PTPN3 expressed in activated T lymphocytes is a candidate for a non-antibody-type immune checkpoint inhibitor.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 20 02 2019
accepted: 23 09 2019
pubmed: 29 9 2019
medline: 26 11 2019
entrez: 29 9 2019
Statut: ppublish

Résumé

It has been shown that protein tyrosine phosphatase non-receptor type (PTPN) 3 inhibits T-cell activation. However, there is no definitive conclusion about how the inhibition of PTPN3 in lymphocytes affects immune functions in human lymphocytes. In the present study, we showed that PTPN3 inhibition significantly contributes to the enhanced activation of activated human lymphocytes. The PTPN3 expression of lymphocytes was significantly increased through the activation process using IL-2 and anti-CD3 mAb. Interestingly, inhibiting the PTPN3 expression in activated lymphocytes significantly augmented the proliferation, migration, and cytotoxicity through the phosphorylation of zeta-chain-associated protein kinase 70 (ZAP-70), lymphocyte-specific protein tyrosine kinase (LCK), and extracellular signal-regulated kinases (ERK). Lymphocyte activation by PTPN3 inhibition was observed only in activated CD3

Identifiants

pubmed: 31562536
doi: 10.1007/s00262-019-02403-y
pii: 10.1007/s00262-019-02403-y
doi:

Substances chimiques

Receptors, Antigen, T-Cell 0
Lymphocyte Specific Protein Tyrosine Kinase p56(lck) EC 2.7.10.2
ZAP-70 Protein-Tyrosine Kinase EC 2.7.10.2
ZAP70 protein, human EC 2.7.10.2
PTPN3 protein, human EC 3.1.3.48
Protein Tyrosine Phosphatase, Non-Receptor Type 3 EC 3.1.3.48

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1649-1660

Subventions

Organisme : KAKENHI
ID : JP15K10055
Organisme : KAKENHI
ID : JP17H04283
Organisme : KAKENHI
ID : JP18K08682

Auteurs

Akiko Fujimura (A)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Kazunori Nakayama (K)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Akira Imaizumi (A)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Makoto Kawamoto (M)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Yasuhiro Oyama (Y)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Shu Ichimiya (S)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Masayo Umebayashi (M)

Fukuoka General Cancer Clinic, Fukuoka, Japan.

Norihiro Koya (N)

Fukuoka General Cancer Clinic, Fukuoka, Japan.

Takashi Morisaki (T)

Fukuoka General Cancer Clinic, Fukuoka, Japan.

Takashi Nakagawa (T)

Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Hideya Onishi (H)

Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. ohnishi@surg1.med.kyushu-u.ac.jp.

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Classifications MeSH