Abstract | BACKGROUND: In the chronic stage of HIV infection T cell proliferative responses to HIV antigens are rare, mostly of low level, and the influence of responses on antiretroviral therapy is not known. OBJECTIVES: To determine a potential correlation between HIV-specific proliferative responses and the subsequent course of infection under antiretroviral therapy. STUDY DESIGN: Proliferation assays were performed with freshly isolated blood mononuclear cells from 45 chronically HIV-infected HAART treated individuals using HIV-p24, other recall antigens, and mitogens as stimulants. Virus load was monitored at the time of stimulation and during 33 months follow-up. RESULTS: A proliferative response to HIV antigen stimulation was detectable in 7 of 45 patients (15.5% responders). This group showed elevated reactions against tetanus toxoid and tuberculin, whereas reactions against standard mitogens were equal in the HIV responder and nonresponder groups. None of the seven HIV-specific responders had a blood virus load rebound of more than 1000 genome copies/ml during follow-up, whereas in 50% of the non-responders higher virus rebounds occurred. CD4 cell levels were slightly higher in the responder group, but mostly independent of virus rebound within the non-responders. Only four patients with high and continuous virus rebound experienced a significant CD4 cell decline. CONCLUSIONS: In patients under HAART, HIV-specific proliferative response is frequently related to anamnestic antigen responses and an enduring control of virus replication.
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Authors | J M Mohm, J-A Rump, J Schulte-Mönting, J Schneider |
Journal | Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
(J Clin Virol)
Vol. 30
Issue 3
Pg. 239-42
(Jul 2004)
ISSN: 1386-6532 [Print] Netherlands |
PMID | 15135742
(Publication Type: Evaluation Study, Journal Article)
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Chemical References |
- HIV Core Protein p24
- Tetanus Toxoid
- Tuberculin
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Topics |
- Antiretroviral Therapy, Highly Active
- CD4 Lymphocyte Count
- Chronic Disease
- HIV Core Protein p24
(immunology, pharmacology)
- HIV Infections
(drug therapy, immunology, physiopathology)
- HIV-1
- Humans
- Leukocytes, Mononuclear
(immunology)
- Lymphocyte Activation
(immunology)
- Prognosis
- Tetanus Toxoid
(pharmacology)
- Tuberculin
(pharmacology)
- Viral Load
- Viremia
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