MPO-ANCA-positive rapidly progressive glomerulonephritis after COVID-19 vaccination during treatment of plaque psoriasis with bimekizumab.

Bimekizumab COVID19 vaccination IL17 antibody MPO-ANCA Psoriasis RPGN

Journal

CEN case reports
ISSN: 2192-4449
Titre abrégé: CEN Case Rep
Pays: Japan
ID NLM: 101636244

Informations de publication

Date de publication:
19 Sep 2024
Historique:
received: 01 04 2024
accepted: 26 08 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 19 9 2024
Statut: aheadofprint

Résumé

A 75-year-old man presented with MPO-ANCA-positive rapidly progressive glomerulonephritis after COVID-19 vaccination during the treatment of plaque psoriasis vulgaris with bimekizumab. Bimekizumab, an anti-IL17 monoclonal antibody, was regularly administered to control the activity of plaque psoriasis. After receiving the sixth COVID-19 vaccine, his kidney function rapidly declined over the course of weeks. Urinalysis showed microscopic hematuria and proteinuria with deformed red blood cells and granular cast. The immunology test was positive for MPO-ANCA. The patient was clinically diagnosed with MPO-ANCA-associated glomerulonephritis. As the patient lost his appetite and developed lower extremity edema with low eGFR (< 15 ml/min/1.73m

Identifiants

pubmed: 39297892
doi: 10.1007/s13730-024-00927-6
pii: 10.1007/s13730-024-00927-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Japanese Society of Nephrology.

Références

Hogan JJ, Markowitz GS, Radhakrishnan J. Drug-induced glomerular disease: immune-mediated injury. Clin J Am Soc Nephrol. 2015;10:1300–10.
doi: 10.2215/CJN.01910215 pubmed: 26092827 pmcid: 4491282
Santoriello D, et al. Anti-neutrophil cytoplasmic antibody associated glomerulonephritis complicating treatment with hydralazine. Kidney Int. 2021;100:440–6.
doi: 10.1016/j.kint.2021.03.029 pubmed: 33857570
Chen CH, Wu MJ, Tsai SF. Safety and effectiveness of COVID-19 vaccines in patients with IgA nephropathy: a retrospective cohort study from the TriNetX global collaborative networks. EClinicalMedicine. 2023;65: 102306.
doi: 10.1016/j.eclinm.2023.102306 pubmed: 38021374 pmcid: 10661495
J. Irure-Ventura et al., Increased induction of de novo serum ANCA and ANCA-associated vasculitis after mass vaccination against SARS-CoV-2. iScience 25, 104847 (2022).
Grewal SK, et al. The risk of IgA nephropathy and glomerular disease in patients with psoriasis: a population-based cohort study. Br J Dermatol. 2017;176:1366–9.
doi: 10.1111/bjd.14961 pubmed: 27518038 pmcid: 5303688
Perkovic D, Simac P, Katic J. IgA vasculitis during secukinumab therapy. Clin Rheumatol. 2021;40:2071–3.
doi: 10.1007/s10067-020-05364-1 pubmed: 32860543
Segawa Y, et al. IgA nephropathy in a patient receiving infliximab for generalized pustular psoriasis. BMC Nephrol. 2020;21:366.
doi: 10.1186/s12882-020-02015-0 pubmed: 32842976 pmcid: 7449059
Windpessl M, et al. COVID-19 vaccines and kidney disease. Nat Rev Nephrol. 2021;17:291–3.
doi: 10.1038/s41581-021-00406-6 pubmed: 33558753 pmcid: 7869766
Diebold M, et al. Incidence of new onset glomerulonephritis after SARS-CoV-2 mRNA vaccination is not increased. Kidney Int. 2022;102:1409–19.
doi: 10.1016/j.kint.2022.08.021 pubmed: 36096267 pmcid: 9462927
Shakoor MT, Birkenbach MP, Lynch M. ANCA-associated vasculitis following Pfizer-BioNTech COVID-19 vaccine. Am J Kidney Dis. 2021;78:611–3.
doi: 10.1053/j.ajkd.2021.06.016 pubmed: 34280507 pmcid: 8285210
Suzuki M, et al. Antineutrophil Cytoplasmic antibody-associated vasculitis after COVID-19 vaccination with Pfizer-BioNTech. Intern Med. 2022;61:2925–9.
doi: 10.2169/internalmedicine.9807-22 pubmed: 36184535 pmcid: 9593166
Sekar A, Campbell R, Tabbara J, Rastogi P. ANCA glomerulonephritis after the Moderna COVID-19 vaccination. Kidney Int. 2021;100:473–4.
doi: 10.1016/j.kint.2021.05.017 pubmed: 34081948 pmcid: 8166044
Campos MAG, et al. ANCA-associated glomerulonephritis and lupus nephritis following COVID-19 vaccination: a case report and literature review. Front Immunol. 2023;14:1298622.
doi: 10.3389/fimmu.2023.1298622 pubmed: 38299140
Canney M, et al. A population-based analysis of the risk of glomerular disease relapse after COVID-19 Vaccination. J Am Soc Nephrol. 2022;33:2247–57.
doi: 10.1681/ASN.2022030258 pubmed: 36332971 pmcid: 9731636
M. Ochi et al., in CEN Case Rep. (Japan, 2019), vol. 8, pp. 200–204.
Ozince RB, Ak T, Erzin YZ, Melikoglu M, Seyahi E. Secukinumab-induced IgA vasculitis in a patient with psoriatic arthritis. Int J Rheum Dis. 2023;26:1811–5.
doi: 10.1111/1756-185X.14667 pubmed: 36929128
Lavoz C, et al. Interleukin-17A blockade reduces albuminuria and kidney injury in an accelerated model of diabetic nephropathy. Kidney Int. 2019;95:1418–32.
doi: 10.1016/j.kint.2018.12.031 pubmed: 30982673
Mehrotra P, et al. IL-17 mediates neutrophil infiltration and renal fibrosis following recovery from ischemia reperfusion: compensatory role of natural killer cells in athymic rats. Am J Physiol Renal Physiol. 2017;312:F385-f397.
doi: 10.1152/ajprenal.00462.2016 pubmed: 27852609
Velden J, et al. Renal IL-17 expression in human ANCA-associated glomerulonephritis. Am J Physiol Renal Physiol. 2012;302:F1663-1673.
doi: 10.1152/ajprenal.00683.2011 pubmed: 22442208
Nogueira E, et al. Serum IL-17 and IL-23 levels and autoantigen-specific Th17 cells are elevated in patients with ANCA-associated vasculitis. Nephrol Dial Transplant. 2010;25:2209–17.
doi: 10.1093/ndt/gfp783 pubmed: 20100727
Gan PY, et al. Th17 cells promote autoimmune anti-myeloperoxidase glomerulonephritis. J Am Soc Nephrol. 2010;21:925–31.
doi: 10.1681/ASN.2009070763 pubmed: 20299361 pmcid: 2900960

Auteurs

Takuya Sugiura (T)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Tomohito Doke (T)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan. tomorurira0220@gmail.com.

Akihito Tanaka (A)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Yuka Sato (Y)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Kayaho Maeda (K)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Kazuhiro Furuhashi (K)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Noritoshi Kato (N)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Tomoki Kosugi (T)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Shoichi Maruyama (S)

Department of Nephrology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Classifications MeSH