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Updated: Aug 8, 2026

Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice
Published on: June 22, 2016
[Inhibitor effect of CD8+CD57+ lymphocytes on cell-mediated cytotoxicity: characterization of suppressor factor]
B Autran1, B Sadat-Sowti, P Debre
1Laboratoire d'Immunologie cellulaire et tissulaire, U.A.-C.N.R.S. n. 186, Paris.
Insights
CD8+CD57+ lymphocytes from HIV patients and transplant recipients suppress immune cell activity. This inhibition is mediated by a heat-resistant, glycosylated soluble factor of 20-30 kD.
Area of Science:
- Immunology
- Cell Biology
Context:
- Human Immunodeficiency Virus (HIV) infection
- Organ transplantation
- Immune system regulation
Purpose:
- Investigate the function of CD8+CD57+ lymphocytes
- Identify novel immunosuppressive mechanisms
Summary:
- CD8+CD57+ lymphocytes from HIV-seropositive patients and allotransplanted recipients exhibit a suppressor function.
- This function inhibits the cytolytic activity of allospecific cytotoxic T lymphocytes (CTL), natural killer (NK) cells, and lymphokine-activated killer (LAK) cells.
- The inhibitory effect is mediated by a non-antigen specific soluble factor, distinct from known mediators like PGE2, TGF-β, and TNF-α/β.
- Preliminary characterization reveals the factor is heat and trypsin resistant, binds to Concanavalin A (suggesting glycosylation), and has a molecular weight of 20-30 kDa.
Impact:
- Elucidates a novel immunosuppressive mechanism involving CD8+CD57+ lymphocytes.
- Potential implications for understanding immune dysregulation in HIV and post-transplant settings.
- Identifies a novel soluble factor with potential therapeutic or diagnostic applications.
Abstract:
We report a new suppressor function of CD8+CD57+ lymphocytes from HIV-seropositive patients or allotransplanted recipients, on the cytolytic activity of allospecific CTL, NK and LAK cells. This inhibitory effect is mediated by a non-antigen specific soluble factor distinct from PGE2, TGF beta and TNF alpha beta. A preliminary biochemical characterization indicates that the CD8+CD57+ inhibitory activity 1. is heat and trypsin resistant, 2. specifically binds to Concanavalin A suggesting its glycosylation, 3. is mediated by a 20-30 kD molecule.
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