scholarly journals Quantifying perinatal transmission of Hepatitis B viral quasispecies by tag linkage deep sequencing

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Yushen Du ◽  
Xiumei Chi ◽  
Chong Wang ◽  
Jing Jiang ◽  
Fei Kong ◽  
...  
1987 ◽  
Vol 21 (4) ◽  
pp. 301-309 ◽  
Author(s):  
Tsang-Ming Ko ◽  
Fon-Jou Hsieh ◽  
Chih-Liang Yaung ◽  
Ding-Shinn Chen ◽  
Kai-Hsin Lin ◽  
...  

PEDIATRICS ◽  
1985 ◽  
Vol 75 (2) ◽  
pp. 362-364
Author(s):  

Infants born to mothers who are hepatitis B surface antigen (HBsAg) positive are frequently infected with hepatitis B virus (HBV). Many of these newborns will become chronic carriers of HBV and will subsequently develop chronic liver disease. Recent studies have demonstrated that perinatal transmission can be prevented by immunization of the newborn. Recommendations for the management of infants at risk are presented. PERINATAL TRANSMISSION OF HBV INFECTIONS Perinatal infection of infants by mothers who are HBsAg positive is most likely to occur if mothers are also hepatitis Be antigen positive. About 90% of infants whose mothers are positive for both markers will become infected and most will become permanent carriers.1 Infants whose mothers are HBeAg negative or who have antibody to HBeAg are at lesser risk, but can still be infected.2 Infected infants usually will not become HBsAg positive until several weeks after birth. Although clinical jaundice or acute hepatitis are rare in infected infants, elevations in transaminase levels are frequent.3 It is estimated that about one in four infants who become chronic carriers following perinatal infection will develop cirrhosis or hepatocellular carcinoma later in life. As they are persistent carriers, later in life they may transmit infection to other family members, to sexual contacts, or to others by transfusions or inoculation of their blood. Infection of female infants may eventually result in transmission of HBV to their own infants. Indeed, transmission from mother to infant is a major method of perpetuation of this virus in hyperendemic areas, eg, the Far East.


PLoS ONE ◽  
2015 ◽  
Vol 10 (12) ◽  
pp. e0144816 ◽  
Author(s):  
Andrea Caballero ◽  
Josep Gregori ◽  
Maria Homs ◽  
David Tabernero ◽  
Carolina Gonzalez ◽  
...  

2013 ◽  
Vol 6 (3) ◽  
pp. 231-236 ◽  
Author(s):  
O. Atinuke Olaleye ◽  
O. Kuti ◽  
N. Olaniyi Makinde ◽  
A.O. Innocent Ujah ◽  
O. Akinyemi Olaleye ◽  
...  

2020 ◽  
Vol 5 (3) ◽  
pp. 108
Author(s):  
Francisca Varpit ◽  
Bruce Gummow

Hepatitis B virus (HBV) infection is a serious problem and earlier studies in Papua New Guinea have reported a high prevalence of hepatitis B virus infection. These studies were undertaken using insensitive tests and before an expanded immunization program. The current HBV status is therefore uncertain. A retrospective study to investigate the HBV status was carried out using blood donor data at Nonga General Hospital, East New Britain Province, Papua New Guinea, from January 2003 to December 2018. Additional data for Human Immunodeficiency Virus, syphilis and hepatitis C virus were also collected. Data were analysed using NCSS statistical software. The mean hepatitis B antigen (HBsAg) sero-prevalence was 21% for the period of study and showed a downward trend over the period of the study, which may reflect the effect of the extended immunization program. HBsAg prevalence in male donors (23%) was significantly higher than females (16%). Donors living in Pomio district had a significantly lower proportion of sero-positive HBsAg donors (7%) than Gazelle (22%), Kokopo (22%) and Rabaul (20%), which was attributed to this district’s geographical isolation. Ethnically, Pomios donors (8%) had significantly lower HBsAg prevalence than the Taulils, (29%), Bainings (21%) and Tolais (21%). Fifteen to nineteen year olds (23%) were the predominant age group affected, and vertical or perinatal transmission was probably the primary transmission route. Our findings call for greater awareness on the part of public policy makers and should be considered when planning future public health campaigns.


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