Asymptomatic memory CD8+ T cells: from development and regulation to consideration for human vaccines and immunotherapeutics

Hum Vaccin Immunother. 2014;10(4):945-63. doi: 10.4161/hv.27762. Epub 2014 Feb 5.

Abstract

Generation and maintenance of high quantity and quality memory CD8(+) T cells determine the level of protection from viral, bacterial, and parasitic re-infections, and hence constitutes a primary goal for T cell epitope-based human vaccines and immunotherapeutics. Phenotypically and functionally characterizing memory CD8(+) T cells that provide protection against herpes simplex virus type 1 and type 2 (HSV-1 and HSV-2) infections, which cause blinding ocular herpes, genital herpes, and oro-facial herpes, is critical for better vaccine design. We have recently categorized 2 new major sub-populations of memory symptomatic and asymptomatic CD8(+) T cells based on their phenotype, protective vs. pathogenic function, and anatomical locations. In this report we are discussing a new direction in developing T cell-based human herpes vaccines and immunotherapeutics based on the emerging new concept of "symptomatic and asymptomatic memory CD8(+) T cells."

Keywords: CD8+ T cells; HSV; asymptomatic; disease; herpes simplex virus; infection; symptomatic; vaccine.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • CD8-Positive T-Lymphocytes / immunology*
  • Herpesvirus Vaccines / immunology*
  • Humans
  • Immunologic Memory
  • Immunotherapy / methods*
  • T-Lymphocyte Subsets / immunology*

Substances

  • Herpesvirus Vaccines