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Endothelial adhesion molecules for nasal-homing T cells in allergy

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Abstract

During the allergic reaction mucosal T cells are activated and a local increase in numbers occurs. In peripheral blood, a concomitant T cell activation and switch towards memory phenotype appears. E-selectin, intercellular adhesion molecule (ICAM)-1 and vascular cell adhesion molecule (VCAM)-1 were studied in nasal mucosal biopsies taken during a time-course provocation study, including patients with seasonal allergic rhinitis and healthy controls. Allergic patients were also studied during the natural pollen season with particular attention to the influence of local corticosteroid treatment. Before provocation allergic patients and controls did not differ concerning the expression of endothelial adhesion molecules. However, the epithelial ICAM-1 expression was increased among allergics (P<0.05). Repetitive allergen provocation induces an increased endothelial expression of VCAM-1 in allergic patients (P<0.01). Similarly, VCAM-1 expression was increased during the natural pollen season (P<0.05). Interestingly, the increased VCAM-1 expression was inhibited by the use of local corticosteroids. The present data demonstrate a putative integrin-VCAM-1 mechanism for selective homing of T memory cells to the allergic nasal mucosa and new in vivo effects of local corticosteroid treatment are demonstrated.

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References

  1. Bentley AM, Durham SR, Robinson DS, et al (1993) Expression of endothelial and leukocyte adhesion molecules intercellular adhesion molecule-1, E-selectin, and vascular cell adhesion molecule-1 in the bronchial mucosa in steady-state and allergen-induced asthma. J Allergy Clin Immunol 92:857–868

    Google Scholar 

  2. Cerf-Bensussan N, Brousse JA, Lisowska-Grospierre B, Guy-Grand D, Griscelli CA (1987) A monoclonal antibody (HML-1) defining a novel membrane molecule present on human intestinal lymphocytes. Eur J Immunol 17:1279–1285

    Google Scholar 

  3. Davidsson Å, Karlsson MG, Hellquist HB (1994) Allergen induced changes of B cell phenotypes in patients with allergic rhinitis. Rhinology 32:890–896

    Google Scholar 

  4. Del Prete G (1992) Human Th1 and Th2 lymphocytes: their role in the pathophysiology of atopy. Allergy 47:450–455

    Google Scholar 

  5. Doukas J, Pober JS (1990) IFN-g enhances endothelial activation induced by tumor necrosis factor but not IL-1. J Immunol 145: 1727–1733

    Google Scholar 

  6. Durham SR, Ying S, Varney VA, et al (1992) Cytokine messenger RNA expression for IL-3, IL-4, IL-5, and granulocyte/macrophage-colony-stimulating factor in the nasal mucosa after local allergen provocation: relationship to tissue eosinophilia. J Immunol 148:2390–2394

    Google Scholar 

  7. Dustin ML, Springer TA (1988) Lymphocyte function associated antigen-1 (LFA-1) interaction with intercellular adhesion molecule-1 (ICAM-1) is one of at least three mechanisms for lymphocyte adhesion to cultured endothelial cells. J Cell Biol 107:321–331

    Google Scholar 

  8. Dustin ML, Rothlein R, Bhan AK, Dinarello CA, Springer TA (1986) Induction by IL-1 and interferon-g: tissue distribution, biochemistry and function of a natural adherence molecule (ICAM-1). J Immunol 137:245–254

    Google Scholar 

  9. Elices MJ, Osborn L, Takada Y, et al (1990) VCAM-1 on activated endothelium interacts with the leukocyte integrin VLA-4 at a site distinct from the VLA-4/fibronectin binding site. Cell 60:577–584

    Google Scholar 

  10. Figdor CF, Kooyk Y van, Keizer GD (1990) On the mode of action of LFA-1. Immunol Today 11:277–280

    Google Scholar 

  11. Fougerolles AR de, Stacker SA, Schwarting R, Springer TA (1991) Characterization of ICAM-2 and evidence for a third counter-receptor for LFA-1.2. J Exp Med 174:253–267

    Google Scholar 

  12. Graber N, Gopal TV, Wilson D, Beall LD, Polte T, Newman W (1990) T cells bind to cytokine-activated endothelial cells via a novel, inducible sialoglycoprotein and endothelial leukocyte adhesion molecule 1. J Immunol 145:819–830

    Google Scholar 

  13. Hellquist HB, Karlsson MG (1992) Nasal memory T lymphocytes capable of producing IL-4 in the allergic reaction. Allergy 47:334–336

    Google Scholar 

  14. Hellquist HB, Karlsson MG (1992) Interaction between memory T cells, Ber-ACT8+ cells, and cytokines — a human nasal MALT? Patologia 15:147

    Google Scholar 

  15. Hemler ME, Huang C, Schwartz L (1987) The VLA family: characterization of five distinct cell surface heterodimers each with a common 130,000 molecular weight b subunit. J Biol Chem 262:3300–3309

    Google Scholar 

  16. Hynes RO (1992) Integrins: versality, modulation, and signalling in cell adhesion. Cell 69:11–25

    Article  CAS  PubMed  Google Scholar 

  17. Karlsson MG, Hellquist HB (1992) Subsets of T lymphocytes in the nasal mucosa — support for a human NALT (abstract). 7th International Congress of Mucosal Immunology, Prague 1992, p 126

  18. Karlsson MG, Hellquist HB (1994) Phenotype switch and activation of T lymphocytes in patients with allergic rhinitis. ORLJ Otorhinolaryngol Relat Spec 56:166–172

    Google Scholar 

  19. Karlsson MG, Davidsson Å, Hellquist HB (1994) Increase of CD4+ and CD45RO+ “memory” T cells in the nasal mucosa of allergic patients. APMIS 102:753–758

    Google Scholar 

  20. Karlsson MG, Davidsson Å, Viale G, Graziani D, Hellquist HB (1995) Nasal messenger RNA expression of IL-2, IL-4 and IL-5 in patients with allergic rhinitis. Diagn Mol Pathol 4:85–92

    Google Scholar 

  21. Kyan-Aung U, Haskard DO, Lee TH (1991) Vascular adhesion molecule-1 and eosinophil adhesion to cultured human umbilical vein endothelial cells in vitro. Am J Respir Cell Mol Biol 5:445–450

    Google Scholar 

  22. Kyan-Aung U, Haskard DO, Poston RN, Thornhill MH, Lee TH (1991) Endothelial leukocyte adhesion molecule-1 and intercellular adhesion molecule-1 mediate the adhesion of eosinophils to endothelial cells in vitro and are expressed by endothelium in allergic cutaneous inflammation in vivo. J Immunol 146:521–528

    Google Scholar 

  23. Landis JR, Koch GG (1977) The measurements of observer agreement for categorial data. Biometrics 33:159–174

    CAS  PubMed  Google Scholar 

  24. Leung DYM, Pober JS, Cotran RS (1991) Expression of endothelial-leukocyte adhesion molecule-1 in elicted late phase allergic reactions. J Clin Invest 87:1805–1809

    Google Scholar 

  25. Lobb RR, Chi-Rosso G, Leone DR, et al (1991) Expression and functional characterization of a soluble form of endothelial-leukocyte adhesion molecule 1. J Immunol 147:124–129

    Google Scholar 

  26. Masinovsky B, Urdal D, Gallatin WM (1990) IL-4 acts synergistically with IL-1b to promote lymphocyte adhesion to microvascular endothelium by induction of vascular cell adhesion molecule-1. J Immunol 145:2886–2895

    Google Scholar 

  27. Masumoto A, Hemler ME (1993) Multiple activation states of VLA-4. Mechanistic differences between adhesion to CS1/fibrinonectin and to vascular cell adhesion molecule-1. J Biol Chem 268:228–234

    Google Scholar 

  28. Micklem KJ, Dong Y, Willis A, et al (1991) HML-1 antigen on mucosa associated T cells, activated cells, and hairy leukemic cells is a new integrin containing the beta7 subunit. Am J Pathol 139:1297–1301

    Google Scholar 

  29. Montefort S, Feather IH, Wilson SJ, et al (1992) The expression of leukocyte-endothelial adhesion molecules is increased in perennial allergic rhinitis. Am J Respir Cell Mol Biol 7:393–398

    Google Scholar 

  30. Picker LJ (1993) Regulation of tissue-selective T-lymphocyte homing receptors during virgin to memory/effector cell transition in human secondary lymphoid tissues. Am Rev Respir Dis 148:S47-S54

    Google Scholar 

  31. Picker LJ, Butcher EC (1992) Physiological and molecular mechanisms of lymphocyte homing. Annu Rev Immunol 10:561–591

    Google Scholar 

  32. Picker LJ, Michie SA, Lusijah SR, Butcher EC (1990) A unique phenotype of skin-associated lymphocytes in humans. Preferential expression of the HECA-452 epitope by benign and malignant T cells at cutaneous sites. Am J Pathol 135:1053–1068

    Google Scholar 

  33. Picker LJ, Terstappen LWMM, Rott LS, Streeter PR, Stein H, Butcher EC (1990) Differential expression of homing-associated adhesion molecules by T cell subsets in man. J Immunol 145:3247–3255

    Google Scholar 

  34. Picker LJ, Kishimoto TK, Smith CW, Warnock RA, Buther EC (1991) ELAM-1 is an adhesion molecule for skin-homing T cells. Nature 349:796–799

    Google Scholar 

  35. Pober JS, Bevilacqua MP, Mendrick DL, Lapierre LA, Fiers LW, Gimbrone MA Jr (1986) Two distinct monokines, interleukin 1 and tumor necrosis factor, each independently induce the biosynthesis and transient expression of the same antigen on the surface of cultured human vascular endothelial cells. J Immunol 136:1680–1687

    Google Scholar 

  36. Pober JS, Gimborne MA Jr, Lapierre LA, et al (1986) Overlapping patterns of activation of human endothelial cells by interleukin 1, tumor necrosis factor, and immune interferon. J Immunol 137:1893–1896

    Google Scholar 

  37. Rice GE, Bevilacqua MP (1989) An inducable endothelial cells surface glycoprotein mediates melanoma adhesion. Science 246:1303–1306

    Google Scholar 

  38. Shimuzi Y, Shaw S, Graber N, et al (1991) Activation independent binding of human memory T cells to adhesion molecule ELAM-1. Nature 341:799–802

    Google Scholar 

  39. Springer TA (1994) Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell 76:301–314

    Article  CAS  PubMed  Google Scholar 

  40. Svanholm H, Straklint H, Gundersen HJG, Fabricius J, Barlebo H, Olsen S (1989) Reproduciability of histomorphometric diagnoses with special reference to kappa statistics. APMIS 97:689–698

    Google Scholar 

  41. Swerlick RA, Lee KH, Li L-J, Sepp NT, Caughman SW, Lawley TJ (1992) Regulation of vascular cell adhesion molecule 1 on human dermal microvascular endothelial cells. J Immunol 149:698–705

    Google Scholar 

  42. Taub DD, Conlon K, Lloyd AR, Oppenheim JJ, Kelvin DJ (1993) Preferential migration of activated CD4+ and CD8+ T cells in response to MIP-1a and MIP-1b. Science 260:355–358

    CAS  PubMed  Google Scholar 

  43. Thornhill MH, Haskard DO (1990) IL-4 regulates endothelial cell activation by IL-1, tumor necrosis factor, or IFN-g. J Immunol 145:865–872

    Google Scholar 

  44. Thornhill MH, Wellicome SM, Mahiouz DL, Lanchbury JSS, Kyan-Aung U, Haskard DO (1991) Tumor necrosis factor combines with IL-4 or IFN-g to selectively enhance endothelial adhesivness for T-cells. The contribution of vascular cell adhesion molecule-1-dependent and independent mechanisms. J Immunol 146:592–598

    Google Scholar 

  45. Wellicome SM, Thornhill MH, Pitzalis C, et al (1990) A monoclonal antibody that detects a novel antigen on endothelial cells that is induced by tumor necrosis factor, IL-1, or lipopolysaccharide. J Immunol 144:2558–2565

    Google Scholar 

  46. Ying S, Durham SR, Jacobson MR, et al (1994) T lymphocytes and mast cells express messenger RNA for interleukin-4 in the nasal mucosa in allergen-induced rhinitis. Immunology 82:200–206

    Google Scholar 

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Karlsson, M.G., Hellquist, H.B. Endothelial adhesion molecules for nasal-homing T cells in allergy. Vichows Archiv A Pathol Anat 429, 49–54 (1996). https://doi.org/10.1007/BF00196820

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  • DOI: https://doi.org/10.1007/BF00196820

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