The role of CD4 +CD25 + regulatory T cells in viral infections

• Published in: Veterinary immunology and immunopathology 2005-10, Vol.108 (1), p.219-225
• Main Authors: Vahlenkamp, Thomas W., Tompkins, Mary B., Tompkins, Wayne A.F.
• Format: Article
• Language: English
• Subjects: Animals; CD4-Positive T-Lymphocytes - immunology; Herpesviridae Infections - immunology; Immune regulation; Immune Tolerance; Immunosuppression; Lymphocyte Activation; Mice; Picornaviridae Infections - immunology; Receptors, Interleukin-2 - metabolism; Regulatory T cells; Retroviridae Infections - immunology; T-Lymphocyte Subsets - immunology; Viral infection; Virus Diseases - immunology
• ISSN: 0165-2427; 1873-2534
• DOI: 10.1016/j.vetimm.2005.07.011

Many virus infections result in the suppression of one or more functions of the immune system. Multiple mechanisms have been proposed to explain viral-induced immunosuppression, including an imbalance in the cellular Th1/Th2 or cytokine profile, induction of anergy, depletion of effector cells and most recently the activation of CD4 +CD25 + regulatory T (T reg) cells. CD4 +CD25 + T reg cells are a subset of circulating CD4 + T cells with suppressive properties. CD4 +CD25 + T reg cells were first identified in mice as cells capable of maintaining self-tolerance by suppressing autoreactive T cells. This review focuses on interactions between CD4 +CD25 + T reg cells and viral pathogens. Most cases in which CD4 +CD25 + T reg cells participate in response to infection reported so far involve chronic or persistent viral infections. Examples have been growing recently and include members of different viral families including retroviridae, herpesviridae and picornaviridae. It is currently not known how microbes are recognized by CD4 +CD25 + T reg cells and whether exoantigen-specific T reg cells are of the same lineage as self-reacting natural T reg cells or represent peripherally induced counterparts derived from CD4 +CD25 − T cells. The findings that T reg cells influence the functional immunity during viral infections, however, might indicate that, in some cases, virus-specific T reg cells not only influence immune pathology or prevent pathogen elimination but also can promote a generalized state of immunosuppression in vivo such that the host is more susceptible to secondary infections with other pathogens or has reduced resistance to tumors. Conceivably, the activities of T reg cells might be one of the contributing reasons why it has been difficult so far to produce effective vaccines against some persisting viral infections.