References
- Mazur LJ, Kim J. Spectrum of noninfectious health effects from molds. Pediatrics 2006; 118: 1909–1926
- Aukrust L, Borch SM, Einarsson R. Mould allergy: spores and mycelium as allergy sources. Allergy 1985; 40: 43–48
- Tariq SM, Matthews SM, Stevens M, Hakim EA. Sensitization to Alternaria and Cladosporium by age of 4 years. Clin Exp Allergy 1996; 26: 794–798
- Vailes L, Sridhara S, Cromwell O, et al. Quantitation of the major fungal allergens, Alt a 1 and Asp f 1, in commercial allergenic products. J Allergy Clin Immunol 2001; 107: 641–646
- Buzina W, Braun H, Freudenschuss K, Lackner A, Stammberger H. Fungal biodiversity – as found in nasal mucus. Med Mycol 2003; 41: 149–161
- Nelson HS, Szefler SJ, Jacobs J, et al. The relationships among environmental allergen sensitization, allergen exposure, pulmonary function, and bronchial hyperresponsiveness in the Childhood Asthma Management Program. J Allergy Clin Immunol 1999; 104: 775–785
- Salo PM, Arbes SJ, Sever M, et al. Exposure to Alternaria alternata in US homes is associated with asthma symptoms. J Allergy Clin Immunol 2006; 118: 892–898
- Pfister G, Stroh CM, Perschinka H, et al. Detection of HSP60 on the membrane surface of stressed human endothelial cells by atomic force and confocal microscopy. J Cell Sci 2005; 118: 1587–1594
- Kopecek P, Raska M, Weigl E. Development of the primer set for the detection of the hsp60 gene in Trichophyton mentagrophytes cDNA. Folia Microbiol 1999; 44: 401–405
- Guillemette T, Sellam A, Simoneau P. Analysis of a nonribosomal peptide synthetase gene from Alternaria brassicae and flanking genomic sequences. Curr Genet 2004; 45: 214–224
- Gosepath J, Brieger J, Vlachtsis K, Mann WJ. Fungal DNA is present in tissue specimens of patients with chronic rhinosinusitis. Am J Rhinol 2004; 18: 9–13
- Shin SH, Ponikau JU, Sherris DA, et al. Chronic rhinosinusitis: an enhanced immune response to ubiquitous airborne fungi. J Allergy Clin Immunol 2004; 114: 1369–1375
- Inoue Y, Matsuwaki Y, Shin SH, Ponikau JU, Kita H. Nonpathogenic, environmental fungi induce activation and degranulation of human eosinophils. J Immunol 2005; 175: 5439–5447
- Chen W, Syldath U, Bellman K, Burkart V, Kolb H. Human 60-kDa heat-shock protein: a danger signal to the innate immune system. J Immunol 1999; 162: 3212–3219
- Kol A, Lichtman AH, Finberg RW, Libby P, Kurt-Jones EA. Cutting edge: heat shock protein (HSP) 60 activates the innate immune response: CD14 is an essential receptor for HSP60 activation of mononuclear cells. J Immunol 2000; 164: 13–17
- Flohe SB, Bruggemann J, Lendemans S, et al. Human heat shock protein 60 induces maturation of dendritic cells versus a Th1-promoting phenotype. J Immunol 2003; 170: 2340–2348
- Osterloh A, Meier-Stiegen F, Veit A, et al. Lipopolysaccharide-free heat shock protein 60 activates T cells. J Biol Chem 2004; 279: 47906–47911
- Ohashi K, Burkar V, Flohe S, Kolb H. Cutting edge: heat shock protein 60 is a putative endogenous ligand of the toll-like receptor-4 complex. J Immunol 2000; 164: 558–561
- Vabulas RM, Ahmad-Nejad P, da Costa C, et al. Endocytosed HSP60s use toll-like receptor 2 (TLR2) and TLR4 to activate the toll/interleukin-1 receptor signaling pathway in innate immune cells. J Biol Chem 2001; 276: 31332–31339
- Bulut Y, Faure E, Thomas L, et al. Chlamydial heat shock protein 60 activates macrophages and endothelial cells through Toll-like receptor 4 and MD2 in a MyD88-dependent pathway. J Immunol 2002; 168: 1435–1440