Active HHV-6 infection in the lymph nodes of HIV-infected patients: In vitro evidence that HHV-6 can break HIV latency

被引:39
作者
Knox, KK [1 ]
Carrigan, DR [1 ]
机构
[1] MED COLL WISCONSIN,DEPT PATHOL,MILWAUKEE,WI 53226
来源
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY | 1996年 / 11卷 / 04期
关键词
HHV-6; lymph node; latency HIV;
D O I
10.1097/00042560-199604010-00007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Studies published previously by this laboratory have demonstrated that patients with AIDS have widely disseminated, active infections with HHV-6 at the time of their death. However, it remains unclear when in the course of the human immunodeficiency virus (HIV) infection the active HHV-6 infection first appears. To address this question, lymph node biopsies from 10 HIV-infected patients were analyzed for active human herpesvirus 6 (HHV-6) infections by immunohistochemical staining. Eight of the biopsies carried the histologic diagnosis of follicular hyperplasia; the other two were characterized as having follicular involution with histiocytosis and reactive lymphadenitis. In total, 10 of 10 (100%) of the lymph nodes studied contained cells productively infected with HHV-6; in contrast, three lymph nodes with follicular hyperplasia and four normal lymph nodes from patients not infected with HIV were negative for HHV-6 infection. Of special note, the absolute CD4(+) lymphocyte counts of 75% (6/8) of the HIV-infected individuals included in these studies were >200/mm(3) at the time of their lymph node biopsy. The A variant of HHV-6 was found to be the predominant form of the virus present in the lymph node biopsies from all of these HIV-infected patients, and in vitro studies demonstrated that exposure of monocytic cells carrying latent HIV to HHV-6A resulted in massive upregulation of HIV replication from latency. Thus, active HHV-6 infections appear relatively early in the course of HIV disease, and in vitro studies suggest that the A variant of HHV-6 is capable of breaking HIV latency, with the potential for helping to catalyze the progression of HIV infection to AIDS.
引用
收藏
页码:370 / 378
页数:9
相关论文
共 43 条
[1]   GENOMIC POLYMORPHISM, GROWTH-PROPERTIES, AND IMMUNOLOGICAL VARIATIONS IN HUMAN HERPESVIRUS-6 ISOLATES [J].
ABLASHI, DV ;
BALACHANDRAN, N ;
JOSEPHS, SF ;
HUNG, CL ;
KRUEGER, GRF ;
KRAMARSKY, B ;
SALAHUDDIN, SZ ;
GALLO, RC .
VIROLOGY, 1991, 184 (02) :545-552
[2]   CO-CULTIVATION OF HUMAN HERPESVIRUS-6 AND HIV1 FROM BLOOD-LYMPHOCYTES [J].
AGUT, H ;
KEROUEDAN, D ;
MPELE, P ;
COLLANDRE, H ;
SAMBALEFEVRE, C ;
ROSENHEIM, M ;
INGRAND, D ;
ITOUANGAPORO, A ;
GENTILINI, M ;
MONTAGNIER, L ;
HURAUX, JM .
RESEARCH IN VIROLOGY, 1989, 140 (01) :23-26
[3]  
AGUT H, 1988, LANCET, V1, P712
[4]   IDENTIFICATION OF PROTEINS SPECIFIC FOR HUMAN HERPESVIRUS-6-INFECTED HUMAN T-CELLS [J].
BALACHANDRAN, N ;
AMELSE, RE ;
ZHOU, WW ;
CHANG, CK .
JOURNAL OF VIROLOGY, 1989, 63 (06) :2835-2840
[5]  
BALACHANDRAN N, 1992, HUMAN HERPESVIRUS 6, P97
[6]   HUMAN HERPESVIRUS-6 (HHV-6)-ASSOCIATED DYSFUNCTION OF BLOOD MONOCYTES [J].
BURD, EM ;
CARRIGAN, DR .
VIRUS RESEARCH, 1993, 29 (01) :79-90
[7]  
BURD EM, 1993, BLOOD, V81, P1645
[8]  
CARRIGAN DR, 1994, BLOOD, V84, P3307
[9]   SUPPRESSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION BY HUMAN HERPESVIRUS-6 [J].
CARRIGAN, DR ;
KNOX, KK ;
TAPPER, MA .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (04) :844-851
[10]   INTERSTITIAL PNEUMONITIS ASSOCIATED WITH HUMAN HERPESVIRUS-6 INFECTION AFTER MARROW TRANSPLANTATION [J].
CARRIGAN, DR ;
DROBYSKI, WR ;
RUSSLER, SK ;
TAPPER, MA ;
KNOX, KK ;
ASH, RC .
LANCET, 1991, 338 (8760) :147-149