We immunohistologically compared the number of intraglomerular infiltrating
cells in 14 children with poststreptococcal acute glomerulonephritis (PSAG
N) and 20 children with immunoglobulin A glomerulonephritis (IgAGN) with hi
stological characteristics similar to those of PSAGN to explain the differe
nce in clinicopathological characteristics between these two diseases. Immu
nohistological study was performed in kidney tissues from these patients by
using monoclonal antibodies of T-cell marker (CD3 and CD45RO), B-cell mark
er (CD20), neutrophil marker (CD15), macrophage marker (CD68), four subclas
ses of macrophages (early-stage, acute-stage, chronic-stage, and mature inf
lammatory macrophage marker), and proliferating cell nuclear antigen (PCNA)
. The 34 patients were classified into three stages according to the time f
rom the detection of urinary abnormalities to biopsy. Intraglomerular immun
opositive cells were expressed as the number of cells per glomerulus. There
were more intraglomerular positive cells of CD15, CD68, and the four macro
phage subclasses In PSAGN than IgAGN. The number of intraglomerular infiltr
ating macrophages decreased with time in PSAGN, whereas the number of macro
phages in IgAGN remained constant at all stages. Intraglomerular infiltrati
on of acute-stage Inflammatory macrophages alone was evident in IgAGN. Both
the number of intraglomerular proliferating macrophages (PCNA-positive plu
s CD68-positive cells) and proportion of proliferating macrophages/total ma
crophages were greater In IgAGN than PSAGN. Normal urinalysis results were
evident in all patients with PSAGN during follow-up, and urinary abnormalit
ies persisted in 18 patients with IgAGN. In conclusion, differences in the
maturity of infiltrating macrophages and number of proliferating macrophage
s are associated with the different clinicopathological characteristics in
children with PSAGN and IgAGN. (C), 2001 by the National Kidney Foundation,
Inc.