Background: Guillain-Barré syndrome (GBS) is an acute polyneuropathy caused by an autoimmune response towards a foreign antigen, notably viral infections. It is characterised by a symmetrical ascending paralysis with treatment remaining largely supportive; however, plasma exchange or intravenous immunoglobulins can be used to shorten recovery time. Case Report: We describe a case of severe acute GBS in a patient post-renal transplantation. The 44-year-old gentleman's induction therapy consisted of methyl prednisolone and basiliximab, with subsequent tacrolimus and mycophenolate mofetil as immunosuppressive agents. Tacrolimus was discontinued immediately on suspicion of a temporal relationship with the patient's condition, and substituted with a combination of ciclosporin, mycophenolate mofetil and prednisolone. Due to extensive patient screening prior to transplant, negative virology/immunology and normal nerve biopsy findings, both tacrolimus and basiliximab may be indicated as causative agents. Conclusion: Immunosuppressive-induced GBS should be considered a differential diagnosis in patients on tacrolimus or basiliximab with acute-onset limb weakness, especially if recently commenced. Discontinuation of tacrolimus and initiation of plasma exchange for the treatment for tacrolimus-associated GBS may be beneficial.

1.
Hughes RA, Hadden RD, Gregson NA, et al: Pathogenesis of Guillain-Barré syndrome. J Neuroimmunol 1999;100:74-97.
2.
Hughes RA, Cornblath DR: Guillain-Barré syndrome. Lancet 2005;366:1653-1666.
3.
J B Winer: Guillain Barré syndrome. Mol Pathol 2001;54:381-385.
4.
Cortese I, Chaudhry V, So YT, et al: Evidence-based guideline update: plasmapheresis in neurologic disorders: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology 2011;76:294-300.
5.
Webster AC, Taylor RRS, Chapman JR, et al: Tacrolimus versus cyclosporin as primary immunosuppression for kidney transplant recipients. Cochrane Database Syst Rev 2005;4:CD003961.
6.
Maccario M, Tarantino A, Nobile-Orazio E, Ponticelli C: Campylobacter jejuni bacteremia and Guillain-Barré syndrome in a renal transplant recipient. Transpl Int 1998;11:439-442.
7.
McMaster P, Mirza DF, Ismail T, et al: Therapeutic drug monitoring of tacrolimus in clinical transplantation. Ther Drug Monit 1995;17:602-605.
8.
Wilson JR, Conwit RA, Eidelman BH, et al: Sensorimotor neuropathy resembling CIDP in patients receiving FK506. Muscle Nerve 1994;17:528-532.
9.
Bhagavati S, Maccabee P, Muntean E, et al: Chronic sensorimotor polyneuropathy associated with tacrolimus immunosuppression in renal transplant patients: case reports. Transplant Proc 2007;39:3465-3467.
10.
Hunt I: Cyclosporine not the only agent to cause Guillain-Barré-like syndrome after solid-organ transplant. J Heart Lung Transplant 2006;25:1387.
11.
Falk JA, Cordova FC, Popescu A, et al: Treatment of Guillain-Barré syndrome induced by cyclosporine in a lung transplant patient. J Heart Lung Transplant 2006;25:140-143.
12.
Hartung HP, Hughes RA, Taylor WA, Heininger K, Reiners K, Toyka KV: T cell activation in Guillain-Barré syndrome and in MS: elevated serum levels of soluble IL-2 receptors. Neurology 1990;40:215-218.
13.
Qureshi AI, Cook AA, Mishu HP, Krendel DA: Guillain-Barré syndrome in immunocompromised patients: a report of three patients and review of literature. Muscle Nerve 1997:20:1002-1007.
14.
Kaya B, Davies CE, Oakervee HE, et al: Guillain-Barré syndrome precipitated by the use of antilymphocyte globulin in the treatment of severe aplastic anaemia. J Clin Pathol 2005;58:994-995.
15.
Gensicke H, Datta AN, Dill P, et al: Increased incidence of Guillain-Barré syndrome after surgery. Eur J Neurol 2012;19:1239-1244.
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