SEARCH

SEARCH BY CITATION

References

  • 1
    Skeen MJ, Ziegler HK. Induction of murine peritoneal γ/δ T cells and their role in resistance to bacterial infection. J Exp Med 1993; 178:97184.
  • 2
    Mombaerts P, Arnoldi J, Russ F, Tonegawa S, Kaufmann SH. Different roles of αβ and γδ T cells in immunity against an intracellular bacterial pathogen. Nature 1993; 365:536.
  • 3
    Ladel CH, Hess J, Daugelat S, Mombaerts P, Tonegawa S, Kaufmann SH. Contribution of α/β and γ/δ T lymphocytes to immunity against Mycobacterium bovis bacillus Calmette Guerin: studies with T cell receptor-deficient mutant mice. Eur J Immunol 1995; 25:83846.
  • 4
    Hayday AC. γ/δ cells: a right time and a right place for a conserved third way of protection. Annu Rev Immunol 2000; 18:9751026.
  • 5
    Kaufmann SH. γ/δand other unconventional T lymphocytes: what do they see and what do they do? Proc Natl Acad Sci USA 1996; 93:22729.
  • 6
    Bender A, Kabelitz D. CD4 CD8 human T cells: phenotypic heterogeneity and activation requirements of freshly isolated ‘double-negative’ T cells. Cell Immunol 1990; 128:54254.
  • 7
    Baldwin CL, Sathiyaseelan T, Naiman B, White AM, Brown R, Blumerman S, Rogers A, Black SJ. Activation of bovine peripheral blood γδ T cells for cell division and IFN-γ production. Vet Immunol Immunopathol 2002; 87:2519.
  • 8
    Sathiyaseelan T, Rogers A, Baldwin CL. Response of bovine γδ T cells to activation through CD3. Vet Immunol Immunopathol 2002; 90:15568.
  • 9
    Fikri Y, Nyabenda J, Denis M, Pastoret PP. Purification and characterization of bovine WC1+γδ T lymphocytes from peripheral blood. Vet Res 2000; 31:22939.
  • 10
    Fikri Y, Pastoret PP, Nyabenda J. Costimulatory molecule requirement for bovine WC1+γδ T cells' proliferative response to bacterial superantigens. Scand J Immunol 2002; 55:37381.
  • 11
    Hanrahan CF, Kimpton WG, Howard CJ, Parsons KR, Brandon MR, Andrews AE, Nash AD. Cellular requirements for the activation and proliferation of ruminant γδ T cells. J Immunol 1997; 159:428794.
  • 12
    Collins RA, Sopp P, Gelder KI, Morrison WI, Howard CJ. Bovine γ/δ TCR+ T lymphocytes are stimulated to proliferate by autologous Theileria annulata-infected cells in the presence of interleukin-2. Scand J Immunol 1996; 44:44452.
  • 13
    Davis WC, Brown WC, Hamilton MJ, Wyatt CR, Orden JA, Khalid AM, Naessens J. Analysis of monoclonal antibodies specific for the γδ TCR. Vet Immunol Immunopathol 1996; 52:27583.
  • 14
    Eberl M, Engel R, Beck E, Jomaa H. Differentiation of human γ−δ T cells towards distinct memory phenotypes. Cell Immunol 2002; 218:16.
  • 15
    Garcia VE, Jullien D, Song M, Uyemura K, Shuai K, Morita CT, Modlin RL. IL-15 enhances the response of human γδ T cells to non-peptide [correction of non-petide] microbial antigens. J Immunol 1998; 160:43229.
  • 16
    Ueta C, Kawasumi H, Fujiwara H, Miyagawa T, Kida H, Ohmoto Y, Kishimoto S, Tsuyuguchi I. Interleukin-12 activates human γδ T cells: synergistic effect of tumour necrosis factor-α. Eur J Immunol 1996; 26:306673.
  • 17
    Wesch D, Glatzel A, Kabelitz D. Differentiation of resting human peripheral blood γδ T cells toward Th1- or Th2-phenotype. Cell Immunol 2001; 212:1107.
  • 18
    Skeen MJ, Ziegler HK. Activation of γδ T cells for production of IFN-γ is mediated by bacteria via macrophage-derived cytokines IL-1 and IL-12. J Immunol 1995; 154:583241.
  • 19
    Wilson RA, Zolnai A, Rudas P, Frenyo LV. T cell subsets in blood and lymphoid tissues obtained from fetal calves, maturing calves and adult bovine. Vet Immunol Immunopathol 1996; 53:4960.
  • 20
    Wyatt CR, Madruga C, Cluff C, Parish S, Hamilton MJ, Goff W, Davis WC. Differential distribution of γδ T cell receptor lymphocyte subpopulations in blood and spleen of young and adult cattle. Vet Immunol Immunopathol 1994; 40:18799.
  • 21
    Mackay CR, Maddox JF, Brandon MR. Three distinct subpopulations of sheep T lymphocytes. Eur J Immunol 1986; 16:1925.
  • 22
    Morrison WI, Davis WC. Individual antigens of cattle. Differentiation antigens expressed predominantly on CD4 CD8 T lymphocytes (WC1, WC2). Vet Immunol Immunopathol 1991; 27:716.
  • 23
    Clevers H, MacHugh ND, Bensaid A et al. Identification of a bovine surface antigen uniquely expressed on CD4 CD8 T cell receptor γδ+ T lymphocytes. Eur J Immunol 1990; 20:80917.
  • 24
    Kirkham PA, Takamatsu HH, Parkhouse RM. Growth arrest of γδ T cells induced by monoclonal antibody against WC1 correlates with activation of multiple tyrosine phosphatases and dephosphorylation of MAP kinase erk2. Eur J Immunol 1997; 27:71725.
  • 25
    Wijngaard PL, Metzelaar MJ, MacHugh ND, Morrison WI, Clevers HC. Molecular characterization of the WC1 antigen expressed specifically on bovine CD4 CD8γδ T lymphocytes. J Immunol 1992; 149:32737.
  • 26
    Brown WC, Davis WC, Choi SH, Dobbelaere DA, Splitter GA. Functional and phenotypic characterization of WC1+γ/δ T cells isolated from Babesia bovis-stimulated T cell lines. Cell Immunol 1994; 153:927.
  • 27
    Sopp P, Howard CJ. IFN-γ and IL-4 production by CD4, CD8 and WC1 γδ TCR (+) T cells from cattle lymph nodes and blood. Vet Immunol Immunopathol 2001; 81:8596.
  • 28
    Rogers AN, Vanburen DG, Hedblom EE, Tilahun ME, Telfer JC, Baldwin CL. γδ T cell function varies with the expressed WC1 coreceptor. J Immunol 2005; 174:338693.
  • 29
    Hope JC, Sopp P, Collins RA, Howard CJ. Differences in the induction of CD8+ T cell responses by subpopulations of dendritic cells from afferent lymph are related to IL-1 α secretion. J Leukoc Biol 2001; 69:2719.
  • 30
    Werling D, Hope JC, Chaplin P, Collins RA, Taylor G, Howard CJ. Involvement of caveolae in the uptake of respiratory syncytial virus antigen by dendritic cells. J Leukoc Biol 1999; 66:508.
  • 31
    Howard CJ, Sopp P, Parsons KR, Finch J. In vivo depletion of BoT4 (CD4) and of non-T4/T8 lymphocyte subsets in cattle with monoclonal antibodies. Eur J Immunol 1989; 19:75764.
  • 32
    Weynants V, Gilson D, Furger A et al. Production and characterization of monoclonal antibodies specific for bovine interleukin-4. Vet Immunol Immunopathol 1998; 66:99112.
  • 33
    Collins RA, Camon EB, Chaplin PJ, Howard CJ. Influence of IL-12 on interferon-γ production by bovine leucocyte subsets in response to bovine respiratory syncytial virus. Vet Immunol Immunopathol 1998; 63:6972.
  • 34
    Hope JC, Thom ML, Villarreal-Ramos B, Vordermeier HM, Hewinson RG, Howard CJ. Vaccination of neonatal calves with Mycobacterium bovis BCG induces protection against intranasal challenge with virulent M. Bovis. Clin Exp Immunol 2005; 139:4856.
  • 35
    Buddle BM, Wedlock DN, Parlane NA, Corner LA, De Lisle GW, Skinner MA. Revaccination of neonatal calves with Mycobacterium bovis BCG reduces the level of protection against bovine tuberculosis induced by a single vaccination. Infect Immun 2003; 71:64119.
  • 36
    Hope JC, Sopp P, Howard CJ. NK-like CD8 (+) cells in immunologically naive neonatal calves that respond to dendritic cells infected with Mycobacterium bovis BCG. J Leukoc Biol 2002; 71:18494.
  • 37
    Hope JC, Thom ML, McCormick PA, Howard CJ. Interaction of antigen presenting cells with mycobacteria. Vet Immunol Immunopathol 2004; 100:18795.
  • 38
    Rhodes SG, Hewinson RG, Vordermeier HM. Antigen recognition and immunomodulation by γδ T cells in bovine tuberculosis. J Immunol 2001; 166:560410.
  • 39
    Smyth AJ, Welsh MD, Girvin RM, Pollock JM. In vitro responsiveness of γδ T cells from Mycobacterium bovis-infected cattle to mycobacterial antigens. predominant involvement of WC1 (+) cells. Infect Immun 2001; 69:8996.
  • 40
    Pollock JM, Welsh MD. The WC1 (+) γδ T cell population in cattle: a possible role in resistance to intracellular infection. Vet Immunol Immunopathol 2002; 89:10514.
  • 41
    Kennedy HE, Welsh MD, Bryson DG, Cassidy JP, Forster FI, Howard CJ, Collins RA, Pollock JM. Modulation of immune responses to Mycobacterium bovis in cattle depleted of WC1 (+) γδ T cells. Infect Immunol 2002; 70:1488500.
  • 42
    Jouanguy E, Doffinger R, Dupuis S, Pallier A, Altare F, Casanova JL. IL-12 and IFN-γ in host defence against mycobacteria and salmonella in mice and men. Curr Opin Immunol 1999; 11:34651.