HIV-1 Tat Suppresses gp120-Specific T Cell Response in IL-10-Dependent Manner

• Published in: The Journal of immunology (1950) 2008-01, Vol.180 (1), p.79-88
• Main Authors: Gupta, Shalini, Boppana, Ramanamurthy, Mishra, Gyan C, Saha, Bhaskar, Mitra, Debashis
• Format: Article
• Language: English
• Subjects: AIDS Vaccines - genetics; AIDS Vaccines - immunology; AIDS Vaccines - therapeutic use; Animals; CD4-Positive T-Lymphocytes - immunology; Cloning, Molecular; Genetic Vectors - genetics; HIV Envelope Protein gp120 - genetics; HIV Envelope Protein gp120 - immunology; HIV Envelope Protein gp120 - therapeutic use; HIV Infections - drug therapy; HIV Infections - prevention & control; HIV-1; Human immunodeficiency virus 1; Immune Tolerance - genetics; Interleukin-10 - genetics; Interleukin-10 - metabolism; Mice; Ovalbumin - immunology; tat Gene Products, Human Immunodeficiency Virus - genetics; tat Gene Products, Human Immunodeficiency Virus - immunology; tat Gene Products, Human Immunodeficiency Virus - therapeutic use
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.180.1.79

A large number of multicomponent vaccine candidates are currently in clinical evaluation, many of which also include the HIV-1 Tat protein, an important regulatory protein of the virus. However, whether Tat, a known immune effector molecule with a well-conserved sequence among different HIV subtypes, affects the immune response to a coimmunogen is not well understood. In this study, using a bicistronic vector expressing both gp120 and Tat, we have analyzed the role of Tat in elicitation of the gp120-specific immune response. The T cell responses to gp120 were greatly diminished in mice coimmunized with Tat as compared with mice immunized with gp120 alone. This immunosuppressive activity of Tat was not confined to viral Ag only because it also suppressed the immune response of unrelated Ag. Analysis of the cytokine profile suggests that Tat induces IL-10 and since IL-10 has been demonstrated to have appreciable T cell inhibitory activity, it is plausible that IL-10 could be responsible for Tat-mediated immunosuppression. Finally, the immunosuppressive effect of Tat was not observed in IL-10-deficient mice, confirming the role of IL-10 in Tat-mediated immunosuppression. Thus, our results demonstrate for the first time that the immunosuppressive effect of Tat is mediated through IL-10 and suggests that Tat-induced IL-10-mediated immune suppression seems to cripple immune surveillance during HIV-1 infection.