Tj. Vyse et al., CONTROL OF MULTIPLE AUTOANTIBODIES LINKED WITH A LUPUS NEPHRITIS SUSCEPTIBILITY LOCUS IN NEW-ZEALAND BLACK MICE, The Journal of immunology, 158(11), 1997, pp. 5566-5574
An NZB locus on distal chromosome 1 has been linked to murine lupus ne
phritis in backcross analyses of New Zealand mice, This locus, designa
ted Nba2 for New Zealand Black autoimmunity 2, was found to colocalize
in both (NZB x SM/J)F-1 x NZW and (B6.H2(z) x NZB)F-1 x NZB backcross
es, and was most likely situated between 92 and 97 cM from the centrom
ere. This region of mouse chromosome 1 encodes several candidate genes
, including the low affinity Fc gamma receptor genes, Both backcrosses
were examined by interval mapping for quantitative trait loci linked
with autoantibody and total Ig production, Nba2 was linked with elevat
ed serum levels of multiple autoantibodies, including a variety of ant
inuclear Abs (anti-dsDNA, antichromatin and anti-histone) and autoanti
bodies to gp70, in both backcrosses. Nba2 was also linked (or showed a
trend for linkage) with hypergammaglobulinemia and IgG1, IgG2a, and/o
r IgG3 levels in each backcross, In the (B6.H2(z) x NZB)F-1 x NZB back
cross, MHC was an additional genetic contribution that interacted with
Nba2 in the production of autoantibodies and the development of nephr
itis, Together, these data provide new insight into the nature of one
important genetic contribution to murine lupus and suggest that Nba2 m
ay act as an immune response gene that influences Ag-driven B cell res
ponses to self and possibly to exogenous Ags.