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Expression of proliferating cell associated protein, Ki-67, supports cellular proliferation in WHO Class IV lupus
P L Cheah1, R Kunaseegaran, L M Looi
1Department of Pathology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Insights
Cellular proliferation significantly increases in diffuse proliferative lupus nephritis (WHO Class IV), confirming its role in glomerular hypercellularity. Ki-67 expression, a marker of cell proliferation, was notably higher in lupus nephritis patients compared to healthy controls.
Area of Science:
- Nephrology
- Immunopathology
- Cell Biology
Background:
- Diffuse proliferative lupus nephritis (WHO Class IV) is characterized by glomerular hypercellularity.
- The cellular basis of this hypercellularity is not fully understood.
- Ki-67 is a reliable marker for cellular proliferation.
Purpose of the Study:
- To investigate the role of cellular proliferation in the pathogenesis of WHO Class IV lupus nephritis.
- To compare Ki-67 expression in lupus nephritis patients with normal controls.
Main Methods:
- Immunohistochemical staining for Ki-67 was performed on renal biopsies from 23 WHO Class IV lupus nephritis patients and 23 normal controls.
- Analysis focused on Ki-67 immunoreactivity in glomeruli.
Main Results:
- Significantly more lupus nephritis patients (69.6%) showed Ki-67 immunoreactivity compared to controls (34.8%) (p<0.05).
- Ki-67 positive glomeruli were significantly higher in lupus nephritis (14.5%) versus controls (0.7%) (p<0.01).
- Increased Ki-67 expression indicates heightened cellular proliferative activity in lupus nephritis.
Conclusions:
- Cellular proliferation, evidenced by Ki-67 expression, is significantly increased in WHO Class IV lupus nephritis.
- This heightened proliferation contributes to the glomerular hypercellularity observed in this condition.
- Ki-67 is a valuable marker for assessing proliferative activity in lupus nephritis.
Abstract:
Ki-67 expression in diffuse proliferative lupus nephritis, WHO Class IV, was compared against normal controls to establish that cellular proliferation is involved in the production of glomerular hypercellularity. Twenty-three histologically confirmed WHO Class IV lupus nephritis and 23 normal control renal tissue were immunohistochemically stained with a polyclonal antibody to Ki-67 (Dako) using the peroxidase labelled streptavidin bioitin kit (Dako). There were 20 females and 3 males, with 17 Chinese and 6 Malays in the WHO Class IV lupus nephritis group. Ages of patients ranged between 10-56 years with a mean of 31.9 years. The normal controls, 20 males and 3 females, and ethnically 9 Indians, 7 Malays, 2 Chinese, and 5 foreign nationals (4 Indonesians and 1 Bangladeshi), had an age range between 15-33 years (mean = 23.3 years). Sixteen (69.6%) WHO Class IV lupus nephritis and 8 (34.8%) normal controls demonstrated Ki-67 immunoreactivity in at least 1 glomerulus (p<0.05). Of the 256 WHO Class IV lupus nephritis non-sclerosed, glomeruli studied, 37 (14.5%) were Ki-67 immunopositive compared with normal controls where 16 (0.7%) of 2159 glomeruli demonstrated Ki-67 (p< 0.01). Cellular proliferative activity, as evidenced by Ki-67 expression, was significantly increased in WHO Class IV lupus nephritis confirming that cell proliferation contributes to glomerular hypercellularity.
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