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Semin Arthritis Rheum. 2004
Dec;34(3):593-601. |
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Intravenous immunoglobulin
and the kidney--a two-edged sword.
Orbach H, Tishler M, Shoenfeld Y.
Department of Medicine B'Wolfram Medical Center,
Holon, Israel.

OBJECTIVES: To review the literature on the use
and efficacy of intravenous immunoglobulin
(IVIG) in glomerulonephritis and to evaluate the
nephrotoxic effect of IVIG. METHODS: A
structured literature search of articles
published on the efficacy of IVIG in the
treatment of nephritis between 1985 and 2003 was
conducted. All articles dealing with lupus
nephritis, IgA nephropathy, Henoch Schonlein
purpura, antineutrophil cytoplasmic antibodies (ANCA)
associated vasculitis, primary membranous
glomerulonephritis, and primary chronic
nephritis were reviewed. The same literature
search was conducted for the nephrotoxic effects
of IVIG. Two groups of patients were defined:
(a) a group of patients with IVIG nephrotoxic
effect published as case reports, and (b) a
group of patients whose data were collected by
the Food and Drug Administration (FDA). All
existing data of both groups were pooled and
compared. RESULTS: One hundred six patients with
lupus nephritis were treated with IVIG. In most
reports proteinuria, nephrotic syndrome, and
values of creatinine clearance were improved. In
3 cases improvement in World Health Organization
(WHO) class was noted, and in 2 cases a
reduction of immune deposits was demonstrated.
In the other forms of autoimmune nephropathy,
although the number of reported cases was small,
improvement was noted in most patients.
Thirty-two reports entailing 78 patients with
IVIG-induced nephrotoxicity were found and their
data were compared with those of 88 patients
reported to the FDA. No specific differences
were noted between the 2 groups of patients, as
their age and indications for using IVIG were
similar. Most of the patients who developed
renal toxicity (72% in the literature and 90% in
the FDA group) received sucrose -containing IVIG
products. A high percentage of patients (31% in
the literature and 40% in the FDA group)
required hemodialysis. Mortality occurred in 10
and 15%, respectively. Renal histology done in a
minority of the cases demonstrated vacuolization
and swelling of the proximal tubules consistent
with osmotic injury. CONCLUSIONS: On one hand,
there are encouraging reports on the efficacy of
IVIG in different types of glomerulonephritis
(mainly lupus nephritis) resistant to
conventional therapy, but the exact success rate
and clinical indications remain undetermined. On
the other hand, IVIG and the kidney is a
two-edged sword, since nephrotoxicity can be a
serious rare complication of IVIG therapy.
Products containing sucrose as a stabilizer are
mainly associated with such injury through the
mechanism of osmotic nephrosis. Preexisting
renal disease, volume depletion, and old age are
risk factors for such toxicity.
Publication Types:
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Intravenous
immunoglobulin (IVIg) therapy in
MPO-ANCA related polyangiitis with
rapidly progressive
glomerulonephritis in Japan.
Muso E, Ito-Ihara T, Ono T, Imai
E, Yamagata K, Akamatsu A, Suzuki K.
Division of Nephrology, Kitano
Hospital, The Tazuke Kofukai Medical
Research Institute, Osaka, Japan.
muso@kitano-hp.or.jp
For 30 myeloperoxidase (MPO)
antineutrophil cytoplasmic antibody
(ANCA) related rapidly progressive
glomerulonephritis patients (male
17, female 13, average age of 68 +/-
11.8 years old), intravenous
immunoglobulin (IVIg) (400
mg/kg/day) was administered for 5
consecutive days before or along
with conventional immunosuppressive
therapy in Japan. Twenty patients
were treated with IVIg before the
start or newly increase of
conventional therapy and evaluated
the independent effect of this
therapy. In these patients, just
after IVIg, significant decrease of
CRP from 8.61 +/- 5.77 to 5.47 +/-
4.50 mg/dl (P < 0.001) was noted
with improvement of elevated serum
creatinine in 12 out of 19 patients
(63%). In the analysis of the
overall outcome of 30 patients, at 3
months after IVIg and following
conventional therapy, no patients
showed renal death except 4 for whom
hemodialysis had been started before
IVIg. At 6 months, renal survival
rate were 92% (newly renal death 2
out of 26) and 2 patients died due
to cerebral bleeding (survival rate
was 93%). No fatal infection was
noted. IVIg might be the potent
inducible therapy which can be
promoted before the beginning of
conventional immunosuppressant
treatment for relatively aged and
lower immunopotent MPO-ANCA patients
in Japan.
Publication Types:
PMID: 15507757 [PubMed - indexed for
MEDLINE]
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Nippon Jinzo Gakkai Shi.
2004 Feb;46(2):79-83. |
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[Successful treatment
of severe ANCA-associated RPGN with
high-dose IVIg therapy]
[Article in Japanese]
Gomada M, Akamatsu A.
Division of Nephrology, Ehime
Prefectural Central Hospital, Ehime,
Japan.
We report a case of anti-neutrophil
cytoplasmic antibody(ANCA)-associated
rapid progressive glomerulonephritis (RPGN)
that was treated with intravenous
immunoglobulin (IVIg) therapy. A
37-year-old woman was admitted to our
hospital because of a low-grade fever,
general malaise, and a poor appetite. At
the time of admission, her renal
function had severely deteriorated
(serum creatinine level 9.5 mg/dl; mean
Ccr 3.3 ml/min) and she had severe
anemia (Hb 6.6 g/dl). An immunological
examination revealed the presence of
ANCA-associated RPGN. A biopsy confirmed
a diagnosis of pauci-immune-type
necrotizing crescentic
glomerulonephritis. After initial
treatment with steroid pulse therapy (methylprednisolone,
1,000 mg/day x 3 days), her general
condition deteriorated and two sessions
of hemodialysis were required. On the
10th hospital day, a high dose of
immunoglobulin was administered
intravenously (IVIg 400 mg/kg/day x 5
days). This therapy immediately improved
her general condition and lowered her
serum titer of MPO-ANCA and her serum
creatinine level. After two IVIg
treatments, her MPO-ANCA titer returned
to a normal level and her serum
creatinine level improved from 9.5 mg/dl
to 3.3 mg/dl. A second biopsy confirmed
clinical improvement. These findings
suggest that IVIg therapy is effective
for cases of ANCA-associated
glomerulonephritis that are difficult to
treat using conventional
immunosuppressive therapy.
Publication Types:
PMID: 15058108 [PubMed - indexed for
MEDLINE]
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riasis, scleroderma and rheumatoid arthritis, he says. |