Constitutive activation of STATs upon in vivo human immunodeficiency virus infection

被引:71
作者
Bovolenta, C
Camorali, L
Lorini, AL
Ghezzi, S
Vicenzi, E
Lazzarin, A
Poli, G
机构
[1] San Raffaele Sci Inst, Labs P2 P3, AIDS Immunophatogenesis Unit, DIBIT, I-20132 Milan, Italy
[2] San Raffaele Sci Inst, Div Infect Dis, Ctr San Luigi, I-20132 Milan, Italy
关键词
D O I
10.1182/blood.V94.12.4202.424k22_4202_4209
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Infection by the human immunodeficiency virus (HIV) either upregulates or downregulates the expression of several cytokines and interferons (IFNs) that use the Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway for signal transduction. However, very little is known on the state of activation of the JAK/STAT pathway after HIV infection either in vivo or in vitro. In this regard, we report here that a constitutive activation of a C-terminal truncated STAT5 (STAT5 Delta) and of STAT1 alpha occurs in the majority (similar to 75%) of individuals with progressive HIV disease. We have further demonstrated that, among peripheral blood mononuclear cells (PBMCs), STAT5 Delta is activated preferentially in CD4(+) T cells. In contrast to a published report, expression of STATs from PBMCs of infected individuals was comparable with that of seronegative donors. In addition, in vitro infection of mitogen-activated PBMCs with a panel of laboratory-adapted and primary HIV strains characterized by differential usage of chemokine coreceptors did not affect STAT protein levels. However, enhanced activation of STAT was observed after in vitro infection of resting PBMCs and nonadherent PBMCs by different viral strains. Thus, constitutive STAT activation in CD4(+) T lymphocytes represents a novel finding of interest also as a potential new marker of immunological reconstitution of HIV-infected individuals. (C) 1999 by The American Society of Hematology.
引用
收藏
页码:4202 / 4209
页数:8
相关论文
共 44 条
[1]  
AMADORI A, 1992, J IMMUNOL, V148, P2709
[2]   Functionally distinct isoforms of STAT5 are generated by protein processing [J].
Azam, M ;
Lee, C ;
Strehlow, I ;
Schindler, C .
IMMUNITY, 1997, 6 (06) :691-701
[3]   ACTIVATION OF JAK KINASES AND STAT PROTEINS BY INTERLEUKIN-2 AND INTERFERON-ALPHA, BUT NOT THE T-CELL ANTIGEN RECEPTOR, IN HUMAN T-LYMPHOCYTES [J].
BEADLING, C ;
GUSCHIN, D ;
WITTHUHN, BA ;
ZIEMIECKI, A ;
IHLE, JN ;
KERR, IM ;
CANTRELL, DA .
EMBO JOURNAL, 1994, 13 (23) :5605-5615
[4]   A new classification for HIV-1 [J].
Berger, EA ;
Doms, RW ;
Fenyö, EM ;
Korber, BTM ;
Littman, DR ;
Moore, JP ;
Sattentau, QJ ;
Schuitemaker, H ;
Sodroski, J ;
Weiss, RA .
NATURE, 1998, 391 (6664) :240-240
[5]   Cellular responses to interferon-gamma [J].
Boehm, U ;
Klamp, T ;
Groot, M ;
Howard, JC .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :749-795
[6]   Positive selection of apoptosis-resistant cells correlates with activation of dominant-negative STAT5 [J].
Bovolenta, C ;
Testolin, L ;
Benussi, L ;
Lievens, PMJ ;
Liboi, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (33) :20779-20784
[7]  
Bovolenta C, 1998, J IMMUNOL, V160, P911
[8]  
Bovolenta C, 1998, J BIOL REG HOMEOS AG, V12, P63
[9]  
Bovolenta C, 1999, J IMMUNOL, V162, P323
[10]   INTRATHECAL SYNTHESIS OF INTERLEUKIN-2 AND SOLUBLE IL-2 RECEPTOR IN ASYMPTOMATIC HIV-1 SEROPOSITIVE INDIVIDUALS - CORRELATION WITH LOCAL PRODUCTION OF SPECIFIC IGM AND IGG ANTIBODIES [J].
CIARDI, M ;
SHARIEF, MK ;
NOORI, MA ;
THOMPSON, EJ ;
SALOTTI, A ;
ROSSI, F ;
VULLO, V ;
CATANIA, S ;
SORICE, F ;
CIRELLI, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1993, 115 (01) :117-122