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. 2019 Jul 1;34(7):1135-1144.
doi: 10.1093/ndt/gfy323.

Modulation of the microbiota by oral antibiotics treats immunoglobulin A nephropathy in humanized mice

Jonathan M Chemouny  1   2   3   4   5 , Patrick J Gleeson  1   2   3 , Lilia Abbad  1   2   3 , Gabriella Lauriero  1   2   3   6 , Erwan Boedec  1   2   3 , Karine Le Roux  5 , Céline Monot  5 , Maxime Bredel  5 , Julie Bex-Coudrat  1   2   3 , Aurélie Sannier  3   7 , Eric Daugas  1   2   3   4 , Francois Vrtovsnik  1   2   3   4 , Loreto Gesualdo  6 , Marion Leclerc  5 , Laureline Berthelot  1   2   3 , Sanae Ben Mkaddem  1   2   3 , Patricia Lepage  5 , Renato C Monteiro  1   2   3   4   8
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Modulation of the microbiota by oral antibiotics treats immunoglobulin A nephropathy in humanized mice

Jonathan M Chemouny et al. Nephrol Dial Transplant. .

Abstract

Background: Immunoglobulin A nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. IgA is mainly produced by the gut-associated lymphoid tissue (GALT). Both experimental and clinical data suggest a role of the gut microbiota in this disease. We aimed to determine if an intervention targeting the gut microbiota could impact the development of disease in a humanized mouse model of IgAN, the α1KI-CD89Tg mice.

Methods: Four- and 12-week old mice were divided into two groups to receive either antibiotics or vehicle control. Faecal bacterial load and proteinuria were quantified both at the beginning and at the end of the experiment, when blood, kidneys and intestinal tissue were collected. Serum mouse immunoglobulin G (mIgG) and human immunoglobulin A1 (hIgA1)-containing complexes were quantified. Renal and intestinal tissue were analysed by optical microscopy after haematoxylin and eosin colouration and immunohistochemistry with anti-hIgA and anti-mouse CD11b antibodies.

Results: Antibiotic treatment efficiently depleted the faecal microbiota, impaired GALT architecture and impacted mouse IgA production. However, while hIgA1 and mIgG serum levels were unchanged, the antibiotic treatment markedly prevented hIgA1 mesangial deposition, glomerular inflammation and the development of proteinuria. This was associated with a significant decrease in circulating hIgA1-mIgG complexes. Notably, final faecal bacterial load strongly correlated with critical clinical and pathophysiological features of IgAN such as proteinuria and hIgA1-mIgG complexes. In addition, treatment with broad-spectrum antibiotics reverted established disease.

Conclusions: These data support an essential role of the gut microbiota in the generation of mucosa-derived nephrotoxic IgA1 and in IgAN development, opening new avenues for therapeutic approaches in this disease.

Keywords: GALT; IgA; IgA nephropathy; antibiotics; gut microbiome.

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