HIV receptors on lymphocytes

被引:3
作者
Garzino-Demo, A [1 ]
Gallo, RC [1 ]
机构
[1] Univ Maryland Biotechnol Inst, Inst Human Virol, Baltimore, MD 21201 USA
关键词
D O I
10.1097/00062752-200307000-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human immunodeficiency virus infection, despite tremendous efforts in research and prevention, is spreading at an increasing speed, especially in developing countries. Currently available therapeutic approaches significantly extend the lifespan of HIV-infected people, but their use is associated with a severe drug regimen, several undesirable side effects, and high cost. Therefore, the scientific community is steadfastly pursuing novel strategies for inhibiting viral replication, promoting a better immune response, and developing an effective vaccine. Recent research on HIV receptors has introduced new concepts in the field, showing that expression of receptors, although necessary for virus entry, is subordinate to quality of expression, so that efficient infection occurs when receptors are properly colocalized. In addition, intracellular signaling triggered by HIV receptors has been shown to play important roles in pathogenesis by inducing apoptosis of bystander cells. Induction of some pathways of intracellular signaling, however, can instead suppress HIV replication, so that modulation of these pathways constitutes an additional target to be exploited for therapy or vaccines. This article reviews the most exciting aspects of these novel findings and discusses their practical application in the fight against HIV infection.
引用
收藏
页码:279 / 283
页数:5
相关论文
共 45 条
[31]   Human immunodeficiency virus type 1 uses lipid raft-colocalized CD4 and chemokine receptors for productive entry into CD4+ T cells [J].
Popik, W ;
Alce, TM ;
Au, WC .
JOURNAL OF VIROLOGY, 2002, 76 (10) :4709-4722
[32]   Amino-terminal truncation of chemokines by CD26/dipeptidylpeptidase IV - Conversion of RANTES into a potent inhibitor of monocyte chemotaxis and HIV-1-infection [J].
Proost, P ;
De Meester, I ;
Schols, D ;
Struyf, S ;
Lambeir, AM ;
Wuyts, A ;
Opdenakker, G ;
De Clercq, E ;
Scharpe, S ;
Van Damme, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (13) :7222-7227
[33]  
ROBBINS SM, 1995, MOL CELL BIOL, V15, P3507
[34]   SIGNAL-TRANSDUCING MOLECULES AND GLYCOSYL-PHOSPHATIDYLINOSITOL-LINKED PROTEINS FORM A CAVEOLIN-RICH INSOLUBLE COMPLEX IN MDCK CELLS [J].
SARGIACOMO, M ;
SUDOL, M ;
TANG, ZL ;
LISANTI, MP .
JOURNAL OF CELL BIOLOGY, 1993, 122 (04) :789-807
[35]   Functional rafts in cell membranes [J].
Simons, K ;
Ikonen, E .
NATURE, 1997, 387 (6633) :569-572
[36]   The association between glycosylphosphatidylinositol-anchored proteins and heterotrimeric G protein alpha subunits in lymphocytes [J].
Solomon, KR ;
Rudd, CE ;
Finberg, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :6053-6058
[37]   GPI-ANCHORED CELL-SURFACE MOLECULES COMPLEXED TO PROTEIN TYROSINE KINASES [J].
STEFANOVA, I ;
HOREJSI, V ;
ANSOTEGUI, IJ ;
KNAPP, W ;
STOCKINGER, H .
SCIENCE, 1991, 254 (5034) :1016-1019
[38]  
Struyf S, 1998, EUR J IMMUNOL, V28, P1262, DOI 10.1002/(SICI)1521-4141(199804)28:04<1262::AID-IMMU1262>3.0.CO
[39]  
2-G
[40]   CD4 cross-linking (CD4XL) induces RAS activation and tumor necrosis factor-alpha secretion in CD4(+) T cells [J].
Tamma, SML ;
Chirmule, N ;
Yagura, H ;
Oyaizu, N ;
Kalyanaraman, V ;
Pahwa, S .
BLOOD, 1997, 90 (04) :1588-1593