Nonconventional CD8+ T cell responses to Listeria infection in mice lacking MHC class Ia and H2-M3

J Immunol. 2011 Jan 1;186(1):489-98. doi: 10.4049/jimmunol.1002639. Epub 2010 Nov 22.

Abstract

CD8(+) T cells restricted to MHC class Ib molecules other than H2-M3 have been shown to recognize bacterial Ags. However, the contribution of these T cells to immune responses against bacterial infection is not well defined. To investigate the immune potential of MHC class Ib-restricted CD8(+) T cells, we have generated mice that lack both MHC class Ia and H2-M3 molecules (K(b-/-)D (b-/-)M3(-/-)). The CD8(+) T cells present in K(b-/-)D (b-/-)M3(-/-) mice display an activated surface phenotype and are able to secrete IFN-γ rapidly upon anti-CD3 and anti-CD28 stimulation. Although the CD8(+) T cell population is reduced in K(b-/-)D (b-/-)M3(-/-) mice compared with that in K(b-/-)D (b-/-) mice, this population retains the capacity to expand significantly in response to primary infection with the bacteria Listeria monocytogenes. However, K(b-/-)D (b-/-)M3(-/-) CD8(+) T cells do not expand upon secondary infection, similar to what has been observed for H2-M3-restricted T cells. CD8(+) T cells isolated from Listeria-infected K(b-/-)D (b-/-)M3(-/-) mice exhibit cytotoxicity and secrete proinflammatory cytokines in response to Listeria-infected APCs. These T cells are protective against primary Listeria infection, as Listeria-infected K(b-/-)D (b-/-)M3(-/-) mice exhibit reduced bacterial burden compared with that of infected β(2)-microglobulin-deficient mice that lack MHC class Ib-restricted CD8(+) T cells altogether. In addition, adoptive transfer of Listeria-experienced K(b-/-)D (b-/-)M3(-/-) splenocytes protects recipient mice against subsequent Listeria infection in a CD8(+) T cell-dependent manner. These data demonstrate that other MHC class Ib-restricted CD8(+) T cells, in addition to H2-M3-restricted T cells, contribute to antilisterial immunity and may contribute to immune responses against other intracellular bacteria.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / microbiology*
  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation
  • Cells, Cultured
  • Cytotoxicity, Immunologic / genetics
  • Disease Models, Animal
  • Female
  • H-2 Antigens / genetics*
  • Histocompatibility Antigen H-2D
  • Histocompatibility Antigens Class I / genetics*
  • Listeria monocytogenes / immunology*
  • Listeriosis / immunology*
  • Listeriosis / metabolism
  • Listeriosis / pathology
  • Lymphocyte Activation / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • beta 2-Microglobulin / deficiency*
  • beta 2-Microglobulin / genetics

Substances

  • H-2 Antigens
  • H-2Kb protein, mouse
  • H2-M3 antigen
  • Histocompatibility Antigen H-2D
  • Histocompatibility Antigens Class I
  • beta 2-Microglobulin