Bi-Directional Activation Between Human Airway Smooth Muscle Cells and T Lymphocytes: Role in Induction of Altered Airway Responsiveness1

Because both T lymphocyte and airway smooth muscle (ASM) cell activation are events fundamentally implicated in the pathobiology of asthma, this study tested the hypothesis that cooperative intercellular signaling between activated T cells and ASM cells mediates proasthmatic changes in ASM responsiveness. Contrasting the lack of effect of resting human T cells, anti-CD3-activated T cells were found to adhere to the surface of naive human ASM cells, increase ASM CD25 cell surface expression, and induce increased constrictor responsiveness to acetylcholine and impaired relaxation responsiveness to isoproterenol in isolated rabbit ASM tissues. Comparably, exposure of resting T cells to ASM cells prestimulated with IgE immune complexes reciprocally elicited T cell adhesion to ASM cells and up-regulated T cell expression of CD25. Extended studies demonstrated that: 1) ASM cells express mRNAs and proteins for the cell adhesion molecules (CAMs)/costimulatory molecules, CD40, CD40L, CD80, CD86, ICAM-1 (CD54), and LFA-1 (CD11a/CD18); 2) apart from LFA-1, ASM cell surface expression of the latter molecules is up-regulated in the presence of activated T cells; and 3) pretreatment of ASM cells and tissues with mAbs directed either against CD11a or the combination of CD40 and CD86 completely abrogated both the activated T cell-induced changes in expression of the above CAMs/costimulatory molecules in ASM cells and altered ASM tissue responsiveness. Collectively, these observations identify the presence of bi-directional cross-talk between activated T cells and ASM cells that involves coligation of specific CAMs/costimulatory molecules, and this cooperative intercellular signaling mediates the induction of proasthmatic-like changes in ASM responsiveness.

[1]  J. Kips,et al.  Cytokines in asthma , 2001, European Respiratory Journal.

[2]  M. Grunstein,et al.  Intrinsic ICAM-1/LFA-1 activation mediates altered responsiveness of atopic asthmatic airway smooth muscle. , 2000, American journal of physiology. Lung cellular and molecular physiology.

[3]  S. Holgate The epidemic of allergy and asthma , 1999, Nature.

[4]  P. Sly,et al.  The role of allergy in the development of asthma , 1999, Nature.

[5]  Cecilia Kim,et al.  Altered expression and action of the low-affinity IgE receptor FcϵRII (CD23) in asthmatic airway smooth muscle , 1999 .

[6]  M. Grunstein,et al.  Autocrine interaction between IL-5 and IL-1beta mediates altered responsiveness of atopic asthmatic sensitized airway smooth muscle. , 1999, The Journal of clinical investigation.

[7]  S. Bromley,et al.  The immunological synapse: a molecular machine controlling T cell activation. , 1999, Science.

[8]  M. Grunstein,et al.  Rhinovirus-mediated changes in airway smooth muscle responsiveness: induced autocrine role of interleukin-1β. , 1999, American journal of physiology. Lung cellular and molecular physiology.

[9]  S. Holgate,et al.  Regulation of pulmonary T cell responses to inhaled antigen: role in Th1- and Th2-mediated inflammation. , 1999, Journal of immunology.

[10]  U. Wahn,et al.  Role of the Th2 Cytokines in the Development of Allergen–Induced Airway Inflammation and Hyperresponsiveness , 1999, International Archives of Allergy and Immunology.

[11]  M. Grunstein,et al.  Regulation of TH1- and TH2-type cytokine expression and action in atopic asthmatic sensitized airway smooth muscle. , 1999, The Journal of clinical investigation.

[12]  M. Grunstein,et al.  Mechanism of rhinovirus-induced changes in airway smooth muscle responsiveness. , 1998, The Journal of clinical investigation.

[13]  M. Grunstein,et al.  Autologously up-regulated Fc receptor expression and action in airway smooth muscle mediates its altered responsiveness in the atopic asthmatic sensitized state. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[14]  R. Djukanović,et al.  The role of ICAM-1 on T-cells in the pathogenesis of asthma. , 1998, The European respiratory journal.

[15]  J. Kirby,et al.  A comparison of the antigen‐presenting capabilities of class II MHC‐expressing human lung epithelial and endothelial cells , 1997, Immunology.

[16]  E. Puré,et al.  Antigen receptor-stimulated peripheral blood and bronchoalveolar lavage-derived T cells induce MHC class II and ICAM-1 expression on human airway smooth muscle. , 1997, American journal of respiratory cell and molecular biology.

[17]  M. Grunstein,et al.  Autocrine role of interleukin 1beta in altered responsiveness of atopic asthmatic sensitized airway smooth muscle. , 1997, The Journal of clinical investigation.

[18]  Q. Hamid,et al.  IL-5 and IL-5 receptor in asthma. , 1997, Memorias do Instituto Oswaldo Cruz.

[19]  M. Schroth ADHESION MOLECULES IN ASTHMA AND ALLERGY , 1996, Radiologic Clinics of North America.

[20]  M. Grunstein,et al.  Mechanism of impaired beta-adrenoceptor responsiveness in atopic sensitized airway smooth muscle. , 1995, The American journal of physiology.

[21]  J. Suttles,et al.  T cell--vascular smooth muscle cell interactions: antigen-specific activation and cell cycle blockade of T helper clones by cloned vascular smooth muscle cells. , 1995, Experimental cell research.

[22]  P. Libby,et al.  Human vascular smooth muscle cells poorly co-stimulate and actively inhibit allogeneic CD4+ T cell proliferation in vitro. , 1995, Journal of immunology.

[23]  M. Jordana,et al.  Immune-inflammatory functions of fibroblasts. , 1994, The European respiratory journal.

[24]  E. Fadden Asthma: Morphologic-Physiologic Interactions , 1994 .

[25]  E. Puré,et al.  T lymphocytes adhere to airway smooth muscle cells via integrins and CD44 and induce smooth muscle cell DNA synthesis , 1994, The Journal of experimental medicine.

[26]  E. R. Mcfadden,et al.  Asthma: morphologic-physiologic interactions. , 1994, American journal of respiratory and critical care medicine.

[27]  J. Pober,et al.  HUMAN CD4+ T CELLS PROLIFERATE TO HLA‐DR+ ALLOGENEIC VASCULAR ENDOTHELIUM: IDENTIFICATION OF ACCESSORY INTERACTIONS , 1993, Transplantation.

[28]  J. D. de Monchy,et al.  Allergen-induced recruitment of inflammatory cells in lavage 3 and 24 h after challenge in allergic asthmatic lungs. , 1993, Chest.

[29]  C. Thompson,et al.  Accessory cell function of keratinocytes for superantigens. Dependence on lymphocyte function-associated antigen-1/intercellular adhesion molecule-1 interaction. , 1993, Journal of immunology.

[30]  A. Mantovani,et al.  Cytokine regulation of endothelial cell function , 1992, Behring Institute Mitteilungen.

[31]  R. Lockey,et al.  A possible role for adhesion molecules in asthma. , 1992, The Journal of allergy and clinical immunology.

[32]  J. Virchow,et al.  Allergic and nonallergic asthmatics have distinct patterns of T-cell activation and cytokine production in peripheral blood and bronchoalveolar lavage. , 1992, The American review of respiratory disease.

[33]  S. Durham,et al.  Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma. , 1992, The New England journal of medicine.

[34]  P. Allavena,et al.  Cytokine regulation of endothelial cell function. , 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[35]  T. Lee,et al.  Asthma: cells and cytokines. , 1992, The Journal of asthma : official journal of the Association for the Care of Asthma.

[36]  S. Romagnani Human TH1 and TH2 subsets: doubt no more. , 1991, Immunology today.

[37]  A. B. Kay,et al.  Asthma and inflammation. , 1991, The Journal of allergy and clinical immunology.

[38]  J. Kelley Cytokines of the lung. , 1992, The American review of respiratory disease.

[39]  M. Hart,et al.  Activation of CD4+ lymphocytes by syngeneic brain microvascular smooth muscle cells. , 1990, Journal of immunology.

[40]  S. Holgate,et al.  Cellular events in the bronchi in mild asthma and after bronchial provocation. , 1989, The American review of respiratory disease.

[41]  A. Clowes,et al.  Gamma-interferon regulates vascular smooth muscle proliferation and Ia antigen expression in vivo and in vitro. , 1988, Circulation research.

[42]  R. Coffman,et al.  The Role of Helper T Cell Products in Mouse B Cell Differentiation and Isotype Regulation , 1988, Immunological reviews.

[43]  K. Chung,et al.  Inflammatory mediators and asthma. , 1988, Pharmacological reviews.

[44]  J. Paterson,et al.  In vitro responsiveness of human asthmatic bronchus to carbachol, histamine, beta-adrenoceptor agonists and theophylline. , 1986, British journal of clinical pharmacology.