The role of inducer cells in mediating in vitro suppression of feline immunodeficiency virus replication

• Published in: Virology (New York, N.Y.) Vol. 320; no. 1; pp. 63 - 74
• Main Authors: Phadke, Anagha P, Choi, In-Soo, Li, Zhongxia, Weaver, Eric, Collisson, Ellen W
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-03-2004
• Subjects: Animals; Biological Factors - pharmacology; CD8 + T lymphocytes; CD8-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - physiology; Cell Communication; Culture Media, Conditioned - pharmacology; Down-Regulation; Feline immunodeficiency virus; Feline skin fibroblasts (FSF); Fibroblasts - physiology; Fibroblasts - virology; FIV; Immunodeficiency Virus, Feline - immunology; Immunodeficiency Virus, Feline - physiology; Inducer cell effector cell contact; Inducer cells; Mice; Time Factors; Virus Replication - immunology; Inducer cells; FIV; CD8 + T lymphocytes; Inducer cell effector cell contact; Feline skin fibroblasts (FSF)
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1016/j.virol.2003.11.016

CD8
+ T-cell-mediated suppression of feline immunodeficiency virus (FIV) replication has been described by several groups, although the mechanisms of activation and conditions for viral suppression vary with the methodologies. We have previously reported that CD8
+ T-cell-mediated suppression of FIV replication required inducer cell stimulation of the effector cells. The focus of the present study was to examine the essential role of inducer cells required for the induction of this soluble anti-FIV activity. Both FIV-PPR-infected T cells and feline skin fibroblasts (FSF) infected with an alphavirus vector expressing FIV capsid or the irrelevant antigen lacZ, stimulated autologous or heterologous effector cells to produce supernatants that suppressed FIV replication. Thus, induction of this suppression of FIV replication did not strictly require autologous inducer cells and did not require the presence of FIV antigen. Anti-viral activity correlated with the presence of CD8
+ T cells. Suppression was maximal when the inducer cells and the effector cells were in contact with each other, because separation of the inducer and effector cells by a 0.45-μm membrane reduced FIV suppression by approximately 50%. These findings emphasize the importance for membrane antigen interactions and cytokines in the optimal induction of effector cell synthesis of the soluble anti-FIV activity.