Db. Borza et al., The goodpasture autoantigen - Identification of multiple cryptic epitopes on the NC1 domain of the alpha 3(IV) collagen chain, J BIOL CHEM, 275(8), 2000, pp. 6030-6037
Goodpasture (GP) disease is an autoimmune disorder in which autoantibodies
against the alpha 3(TV) chain of type TV collagen bind to the glomerular an
d alveolar basement membranes, causing progressive glomerulonephritis and p
ulmonary hemorrhage, Two major conformational epitope regions have been ide
ntified on the noncollagenous domain of type IV collagen (NC1 domain) of th
e alpha 3(IV) chain as residues 17-31 (E-A) and 127-141 (E-B) (Netzer, K.-O
. et al. (1999) J. Biol. Chem. 274, 11267-11274), To determine whether thes
e regions are two distinct epitopes or form a single epitope, three GP sera
were fractionated by affinity chromatography on immobilized NC1 chimeras c
ontaining the E-A and/or the E-B region. Four subpopulations of GP antibodi
es with distinct epitope specificity for the alpha 3(IV)NC1 domain were thu
s separated and characterized. They were designated GP(A), GP(B), GP(AB) an
d GP(X), to reflect their reactivity with E-A only, E-B only, both regions,
and neither, respectively. Hence, regions E-A and E-B encompass critical a
mino acids that constitute three distinct epitopes for GP(A), GP(B), and GP
(AB) antibodies, respectively, whereas the epitope for GP, antibodies is lo
cated in a different unknown region. The GP(A) antibodies were consistently
immunodominant, accounting for 60-65% of the total immunoreactivity to alp
ha 3(IV)NC1; thus, they probably play a major role in pathogenesis. Regions
E-A and E-B are held in close proximity because they jointly form the epit
ope for Mab3, a monoclonal antibody that competes for binding with GP autoa
ntibodies. All GP epitopes are sequestered in the hexamer configuration of
the NC1 domain found in tissues and are inaccessible for antibody binding u
nless dissociation of the hexamer occurs, suggesting a possible mechanism f
or etiology of GP disease. GP antibodies have the capacity to extract alpha
3(IV)NC1 monomers, but not dimers, from native human glomerular basement m
embrane hexamers, a property that may be of fundamental importance for the
pathogenesis of the disease.