Abbas F, El Kossi M, Jin JK, Sharma A, Halawa A. De novo glomerular diseases after renal transplantation: How is it different from recurrent glomerular diseases? World J Transplant 2017; 7(6): 285-300 [PMID: 29312858 DOI: 10.5500/wjt.v7.i6.285]
Corresponding Author of This Article
Ahmed Halawa, FRCS (Gen Surg), MD, MSc, Surgeon, Consultant Transplant Surgeon, Department of Transplantation Surgery, Sheffield Teaching Hospitals, Herries Road, Sheffield S5 7AU, United Kingdom. ahmed.halawa@sth.nhs.uk
Research Domain of This Article
Transplantation
Article-Type of This Article
Review
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This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Transplant. Dec 24, 2017; 7(6): 285-300 Published online Dec 24, 2017. doi: 10.5500/wjt.v7.i6.285
Table 1 Prevalence of the de novo vs recurrent membranoproliferative glomerulonephritis according to the new membranoproliferative glomerulonephritis pathological classification depending on the mechanism of glomerular injury instead of deposits distribution[14,59]
No.
MPGN subtype
Pathological criteria
Recurrent MPGN
De novo MPGN
1
ICGN (immune complex-mediated GN)
Contains immune complexes + complement compounds
More common (most of the recurrent cases are ICGN)
Table 3 Main characteristics of the more frequent de novo glomerulonephritis after transplantation (minimal change disease, nephrotic syndrome, membranous nephropathy, membranoproliferative glomerulonephritis, hepatitis C virus, IgAN)
Disease
Presentation
Time of onset
Difference with native GN
Treatment
Prognosis
MN
Proteinuria sometimes in nephrotic range
Late after transplant
Associated with trans-plant complications; IgG1 deposits instead of IgG4
No specific treatment
Slowly progressive
MPGN
Proteinuria, hematuria, NS, nephritic sediment
Months or years after transplant
Often associated with HCV, or with other diseases
Steroids + cytotoxic drugs if crescentic GN (?)
Slowly progressive; poor with many crescents.
FSGS
Proteinuria, rarely in nephrotic range
Months or years after transplant
NS is rare; signs of rejection or CNI toxicity at biopsy
Removal of associated events
Usually poor, particularly in collapsing GN
MCD
NS
Early after transplant
Mild mesangial sclerosis, hypercellularity
Steroids
Good
Table 4 The risk of recurrence of de novo glomerulonephritis after retransplantation is unknown
Disease
Indications to retransplant
MN
In view of the slow progression, there is no contraindication to retransplant
MPGN
The risk of recurrence is high in carriers of HCV, active autoimmune disease, or monoclonal gammopathy. These risk factors should be removed or inactivated before retransplant
FSGS
If FSGS was caused by calcineurin inhibitor or mTOR inhibitor toxicity, there is no contraindication to retransplant, but the dosage of the offending drug should be minimized. If FSGS was associated with AMR, the risk of recurrence is increased. Circulating antibodies should be removed before retransplant
Collapsing nephropathy
Risk of recurrence is probably high. Antiviral and/or removal of circulating AB before retransplant are recommended according to the possible role played by virus infection or AMR in the 1st transplant
MCD
In view of the favorable prognosis, there is no contraindication to retransplant
IgAN
No contraindication to retransplant
Citation: Abbas F, El Kossi M, Jin JK, Sharma A, Halawa A. De novo glomerular diseases after renal transplantation: How is it different from recurrent glomerular diseases? World J Transplant 2017; 7(6): 285-300