Human cytomegalovirus particles directly suppress CD4 T-lymphocyte activation and proliferation

Immunobiology. 2013 Aug;218(8):1034-40. doi: 10.1016/j.imbio.2013.01.002. Epub 2013 Jan 16.

Abstract

CD4 T cells are important regulators of the immune system and are vital for mounting a strong immune response against viral infections. Human cytomegalovirus (HCMV) is known to be a strong modulator of the innate as well as adaptive immune responses. In this study, we found that HCMV directly inhibited proliferation of CD4 T cells and rendered them unresponsive to immunological stimuli. This effect was not observed when CD4 T cells were treated with herpes simplex virus-1/2 or measles virus. When stimulated with phytohemagglutinin, concanavalin A, or phorbol myristate acetate, HCMV-treated T cells were unable to proliferate, revealing an ability of HCMV to inhibit CD4 T cell response. Furthermore, HCMV also prevented proliferation of leukemic T-cell lines. HCMV-treated CD4 T cells expressed the activation markers CD45RO and CD69, were not apoptotic and produced decreased levels of the cytokines IL-4, IFN-γ and TNF-α, compared to untreated controls. The inhibitory effect of HCMV on CD4 T cell proliferation was not mediated by HCMV gH, gB or other immunogenic glycoproteins, since intravenous immunoglobulins or gB- or gH-specific neutralizing antibodies did not prevent the suppression of T-cell proliferation. Our observations show that HCMV inhibits CD4 T cell function with potential clinical consequences for both humoral and cell-mediated immune responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Viral / immunology
  • Antigens, CD / biosynthesis
  • Antigens, Differentiation, T-Lymphocyte / biosynthesis
  • CD4-Positive T-Lymphocytes / immunology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Concanavalin A
  • Cytomegalovirus / immunology*
  • Cytomegalovirus Infections / immunology*
  • Cytomegalovirus Infections / virology
  • Herpesvirus 1, Human / immunology
  • Herpesvirus 2, Human / immunology
  • Humans
  • Interferon-gamma / biosynthesis
  • Interleukin-4 / biosynthesis
  • K562 Cells
  • Lectins, C-Type / biosynthesis
  • Leukocyte Common Antigens / biosynthesis
  • Leukocytes, Mononuclear / immunology
  • Lymphocyte Activation / immunology*
  • Macrophages / immunology
  • Measles virus / immunology
  • Phytohemagglutinins
  • Tetradecanoylphorbol Acetate
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Antibodies, Viral
  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD69 antigen
  • Lectins, C-Type
  • Phytohemagglutinins
  • Tumor Necrosis Factor-alpha
  • Concanavalin A
  • Interleukin-4
  • Interferon-gamma
  • Leukocyte Common Antigens
  • Tetradecanoylphorbol Acetate