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Prognostic value of proliferative responses to HIV-1 antigen in chronically HIV-infected patients under antiretroviral therapy.

AbstractBACKGROUND:
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.
AuthorsJ M Mohm, J-A Rump, J Schulte-Mönting, J Schneider
JournalJournal 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
PMID15135742 (Publication Type: Evaluation Study, Journal Article)
Chemical References
  • HIV Core Protein p24
  • Tetanus Toxoid
  • Tuberculin
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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