The Efficacy of T Cell-Mediated Immune Responses Is Reduced by the Envelope Protein of the Chimeric HIV-1/SIV-KB9 Virus In Vivo

• DOI: 10.4049/jimmunol.181.8.5510
• Publication Date: 2014-04-18T23:47:01Z
• Authors: Liljana Stevceva; Victor Yoon; Angela Carville; Beatriz Pacheco; Michael Santosuosso; Birgit Korioth-Sc...; Keith Mansfield; Mark C. Poznansky
• Keywords: Acquired Immunodeficiency Syndrome; Immunity, Cellular; 0303 health sciences; Membrane Glycoproteins; Lymphoid Tissue; Simian Acquired Immunodeficiency Syndrome; CHO Cells; CD8-Positive T-Lymphocytes; HIV Envelope Protein gp120; Macaca mulatta; T-Lymphocytes, Regulatory; 3. Good health; 03 medical and health sciences; Cricetulus; Viral Envelope Proteins; Transforming Growth Factor beta; Cricetinae; HIV-1; Animals; Humans; Simian Immunodeficiency Virus

Abstract Gp120 is a critical component of the envelope of HIV-1. Its role in viral entry is well described. In view of its position on the viral envelope, gp120 is a part of the retrovirus that immune cells encounter first and has the potential to influence antiretroviral immune responses. We propose that high levels of gp120 are present in tissues and may contribute to the failure of the immune system to fully control and ultimately clear the virus. Herein, we show for the first time that lymphoid tissues from acutely HIV-1/SIV (SHIV)-KB9-infected macaques contain deposits of gp120 at concentrations that are high enough to induce suppressive effects on T cells, thus negatively regulating the antiviral CTL response and contributing to virus survival and persistence. We also demonstrate that SHIV-KB9 gp120 influences functional T cell responses during SHIV infection in a manner that suppresses degranulation and cytokine secretion by CTLs. Finally, we show that regulatory T cells accumulate in lymphoid tissues during acute infection and that they respond to gp120 by producing TGFβ, a known suppressant of cytotoxic T cell activity. These findings have significant implications for our understanding of the contribution of non-entry-related functions of HIV-1 gp120 to the pathogenesis of HIV/AIDS.