Lytic replication of Epstein-Barr virus in the peripheral blood: Analysis of viral gene expression in B lymphocytes during infectious mononucleosis and in the normal carrier state

被引:74
作者
Prang, NS
Hornef, MW
Jager, M
Wagner, HJ
Wolf, H
Schwarzmann, FM
机构
[1] UNIV REGENSBURG,INST MED MIKROBIOL & HYG,D-93053 REGENSBURG,GERMANY
[2] UNIV LUBECK,INST IMMUNOL & TRANSFUS MED,D-2400 LUBECK,GERMANY
关键词
D O I
10.1182/blood.V89.5.1665.1665_1665_1677
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epstein-Barr virus (EBV) has been shown to establish latency in resting B lymphocytes of the peripheral blood, This creates a virus reservoir in contrast to lytic virus replication, which is thought to be restricted to differentiated epithelial cells in vivo. So far, the route of transmission between B cells and the production of progeny virus in the epithelial tissue has remained unclear. Reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemistry analysis of 16 patients with acute infectious mononucleosis (IM) and 25 healthy seropositive donors was performed to detect lytic replication gene products in B lymphocytes of the peripheral blood, Transcriptional activity was found in peripheral blood B lymphocytes (PBLs) for BZLF1 in 88%, BALF2 in 50%, and BcLF1 in 25% of the tested IM patients. All positive results were further confirmed in enriched B-cell populations by antigen determination using immunostaining with the APAAP technique. Furthermore, we detected transcripts for BZLF1 in 72% and for BALF2 in 16% of peripheral B lymphocytes of healthy seropositive donors. In contrast to patients with IM, no signals for BcLF1 were ever found in healthy seropositive donors, In these individuals, lytic replication of EBV is probably restricted by immunologic and gene regulatory mechanisms, whereas in the absence of immunologic control, reflected here by IM patients, the production of infectious virus becomes visible in PBLs, (C) 1997 by The American Society of Hematology.
引用
收藏
页码:1665 / 1677
页数:13
相关论文
共 67 条
[1]   MORPHOLOGY, IMMUNOPHENOTYPE, AND DISTRIBUTION OF LATENTLY AND/OR PRODUCTIVELY EPSTEIN-BARR VIRUS-INFECTED CELLS IN ACUTE INFECTIOUS-MONONUCLEOSIS - IMPLICATIONS FOR THE INTERINDIVIDUAL INFECTION ROUTE OF EPSTEIN-BARR-VIRUS [J].
ANAGNOSTOPOULOS, I ;
HUMMEL, M ;
KRESCHEL, C ;
STEIN, H .
BLOOD, 1995, 85 (03) :744-750
[2]   CD28 INTERACTION WITH B7-COSTIMULATES PRIMARY ALLOGENEIC PROLIFERATIVE RESPONSES AND CYTOTOXICITY MEDIATED BY SMALL, RESTING LYMPHOCYTES-T [J].
AZUMA, M ;
CAYABYAB, M ;
BUCK, D ;
PHILLIPS, JH ;
LANIER, LL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (02) :353-360
[3]   EPSTEIN-BARR VIRUS-INDUCED CELL-FUSION [J].
BAYLISS, GJ ;
WOLF, H .
NATURE, 1980, 287 (5778) :164-165
[4]   EXPRESSION OF PROTEINS ENCODED BY EPSTEIN-BARR-VIRUS TRANSACTIVATOR GENES DEPENDS ON THE DIFFERENTIATION OF EPITHELIAL-CELLS IN ORAL HAIRY LEUKOPLAKIA [J].
BECKER, J ;
LESER, U ;
MARSCHALL, M ;
LANGFORD, A ;
JILG, W ;
GELDERBLOM, H ;
REICHART, P ;
WOLF, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8332-8336
[5]  
BLAZAR BA, 1990, CLIN EXP IMMUNOL, V80, P62
[6]   SPECIFIC CYTOTOXIC T-LYMPHOCYTES RECOGNIZE THE IMMEDIATE-EARLY TRANSACTIVATOR ZTA OF EPSTEIN-BARR-VIRUS [J].
BOGEDAIN, C ;
WOLF, H ;
MODROW, S ;
STUBER, G ;
JILG, W .
JOURNAL OF VIROLOGY, 1995, 69 (08) :4872-4879
[7]  
BORYSIEWICZ LK, 1986, Q J MED, V58, P111
[8]  
BURKITT DP, SCI BASIS MED ANN, V1969, P82
[9]   AN EPSTEIN-BARR VIRUS-SPECIFIC CYTOTOXIC T-CELL EPITOPE PRESENT ON A-TYPE AND B-TYPE TRANSFORMANTS [J].
BURROWS, SR ;
MISKO, IS ;
SCULLEY, TB ;
SCHMIDT, C ;
MOSS, DJ .
JOURNAL OF VIROLOGY, 1990, 64 (08) :3974-3976
[10]   EXPRESSION OF THE EPSTEIN-BARR-VIRUS IMMEDIATE-EARLY GENE, BZLF1, IN NASOPHARYNGEAL CARCINOMA TUMOR-CELLS [J].
COCHET, C ;
MARTELRENOIR, D ;
GRUNEWALD, V ;
BOSQ, J ;
COCHET, G ;
SCHWAAB, G ;
BERNAUDIN, JF ;
JOAB, I .
VIROLOGY, 1993, 197 (01) :358-365