Cytotoxic T Cell Functions Accumulate When CD4 Is Downregulated by CD4 + T Cells in African Green Monkeys

• Published in: The Journal of immunology (1950) 2017-06, Vol.198 (11), p.4403-4412
• Main Authors: Vinton, Carol L, Ortiz, Alexandra M, Calantone, Nina, Mudd, Joseph C, Deleage, Claire, Morcock, David R, Whitted, Sonya, Estes, Jacob D, Hirsch, Vanessa M, Brenchley, Jason M
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; AIDS; Alveoli; Animals; Bronchoalveolar Lavage; Bronchus; CD4 antigen; CD4 Antigens - genetics; CD4 Antigens - immunology; CD4-Positive T-Lymphocytes - immunology; CD4-Positive T-Lymphocytes - metabolism; CD4-Positive T-Lymphocytes - virology; CD8 antigen; Chlorocebus aethiops; Cytotoxicity; Down-Regulation; Follicles; Immune response; Lentivirus; Lymph nodes; Lymph Nodes - anatomy & histology; Lymph Nodes - cytology; Lymph Nodes - immunology; Lymph Nodes - virology; Lymphocytes; Lymphocytes T; Lymphoid tissue; Macaca mulatta; Major histocompatibility complex; Monkeys; Peripheral blood; Retroviridae; Simian Acquired Immunodeficiency Syndrome - immunology; Simian Immunodeficiency Virus - immunology; T-Lymphocytes, Cytotoxic - immunology; T-Lymphocytes, Cytotoxic - metabolism; Tissues
• ISSN: 0022-1767; 1550-6606; 1550-6606
• DOI: 10.4049/jimmunol.1700136

African green monkeys (AGMs) are a natural host of SIV that do not develop simian AIDS. Adult AGMs naturally have low numbers of CD4 T cells and a large population of MHC class II-restricted CD8αα T cells that are generated through CD4 downregulation in CD4 T cells. In this article, we study the functional profiles and SIV infection status in vivo of CD4 T cells, CD8αα T cells, and CD8αβ T cells in lymph nodes, peripheral blood, and bronchoalveolar lavage fluid of AGMs and rhesus macaques (in which CD4 downregulation is not observed). We show that, although CD8αα T cells in AGMs maintain functions associated with CD4 T cells (including Th follicular functionality in lymphoid tissues and Th2 responses in bronchoalveolar lavage fluid), they also accumulate functions normally attributed to canonical CD8 T cells. These hyperfunctional CD8αα T cells are found to circulate peripherally, as well as reside within the lymphoid tissue. Due to their unique combination of CD4 and CD8 T cell effector functions, these CD4 CD8αα T cells are likely able to serve as an immunophenotype capable of Th1, follicular Th, and CTL functionalities, yet they are unable to be infected by SIV. These data demonstrate the ambiguity of CD4/CD8 expression in dictating the functional capacities of T cells and suggest that accumulation of hyperfunctional CD8αα T cells in AGMs may lead to tissue-specific antiviral immune responses in lymphoid follicles that limit SIV replication in this particular anatomical niche.