JAC Advance Access originally published online on July 28, 2004
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Journal of Antimicrobial Chemotherapy 2004 54(3):582-586; doi:10.1093/jac/dkh396
JAC vol.54 no.3 © The British Society for Antimicrobial Chemotherapy 2004; all rights reserved.
Leading article |
Cytomegalovirus infection in the era of HAART: fewer reactivations and more immunity
Departments of 1 Medicine and 2 Pediatrics, University of Colorado School of Medicine, Denver, Colorado, USA
* Correspondence address. UCHSC, 4200 E 9th Ave., Denver, CO 80262, USA. Tel: +1-303-315-4624; Fax: +1-303-315-1787; Email: adrianna.weinberg{at}uchsc.edu
The incidence of cytomegalovirus (CMV) disease, once the most common and highly feared viral complication of AIDS, has dramatically decreased with the advent of highly active antiretroviral therapy (HAART). HAART-associated changes in the epidemiology of CMV disease resulted from the increase in CMV-specific immune responses coupled with the decrease in CMV reactivation. However, CMV disease continues to afflict HIV-infected patients on HAART when CD4+ cell counts fail to rise above 100 cells/mm3 and when reconstitution of normal CMV-specific immune responses does not occur. The latter scenario may lead to recurrent or de novo CMV end-organ disease, or to the recently described CMV immune recovery vitritis. HAART-associated immune reconstitution offers unique opportunities to investigate the virological and immunological correlates of protection against CMV disease. Although the full extent of CMV-specific immune reconstitution has not been defined thus far, CMV-specific interferon-
production has been shown to be significantly associated with protection against CMV reactivation and recurrent disease.
Keywords: HIV , immune reconstitution , AIDS , opportunistic infections
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
B. Kahaleh The microvascular endothelium in scleroderma Rheumatology, October 1, 2008; 47(suppl_5): v14 - v15. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. J. Ryckman, B. L. Rainish, M. C. Chase, J. A. Borton, J. A. Nelson, M. A. Jarvis, and D. C. Johnson Characterization of the Human Cytomegalovirus gH/gL/UL128-131 Complex That Mediates Entry into Epithelial and Endothelial Cells J. Virol., January 1, 2008; 82(1): 60 - 70. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. S. Miller, J. R. Berger, Y. Mootoor, S. A. Avdiushko, H. Zhu, and R. J. Kryscio High prevalence of multiple human herpesviruses in saliva from human immunodeficiency virus-infected persons in the era of highly active antiretroviral therapy. J. Clin. Microbiol., July 1, 2006; 44(7): 2409 - 2415. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. F. Stone, P. Price, and M. A. French Cytomegalovirus (CMV)-specific CD8+ T cells in individuals with HIV infection: correlation with protection from CMV disease J. Antimicrob. Chemother., April 1, 2006; 57(4): 585 - 588. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. P. Tchesnokov, C. Gilbert, G. Boivin, and M. Gotte Role of Helix P of the Human Cytomegalovirus DNA Polymerase in Resistance and Hypersusceptibility to the Antiviral Drug Foscarnet J. Virol., February 1, 2006; 80(3): 1440 - 1450. [Abstract] [Full Text] [PDF] |
||||



