Perforin expression can define CD8 positive lymphocyte subsets in pigs allowing phenotypic and functional analysis of Natural Killer, Cytotoxic T, Natural Killer T and MHC un-restricted cytotoxic T-cells

• Published in: Veterinary Immunology and Immunopathology 2006-04, Vol.110 (3), p.279-292
• Main Authors: Denyer, Michael S., Wileman, Thomas E., Stirling, Catrina M.A., Zuber, Bartek, Takamatsu, Haru-Hisa
• Format: Article
• Language: English
• Subjects: Animals; Antigens, CD - metabolism; CD8-positive T-lymphocytes; CTL; cytotoxic T-lymphocytes; gene expression; Gene Expression Regulation; genetic variation; Killer Cells, Natural - immunology; Killer Cells, Natural - metabolism; Lymphoid Tissue - metabolism; major histocompatibility complex; Major Histocompatibility Complex - immunology; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; messenger RNA; natural killer cells; NKT; Perforin; Phenotype; Pig; Pore Forming Cytotoxic Proteins; receptors; swine; Swine - immunology; T-Lymphocyte Subsets - immunology; T-Lymphocyte Subsets - metabolism; T-lymphocytes; T-Lymphocytes, Cytotoxic - immunology; T-Lymphocytes, Cytotoxic - metabolism
• ISSN: 0165-2427; 1873-2534; 1365-2567
• DOI: 10.1016/j.vetimm.2005.10.005

In this study we have used the expression of perforin to characterize subsets of porcine cytotoxic lymphocytes. Perforin positive lymphocytes expressed both CD2 and CD8α, most were small dense lymphocytes (SDL) and up to 90% were CD3 negative. However, the numbers of perforin positive T-cells increased with the age of the animal and their populations increased after specific antigen stimulation in vitro . The remaining perforin positive lymphocytes were large and granular and contained more CD3 +CD5 +CD6 + T-cells (−40%) of which a substantial proportion also co-expressed CD4. Perforin was expressed in subpopulations of both CD8αα and CD8αβ lymphocytes, but was not expressed in γδ T-cells or monocyte/macrophages. The perforin positive CD3 − subset was phenotypically homogeneous and defined as CD5 −CD6 −CD8β −CD16 +CD11b +. This population had NK activity and expressed mRNA for the NK receptor NKG2D, and adaptors DAP10 and DAP12. Perforin positive T-cells (CD3 +) could be divided into at least three subsets. The first subset was CD4 −CD5 +CD6 +CD11b −CD16 − most were small dense lymphocytes with cytotoxic T-cell activity but not all expressed CD8β. The second subset was mainly observed in the large granular lymphocytes. Their phenotype was CD4 +CD5 +CD6 +CD8β +CD16 −CD11b − and also showed functional CTL activity. Thus not all of double positive T-cells are memory helper T-cells. The third subset did not express the T-cell co-receptor CD6, but up to half of them expressed another T-cell co-receptor CD5. The majority of this subset expressed CD11b and CD16, thus the third perforin positive T-cell subset was CD3 +CD4 −CD5 +CD6 −CD8β ±CD11b +CD16 +, and possessed MHC-unrestricted cytotoxicity and LAK activity.