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Expression of Intratumoral Forkhead Box Protein 3 in Posttransplant Lymphoproliferative Disorders : Clinical Features and Survival Outcomes

Berglund, David (författare)
Uppsala universitet,Klinisk immunologi,Transplantationskirurgi
Kinch, Amelie, 1973- (författare)
Uppsala universitet,Infektionssjukdomar
Edman, Elin (författare)
Halmstad Hospital
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Backlin, Carin (författare)
Uppsala universitet,Reumatologi
Enblad, Gunilla (författare)
Uppsala universitet,Enheten för onkologi
Larsson, Erik (författare)
Uppsala universitet,Molekylär och morfologisk patologi
Molin, Daniel (författare)
Uppsala universitet,Enheten för onkologi
Pauksens, Karlis (författare)
Uppsala universitet,Infektionssjukdomar
Sundström, Christer (författare)
Uppsala universitet,Klinisk och experimentell patologi,Rose-Marie Amini
Baecklund, Eva (författare)
Uppsala universitet,Reumatologi
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 (creator_code:org_t)
Lippincott Williams & Wilkins, 2015
2015
Engelska.
Ingår i: Transplantation. - : Lippincott Williams & Wilkins. - 0041-1337 .- 1534-6080. ; 99:5, s. 1036-1042
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background. The infiltration of regulatory T cells (Tregs) in lymphomas is associated with better prognosis for some types of lymphomas, but knowledge of their role in posttransplant lymphoproliferative disorders (PTLDs) is limited. We therefore investigated the association between the expression of the Treg marker forkhead box protein 3 (FoxP3) in biopsies of PTLDs and survival, PTLD subtype, and clinical characteristics.Methods. Seventy-four cases of PTLD after solid organ transplantation with sufficient material for further analysis were included from a population-based study of PTLDs in Sweden. The PTLD biopsies were reevaluated and stained with the 236A/E7 antibody to detect FoxP3 in lymphoma tissue. Detailed clinical data were collected retrospectively from medical records.Results. Based on a cutoff level of 29 FoxP3+ cells per mm2, most (80%) of the PTLDs were FoxP3-. Forty-seven of 74 PTLDs displayed no FoxP3+ cells at all. The frequency of FoxP3+ cells did not influence median overall survival. The FoxP3- PTLDs were more frequently of T-cell phenotype (P=0.04), located at the graft (P=0.03), occurred earlier after transplantation (P=0.04), were more likely to develop in lung recipients (P=0.04), and in patients that had received anti T-cell globulin as induction therapy (P=0.02). The FoxP3+ PTLDs were associated with hepatitis C seropositivity (P=0.03). In multivariate analysis, B-cell PTLD and hepatitis C infection were independent predictors of FoxP3 positivity.Conclusion. Our findings suggest that intratumoral FoxP3+ Tregs do not influence survival in patients with PTLD. FoxP3+ Tregs are rare in PTLD, possibly because of heavy immunosuppression.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Klinisk laboratoriemedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Clinical Laboratory Medicine (hsv//eng)

Nyckelord

Regulatory T cell
FoxP3
Posttransplant lymphoproliferative disorders
lymphoma
microenvironment
survival
clinical features
hepatitis C
Treg
immunosuppression
antithymocyte globulin
Medicinsk vetenskap
Medical Science
Patologi
Pathology

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