Age influence on hypersensitivity pneumonitis induced in mice by exposure to Pantoea agglomerans

References

• Aujla SJ, Chan YR, Zheng M, et al. (2008). IL-22 mediates mucosal host defense against Gram-negative bacterial pneumonia. Nat Med 14:275–81
   PubMed Web of Science ®Google Scholar
• Bertorelli G, Bocchino V, Olivieri D. (2000). Hypersensitivity pneumonitis. Eur Respir Mon 14:120–36
   Google Scholar
• Biondi PA, Chiesa LM, Storelli MR, Renon P. (1997). A new procedure for the specific high-performance liquid chromatographic determination of hydroxyproline. J Chromatogr Sci 35:509–12
   PubMed Web of Science ®Google Scholar
• Bourke SJ, Dalphin JC, Boyd G, et al. (2001). Hypersensitivity pneumonitis: current concepts. Eur Respir J 18:81–92
   Web of Science ®Google Scholar
• Bruunsgaard H. (1999). A high plasma concentration of TNF-α is associated with dementia in centenarians. J Gerontol A Biol Sci Med Sci 54:M357–64
   PubMedGoogle Scholar
• Carbonetti NH. (2007). Immunomodulation in the pathogenesis of Bordetella pertussis infection and disease. Curr Opin Pharmacol 7:272–8
   Google Scholar
• Caruso C, Candore G, Cigna D, et al. (1996). Cytokine production pathway in the elderly. Immunol Res 15:84–90
   PubMed Web of Science ®Google Scholar
• Caruso R, Fina D, Paoluzi OA, et al. (2008). IL-23-mediated regulation of IL-17 production in Helicobacter pylori-infected gastric mucosa. Eur J Immunol 38:470–8
   PubMed Web of Science ®Google Scholar
• Cooke A. (2006). Th17 cells in inflammatory conditions. Rev Diabet Stud 3:72–5
   PubMedGoogle Scholar
• DeLucca AJ, Godshall MA, Palmgren MS. (1984). Gram-negative bacterial endotoxins in grain elevator dusts. Am Ind Hyg Assoc J 45:336–9
   PubMed Web of Science ®Google Scholar
• DeLucca AJ, Palmgren MS. (1986). Mesophilic microorganisms and endotoxin levels on developing cotton plants. Am Ind Hyg Assoc J 47:437–42
   PubMed Web of Science ®Google Scholar
• Denis M, Bisson D. (1995). Antigen-induced alveolitis: cytokine production in a mouse model. Inflammation 19:157–77
   Google Scholar
• Dutkiewicz J. (1976). Studies on endotoxins of Erwinia herbicola and their biological activity. Zbl Bakt Hyg I Abt Orig A 236:487–508
   Google Scholar
• Dutkiewicz J. (1978a). Exposure to dust-borne bacteria in agriculture. I. Environmental studies. Arch Environ Health 33:250–9
   PubMed Web of Science ®Google Scholar
• Dutkiewicz J. (1978b). Exposure to dust-borne bacteria in agriculture. II. Immunological survey. Arch Environ Health 33:260–70
   PubMed Web of Science ®Google Scholar
• Dutkiewicz J, Kuś L, Dutkiewicz E, Warren CPW. (1985). Hypersensitivity pneumonitis in grain farmers due to sensitization to Erwinia herbicola. Ann Allergy 54:65–8
   Google Scholar
• Dutkiewicz J. (1986). Microbial hazards in plants processing grain and herbs. Am J Ind Med 10:300–2
   PubMed Web of Science ®Google Scholar
• Dutkiewicz J. (1987). Bacteria in farming environment. Eur J Respir 71:71–88
   Google Scholar
• Dutkiewicz J, Tucker J, Woodfork K, Burrell R. (1989). The identification of extracellular endotoxin molecules by immunoelectron microscopy. In: Jacobs RR, Wakelyn PJ. (eds.) Cotton Dust. Proceedings of the 13th Cotton Dust Research Conference, Nashville, Tennessee, 5–6 January 1989. Memphis, TN: National Cotton Council, 111–14
   Google Scholar
• Dutkiewicz J, Tucker J, Burrell R, et al. (1992). Ultrastructure of the endotoxin produced by Gram-negative bacteria associated with organic dusts. System Appl Microbiol 15:474–85
   Google Scholar
• Dutkiewicz J, Krysińska-Traczyk E, Skórska C, et al. (2000). Exposure of agricultural workers to airborne microorganisms and endotoxin during handling of various vegetable products. Aerobiologia 16:193–8
   Google Scholar
• Dutkiewicz J, Skórska C, Burrell R, et al. (2005). Immunostimulative effects of repeated inhalation exposure to microvesicle-bound endotoxin of Pantoea agglomerans. Ann Agric Environ Med 12:289–94
   Google Scholar
• Gell PGH, Coombs RRA. (1963). The classification of allergic reactions underlying disease. In: Coombs RRA, Gells PGH. (ed.) Clinical aspects of immunology. Oxford: Blackwell Science
   Google Scholar
• Ginaldi L, Loreto MF, Corsi MP, et al. (2001). Immunosenescence and infectious diseases. Microbes Infect 3:851–7
   PubMed Web of Science ®Google Scholar
• Goetzl EJ, Huang MC, Kon J, et al. (2010). Gender specificity of altered human immune cytokine profiles in aging. FASEB J 24:3580–9
   PubMed Web of Science ®Google Scholar
• Golec M, Skórska C, Mackiewicz B, Dutkiewicz J. (2004). Immunologic reactivity to work-related airborne allergens in people occupationally exposed to dust from herbs. Ann Agric Environ Med 11:121–7
   Google Scholar
• Golec M, Skórska C, Lemieszek M, Dutkiewicz J. (2009). A novel inhalation challege to study animal model of allergic alveolitis. Ann Agric Environ Med 16:173–5
   Google Scholar
• Gomez CR, Nomellini V, Faunce DE, Kovacs EJ. (2008). Innate immunity and aging. Exp Gerontol 43:718–28
   PubMed Web of Science ®Google Scholar
• Hanak V, Golbin JM, Ryu JH. (2007). Causes and presenting features in 85 consecutive patients with hypersensitivity pneumonitis. Mayo Clin Proc 82:812–16
   PubMed Web of Science ®Google Scholar
• Hanak V, Golbin JM, Hartman TE, Ryu JH. (2008). High-resolution CT findings of parenchymal fibrosis correlate with prognosis in hypersensitivity pneumonitis. Chest 134:133–8
   PubMed Web of Science ®Google Scholar
• Haynes L, Maué AC. (2009). Effects of aging on T cell function. Curr Opin Immunol 21:414–17
   PubMed Web of Science ®Google Scholar
• Jiang D, Liang J, Hodge J, et al. (2004). Regulation of pulmonary fibrosis by chemokine receptor CXCR3. J Clin Invest 114:291–9
   PubMed Web of Science ®Google Scholar
• Joshi AD, Fong DJ, Oak SR, et al. (2009). IL-17 mediated immunopathogenesis in experimental hypersensitivity pneumonitis. Am J Respir Crit Care Med 179:705–16
   PubMed Web of Science ®Google Scholar
• Khader SA, Gaffen SL, Kolls JK. (2009). Th17 cells at the crossroads of innate and adaptive immunity against infectious diseases at the mucosa. Mucosal Immunol 2:403–11
   PubMed Web of Science ®Google Scholar
• Kim JH, Kim HY, Kim S, et al. (2005). Natural killer T (NKT) cells attenuate bleomycin-induced pulmonary fibrosis by producing interferon-gamma. Am J Pathol 167:1231–41
   PubMed Web of Science ®Google Scholar
• Kovacs EJ, Palmer JL, Fortin CF, et al. (2009). Aging and innate immunity in the mouse: impact of intrinsic and extrinsic factors. Trends Immunol 30:319–24
   PubMedGoogle Scholar
• Krysińska-Traczyk E, Skórska C, et al. (2004). Exposure to airborne microorganisms, dust and endotoxin during flax scutching on farms. Ann Agric Environ Med 11:309–17
   Google Scholar
• Kuś L. (1980). Allergic alveolitis after exposure to antigens occurring in grain dust in the light of the own clinical and experimental studies. Med Wiejska 15:73–80
   Google Scholar
• Lantz RC, Birch K, Hinton DE, Burrell R. (1985). Morphometric changes of the lung induced by inhaled bacterial endotoxin. Exp Molec Pathol 43:305–20
   PubMed Web of Science ®Google Scholar
• Lemieszek M, Chilosi M, Golec M, et al. (2011). Mouse model of hypersensitivity pneumonitis after inhalation exposure to different microbial antigens associated with organic dust. Ann Agric Environ Med 18:159–68
   Google Scholar
• Lewis DM. (1985). Stimulation of interleukin 1 production by alveolar macrophages by endotoxin from various bacterial species. In: Wakelyn PJ, Jacobs RR. (eds.) Proceedings of the 9th Cotton Dust Research Conference. Memphis, TN: National Cotton Council, 157–9
   Google Scholar
• Lima MS, Coletta EN, Ferreira RG, et al. (2009). Subacute and chronic hypersensitivity pneumonitis: histopathological patterns and survival. Respir Med 103:508–15
   PubMed Web of Science ®Google Scholar
• Linton PJ, Dorshkind K. (2004). Age-related changes in lymphocyte development and function. Nat Immunol 5:133–9
   PubMed Web of Science ®Google Scholar
• Mackiewicz B, Skórska C, Dutkiewicz J, et al. (1999). Allergic alveolitis due to herb dust exposure. Ann Agric Environ Med 6:167–70
   PubMed Web of Science ®Google Scholar
• Mangan PR, Harrington LE, O’Quinn DB, et al. (2006). Transforming growth factor-beta induces development of the T(H)17 lineage. Nature 441:231–4
   PubMed Web of Science ®Google Scholar
• Milanowski J. (1992). Immunological investigations in Polish farm workers with extrinsic allergic alveolitis. Ann Allergy 68:89
   Google Scholar
• Milanowski J. (1994a). Effects of Pantoea agglomerans on the respiratory system. Part I. Studies in vitro. Ann Agric Environ Med 1:44–51
   Google Scholar
• Milanowski J. (1994b). Effects of Pantoea agglomerans on the respiratory system. Part II. Studies in vivo. Ann Agric Environ Med 1:52–6
   Google Scholar
• Milanowski J, Dutkiewicz J, Potoczna H, et al. (1998). Allergic alveolitis among agricultural workers in eastern Poland: a study of twenty cases. Ann Agric Environ Med 5:31–43
   Google Scholar
• Nance S, Cross R, Yi AK, Fitzpatrick EA. (2005). IFN-gamma production by innate immune cells is sufficient for development of hypersensitivity pneumonitis. Eur J Immunol 35:1928–38
   PubMed Web of Science ®Google Scholar
• Patel AM, Ryu JH, Reed CE. (2001). Hypersensitivity pneumonitis: current concepts and future questions. J Allergy Clin Immunol 108:661–70
   PubMed Web of Science ®Google Scholar
• Pepys J. (1969). Hypersensitivity diseases of the lungs due to fungi and organic dusts. Basel: S. Karger; 1969
   Google Scholar
• Reynolds HY. (1988). Hypersensitivity pneumonitis: correlation of cellular and immunologic changes with clinical phases of disease. Lung 166:189–208
   Google Scholar
• Rose C, King TE Jr. (1992). Controversies in hypersensitivity pneumonitis. Am Rev Respir Dis 145:2–4
   Google Scholar
• Rylander R. (1987). The role of endotoxin for reactions after exposure to cotton dust. Am J Ind Med 12:687–97
   PubMed Web of Science ®Google Scholar
• Rylander R, Lundholm M. (1978). Bacteria contamination of cotton and cotton dust and effects on the lung. Br J Ind Med 35:204–7
   PubMedGoogle Scholar
• Sahin H, Brown KK, Curran-Everett D, et al. (2007). Chronic hypersensitivity pneumonitis: CT features comparison with pathologic evidence of fibrosis and survival. Radiology 244:591–8
   PubMed Web of Science ®Google Scholar
• Shanley TP, Peters JL, Jones ML, et al. (1996). Regulatory effects of endogenous interleukin-1 receptor antagonist protein in immunoglobulin G immune complex-induced lung injury. J Clin Invest 97:963–70
   PubMed Web of Science ®Google Scholar
• Siciliano NA, Skinner JA, Yuk MH. (2006). Bordetella bronchiseptica modulates macrophage phenotype leading to the inhibition of CD4+ T cell proliferation and the initiation of a Th17 immune response. J Immunol 177:7131–8
   PubMed Web of Science ®Google Scholar
• Simonian PL, Roark CL, Wehrmann F, et al. (2009). Th17-polarized immune response in a murine model of hypersensitivity pneumonitis and lung fibrosis. J Immunol 182:657–65
   PubMed Web of Science ®Google Scholar
• Skórska C, Mackiewicz B, Dutkiewicz J. (2000). Effects of exposure to flax dust in Polish farmers: work-related symptoms and immunologic response to microbial antigens associated with dust. Ann Agric Environ Med 7:111–18
   Google Scholar
• Skórska C, Golec M, Mackiewicz B, et al. (2005a). Health effects of exposure to herb dust in valerian growing farmers. Ann Agric Environ Med 12:247–52
   PubMed Web of Science ®Google Scholar
• Skórska C, Sitkowska J, Krysińska-Traczyk E, et al. (2005b). Exposure to airborne microorganisms, dust and endotoxin during processing of peppermint and chamomile herbs on farms. Ann Agric Environ Med 12:281–8
   PubMed Web of Science ®Google Scholar
• Suga M, Yamasaki H, Nakagawa K, et al. (1997). Mechanisms accounting for granulomatous responses in hypersensitivity pneumonitis. Sarcoidosis Vasc Diffuse Lung Dis 14:131–8
   Google Scholar
• Trzonkowski P, Myśliwska J, Godlewska B, et al. (2004). Immune consequences of the spontaneous pro-inflammatory status in depressed elderly patients. Brain Behav Immun 18:135–48
   PubMed Web of Science ®Google Scholar
• Veldhoen M, Hocking RJ, Atkins CJ, et al. (2006). TGFbeta in the context of an inflammatory cytokine milieu supports de novo differentiation of IL-17-producing T cells. Immunity 24:179–89
   PubMed Web of Science ®Google Scholar
• Wilson NJ, Boniface K, Chan JR, et al. (2007). Development, cytokine profile and function of human interleukin 17-producing helper T cells. Nat Immunol 8:950–7
   PubMed Web of Science ®Google Scholar
• Yamasaki H, Ando M, Brazer W, et al. (1999). Polarized type 1 cytokine profile in bronchoalveolar lavage T cells of patients with hypersensitivity pneumonitis. J Immunol 163:3516–23
   PubMed Web of Science ®Google Scholar
• Yoshikawa TT. (2000). Epidemiology and unique aspects of aging and infectious diseases. Clin Infect Dis 30:931–3
   PubMed Web of Science ®Google Scholar