype C-derived vaccine, one was inoculated with the genotype A-derived vaccine, and one was inoculated with both the A- and C-derived vaccines. Information on the type of vaccine given to the remaining three children was not available. The serum levels of HB surface antigen (HBsAg), antibody to HBsAg (anti-HBs), and antibody to HB core (anti-HBc) of the children, as well as HBV markers of the mothers, were examined. Results All mothers were positive for HBsAg (6,563±11,005 IU/mL), negative for HBeAg, and positive for anti-HBe. HBV-DNA levels (log IU/mL) were <3.3 in 7 mothers, 3.3-4.3 in 9 mothers, and >4.3 in one mother. HBsAg and anti-HBc were negative in all children, regardless of the type of vaccine used. Anti-HBs were positive in 13 children and negative in 12. Conclusion All children born to mothers infected with genotype D, including 20 who were inoculated with the genotype C-derived vaccine, were negative for both HBsAg and anti-HBc. These results suggest that the genotype C-derived HB vaccine is effective in preventing mother-to-child transmission from mothers infected with HBV genotype D. Objective There is a paucity of information on whether the hepatitis B virus (HBV) vaccine, derived from HBV genotype C, can prevent mother-to-child transmission of HBV genotype D. The aim of this study was to clarify this issue. Methods The subjects consisted of 25 children (8.5±4.1 years old, 7 males, 18 females), born to 17 mothers who were chronically infected with HBV genotype D. Of these, 20 children were inoculated with the genotype C-derived vaccine, one was inoculated with the genotype A-derived vaccine, and one was inoculated with both the A- and C-derived vaccines. Information on the type of vaccine given to the remaining three children was not available. The serum levels of HB surface antigen (HBsAg), antibody to HBsAg (anti-HBs), and antibody to HB core (anti-HBc) of the children, as well as HBV markers of the mothers, were examined. Results All mothers were positive for HBsAg (6,563±11,005 IU/mL), negative for HBeAg, and positive for anti-HBe. HBV-DNA levels (log IU/mL) were <3.3 in 7 mothers, 3.3-4.3 in 9 mothers, and >4.3 in one mother. HBsAg and anti-HBc were negative in all children, regardless of the type of vaccine used. Anti-HBs were positive in 13 children and negative in 12. Conclusion All children born to mothers infected with genotype D, including 20 who were inoculated with the genotype C-derived vaccine, were negative for both HBsAg and anti-HBc. These results suggest that the genotype C-derived HB vaccine is effective in preventing mother-to-child transmission from mothers infected with HBV genotype D.Objective There is a paucity of information on whether the hepatitis B virus (HBV) vaccine, derived from HBV genotype C, can prevent mother-to-child transmission of HBV genotype D. The aim of this study was to clarify this issue. Methods The subjects consisted of 25 children (8.5±4.1 years old, 7 males, 18 females), born to 17 mothers who were chronically infected with HBV genotype D. Of these, 20 children were inoculated with the genotype C-derived vaccine, one was inoculated with the genotype A-derived vaccine, and one was inoculated with both the A- and C-derived vaccines. Information on the type of vaccine given to the remaining three children was not available. The serum levels of HB surface antigen (HBsAg), antibody to HBsAg (anti-HBs), and antibody to HB core (anti-HBc) of the children, as well as HBV markers of the mothers, were examined. Results All mothers were positive for HBsAg (6,563±11,005 IU/mL), negative for HBeAg, and positive for anti-HBe. HBV-DNA levels (log IU/mL) were <3.3 in 7 mothers, 3.3-4.3 in 9 mothers, and >4.3 in one mother. HBsAg and anti-HBc were negative in all children, regardless of the type of vaccine used. Anti-HBs were positive in 13 children and negative in 12. Conclusion All children born to mothers infected with genotype D, including 20 who were inoculated with the genotype C-derived vaccine, were negative for both HBsAg and anti-HBc. These results suggest that the genotype C-derived HB vaccine is effective in preventing mother-to-child transmission from mothers infected with HBV genotype D. |
| Author | Ohno, Naofumi Hiasa, Yoichi Michitaka, Kojiro Tokumoto, Yoshio Ninomiya, Tomoyuki Hiraoka, Atsushi Watanabe, Takao Abe, Masanori Yoshida, Osamu |
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| Cites_doi | 10.1111/jgh.13030 10.1046/j.1440-1746.2003.03092.x 10.1099/0022-1317-73-5-1201 10.1111/j.1872-034X.2007.00043.x 10.1053/j.gastro.2016.05.048 10.1093/infdis/151.2.287 10.2957/kanzo.56.675 10.1111/j.1872-034X.2007.00120.x 10.1586/erv.11.151 10.1002/jmv.21035 10.1056/NEJMoa1007644 10.1007/s00535-017-1316-3 10.1016/S1386-6346(03)00168-2 10.1093/infdis/jiv750 10.1002/hep.29800 10.1053/j.gastro.2007.02.055 10.1001/jama.1996.03540110060032 10.2957/kanzo.30.836 10.1053/jhep.2001.27221 10.1002/jmv.20502 |
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| Keywords | anti-HBc vaccine hepatitis B virus genotype mother-to-child transmission |
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| References | 9. Kato M, Hamada-Tsutsumi S, Okuse C, et al. Effects of vaccine-acquired polyclonal anti-HBs antibodies on the prevention of HBV infection of non-vaccine genotypes. J Gastroenterol 52: 1051-1063, 2017. 1. World Health Organization. Hepatitis B [Internet]. [cited 2019 Jul 18]. Available from: https://www.who.int/news-room/fact-sheets/detail/hepatitis-b 19. Cassidy A, Mossman S, Olivieri A, De Ridder M, Leroux-Roels G. Hepatitis B vaccine effectiveness in the face of global HBV genotype diversity. Expert Rev Vaccines 10: 1709-1715, 2011. 6. Noto H, Terao T, Ryou S, et al. Combined passive and active immunoprophylaxis for preventing perinatal transmission of the hepatitis B virus carrier state in Shizuoka, Japan during 1980-1994. J Gastroenterol Hepatol 18: 943-949, 2003. 25. Ni YH, Huang LM, Chang MH, et al. Two decades of universal hepatitis B vaccination in Taiwan: impact and implication for future strategies. Gastroenterology 132: 1287-1293, 2007. 24. Van Damme P. Long-term protection after hepatitis B vaccine. J Infect Dis 214: 1-3, 2016. 26. Horiike N, Onji M, Ogawa Y, Michitaka K, Murota T, Ohta Y. Study of long-term prospective effect on family inhabitants of HBV carriers by administration of hepatitis B vaccine, with a special reference to the different subtype of HBV. Kanzo 30: 836-840, 1989 (in Japanese, Abstract in English). 20. Yotsuyanagi H, Takano T, Tanaka M, et al. Hepatitis B virus-related hepatocellular carcinoma in young adults: Efficacy of nationwide selective vaccination. Hepatol Res 50: 182-189, 2020. 15. Michitaka K, Tanaka Y, Horiike N, et al. Tracing the history of hepatitis B virus genotype D in western Japan. J Med Virol 78: 44-52, 2006. 12. Terrault NA, Lok ASF, McMahon BJ, et al. Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance. Hepatology 67: 1560-1599, 2018. 16. Matsuura K, Michitaka K, Yamauchi K, et al. Characteristics of geographic distributions and route of infection for hepatitis B virus genotype D in Ehime area in western Japan. Hepatol Res 37: 255-262, 2007. 18. Chang MH, You SL, Chen CJ, et al. Long-term effects of hepatitis B immunization of infants in preventing liver cancer. Gastroenterology 151: 472-480, 2016. 13. Orito E, Ichida T, Sakugawa H, et al. Geographic distribution of hepatitis B virus (HBV) genotype in patients with chronic HBV infection in Japan. Hepatology 34: 590-594, 2001. 4. Kanai K, Takehiro A, Noto H, et al. Prevention of perinatal transmission of hepatitis B virus (HBV) to children of e antigen-positive HBV carrier mothers by hepatitis B immune globulin and HBV vaccine. J Infect Dis 151: 287-290, 1985. 5. Koyama T, Matsuda I, Sato S, Yoshizawa H. Prevention of perinatal hepatitis B virus transmission by combined passive-active immunoprophylaxis in Iwate, Japan (1981-1992) and epidemiological evidence for its efficacy. Hepatol Res 26: 287-292, 2003. 14. Ito K, Yotsuyanagi H, Sugiyama M, et al. Geographic distribution and characteristics of genotype A hepatitis B virus infection in acute and chronic hepatitis B patients in Japan. J Gastroenterol Hepatol 31: 180-189, 2016. 7. Chen HL, Chang MH, Ni YH, et al. Seroepidemiology of hepatitis B virus infection in children: ten years of mass vaccination in Taiwan. JAMA 276: 906-908, 1996. 23. Sodeyama T, Kobayashi M. Efficacy of HB vaccine. Nippon Rinsho 62 (Suppl 8): 216-221, 2004 (in Japanese). 21. Avazova D, Kurbanov F, Tanaka Y, et al. Hepatitis B virus transmission pattern and vaccination efficiency in Uzbekistan. J Med Virol 80: 217-224, 2008. 10. Stramer SL, Wend U, Candotti D, et al. Nucleic acid testing to detect HBV infection in blood donors. N Engl J Med 364: 236-247, 2011. 11. Norder H, Hammas B, Löfdahl S, et al. Comparison of the amino acid sequences of nine different serotypes of hepatitis B surface antigen and genomic classification of the corresponding hepatitis B virus strains. J Gen Virol 73: 1201-1208, 1992. 8. Aono J, Yotsuyanagi H, Miyoshi H, et al. Amino acid substitutions in the S region of hepatitis B virus in sera from patients with acute hepatitis. Hepatol Res 37: 731-739, 2007. 17. Ogawa M, Akine D, Sasahara T. Comparison of hepatitis B vaccine efficacy in Japanese students: a retrospective study. Environ Health Prev Med 24: 80, 2019. 3. World Health Organization. Hepatitis B vaccines: WHO position paper-July 2017. Weekly epidemiological record [Internet]. 2017 [cited 2020 Mar 1]; 92: 369-392. Available from: https://www.who.int/wer 22. Nommensen FE, Go ST, Maclaren DM. Half-life of HBs antibody after hepatitis B vaccination: an aid to timing of booster vaccination. Lancet 2: 847-849, 1989. 27. Komatsu H, Iwasawa K, Inui A, et al. Effectiveness of genotype C-derived hepatitis B vaccine in preventing perinatal transmission in children born to hepatitis B virus carrier mothers infected with genotype A. Kanzo 56: 675-677, 2015 (in Japanese, Abstract in English). 2. Schillie S, Vellozzi C, Reingold A, et al. Prevention of hepatitis B virus infection in the United States: recommendations of the advisory committee on immunization practices. MMWR Recomm Rep 67: 1-31, 2018. 22 23 24 25 26 27 HL Chen (7) 1996; 276 10 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 8 9 20 21 |
| References_xml | – reference: 9. Kato M, Hamada-Tsutsumi S, Okuse C, et al. Effects of vaccine-acquired polyclonal anti-HBs antibodies on the prevention of HBV infection of non-vaccine genotypes. J Gastroenterol 52: 1051-1063, 2017. – reference: 22. Nommensen FE, Go ST, Maclaren DM. Half-life of HBs antibody after hepatitis B vaccination: an aid to timing of booster vaccination. Lancet 2: 847-849, 1989. – reference: 27. Komatsu H, Iwasawa K, Inui A, et al. Effectiveness of genotype C-derived hepatitis B vaccine in preventing perinatal transmission in children born to hepatitis B virus carrier mothers infected with genotype A. Kanzo 56: 675-677, 2015 (in Japanese, Abstract in English). – reference: 24. Van Damme P. Long-term protection after hepatitis B vaccine. J Infect Dis 214: 1-3, 2016. – reference: 3. World Health Organization. Hepatitis B vaccines: WHO position paper-July 2017. Weekly epidemiological record [Internet]. 2017 [cited 2020 Mar 1]; 92: 369-392. Available from: https://www.who.int/wer – reference: 19. Cassidy A, Mossman S, Olivieri A, De Ridder M, Leroux-Roels G. Hepatitis B vaccine effectiveness in the face of global HBV genotype diversity. Expert Rev Vaccines 10: 1709-1715, 2011. – reference: 13. Orito E, Ichida T, Sakugawa H, et al. Geographic distribution of hepatitis B virus (HBV) genotype in patients with chronic HBV infection in Japan. Hepatology 34: 590-594, 2001. – reference: 6. Noto H, Terao T, Ryou S, et al. Combined passive and active immunoprophylaxis for preventing perinatal transmission of the hepatitis B virus carrier state in Shizuoka, Japan during 1980-1994. J Gastroenterol Hepatol 18: 943-949, 2003. – reference: 21. Avazova D, Kurbanov F, Tanaka Y, et al. Hepatitis B virus transmission pattern and vaccination efficiency in Uzbekistan. J Med Virol 80: 217-224, 2008. – reference: 11. Norder H, Hammas B, Löfdahl S, et al. Comparison of the amino acid sequences of nine different serotypes of hepatitis B surface antigen and genomic classification of the corresponding hepatitis B virus strains. J Gen Virol 73: 1201-1208, 1992. – reference: 12. Terrault NA, Lok ASF, McMahon BJ, et al. Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance. Hepatology 67: 1560-1599, 2018. – reference: 14. Ito K, Yotsuyanagi H, Sugiyama M, et al. Geographic distribution and characteristics of genotype A hepatitis B virus infection in acute and chronic hepatitis B patients in Japan. J Gastroenterol Hepatol 31: 180-189, 2016. – reference: 25. Ni YH, Huang LM, Chang MH, et al. Two decades of universal hepatitis B vaccination in Taiwan: impact and implication for future strategies. Gastroenterology 132: 1287-1293, 2007. – reference: 26. Horiike N, Onji M, Ogawa Y, Michitaka K, Murota T, Ohta Y. Study of long-term prospective effect on family inhabitants of HBV carriers by administration of hepatitis B vaccine, with a special reference to the different subtype of HBV. Kanzo 30: 836-840, 1989 (in Japanese, Abstract in English). – reference: 18. Chang MH, You SL, Chen CJ, et al. Long-term effects of hepatitis B immunization of infants in preventing liver cancer. Gastroenterology 151: 472-480, 2016. – reference: 20. Yotsuyanagi H, Takano T, Tanaka M, et al. Hepatitis B virus-related hepatocellular carcinoma in young adults: Efficacy of nationwide selective vaccination. Hepatol Res 50: 182-189, 2020. – reference: 15. Michitaka K, Tanaka Y, Horiike N, et al. Tracing the history of hepatitis B virus genotype D in western Japan. J Med Virol 78: 44-52, 2006. – reference: 8. Aono J, Yotsuyanagi H, Miyoshi H, et al. Amino acid substitutions in the S region of hepatitis B virus in sera from patients with acute hepatitis. Hepatol Res 37: 731-739, 2007. – reference: 16. Matsuura K, Michitaka K, Yamauchi K, et al. Characteristics of geographic distributions and route of infection for hepatitis B virus genotype D in Ehime area in western Japan. Hepatol Res 37: 255-262, 2007. – reference: 23. Sodeyama T, Kobayashi M. Efficacy of HB vaccine. Nippon Rinsho 62 (Suppl 8): 216-221, 2004 (in Japanese). – reference: 2. Schillie S, Vellozzi C, Reingold A, et al. Prevention of hepatitis B virus infection in the United States: recommendations of the advisory committee on immunization practices. MMWR Recomm Rep 67: 1-31, 2018. – reference: 5. Koyama T, Matsuda I, Sato S, Yoshizawa H. Prevention of perinatal hepatitis B virus transmission by combined passive-active immunoprophylaxis in Iwate, Japan (1981-1992) and epidemiological evidence for its efficacy. Hepatol Res 26: 287-292, 2003. – reference: 17. Ogawa M, Akine D, Sasahara T. Comparison of hepatitis B vaccine efficacy in Japanese students: a retrospective study. Environ Health Prev Med 24: 80, 2019. – reference: 1. World Health Organization. Hepatitis B [Internet]. [cited 2019 Jul 18]. Available from: https://www.who.int/news-room/fact-sheets/detail/hepatitis-b – reference: 7. Chen HL, Chang MH, Ni YH, et al. Seroepidemiology of hepatitis B virus infection in children: ten years of mass vaccination in Taiwan. JAMA 276: 906-908, 1996. – reference: 4. Kanai K, Takehiro A, Noto H, et al. Prevention of perinatal transmission of hepatitis B virus (HBV) to children of e antigen-positive HBV carrier mothers by hepatitis B immune globulin and HBV vaccine. J Infect Dis 151: 287-290, 1985. – reference: 10. Stramer SL, Wend U, Candotti D, et al. Nucleic acid testing to detect HBV infection in blood donors. N Engl J Med 364: 236-247, 2011. – ident: 2 – ident: 14 doi: 10.1111/jgh.13030 – ident: 6 doi: 10.1046/j.1440-1746.2003.03092.x – ident: 11 doi: 10.1099/0022-1317-73-5-1201 – ident: 16 doi: 10.1111/j.1872-034X.2007.00043.x – ident: 18 doi: 10.1053/j.gastro.2016.05.048 – ident: 4 doi: 10.1093/infdis/151.2.287 – ident: 27 doi: 10.2957/kanzo.56.675 – ident: 8 doi: 10.1111/j.1872-034X.2007.00120.x – ident: 19 doi: 10.1586/erv.11.151 – ident: 20 – ident: 21 doi: 10.1002/jmv.21035 – ident: 10 doi: 10.1056/NEJMoa1007644 – ident: 9 doi: 10.1007/s00535-017-1316-3 – ident: 22 – ident: 17 – ident: 3 – ident: 5 doi: 10.1016/S1386-6346(03)00168-2 – ident: 1 – ident: 24 doi: 10.1093/infdis/jiv750 – ident: 12 doi: 10.1002/hep.29800 – ident: 25 doi: 10.1053/j.gastro.2007.02.055 – volume: 276 start-page: 906 issn: 0098-7484 year: 1996 ident: 7 publication-title: JAMA The Journal of the American Medical Association doi: 10.1001/jama.1996.03540110060032 – ident: 26 doi: 10.2957/kanzo.30.836 – ident: 13 doi: 10.1053/jhep.2001.27221 – ident: 15 doi: 10.1002/jmv.20502 – ident: 23 |
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| SubjectTerms | Adult anti-HBc Child Child, Preschool Children DNA, Viral - genetics Female Genotype Genotype & phenotype Genotypes Hepatitis Hepatitis B Hepatitis B - genetics Hepatitis B - immunology Hepatitis B - prevention & control Hepatitis B Antibodies - blood Hepatitis B e antigen Hepatitis B surface antigen Hepatitis B Surface Antigens - blood Hepatitis B Vaccines - immunology hepatitis B virus Humans Infants Infectious Disease Transmission, Vertical - prevention & control Internal medicine Japan Male mother-to-child transmission Mothers Original Serum levels vaccine Vaccines |
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| Title | The Effect of the Hepatitis B Vaccine Derived from Genotype C on Infants Born to Mothers Infected with Genotype D |
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