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Vasculitis is a group of diseases featuring inflammation of the wall of

blood vessels due to leukocyte migration and resultant damage. While

most vasculitides are rare, they generally affect several organ systems

and can cause severe disability.

PR-3

There is a strong association between anti-PR3 antibodies and Wegener’s

granulomatosis. Specificity has been found of 95-98%. Sensitivity

depends on the phase and the activity of the disease, and has been

found around 90% for expanded Wegener’s granulomatosis (i.e. with

necrotizing glomerulonephritis, systemic vasculitis and granulomatous

inflammation of the respiratory tract), and around 75% for limited

Wegener’s granulomatosis (i.e. without renal involvement).

MPO

High levels of anti-MPO antibodies are found in 65% of patients with

idiopathic necrotizing glomerulonephritis, 60% of patients with Churg-

Strauss syndrome, 30-40% of patients with Goodpasture’s syndrome and

10% of patients with Wegener’s granulomatosis. Specificity for systemic

vasculitis and idiopathic necrotizing glomerulonephritis goes up to 95%.

ANTI-NEUTROPHIL CYTOPLASMANTIBODIES (ANCA)

44850

Ethanol fixed, IFA Complete kit, 4 slides x 6 wells

44851

Ethanol fixed, IFA Complete kit ,10 slides x 6 wells

44852

Ethanol fixed, IFA Slide Box ,10 slides x 6 wells

44878

Formalin fixed, IFA Slide Box, 10 slides x 6 wells

44898

Formalin fixed, IFA Complete kit, 10 slides x 6 wells

ANTI-PR3 ANTIBODIES (C-ANCA)

44791

ELISA 96 T

Purified human antigen

ANTI-MPO ANTIBODIES (P-ANCA)

44790

ELISA 96 T

Purified human antigen

Vasculitis

Glomerular basement membrane antibodies

Monkey kidney

GBM

Indirect immmunofluorescence assay is the conventional method for

the determination of anti-glomerular basement membrane antibodies

(GBMA). Antibodies to GBM are present in patients with Goodpasture’s

syndrome. The disease presents a progressive glomerulonephritis with or

without massive pulmonary hemorrhage. The finding of GBMA confirms

a diagnosis of a life threatening disease that causes loss of kidney, and

indicates a grave prognosis. Results obtained in a comparative study do

not show significant systematic differences compared to an ELISA for

anti-type IV collagen alpha chain antibodies.

ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODIES

(GBMA)

44588

IFA – Slide box, 12 slides x 4 wells

Monkey Kidney

44870

ELISA kit 96 T

Highly purified antigen

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