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Renal transplantation in patients with human T-cell lymphotropic virus type 1.

Abstract

BACKGROUND
Renal transplantation (RTx) in carriers of human T-cell lymphotropic virus type 1 (HTLV-1) has a risk of developing overt leukemia upon immunosuppression. Although there have been a few reports of such cases, it is unclear HTLV-1 carrier if patients on the modern immunosuppressants would develop HTLV-1-associated myelopathy or adult T-cell leukemia lymphoma.
METHODS
We retrospectively reviewed the clinical outcomes of RTx in nine HTLV-1 carriers to assess a risk of developing leukemia from 2002 to 2011 using immunosuppression with a calcineurin inhibitor, mycophenolate mofetil (MMF), and steroid. The anti-CD25 monoclonal antibody basiliximab was used for induction. In two cases of ABO-incompatible RTx, the rituximab was also administered before RTx.
RESULTS
The ratio of male to female subjects was 2 to 7 with an overall mean recipient age of 54.3 ± 8.1 years. We prescribed cyclosporine (n = 5) or tacrolimus (n = 4). There was only one graft loss due to the death caused by aspiration pneumonia with a functioning graft. No one developed overt leukemia with combined treatment with MMF, basiliximab and rituximab.
CONCLUSION
We concluded that RTx in HTLV-1 carriers could be performed using a modern immunosuppressive regimen, without the risk of developing leukemia.

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  • Publisher Full Text
  • Authors

    Shirai H, Suzuki M, Tomita Y, Iwadoh K, Kai K, Sannomiya A, Koyama I, Nakajima I, Fuchinoue S

    Institution

    Department of Surgery III, Tokyo Women's Medical University, Tokyo, Japan.

    Source

    Transplantation proceedings 44:1 2012 Jan pg 83-6

    MeSH

    Aged
    Drug Therapy, Combination
    Female
    Graft Survival
    HTLV-I Infections
    Human T-lymphotropic virus 1
    Humans
    Immunosuppressive Agents
    Japan
    Kidney Transplantation
    Leukemia-Lymphoma, Adult T-Cell
    Male
    Middle Aged
    Paraparesis, Tropical Spastic
    Retrospective Studies
    Risk Assessment
    Risk Factors
    Survival Analysis
    Time Factors
    Treatment Outcome
    Virus Activation

    Pub Type(s)

    Journal Article

    Language

    eng

    PubMed ID

    22310586