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A quantitative study on the activation of the alternative pathway of complement by mouldy hay dust and thermophilic actinomycetes
Author(s) -
EDWARDS J. H.
Publication year - 1976
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1111/j.1365-2222.1976.tb01408.x
Subject(s) - zymosan , hay , chemistry , magnesium , alternative complement pathway , acetic acid , complement system , biochemistry , food science , chromatography , biology , zoology , antibody , immunology , organic chemistry , in vitro
Summary Materials associated with the induction of farmer's lung were incubated with fresh normal human serum in the presence of magnesium ethylene glycol tetra‐acetic acid (MgEGTA) or ethylene diamine tetra‐acetic acid (EDTA) and results compared with material known to activate the alternative pathway of complement—zymosan. Results show that Micropolyspora faeni organisms are as active as zymosan in reducing complement (C) levels in the presence of MgEGTA, with a 50% reduction in CH50 at approximately 140 μg/ml. Thermoactinomyces vulgaris organisms produced a 50% CH50 reduction at approximately 1.25 mg/ml and two samples of respirable mouldy hay dust (MHD) at approximately 5.6 mg/ml whereas extracts of M. faeni and T. vulgaris reduced the CH50 titre by 17% and 39% respectively at 16 mg/ml in the presence of MgEGTA. Organisms and extracts did not reduce the CH50 titre in the presence of EDTA even at the maximum concentration quoted by more than 3%, thus it is considered that alternative pathway activation was responsible for C utilization in the presence of MgEGTA. Respirable MHD used less than 4% available C at 4 mg/ml in the presence of EDTA but at 8 mg/ml dust 11% and 28% available CH50 were used compared with 79% and 81% respectively in the presence of MgEGTA. The elution of immunoglobulin binding material from MHD may be responsible for apparent CH50 consumption in the presence of EDTA.