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Post-transplant lymphoproliferative disorder

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Title: Post-transplant lymphoproliferative disorder  
Author: World Heritage Encyclopedia
Language: English
Subject: Lymphoproliferative disorders, Lung transplantation, Transplant rejection, PTLD, Anti-lymphocyte globulin
Collection: Epstein–barr Virus-Associated Diseases, Lymphoma, Transplantation Medicine
Publisher: World Heritage Encyclopedia

Post-transplant lymphoproliferative disorder

Post-transplant lymphoproliferative disorder
Classification and external resources
ICD-9-CM 238.77
ICD-O M9970/1
DiseasesDB 34154
eMedicine ped/2851

Post-transplant lymphoproliferative disorder (PTLD) is the name given to a B-cells may undergo mutations which will render them malignant, giving rise to a lymphoma.

In some patients, the malignant cell clone can become the dominant proliferating cell type, leading to frank lymphoma, a group of organ transplant.


The disease is an uncontrolled proliferation of B cell lymphocytes latently infected with Epstein-Barr virus.[1][2] Production of an interleukin-10, an endogenous, pro-regulatory cytokine, has also been implicated.

In immunocompetent patients, Epstein-Barr virus can cause infectious mononucleosis in adolescent, which is otherwise asymptomatic in children during their childhood. However in immunosuppressed transplant patients, the lack of T-cell immunosurveillance can lead to the proliferation of these EBV-infected of B-lymphocytes.

However, calcineurin inhibitors (T cell function, and can prevent the control of the B cell proliferation.

Depletion of T cells by use of anti-T cell antibodies in the prevention or treatment of transplant rejection further increases the risk of developing post-transplant lymphoproliferative disorder. Such antibodies include ATG, ALG and OKT3.

Polyclonal PTLD may form tumor masses and present with symptoms due to a mass effect, e.g. symptoms of bowel obstruction. Monoclonal forms of PTLD tend to form a disseminated malignant lymphoma.


PTLD may spontaneously regress on reduction or cessation of immunosuppressant medication,[3] and can also be treated with addition of anti-viral therapy. In some cases it will progress to non-Hodgkin's lymphoma and may be fatal. A phase 2 study of adoptively transferred EBV-specific T cells demonstrated high efficacy with minimal toxicity.[4]


  1. ^ Gottschalk S, Rooney CM, Heslop HE (2005). "Post-transplant lymphoproliferative disorders". Annu. Rev. Med. 56 (1): 29–44.  
  2. ^ Nourse, JP; Jones K; Gandhi MK. (May 2011). "Epstein-Barr Virus-related post-transplant lymphoproliferative disorders: pathogenetic insights for targeted therapy.". Am J Transplant 11 (5): 888–95.  
  3. ^ "Hematopathology". 
  4. ^ Haque, T; Haque T, Wilkie GM, Jones MM, Higgins CD, Urquhart G, Wingate P, Burns D, McAulay K, Turner M, Bellamy C, Amlot PL, Kelly D, MacGilchrist A, Gandhi MK, Swerdlow AJ, Crawford DH. (Aug 2007). "Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial." (PDF). Blood 110 (4): 1123–31.  
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