Abstract :
We read with interest the recently published article by Tipu et al. entitled “Clinical,
histopathological and immunofluorescent findings of IgA nephropathy”, in the esteemed
Iranian Journal of Immunology (1). The study described frequency of different clinical,
histopathological and immunofluorescent characteristics of IgA nephropathy. The
authors should be applauded for their findings; however, we would like to remind a few
points about IgA nephropathy (IgAN). After popularization of Oxford classification of
IgAN on July 2009 (2), it is necessary to describe the morphologic lesions in the cadre
of this classification. Thus, it is indispensable to change the morphologic lesions of
table 2 of the mentioned work, according to the MEST variables. In the materials and
methods section, the authors stated that, specimen for immunofluorescence, stained for
antibodies of IgA, IgG, IgM, C3, C4 and fibrinogen. However, the definition of IgAN
requires the presence of IgA deposits which were graded ≥ 2+ and the absence of C1q
deposition (2,3). Hence, the specimens for C1q antibody must be stained and its strict
negative, brightness should be stated in the paper as an important part of definition of
IgAN following ≥ 2+ brightness of IgA antibody deposits (1-5). Since IgAN has various
morphologic features, it is indispensable to rule out the lupus nephritis. While in the
later, there is a prominent deposit of C1q. As the authors also mentioned, IgA
nephropathy (IgAN) is very common form of primary glomerulonephritis and occurs
worldwide (4-9) and the disease may have distinct morphologic and clinical
presentation in different regions (1). Therefore these kinds of studies are crucial in our
region to further understand the presentations of immunoglobulin A nephropathy.
Keywords :
LETTER TO THE EDITOR , Clinical , Histopathological , Immunofluorescent Findings of IgA Nephropathy