Perforin-dependent CD4+ T-cell cytotoxicity contributes to control a murine poxvirus infection.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 22665800.
- Also identified by DOI 10.1073/pnas.1202143109 and PMC identifier 3382508.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
CD4(+) T cells are generally regarded as helpers and regulators of the immune response. Although cytolytic CD4(+) T cells have been described, whether those generated during the course of a viral infection play a role in virus control remains unknown. Here we show that during acute infection with ectromelia virus, the mouse homolog of the human virus of smallpox, large numbers of CD4(+) T cells in the draining lymph node and liver of resistant mice have a cytotoxic phenotype. We also show that these cells kill targets in vivo in a perforin-dependent manner and that mice with specific deficiency of perforin in CD4(+) T cells have impaired virus control. Thus, perforin-dependent CD4(+) T-cell killing of infected cells is an important mechanism of antiviral defense.
Medical subject headings
- CD4-Positive T-Lymphocytes
- Cytotoxicity, Immunologic
- Ectromelia virus
- Perforin