Renal TGF-β in HIV-associated kidney diseases

• Published in: Kidney international Vol. 51; no. 5; pp. 1568 - 1577
• Main Authors: Bódi, Istvan, Kimmel, Paul L., Abraham, Andrew A., Svetkey, Laura P., Klotman, Paul E., Kopp, Jeffrey B.
• Format: Journal Article Conference Proceeding
• Language: English
• Published: New York, NY Elsevier Inc 01.05.1997; Nature Publishing
• Subjects: AIDS/HIV; Biological and medical sciences; HIV Infections - metabolism; Humans; Immunodeficiencies; Immunodeficiencies. Immunoglobulinopathies; Immunohistochemistry; Immunopathology; Kidney - chemistry; Kidney Diseases - metabolism; Leukocyte Common Antigens - analysis; Medical sciences; Transforming Growth Factor beta - analysis; Infection; Human; Kidney disease; Immunopathology; Urinary system disease; Immunological investigation; Pathogenesis; Viral disease; Cytokine; Tumor necrosis factor β; AIDS; Immune deficiency
• ISSN: 0085-2538; 1523-1755
• DOI: 10.1038/ki.1997.215

Renal TGF-β in HIV-associated kidney diseases. Human immunodeficiency virus (HIV)-1 infection may be complicated by progressive renal glomerular disease, including focal segmental glomerulosclerosis (FSGS) and proliferative glomerulonephritis. We examined renal tissue from 71 patients, including biopsies and autopsies from patients in the presence and absence of HIV-1 infection. We assessed the extent of TGF-β, interstitial fibrosis, and interstitial CD45-positive cellular infiltrate using immunohistochemistry. Extracellular TGF-β1/03 was largely confined to the renal interstitium, with the highest scores in HIV-seropositive renal disease and crescentic nephritis. Among all biopsies, the TGFβ1/β3 score correlated with the fibrosis score (r = 0.79, P < 0.0001) and with the CD45 score (r = 0.60, P < 0.0001). Biopsies from HIV-infected patients, taken together, showed marginally more TGF-β/1β3 compared to biopsies from HIV-uninfected patients (P = 0.05); similarly, HIV-associated FSGS showed marginally more TGF-β1/β3 compared to FSGS biopsies obtained from HIV-uninfected patients (P = 0.05). Intracellular TGF-β1 and TGF-β3 were both expressed by renal tubular epithelial cells and in extraglomerular crescents, whereas TGF-β3 was also present within interstitial mononuclear cells and eosinophils, and, exclusively in HIV-infected patients, within glomerular cells. In conclusion, TGF-β expression was increased in several progressive glomerular diseases, and was particularly but not uniquely elevated in HIV-associated renal diseases.