Related Experiment Video
Updated: Aug 8, 2026

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay
Published on: September 14, 2014
Recognition of envelope protein by dengue virus serotype-specific human CD4+ CD8- cytotoxic T-cell clones
P G Livingston1, I Kurane, C J Lai
1Department of Medicine, University of Massachusetts Medical Center, Worcester 01655.
Insights
This study analyzed dengue virus-specific CD4+ cytotoxic T lymphocytes (CTL) to understand their role in infection. E protein-specific CD4+ CTLs, restricted by HLA-DR7, may aid virus clearance during reinfection.
Area of Science:
- Immunology
- Virology
- T cell biology
Background:
- Dengue virus infections pose a significant global health challenge.
- Understanding the role of cytotoxic T lymphocytes (CTLs) in dengue pathogenesis is crucial for vaccine development.
Purpose of the Study:
- To analyze dengue virus-specific CD4+ CTLs at the clonal level.
- To investigate the specificity and HLA restriction of these CTLs in dengue virus type 4 (D4V) infections.
Main Methods:
- Stimulation of peripheral blood mononuclear cells from D4V-immune donors.
- Generation and characterization of CD4+ CTL clones.
- Assays for specific lysis of antigen-treated target cells.
- Analysis of HLA restriction and cross-reactivity.
Main Results:
- 17 HLA class II-restricted CD4+ CTL clones were generated.
- Clones showed varying specificities: D4V-specific, D2V/D4V cross-reactive, and D1V/D3V/D4V cross-reactive.
- Antigen recognition by several clones was restricted by HLA-DR7.
- E protein-specific CD4+ CTLs demonstrated serotype specificity and HLA-DR7 restriction.
Conclusions:
- E protein-specific CD4+ CTLs are important mediators of virus clearance, particularly during homologous serotype reinfection.
- These CTLs may provide help for antibody production and lysis of infected cells.
- A common epitope on the E protein may be recognized by these CTLs.
Abstract:
We analyzed dengue virus-specific CD4+ CD8- cytotoxic T lymphocytes (CTL) at the clonal level to further understand their role in dengue virus infections. Stimulation of peripheral blood mononuclear cells from two dengue virus type 4 (D4V)-immune donors with live D4V or noninfectious D4V antigen generated 17 HLA class II-restricted CD4+ CTL capable of specific lysis of dengue virus antigen-treated autologous lymphoblastoid cell lines. Thirteen clones were D4V specific, three clones were cross-reactive for D2V and D4V, and one clone was cross-reactive for D1V, D3V, and D4V. Antigen recognition by six D4V-specific clones and three D2V- and D4V-cross-reactive clones was restricted by HLA-DR7. Five D4V-specific CD4+ CTL clones lysed autologous lymphoblastoid cell lines infected with a dengue virus-vaccinia virus recombinant containing the E gene of D4V, whereas three serotype-cross-reactive CTL clones did not. These results indicate that E-specific clones are serotype specific and HLA-DR7 restricted in these two donors and suggest that a common epitope on E protein may be recognized. E protein-specific CD4+ CTL may be important mediators of virus clearance especially during reinfection with the same serotype as that in primary infection by providing help for virus-specific antibody production and lysis of virus-infected cells.
More Related Videos
Related Concept Videos
T Cell Activation and Clonal Selection
Naive T cells that have not yet encountered an antigen express two primary CD...
Cytotoxic T Cells-mediated Immune Response
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
Immune Response Against Viral Pathogens
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...

