Tumor Microenvironment in T-Cell Lymphomas.
CD47-SIRPalpha axis
Checkpoint blockade
Helper T-cells
Immunotherapy
Regulatory T-cells
T-cell lymphoma
Tumor microenvironment
Journal
Cancer treatment and research
ISSN: 0927-3042
Titre abrégé: Cancer Treat Res
Pays: United States
ID NLM: 8008541
Informations de publication
Date de publication:
Historique:
entrez:
1
1
2019
pubmed:
1
1
2019
medline:
2
7
2019
Statut:
ppublish
Résumé
T-cell lymphomas (TCL) are uncommon non-Hodgkin lymphomas that often have an aggressive clinical course. Patients typically have limited treatment options upon relapse and a dismal prognosis after progression despite newly approved therapies. New therapeutic approaches for these orphan diseases are very much needed and a greater understanding of the role of nonmalignant immune cells in the tumor microenvironment may allow for an improved antitumor immune response. The tumor microenvironment is a key component in tumor evasion and typically results in an ineffective T-cell response to the tumor cells despite a significant inflammatory response. A better understanding of the tumor microenvironment therefore, in an effort to overcome the barriers to an effective immune response, would help in developing novel therapeutic approaches to treat and improve outcomes of these diseases. Immune checkpoint blockade to reinvigorate suppressed T-cell, or modulation of the CD47-SIRPalpha axis to promote macrophage phagocytosis, would be such targets. However, whether modulating the immune response using each pathway alone or whether a combination approach is necessary has yet to be determined.
Identifiants
pubmed: 30596213
doi: 10.1007/978-3-319-99716-2_3
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM