Cigarette smoke-induced emphysema: A role for the B cell?

RATIONALE Little is known about what drives the inflammatory reaction in the development of chronic obstructive lung disease. B cells have been found. OBJECTIVE To study the involvement of B cells in the development of emphysema. METHODS The presence of B-cell follicles and their interaction with other cells were investigated in lungs of patients with chronic obstructive pulmonary disease and of smoking mice. B cells were isolated from lymphoid follicles by laser microdissection and analyzed for the presence of immunoglobulin rearrangements and somatic mutations. MAIN RESULTS Lymphoid follicles consisting of B cells and follicular dendritic cells with adjacent T cells were demonstrated both in the parenchyma and in bronchial walls of patients with emphysema. A clonal process was observed in all follicles and the presence of ongoing somatic mutations was observed in 75% of the follicles, indicating oligoclonal, antigen-specific proliferation. Similar lymphoid follicles were detected in mice that had developed pulmonary inflammation and progressive alveolar airspace enlargement after smoking. The increase in the number of B-cell follicles was progressive with time and correlated with the increase in mean linear intercept. Specific bacterial or viral nucleic acids could not be detected. CONCLUSIONS B-cell follicles with an oligoclonal, antigen-specific reaction were found in men and mice with emphysema. In mice, the development was progressive with time and correlated with the increase in airspace enlargement. We hypothesize that these B cells contribute to the inflammatory process and/or the development and perpetuation of emphysema by producing antibodies against either tobacco smoke residues or extracellular matrix components.

[1]  Christopher M Overall,et al.  Proteomics Discovery of Metalloproteinase Substrates in the Cellular Context by iTRAQ™ Labeling Reveals a Diverse MMP-2 Substrate Degradome*S , 2007, Molecular & Cellular Proteomics.

[2]  J. Hogg,et al.  Pathophysiology of airflow limitation in chronic obstructive pulmonary disease , 2004, The Lancet.

[3]  P. Paré,et al.  The nature of small-airway obstruction in chronic obstructive pulmonary disease. , 2004, The New England journal of medicine.

[4]  A. M. Houghton,et al.  Neutrophil elastase contributes to cigarette smoke-induced emphysema in mice. , 2003, The American journal of pathology.

[5]  M. Manns,et al.  Autoimmunity and hepatitis C. , 2003, Autoimmunity reviews.

[6]  M. Cosio,et al.  Hypothesis: Does COPD have an autoimmune component? , 2003, Thorax.

[7]  D. Gray,et al.  Antigen-capturing Cells Can Masquerade as Memory B Cells , 2003, The Journal of experimental medicine.

[8]  I. Kawase,et al.  Sustained interleukin‐6 signalling leads to the development of lymphoid organ‐like structures in the lung , 2003, The Journal of pathology.

[9]  M. Salmon,et al.  Why does inflammation persist: a dominant role for the stromal microenvironment? , 2002, Expert Reviews in Molecular Medicine.

[10]  D. Phillips Smoking-related DNA and protein adducts in human tissues. , 2002, Carcinogenesis.

[11]  C. Berek,et al.  Morphological and molecular pathology of the B cell response in synovitis of rheumatoid arthritis , 2002, Virchows Archiv.

[12]  Jin Dai,et al.  Tumor necrosis factor-alpha is central to acute cigarette smoke-induced inflammation and connective tissue breakdown. , 2002, American journal of respiratory and critical care medicine.

[13]  T. Seemungal,et al.  Relationship between bacterial colonisation and the frequency, character, and severity of COPD exacerbations , 2002, Thorax.

[14]  A. Churg,et al.  Acute cigarette smoke-induced connective tissue breakdown requires both neutrophils and macrophage metalloelastase in mice. , 2002, American journal of respiratory cell and molecular biology.

[15]  B. Beghé,et al.  Airway inflammation in severe chronic obstructive pulmonary disease: relationship with lung function and radiologic emphysema. , 2002, American journal of respiratory and critical care medicine.

[16]  W. Bailey,et al.  Global initiative for chronic obstructive lung disease. , 2002, Journal of cardiopulmonary rehabilitation.

[17]  M. Sopori,et al.  Effects of cigarette smoke on the immune system , 2002, Nature Reviews Immunology.

[18]  A. van den Berg,et al.  TP53 gene mutations in Hodgkin lymphoma are infrequent and not associated with absence of Epstein‐Barr virus , 2001, International journal of cancer.

[19]  P. Paré,et al.  Amplification of inflammation in emphysema and its association with latent adenoviral infection. , 2001, American journal of respiratory and critical care medicine.

[20]  M. Cosio,et al.  Lymphocyte population and apoptosis in the lungs of smokers and their relation to emphysema. , 2001, The European respiratory journal.

[21]  U. Sack,et al.  Human Monoclonal Rheumatoid Synovial B Lymphocyte Hybridoma with a New Disease-Related Specificity for Cartilage Oligomeric Matrix Protein1 , 2001, The Journal of Immunology.

[22]  B. Ma,et al.  Inducible targeting of IL-13 to the adult lung causes matrix metalloproteinase- and cathepsin-dependent emphysema. , 2000, The Journal of clinical investigation.

[23]  L. Klareskog,et al.  IFN-γ production in response to in vitro stimulation with collagen type II in rheumatoid arthritis is associated with HLA-DRB1*0401 and HLA-DQ8 , 1999, Arthritis Research.

[24]  L. Fabbri,et al.  CD8+ve cells in the lungs of smokers with chronic obstructive pulmonary disease. , 1999, American journal of respiratory and critical care medicine.

[25]  D. Postma,et al.  Proteoglycan changes in the extracellular matrix of lung tissue from patients with pulmonary emphysema. , 1999, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

[26]  M. Ko,et al.  Effects of depletion of neutrophils or macrophages on development of cigarette smoke-induced emphysema. , 1999, American journal of physiology. Lung cellular and molecular physiology.

[27]  M. Horton,et al.  Induction and regulation of macrophage metalloelastase by hyaluronan fragments in mouse macrophages. , 1999, Journal of immunology.

[28]  Dirkje S Postma,et al.  Ongoing airway inflammation in patients with COPD who do not currently smoke , 1999, Chest.

[29]  D. Patel,et al.  Fractalkine and CX3CR1 Mediate a Novel Mechanism of Leukocyte Capture, Firm Adhesion, and Activation under Physiologic Flow , 1998, The Journal of experimental medicine.

[30]  T. Schall,et al.  Identification and Molecular Characterization of Fractalkine Receptor CX3CR1, which Mediates Both Leukocyte Migration and Adhesion , 1997, Cell.

[31]  L. Fabbri,et al.  Inflammatory cells in the bronchial glands of smokers with chronic bronchitis. , 1997, American journal of respiratory and critical care medicine.

[32]  S. Shapiro,et al.  Requirement for macrophage elastase for cigarette smoke-induced emphysema in mice. , 1997, Science.

[33]  M. Nagarkatti,et al.  Hyaluronate-CD44 interactions can induce murine B-cell activation. , 1997, Blood.

[34]  D. Postma,et al.  Peripheral blood lymphocyte cell subsets in subjects with chronic obstructive pulmonary disease: association with smoking, IgE and lung function. , 1997, Respiratory medicine.

[35]  M. Burdick,et al.  Hyaluronan (HA) fragments induce chemokine gene expression in alveolar macrophages. The role of HA size and CD44. , 1996, The Journal of clinical investigation.

[36]  W. MacNee,et al.  Oxidant/antioxidant imbalance in smokers and chronic obstructive pulmonary disease. , 1996, Thorax.

[37]  S. Nikkari,et al.  Virus‐specific, antibody‐secreting cells during upper respiratory infections , 1995, Journal of medical virology.

[38]  J C Yernault,et al.  Optimal assessment and management of chronic obstructive pulmonary disease (COPD). The European Respiratory Society Task Force. , 1995, The European respiratory journal.

[39]  T. Tetley New perspectives on basic mechanisms in lung disease. 6. Proteinase imbalance: its role in lung disease. , 1993, Thorax.

[40]  J. Hogg,et al.  Characterization of the inflammatory reaction in the peripheral airways of cigarette smokers using immunocytochemistry. , 1992, The American review of respiratory disease.

[41]  R. B. Griffith,et al.  Simultaneous mainstream-sidestream smoke exposure systems II. The rat exposure system. , 1985, Toxicology.

[42]  R. Hancock,et al.  Simultaneous mainstream-sidestream smoke exposure systems I. Equipment and procedures. , 1985, Toxicology.

[43]  C. G. Becker,et al.  Activation of factor XII by tobacco glycoprotein , 1977, The Journal of experimental medicine.

[44]  I. W. Mclean,et al.  PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY , 1974, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[45]  Thurlbeck Wm Measurement of pulmonary emphysema. , 1967 .

[46]  J. Platt,et al.  Evolutionary clues to the functions of the Toll-like family as surveillance receptors. , 2003, Trends in immunology.

[47]  Xiang‐Dong Wang,et al.  Emphysematous lung destruction by cigarette smoke. The effects of latent adenoviral infection on the lung inflammatory response. , 2002, American journal of respiratory cell and molecular biology.

[48]  W. Timens,et al.  Germinal center reaction and B lymphocytes: morphology and function. , 1990, Current topics in pathology. Ergebnisse der Pathologie.

[49]  Paul J. Sheffield,et al.  Equipment and Procedures , 1984 .