| Literature DB >> 24499824 |
Arif Azam Khan1, Ruchi Srivastava1, Patricia Prado Lopes2, Christine Wang1, Thanh T Pham1, Justin Cochrane1, Nhi Thi Uyen Thai1, Lucas Gutierrez1, Lbachir Benmohamed3.
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."Entities:
Keywords: CD8+ T cells; HSV; asymptomatic; disease; herpes simplex virus; infection; symptomatic; vaccine
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Year: 2014 PMID: 24499824 PMCID: PMC4896594 DOI: 10.4161/hv.27762
Source DB: PubMed Journal: Hum Vaccin Immunother ISSN: 2164-5515 Impact factor: 3.452