Experimental T cell-mediated inflammatory reactions in the murine oral mucosa. II. Immunohistochemical characterization of resident and infiltrating cells

Clinical and Experimental Immunology

Volumn 104, Issue 2, 1996, Pages 297-305

  Ahlfors, E ^a   Jonsson, R ^b   Czerkinsky, C ^a,c  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

^b Department of Medical Microbiology ^*  (Norway)

^c EDOUARD HERRIOT HOSPITAL   (France)

Author keywords

Delayed type hypersensitivity; Immunohistochemistry; Mouse; Oral mucosa

Indexed keywords

CD11 ANTIGEN; CD4 ANTIGEN; CD8 ANTIGEN; INTERLEUKIN 2 RECEPTOR; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; OXAZOLONE;

ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; DELAYED HYPERSENSITIVITY; FEMALE; IMMUNOHISTOCHEMISTRY; LYMPHOCYTIC INFILTRATION; MALE; MOUSE; MOUTH INFLAMMATION; MOUTH MUCOSA; NONHUMAN; PRIORITY JOURNAL; T LYMPHOCYTE;

EID: 0029924464     PISSN: 00099104     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2249.1996.967659.x     Document Type: Article

References (39)

1. Brandtzaeg P. Basic mechanisms of mucosal immunity: a major adaptive defence system. Immunologist 1995; 3:89-96.
2. Bienenstock J, Befus AD, McDermott M et al. The mucosal immunological network: compartmentalization of lymphocytes, natural killer cells, and mast cells. Ann N Acad Sci 1982; 409:164-73.
3. Mowat AM, Ferguson A. Hypersensitivity reactions in the small intestine. VI. Pathogenesis of the graft-vs.-host reaction in the small intestinal mucosa. Transplantation 1981; 32:238-50.
4. Sanchez R, Ahlfors E, Backman K et al. Oral lesions of lupus erythematosus patients in relation to other chronic inflammatory oral diseases: an immunologic study. Scand J Dent Res 1988; 122:569-77.
5. Seymour GJ, Gemmell E, Walsh LJ et al. Immunohistological analysis of experimental gingivitis in humans. Clin Exp Immunol 1988; 71:132-8.
6. Ahlfors E, Czerkinsky C. Contact sensitivity in the murine oral mucosa. I. An experimental model of delayed contact hypersensitivity at mucosal surfaces. Clin Exp Immunol 1991; 86:449-56.
7. Springer T, Yolfre G, Secher DS et al. Mac-1: a macrophage differentiation antigen identified by monoclonal antibody. Eur J Immunol 1979; 9:301-7.
8. Pierres A, Naquet P, van Agthoven A et al. A rat anti-mouse T4 monoclonal antibody (H129.19) inhibits the proliferation of Ia-reactive T cell clones and delineates two phenotypically distinct subsets among anti-Ia cytolytic T cell clones. J Immunol 1984; 132:2775-81.
9. Ledbetter JR, Herzenberg LA. Xenogeneic monoclonal antibodies to mouse lymphoid differentiation antigens. Immunological Rev 1979; 47:63-90.
10. Ledbetter JR, Rouse RB, Micklem HS et al. T cell subsets defined by expression of Lyt-1,2,3 and Thy-1 antigens. J Exp Med 1980; 152:280-9.
11. Ortega, GR, Robb RJ, Shevach EM et al. The murine IL-2 receptor. I. Monoclonal antibodies that define distinct functional epitopes on activated T cells and react with activated B cells. J Immunol 1984; 133:1970-5.
12. Lemke H, Hämmerling GJ, Hämmerling U. Fine specificity analysis with monoclonal antibodies of antigens controlled by the major histocompatibility complex and by the Qa/TL region in mice. Immunological Rev 1979; 47:175-90.
13. Mosmann TH, Cherwinsky M, Bond M et al. Two types of murine helper T cell clone: I. Definitions according to profiles of lymphokine activities and secreted proteins. J Immunol 1986; 136:2348-57.
14. Cherwinsky HM, Schumacher JH, Brown KD et al. Two types of mouse helper T cell clone: III Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies. J Exp Med 1987; 166:1229-44.
15. Konttinen YT, Segerberg-Konttinen A, Nordström D et al. An immunoperoxidase-autoradiography double labelling method for analysis of lymphocyte activation markers and DNA synthesis. J Immunol Methods 1988; 110:19-27.
16. Gawkrodger DJ, McVittie E, Carr MM et al. Phenotypic characterization of the early cellular responses in allergic and irritant contact dermatitis. Clin Exp Immunol 1986; 66:590-8.
17. Herzog W-R, Millet I, Ferreri NS et al. An antigen-specific DTH-initiating cell clone. Functional, phenotypical and partial molecular characterization. J Immunol 1990; 144:3667-76.
18. 4-specific DTH-initiating cells with an unusual mixed phenotype for an antigen-specific cell. Cell Immunol 1995; 161:244-55.
19. Van Loveren H, Meade R, Askenase PW. An early component of delayed-type hypersensitivity mediated by T cells and mast cells. J Exp Med 1983; 157:1604-17.
20. Picker L, Butcher EC. Physiological and molecular mechanisms of lymphocyte homing. Annu Rev Immunol 1992; 10:561-91.
21. 2-terminal sequence-characterized human monokine possessing neutrophil chemotactic, skin-reactive, and granulocytosis-promoting activity. J Exp Med 1988; 167:1364-76.
22. Yoshimura T, Matsushima K, Tanaka S et al. Purification of a human monocyte-derived neutrophil chemotactic factor that has peptide sequence similarity to other host defence cytokines. Proc Natl Acad Sci USA 1987; 84:9233-7.
23. Sauder DN, Mounessa NL, Katz SI, Dinarello CA, Gallin JI. Chemotactic cytokines: the role of leukocytic pyrogen and epidermal cell thymocyte-activating factor in neutrophil chemotaxis. J Immunol 1984; 132:828-32.
24. Barker JNWN, Sarma V, Mitra RS et al. Marked synergism between tumor necrosis factor-α and interferon-γ in regulation of keratinocyte-derived adhesion molecules and chemotactic factors. J Clin Invest 1990; 85:605-8.
25. Strieter RM, Kunkel SL, Showell HJ et al. Endothelial cell gene expression of a neutrophil chemotactic factor by TNF-α, LPS, and IL1-β. Science 1989; 243:1467-9.
26. Larsen CG, Anderson AO, Oppenheim JJ et al. Production of interleukin-8 by human dermal fibroblasts and keratinocytes in response to interleukin-1 or tumour necrosis factor. Immunology 1989; 68:31-36.
27. Rampart M, Van Damme J, Zonnekeyn L et al. Granulocyte chemotactic protein/interleukin-8 induces plasma leakage and neutrophil accumulation in rabbit skin. Am J Pathol 1989; 135:21-25.
28. Daynes RA, Araneo BA, Dowell TA et al. Regulation of murine lymphokine production in vivo. III. The lymphoid tissue microenvironment exerts regulatory influences over T helper cell function. J Exp Med 1990; 171:979-96.
29. Cher DJ, Mossman TR. Two types of murine helper T cell clones. II. Delayed-type hypersensitivity is mediated by TH1 clones. J Immunol 1990; 138:3688-94.
30. Askenase PW, Szczepanik M, Ptak M at al. γδ T cells in normal spleen assist immunized αβ T cells in the adoptive cell transfer of contact sensitivity. J Immunol 1995; 154:3644-53.
31. Dieli F, Asherson GL, Romano GC et al. IL-4 is essential for the systemic transfer of delayed hypersensitivity by T cell lines. Role of γδ cells. J Immunol 1994; 152:2698-704.
32. Suitters AJ, Lamport IA. Expression of Ia antigen on epidermal keratinocytes is a consequence of cellular immunity. Br J Exp Pathol 1982; 63:207-13.
33. Scheynius A, Klareskog L, Forsum U. In situ identification of T lymphocyte subsets and HLA-DR expressing cells in the human skin tuberculin reaction. Clin Exp Immunol 1982; 49:325-30.
34. Scheynius A, Fischer T, Forsum U, Klareskog L. Phenotypic characterization in situ of inflammatory cells in allergic and irritant contact dermatitis in man. Clin Exp Immunol 1984; 55:81-90.
35. Roberts LK, Spangrude GJ, Daynes RA, Krueger GG. Correlation between keratinocyte expression of Ia and the intensity and duration of contact hypersensitivity responses in mice. J Immunol 1985; 135:2929-36.
36. Warfvinge G, Larsson Å. Immunocytochemical analysis of early focal cellular infiltrates in experimental oral contact hypersensitivity. Acta Derm Venereol 1991; 71:377-83.
37. Scheynius A, Tjernlund U. Human keratinocytes express HLA-DR antigens in the tuberculin reaction. Scand J Immunol 1984; 19:141-7.
38. Nickoloff BJ, Turka LA. Immunological functions of non-professional antigen-presenting cells: new insights from studies of T-cell interactions with keratinocytes. Immunol Today 1994; 15:464-9.
39. van Wilsem EJG, van Hoogstraten IMW, Breve J et al. Dendritic cells of the oral mucosa and the induction of oral tolerance. A local affair. Immunology 1994; 83:128-32.