The diphasic effects of proteases on serum complement

Innerfield, Irving

doi:10.1007/bf01970256

Cited by 1 publication

(1 citation statement)

References 13 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Other studies have shown that complement activity can be consumed in a manner which requires neither antibody nor properdin. These include bacterial [6,37] and fungal [16] proteinases, polyanions [4], fungal ex tracts [3], plicatic acid [5], and house dust allergen [2]. More recently, Marx el al.…”

Section: Discussionmentioning

confidence: 99%

Antibody-Independent Complement Consumption by <i>Micropolyspora Faeni</i>

Marx¹,

Motszko²,

Roberts³

1980

Int Arch Allergy Immunol

View full text Add to dashboard Cite

Micropolyspora faeni is an etiologic agent of hypersensitivity pneumonitis, a disease with an ill-defined mechanism of pathogenesis. Many reports have suggested an immunologic mechanism. A number of laboratories have demonstrated a nonantibody-mediated activation of the complement cascade. This study was undertaken to define the pathway of the complement consumption induced by M. faeni. We utilized an extract of M. faeni grown on synthetic media rather than the more common double dialysis extracts. Complement consumption by this extract was easily demonstrable in the absence of detectable antibody, but was inhibited by EDTA and MgEGTA. With the exception of C1, all of the early components of the classical pathway were markedly reduced following incubation of normal human serum with this extract. C1 was poorly consumed. In addition, factor B conversion to B was not inhibited by 10 mM MgEGTA suggests that the alternative pathway may also be affected. The generation of M. faeni-dependent chemotactic factor(s) from serum demonstrates that the complement cascade is being activated rather than inhibited.

show abstract