IFN-γ-Producing Dendritic Cells Are Important for Priming of Gut Intraepithelial Lymphocyte Response Against Intracellular Parasitic Infection1

The importance of intraepithelial lymphocytes (IEL) in immunoprotection against orally acquired pathogens is being increasingly recognized. Recent studies have demonstrated that Ag-specific IEL can be generated and can provide an important first line of defense against pathogens acquired via oral route. However, the mechanism involved in priming of IEL remains elusive. Our current study, using a microsporidial model of infection, demonstrates that priming of IEL is dependent on IFN-γ-producing dendritic cells (DC) from mucosal sites. DC from mice lacking the IFN-γ gene are unable to prime IEL, resulting in failure of these cells to proliferate and lyse pathogen-infected targets. Also, treatment of wild-type DC from Peyer’s patches with Ab to IFN-γ abrogates their ability to prime an IEL response against Encephalitozoon cuniculi in vitro. Moreover, when incubated with activated DC from IFN-γ knockout mice, splenic CD8+ T cells are not primed efficiently and exhibit reduced ability to home to the gut compartment. These data strongly suggest that IFN-γ-producing DC from mucosal sites play an important role in the generation of an Ag-specific IEL response in the small intestine. To our knowledge, this report is the first demonstrating a role for IFN-γ-producing DC from Peyer’s patches in the development of Ag-specific IEL population and their trafficking to the gut epithelium.

[1]  Mamoru Ito,et al.  Interleukin 12–dependent Interferon γ Production by CD8α+Lymphoid Dendritic Cells , 1999, The Journal of experimental medicine.

[2]  J. Kraehenbuhl,et al.  A recombinant Salmonella typhimurium vaccine strain is taken up and survives within murine Peyer's patch dendritic cells , 2000, Cellular microbiology.

[3]  S. London,et al.  Reovirus Serotype 1/Strain Lang-Stimulated Activation of Antigen-Specific T Lymphocytes in Peyer’s Patches and Distal Gut-Mucosal Sites: Activation Status and Cytotoxic Mechanisms1 , 2005, The Journal of Immunology.

[4]  S. Dandekar,et al.  Intestinal Intraepithelial Lymphocytes Are Primed for Gamma Interferon and MIP-1β Expression and Display Antiviral Cytotoxic Activity despite Severe CD4+ T-Cell Depletion in Primary Simian Immunodeficiency Virus Infection , 1998, Journal of Virology.

[5]  M. Moser Regulation of Th1/Th2 development by antigen-presenting cells in vivo. , 2001, Immunobiology.

[6]  S. Müller,et al.  Intestinal Intraepithelial Lymphocytes Exert Potent Protective Cytotoxic Activity During an Acute Virus Infection1 , 2000, The Journal of Immunology.

[7]  Ira Mellman,et al.  Dendritic Cells Specialized and Regulated Antigen Processing Machines , 2001, Cell.

[8]  K. Sayama,et al.  Essential Roles of Perforin in Antigen-Specific Cytotoxicity Mediated by Human CD4+ T Lymphocytes: Analysis Using the Combination of Hereditary Perforin-Deficient Effector Cells and Fas-Deficient Target Cells 1 , 2003, The Journal of Immunology.

[9]  A. Iwasaki,et al.  Localization of Distinct Peyer's Patch Dendritic Cell Subsets and Their Recruitment by Chemokines Macrophage Inflammatory Protein (Mip)-3α, Mip-3β, and Secondary Lymphoid Organ Chemokine , 2000, The Journal of experimental medicine.

[10]  A. Adjei,et al.  Differential intra-epithelial lymphocyte phenotypes following Cryptosporidium parvum challenge in susceptible and resistant athymic strains of mice. , 2000, Parasitology international.

[11]  A. Nel,et al.  Intestinal intraepithelial lymphocytes are activated and cytolytic but do not proliferate as well as other T cells in response to mitogenic signals. , 1993, Journal of immunology.

[12]  T. Hibi,et al.  Gut cryptopatches: direct evidence of extrathymic anatomical sites for intestinal T lymphopoiesis. , 2000, Immunity.

[13]  J. Trapani,et al.  Unlocking the secrets of cytotoxic granule proteins , 2001, Journal of leukocyte biology.

[14]  P. Ashton‐Rickardt The granule pathway of programmed cell death. , 2005, Critical reviews in immunology.

[15]  A. Iwasaki,et al.  Freshly Isolated Peyer's Patch, but Not Spleen, Dendritic Cells Produce Interleukin 10 and Induce the Differentiation of T Helper Type 2 Cells , 1999, The Journal of experimental medicine.

[16]  R. Mosley,et al.  Proliferative properties of murine intestinal intraepithelial lymphocytes (IEL): IEL expressing TCRαβ or TCRτδ are largely unresponsive to proliferative signals mediated via conventional stimulation of the CD3-TCR complex , 1991 .

[17]  P. Scott Development and regulation of cell-mediated immunity in experimental Leishmaniasis , 2003, Immunologic research.

[18]  Wolfgang Weninger,et al.  Selective imprinting of gut-homing T cells by Peyer's patch dendritic cells , 2003, Nature.

[19]  Z. Fan,et al.  Molecular mechanisms of lymphocyte-mediated cytotoxicity. , 2005, Cellular & molecular immunology.

[20]  T. Shimamura,et al.  Development of intestinal intraepithelial T lymphocytes is independent of Peyer's patches and lymph nodes in aly mutant mice. , 1994, Journal of immunology.

[21]  A. Iwasaki,et al.  Involvement of Dendritic Cell Subsets in the Induction of Oral Tolerance and Immunity , 2004, Annals of the New York Academy of Sciences.

[22]  J. O’Shea,et al.  Inducible Expression of Stat4 in Dendritic Cells and Macrophages and Its Critical Role in Innate and Adaptive Immune Responses1 , 2001, The Journal of Immunology.

[23]  C Caux,et al.  Immunobiology of dendritic cells. , 2000, Annual review of immunology.

[24]  T. Gyorkos,et al.  Modified technique for efficient detection of microsporidia , 1994, Journal of clinical microbiology.

[25]  J. Schwartzman,et al.  γδ T Cell-Deficient Mice Have a Down-Regulated CD8+ T Cell Immune Response Against Encephalitozoon cuniculi Infection1 , 2001, The Journal of Immunology.

[26]  W. Strober,et al.  Distinct populations of dendritic cells are present in the subepithelial dome and T cell regions of the murine Peyer's patch , 1996, The Journal of experimental medicine.

[27]  D. Bout,et al.  Gut-derived intraepithelial lymphocytes induce long term immunity against Toxoplasma gondii. , 1998, Journal of immunology.

[28]  U. Boehm,et al.  Cellular responses to interferon-gamma. , 1997, Annual review of immunology.

[29]  S. Nishikawa,et al.  Visualization of peptide presentation following oral application of antigen in normal and Peyer's patches‐deficient mice , 2003, European journal of immunology.

[30]  F. Geissmann,et al.  Dendritic cells are early cellular targets of Listeria monocytogenes after intestinal delivery and are involved in bacterial spread in the host , 2001, Cellular microbiology.

[31]  M. Munder,et al.  Direct stimulation of macrophages by IL-12 and IL-18 - a bridge built on solid ground. , 2001, Immunology letters.

[32]  S. Matsuda,et al.  Synergistic Effects of IL-4 and IL-18 on IL-12-Dependent IFN-γ Production by Dendritic Cells1 , 2000, The Journal of Immunology.

[33]  J. Reimann,et al.  IL-12/IL-18-Dependent IFN-γ Release by Murine Dendritic Cells1 , 2001, The Journal of Immunology.

[34]  F. Shanahan,et al.  The Fas counterattack: Fas-mediated T cell killing by colon cancer cells expressing Fas ligand , 1996, The Journal of experimental medicine.

[35]  E. Pamer Immune responses to Listeria monocytogenes , 2004, Nature Reviews Immunology.

[36]  I. Khan,et al.  Induction of a Rapid and Strong Antigen-Specific Intraepithelial Lymphocyte Response during Oral Encephalitozoon cuniculi Infection1 , 2004, The Journal of Immunology.

[37]  P. Kourilsky,et al.  Identical T Cell Clones Are Located within the Mouse Gut Epithelium and Lamina Propria and Circulate in the Thoracic Duct Lymph , 2000, The Journal of experimental medicine.

[38]  A. Iwasaki,et al.  Unique Functions of CD11b+, CD8α+, and Double-Negative Peyer’s Patch Dendritic Cells1 , 2001, The Journal of Immunology.

[39]  A. Hayday,et al.  Intraepithelial lymphocytes: exploring the Third Way in immunology , 2001, Nature Immunology.

[40]  柳井 文男 Essential roles of perforin in antigen-specific cytotoxicity mediated by human CD4[+] T lymphocytes : analysis using the combination of hereditary perforin-deficient effector cells and Fas-deficient target cells , 2004 .

[41]  Mamoru Ito,et al.  Interleukin 12-dependent interferon gamma production by CD8alpha+ lymphoid dendritic cells. , 1999 .

[42]  I. Khan,et al.  Lack of CD4+ T Cells Does Not Affect Induction of CD8+ T-Cell Immunity against Encephalitozoon cuniculi Infection , 2000, Infection and Immunity.

[43]  C. Johansson,et al.  Phenotype and function of intestinal dendritic cells. , 2005, Seminars in immunology.

[44]  I. Khan,et al.  Augmentation of the CD8+ T cell response by IFN-gamma in IL-12-deficient mice during Toxoplasma gondii infection. , 1999, Journal of immunology.

[45]  J. Chai,et al.  ROLE OF MURINE INTESTINAL INTRAEPITHELIAL LYMPHOCYTES AND LAMINA PROPRIA LYMPHOCYTES AGAINST PRIMARY AND CHALLENGE INFECTIONS WITH CRYPTOSPORIDIUM PARVUM , 2003, The Journal of parasitology.

[46]  S. Dandekar,et al.  An early expansion of CD8αβ T cells, but depletion of resident CD8αα T cells, occurs in the intestinal epithelium during primary simian immunodeficiency virus infection , 2000 .

[47]  D. Rubin,et al.  Developmental relationship between cytotoxic α/β T cell receptor‐positive intraepithelial lymphocytes and Peyer's patch lymphocytes , 1993 .

[48]  P. Hertzog,et al.  Differential Production of IL-12, IFN-α, and IFN-γ by Mouse Dendritic Cell Subsets1 , 2001, The Journal of Immunology.

[49]  W. Agace,et al.  CCL25/CCR9 promotes the induction and function of CD103 on intestinal intraepithelial lymphocytes , 2004, European journal of immunology.

[50]  T. Curiel,et al.  NK Cells Help To Induce CD8+-T-Cell Immunity against Toxoplasma gondii in the Absence of CD4+ T Cells , 2005, Infection and Immunity.

[51]  G. Trinchieri Interleukin-12: a proinflammatory cytokine with immunoregulatory functions that bridge innate resistance and antigen-specific adaptive immunity. , 1995, Annual review of immunology.