High numbers of programmed cell death-1-positive tumor infiltrating lymphocytes correlate with early onset of post-transplant lymphoproliferative disorder.


Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 16 12 2020
accepted: 09 03 2021
revised: 05 03 2021
pubmed: 26 3 2021
medline: 29 6 2021
entrez: 25 3 2021
Statut: ppublish

Résumé

Post-transplant lymphoproliferative disorder (PTLD) is a life-threatening complication of transplantation. In addition to reactivation of Epstein-Barr virus in immunocompromised patients, impaired tumor immunity is suggested to be a risk factor for PTLD. However, it remains unclear whether immune suppressive tumor-infiltrating lymphocytes (TILs) correlate with the occurrence or prognosis of PTLD. We analyzed TILs in 26 patients with PTLD to elucidate the clinicopathological significance of the expression of PD-1 and FoxP3, which are associated with exhausted T-cells and regulatory T-cells (Tregs), respectively. Numbers of PD-1

Identifiants

pubmed: 33765256
doi: 10.1007/s12185-021-03129-3
pii: 10.1007/s12185-021-03129-3
doi:

Substances chimiques

FOXP3 protein, human 0
Forkhead Transcription Factors 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-64

Subventions

Organisme : KAKENHI
ID : 19K07450

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Auteurs

Hideaki Saito (H)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Hiroaki Miyoshi (H)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

Hirohiko Shibayama (H)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan. hiro@bldon.med.osaka-u.ac.jp.

Jun Toda (J)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Shinsuke Kusakabe (S)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Michiko Ichii (M)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Jiro Fujita (J)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Kentaro Fukushima (K)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Tetsuo Maeda (T)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.
Department of Hematology, Suita Municipal Hospital, Osaka, Japan.

Masao Mizuki (M)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Kenji Oritani (K)

Department of Hematology, Graduate School of Medical Sciences, International University of Health and Welfare, Chiba, Japan.

Masao Seto (M)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

Takafumi Yokota (T)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Yuzuru Kanakura (Y)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.
Department of Hematology, Sumitomo Hospital, Osaka, Japan.

Naoki Hosen (N)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, 565-0871, Japan.

Koichi Ohshima (K)

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

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