PERSISTENCE OF HEPATITIS-A VIRUS IN FULMINANT-HEPATITIS AND AFTER LIVER-TRANSPLANTATION

被引:48
作者
FAGAN, E
YOUSEF, G
BRAHM, J
GARELICK, H
MANN, G
WOLSTENHOLME, A
PORTMANN, B
HARRISON, T
MOWBRAY, JF
MOWAT, A
ZUCKERMAN, A
WILLIAMS, R
机构
[1] UNIV LONDON KINGS COLL HOSP,LIVER UNIT,DENMARK HILL,LONDON SE5 8RX,ENGLAND
[2] ST MARYS HOSP,SCH MED,DEPT EXPTL PATHOL,LONDON,ENGLAND
[3] UNIV LONDON LONDON SCH HYG & TROP MED,DEPT MED MICROBIOL,LONDON WC1E 7HT,ENGLAND
[4] UNIV LONDON KINGS COLL HOSP,DEPT CHILD HLTH,LONDON SE5 8RX,ENGLAND
关键词
DNA probe; fulminant hepatic failure; monoclonal antibodies; persistent virus infection;
D O I
10.1002/jmv.1890300210
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A peroxidase‐labelled, specific mouse monoclonal antibody to hepatitis A virus (HAV) and an in situ hybridization technique (streptavidin‐biotin‐horseradish peroxidase reaction) with an HAV‐specific cDNA probe (recombinant plasmid pAWHA comprising 1.8 kb of the HAV‐specific cDNA, located toward the 3′ end of the genome) were used to detect HAV in liver tissues in two patients with fulminant viral hepatitis type A treated by liver transplantation after a protracted (day 40: case 1) and relapsing (day 60: case 2) clinical course. HAV antigens and HAV‐specific genomic sequences were detected in the hepatectomy tissues and in serial biopsies of the liver grafts through to final follow‐up at 2 months (case 2) or death at 7 months after re‐grafting for chronic rejection (case 1). In the fulminant liver parenchyma, numerous degenerating and some surviving hepatocytes were positive and randomly scattered. The immunoperoxidase staining was predominantly cytoplasmic and often granular. The localization of the cDNA probe was predominantly nuclear/perinuclear but was occasionally cytoplasmic. High‐titre IgM‐anti‐HAV antibodies persisted until death (case 1) or resolution (5 months) of an acute hepatitis (case 2), which occurred at 2 months, accompanied by HAV antigen (ELISA), in stool. Intact replicating virus particles must have been present in one or more sites in each case, including extrahepatic locations, with a viraemia as the most likely explanation for subsequent reinfection of the grafts. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:131 / 136
页数:6
相关论文
共 30 条
[1]   PRIMARY ISOLATION AND SERIAL PASSAGE OF HEPATITIS-A VIRUS-STRAINS IN PRIMATE CELL-CULTURES [J].
BINN, LN ;
LEMON, SM ;
MARCHWICKI, RH ;
REDFIELD, RR ;
GATES, NL ;
BANCROFT, WH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 20 (01) :28-33
[2]  
BOWLES NE, 1987, LANCET, V1, P1004
[3]  
BOWLES NE, 1986, LANCET, V1, P1120
[4]   MULTIPLICATION OF HEPATITIS-B VIRUS IN FULMINANT HEPATITIS-B [J].
BRECHOT, C ;
BERNUAU, J ;
THIERS, V ;
DUBOIS, F ;
GOUDEAU, A ;
RUEFF, B ;
TIOLLAIS, P ;
BENHAMOU, JP .
BMJ-BRITISH MEDICAL JOURNAL, 1984, 288 (6413) :270-271
[5]   A BIPHASIC ILLNESS ASSOCIATED WITH ACUTE HEPATITIS - A VIRUS-INFECTION [J].
COBDEN, I ;
JAMES, OFW .
JOURNAL OF HEPATOLOGY, 1986, 2 (01) :19-23
[6]   PROPAGATION OF HUMAN HEPATITIS-A VIRUS IN AFRICAN-GREEN MONKEY KIDNEY-CELL CULTURE - PRIMARY ISOLATION AND SERIAL PASSAGE [J].
DAEMER, RJ ;
FEINSTONE, SM ;
GUST, ID ;
PURCELL, RH .
INFECTION AND IMMUNITY, 1981, 32 (01) :388-393
[7]  
DELELLIS SR, 1979, AM J CLIN PATHOL, V7, P483
[8]   PROPAGATION OF HUMAN HEPATITIS-A VIRUS IN A HEPATOMA-CELL LINE [J].
FROSNER, GG ;
DEINHARDT, F ;
SCHEID, R ;
GAUSSMULLER, V ;
HOLMES, N ;
MESSELBERGER, V ;
SIEGL, G ;
ALEXANDER, JJ .
INFECTION, 1979, 7 (06) :303-305
[9]  
GARELICK H, 1988, VIRAL HEPATITIS LIVE, P12
[10]  
GAUSSMULLER V, 1984, P SOC EXP BIOL MED, V175, P10, DOI 10.3181/00379727-175-41757