Differential Effects of Type I IFNs on the Growth of WC1− CD8+ γδ T Cells and WC1+ CD8− γδ T Cells In Vitro

Type I IFNs have a broad array of immunoregulatory functions that include up-regulation of type 1 immune responses through enhancing differentiation and activation of CD8+ T cells and CD4+ Th1 cells. Ovine trophoblast IFN-τ is a recently described type I IFN with the potential for therapeutic use, based on its potent antiviral activity yet low toxicity. Studies were designed to determine the immunoregulatory effects of IFN-τ on Ag-stimulated T cells, and a novel effect of type I IFNs on γδ T cells was observed. In cultures of parasite Ag-stimulated bovine T cells that contained a mixture of αβ and γδ T cells, both IFN-τ and IFN-α suppressed the expansion of WC1+ CD2− CD6− CD8− γδ T cells, yet stimulated the growth of WC1− CD2+ CD6+ CD8+ γδ T cells and CD8+ αβ T cells. The CD8+ γδ T cell subset expressed high levels of the IL-2R α-chain. Furthermore, we showed that type I IFN enhanced IL-2 production by these Ag-stimulated T cell lines. In short term cultures of PBMC, IL-2 stimulated an expansion of WC1− CD6+ CD8+ γδ T cells, which was significantly increased by IFN-τ, even though IFN-τ alone did not support cell survival. These studies demonstrate for the first time that type I IFNs differentially modulate the proliferation of different subsets of γδ T cells, which appears to act in part via IL-2.

[1]  F. Bazer,et al.  Trophoblast IFN-tau differentially induces lymphopenia and neutropenia in lambs. , 1998, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

[2]  A. Alberti,et al.  Therapy of hepatitis C: Re‐treatment with alpha interferon , 1997, Hepatology.

[3]  P. Ricciardi-Castagnoli,et al.  Production of Interferon‐α/β by Murine Dendritic Cell Lines Stimulated by Virus and Bacteria , 1997, Scandinavian journal of immunology.

[4]  J. Sprent,et al.  T Cell Stimulation In Vivo by Lipopolysaccharide (LPS) , 1997, The Journal of experimental medicine.

[5]  L. Dudler,et al.  TCR γδ+ cells are prominent in normal bovine skin and express a diverse repertoire of antigen receptors , 1997, Immunology.

[6]  G. Asherson,et al.  Development of IFN-gamma-producing CD8+ gamma delta+ T lymphocytes and IL-2-producing CD4+ alpha beta+ T lymphocytes during contact sensitivity. , 1997, Journal of immunology.

[7]  L. Harrison,et al.  Aerosol Insulin Induces Regulatory CD8 γδ T Cells That Prevent Murine Insulin-dependent Diabetes , 1996, The Journal of experimental medicine.

[8]  P. Sopp,et al.  Bovine γ/δ TcR+ T Lymphocytes are Stimulated to Proliferate by Autologous Theileria annulata‐Infected Cells in the Presence of Interleukin‐2 , 1996, Scandinavian journal of immunology.

[9]  H. C. van der Heyde,et al.  Human gamma delta T cell subset-proliferative response to malarial antigen in vitro depends on CD4+ T cells or cytokines that signal through components of the IL-2R. , 1996, Journal of immunology.

[10]  J. Naessens Introduction and summary of workshop findings , 1996 .

[11]  M. Cooper,et al.  Expression of an avian CD6 candidate is restricted to αβ T cells, splenic CD8+ γδ T cells and embryonic natural killer cells , 1996, European journal of immunology.

[12]  J. Sprent,et al.  Induction of Bystander T Cell Proliferation by Viruses and Type I Interferon in Vivo , 1996, Science.

[13]  W. Davis,et al.  Identification of γδT lymphocyte subsets that populate calf ileal mucosa after birth , 1996, Veterinary Immunology and Immunopathology.

[14]  B. Ruef,et al.  CD4+ T-helper lymphocyte responses against Babesia bigemina rhoptry-associated protein I , 1996, Infection and immunity.

[15]  M. Jutila,et al.  Generation of a new gamma delta T cell-specific monoclonal antibody (GD3.5). Biochemical comparisons of GD3.5 antigen with the previously described Workshop Cluster 1 (WC1) family. , 1996, Journal of immunology.

[16]  O. J. Trask,et al.  Modulation of WC1, a lineage‐specific cell surface molecule of γ/δ T cells, augments cellular proliferation , 1996 .

[17]  M. Kagnoff Mucosal immunology: new frontiers. , 1996, Immunology today.

[18]  P. Subramaniam,et al.  Differential recognition of the type I interferon receptor by interferons tau and alpha is responsible for their disparate cytotoxicities. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[19]  P. Subramaniam,et al.  The IFN pregnancy recognition hormone IFN-tau blocks both development and superantigen reactivation of experimental allergic encephalomyelitis without associated toxicity. , 1995, Journal of immunology.

[20]  B. Haynes,et al.  Cloning, mapping, and characterization of activated leukocyte-cell adhesion molecule (ALCAM), a CD6 ligand , 1995, The Journal of experimental medicine.

[21]  P. Askenase,et al.  Gamma delta T cells in normal spleen assist immunized alpha beta T cells in the adoptive cell transfer of contact sensitivity. Effect of Bordetella pertussis, cyclophosphamide, and antibodies to determinants on suppressor cells. , 1995, Journal of immunology.

[22]  B. Haynes,et al.  Characterization of a CD6 ligand(s) expressed on human- and murine-derived cell lines and murine lymphoid tissues. , 1994, Cellular immunology.

[23]  V. Holan,et al.  Interleukin-1 and interferon-alpha augment interleukin-2 (IL-2) production by distinct mechanisms at the IL-2 mRNA level. , 1994, Cellular immunology.

[24]  F. Jongejan,et al.  Production of alpha interferon in Cowdria ruminantium-infected cattle and its effect on infected endothelial cell cultures , 1994, Infection and immunity.

[25]  B. Szente,et al.  How interferons fight disease. , 1994, Scientific American.

[26]  C. Cluff,et al.  Differential distribution of γδT-cell receptor lymphocyte subpopulations in blood and spleen of young and adult cattle , 1994 .

[27]  D. Dobbelaere,et al.  CD4+ T-cell clones obtained from cattle chronically infected with Fasciola hepatica and specific for adult worm antigen express both unrestricted and Th2 cytokine profiles , 1994, Infection and immunity.

[28]  J U Gutterman,et al.  Cytokine therapeutics: lessons from interferon alpha. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[29]  M. Kronenberg,et al.  Antigens recognized by gamma delta T cells. , 1994, Current opinion in immunology.

[30]  D. Dobbelaere,et al.  Functional and Phenotypic Characterization of WC1+ γ/δ T Cells Isolated from Babesia bovis-Stimulated T Cell Lines , 1994 .

[31]  V. Holan,et al.  Interleukin-2 production by T cells : a study of the immunoregulatory actions of interferon-α, interferon-γ, and tumor necrosis factor-α in phenotypically different T cell clones , 1993 .

[32]  S. Tonegawa,et al.  Different roles of αβ and γδ T cells in immunity against an intracellular bacterial pathogen , 1993, Nature.

[33]  E. A. Havell Listeria monocytogenes-Induced Interferon-v Primes the Host for Production of Tumor Necrosis Factor and Interferon-α/β , 1993 .

[34]  M. Brandon,et al.  Activation of uterine intraepithelial γδ T cell receptor‐positive lymphocytes during pregnancy , 1993 .

[35]  F. Bazer,et al.  Natural Killer Cell Activity of Lymphocytes Exposed to Ovine, Type I, Trophoblast Interferon , 1993, American journal of reproductive immunology.

[36]  S. Tonegawa,et al.  Gamma/delta cells. , 1993, Annual review of immunology.

[37]  H. Clevers,et al.  Molecular characterization of the WC1 antigen expressed specifically on bovine CD4-CD8- gamma delta T lymphocytes. , 1992, Journal of immunology.

[38]  W. Brown,et al.  Bovine helper T cell clones recognize five distinct epitopes on Babesia bovis merozoite antigens , 1992, Infection and immunity.

[39]  R. Roberts,et al.  Interferons as hormones of pregnancy. , 1992, Endocrine reviews.

[40]  C. Martínez-A,et al.  Functionally distinct subsets of human γ/δ T cells , 1991 .

[41]  F. Bazer,et al.  Cloning and expression in Saccharomyces cerevisiae of a synthetic gene for the type-I trophoblast interferon ovine trophoblast protein-1: purification and antiviral activity. , 1991, Journal of interferon research.

[42]  K. Kohno,et al.  Natural human interferon-alpha augments interleukin-2 production by a direct action on the activated IL-2-producing T cells. , 1991, Journal of interferon research.

[43]  J. Bluestone,et al.  Novel function for intestinal intraepithelial lymphocytes. Murine CD3+, gamma/delta TCR+ T cells produce IFN-gamma and IL-5. , 1991, Journal of immunology.

[44]  P. Kourilsky,et al.  Induction of CD8 molecules on thymic γ/δ T cells in vitro is dependent upon α/β T cells , 1991 .

[45]  C. Snapper,et al.  Regulation by interferon alpha of immunoglobulin isotype selection and lymphokine production in mice , 1991, The Journal of experimental medicine.

[46]  F. Bazer,et al.  Type I Conceptus Interferons: Maternal Recognition of Pregnancy Signals and Potential Therapeutic Agents , 1991, American journal of reproductive immunology.

[47]  W. Brown,et al.  Cell-mediated immune responses to Babesia bovis merozoite antigens in cattle following infection with tick-derived or cultured parasites , 1991, Infection and immunity.

[48]  C. Mackay,et al.  Prominence of γδ T cells in the ruminant immune system , 1991 .

[49]  G. Pawelec,et al.  Monoclonal antibodies to CD6 preferentially stimulate T-cell clones with γ/δ rather than α/β aantigen receptors , 1991 .

[50]  C. Bron,et al.  Selective expression of CD8α (Ly‐2) subunit on activated thymic γ/δ cells , 1990 .

[51]  G. Palmer,et al.  Immune serum against Anaplasma marginale initial bodies neutralizes infectivity for cattle. , 1984, Journal of immunology.