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 inInternal Medicine Vol. 59; no. 22; pp. 2825 - 2830
Main Authors Michitaka, Kojiro, Ohno, Naofumi, Hiasa, Yoichi, Watanabe, Takao, Tokumoto, Yoshio, Abe, Masanori, Yoshida, Osamu, Hiraoka, Atsushi, Ninomiya, Tomoyuki
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society of Internal Medicine 15.11.2020
Japan Science and Technology Agency
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Online AccessGet full text
ISSN0918-2918
1349-7235
1349-7235
DOI10.2169/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.
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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  fullname: Michitaka, Kojiro
  organization: Gastroenterology Center, Ehime Prefectural Central Hospital, Japan
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  fullname: Ohno, Naofumi
  organization: Ohno Naika-Shokakika, Japan
– sequence: 1
  fullname: Hiasa, Yoichi
  organization: Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Japan
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  fullname: Watanabe, Takao
  organization: Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Japan
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  fullname: Tokumoto, Yoshio
  organization: Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Japan
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  fullname: Abe, Masanori
  organization: Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Japan
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Cites_doi 10.1111/jgh.13030
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Issue 22
Keywords anti-HBc
vaccine
hepatitis B virus
genotype
mother-to-child transmission
Language English
License The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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Correspondence to Dr. Kojiro Michitaka, c-kmichitaka@eph.pref.ehime.jp
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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.
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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
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Snippet 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...
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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
URI https://www.jstage.jst.go.jp/article/internalmedicine/59/22/59_5090-20/_article/-char/en
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