YEN-HSUAN NIHO-HSIUNG LINPEI-JER CHENHONG-YUAN HSUChen D.-S.MEI-HWEI CHANG2021-07-032021-07-0319940168-8278https://www.scopus.com/inward/record.uri?eid=2-s2.0-0028302817&doi=10.1016%2fS0168-8278%2805%2980353-8&partnerID=40&md5=ed3047aad1f7747709470c2b7f746a3bhttps://scholars.lib.ntu.edu.tw/handle/123456789/568892To investigate mother-to-infant transmission of hepatitis C virus, serial follow-up of anti-HCV and hepatitis C virus RNA was undertaken in 11 infants born to hepatitis C virus-infected mothers who had been screened from 11 688 pregnant women. None of the hepatitis C virus-infected mothers was infected by human immunodeficiency virus. Anti-HCV was checked by the second-generation enzyme immunoassay kit, and hepatitis C virus RNA was examined by reverse transcriptase-nested polymerase chain reaction. Hepatitis C virus RNA was found in more than two serum samples in two of these 11 infants; those two infants were regarded as hepatitis C virus-infected. One of the two had hepatitis C virus RNA at the age of 1, 3, and 6 months, but not later. The course of hepatitis C virus RNA and anti-HCV in this baby may reflect fluctuating viral replication in chronic infectious disease or viral clearance in acute infection. The other infant had hepatitis C virus RNA detectable at the age of 3 months and at 15, 18 and 24 months. In the other nine non-hepatitis C virus-infected infants, maternally acquired anti-HCV gradually disappeared by the age of 6 months. The liver function profile fell to the normal range in all the infants, including the two hepatitis C virus-infected infants. This may indicate the subclinical nature of hepatitis C virus infection in infancy. Seven fathers and four siblings of these 11 infants were checked for anti-HCV and liver function tests; none had evidence of hepatitis C virus infection. These results show that the rate of mother-to-infant transmission of hepatitis C virus from mothers without human immunodeficiency virus coinfection is about 18% and that hepatitis C virus infection in these patients seemed to run a subclinical course. ? 1994 Journal of Hepatology.[SDGs]SDG3antibody response; article; clinical article; controlled study; follow up; hepatitis c; hepatitis c virus; human; human immunodeficiency virus infection; infant; polymerase chain reaction; priority journal; taiwan; vertical transmission; virus genome; Base Sequence; Female; Genome, Viral; Hepacivirus; Hepatitis Antibodies; Hepatitis C; HIV Infections; Human; Infant, Newborn; Maternal-Fetal Exchange; Molecular Probes; Molecular Sequence Data; Polymerase Chain Reaction; Pregnancy; Pregnancy Complications, Infectious; RNA, Viral; Support, Non-U.S. Gov't; Time Factors; Transcription, Geneticjournal article10.1016/S0168-8278(05)80353-880715412-s2.0-0028302817