Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection

• Published in: Frontiers in immunology Vol. 9; p. 1095
• Main Authors: Xiao, Minglu, Chen, Xiangyu, He, Ran, Ye, Lilin
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 22.05.2018
• Subjects: B-cell follicles; CXCR5+CD8 T cells; follicular CD8 T cells; human immunodeficiency virus infections; human immunodeficiency virus reservoir; Immunology; follicular CD8 T cells; CXCR5+CD8 T cells; B-cell follicles; human immunodeficiency virus reservoir; human immunodeficiency virus infections
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2018.01095

The combination antiretroviral therapeutic (cART) regime effectively suppresses human immunodeficiency virus (HIV) replication and prevents progression to acquired immunodeficiency diseases. However, cART is not a cure, and viral rebound will occur immediately after treatment is interrupted largely due to the long-term presence of an HIV reservoir that is composed of latently infected target cells that maintain a quiescent state or persistently produce infectious viruses. CD4 T cells that reside in B-cell follicles within lymphoid tissues, called follicular helper T cells (TFH), have been identified as a major HIV reservoir. Due to their specialized anatomical structure, HIV-specific CD8 T cells are largely insulated from this TFH reservoir. It is increasingly clear that the elimination of TFH reservoirs is a key step toward a functional cure for HIV infection. Recently, several studies have suggested that a fraction of HIV-specific CD8 T cells can differentiate into a CXCR5-expressing subset, which are able to migrate into B-cell follicles and inhibit viral replication. In this review, we discuss the differentiation and functions of this newly identified CD8 T-cell subset and propose potential strategies for purging TFH HIV reservoirs by utilizing this unique population.