CMV retinitis recurs after stopping treatment in virological and immunological failures of potent antiretroviral therapy

Details

Serval ID
serval:BIB_544B5EEDF55A
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
CMV retinitis recurs after stopping treatment in virological and immunological failures of potent antiretroviral therapy
Journal
AIDS
Author(s)
Torriani  F. J., Freeman  W. R., Macdonald  J. C., Karavellas  M. P., Durand  D. M., Jeffrey  D. D., Meylan  P. R., Schrier  R. D.
ISSN
0269-9370 (Print)
Publication state
Published
Issued date
01/2000
Volume
14
Number
2
Pages
173-80
Notes
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: Jan 28
Abstract
OBJECTIVES: To determine predictors of clinical relapse of cytomegalovirus (CMV) end-organ disease in a cohort of 17 HIV-infected patients with healed and treated CMV retinitis (CMVR) who responded to HAART with an increase in CD4 cell counts to above 70 cells/mm3 and discontinued CMV maintenance therapy (MT). DESIGN: Seventeen patients were monitored for reactivation of retinitis. The CD4 cell counts, HIV RNA and peripheral blood mononuclear cell (PBMC) lymphoproliferative assays to CMV at 3 month intervals were compared between patients with and without reactivation of CMVR. Positive lymphoproliferative responses were defined as a stimulation index of 3 or greater. RESULTS: Five out of 17 (29%) patients experienced a recurrence of CMVR a mean of 14.5 months after stopping CMV MT and between 8 days and 10 months after CD4 cell counts fell below 50 cells/mm3. Median CD4 cell counts and plasma HIV RNA at reactivation were 37 cells/mm3 and 5.3 log10 copies/ml. Three patients recurred at a previously active site of the retina, one had contralateral CMVR, and one a recurrence of retinitis and pancreatitis simultaneously. Mean lymphoproliferative responses to CMV were 2.4 in patients with reactivation versus 21.0 stimulation index (SI) in patients without reactivation (P= 0.01). A model incorporating four variables (CD4 cell counts and HIV RNA at maintenance discontinuation, highest CD4 cell count, nadir HIV RNA and median lymphoproliferative responses) identified correctly 88% of patients with and without reactivation. CONCLUSION: CMV disease recurs after virological and immunological failure of HAART if CD4 cell counts drop below 50. In this situation, anti-CMV agents should be resumed before clinical reactivation ensues, because of the risk of contralateral retinal involvement and systemic disease.
Keywords
AIDS-Related Opportunistic Infections/*drug therapy/immunology/virology Adult Anti-HIV Agents/*therapeutic use CD4 Lymphocyte Count/drug effects Cohort Studies Cytomegalovirus/drug effects Cytomegalovirus Retinitis/*drug therapy/prevention & control Female *HIV/drug effects/genetics Humans Lymphocyte Activation Male Middle Aged Prospective Studies RNA, Viral/blood Recurrence Risk Factors T-Lymphocytes/immunology Treatment Failure Viral Load
Pubmed
Web of science
Create date
25/01/2008 15:33
Last modification date
20/08/2019 15:09
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