Aggressive immunosuppressive therapy should be considered for patients with
proliferative lupus nephritis as the risk for progression to end stage ren
al disease is high. intermittent intravenous cyclophosphamide therapy impro
ves renal survival; longer duration of therapy is associated with fewer rel
apse of nephritis and decreased risk of diminished renal function. While az
athioprine therapy does not differ statistically from steroids alone in pro
longing renal survival, this therapy may be considered in patients with few
risk factors for progression to renal insufficiency. Methylprednisolone as
a single therapy does not prolong renal survival compared with regimens in
cluding cyclophosphamide. Plasmapheresis remains under study but has not sh
own additional benefit in treatment of severe lupus nephritis. The potentia
l roles for cyclosporin A and mycophenylate mofetil in the therapy of proli
ferative lupus nephritis remain to be defined. Supportive care including ri
gorous control of hypertension, consideration of angiotensin receptor inhib
ition or blockade to reduce proteinuria and prolong renal function, control
of hyperlipidemia, prevention of osteoporosis, and prevention of pregnancy
remain important clinical goals. Current research efforts focus on genetic
and socioeconomic factors involved in racial differences in expression of
lupus nephritis, hormonal manipulation to preserve gonadal function during
cyclophosphamide therapy, and the potential impact on lupus activity of est
rogen-containing oral contraceptives or postmenopausal hormone replacement
therapy.