Abstract
Chronic immune activation is associated with impaired signal transduction. Since such activation is commonly found during HIV-1 infection, we studied cellular responses to non-specific T-cell receptor stimulation of PBMC obtained from 20 HIV-1 non-infected individuals and 23 highly or partially immune activated HIV-1 infected individuals. PBMC proliferation and ERK-1/2 phosphorylation following anti-CD3 stimulation, and constitutive levels of Cbl-b, were determined. Increased levels of Cbl-b, decreased proliferation, and lower ERK-1/2 phosphorylation were found in PBMC of highly immune activated HIV-1 infected individuals. The elevated expression of Cbl-b and impaired phosphorylation of ERK-1/2 associated with immune activation probably contribute to the attenuated proliferative and cellular responses characteristic of HIV-1 infection. Therefore, targeting immune negative modulators, such as Cbl-b, may serve as a novel approach for controlling HIV-1 disease progression.
Original language | English |
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Pages (from-to) | 464-467 |
Number of pages | 4 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 298 |
Issue number | 4 |
DOIs | |
State | Published - 1 Jan 2002 |
Externally published | Yes |
Keywords
- AIDS
- Anti-CD3 stimulation
- CTLA-4
- Cbl-b
- ERK
- HIV-1
- Immune activation
- Proliferation
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology