Immune Regulatory Processes of the Tumor Microenvironment under Malignant Conditions.

TME targeting therapy anti-tumor immune responses antigen presentation cytokines immune checkpoint immune evasion metabolism tumor microenvironment

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
10 Dec 2021
Historique:
received: 22 09 2021
revised: 03 12 2021
accepted: 05 12 2021
entrez: 24 12 2021
pubmed: 25 12 2021
medline: 11 1 2022
Statut: epublish

Résumé

The tumor microenvironment (TME) is a critical regulator of tumor growth, progression, and metastasis. Since immune cells represent a large fraction of the TME, they play a key role in mediating pro- and anti-tumor immune responses. Immune escape, which suppresses anti-tumor immunity, enables tumor cells to maintain their proliferation and growth. Numerous mechanisms, which have been intensively studied in recent years, are involved in this process and based on these findings, novel immunotherapies have been successfully developed. Here, we review the composition of the TME and the mechanisms by which immune evasive processes are regulated. In detail, we describe membrane-bound and soluble factors, their regulation, and their impact on immune cell activation in the TME. Furthermore, we give an overview of the tumor/antigen presentation and how it is influenced under malignant conditions. Finally, we summarize novel TME-targeting agents, which are already in clinical trials for different tumor entities.

Identifiants

pubmed: 34948104
pii: ijms222413311
doi: 10.3390/ijms222413311
pmc: PMC8706102
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : DOC Fellowship Programme of the Austrian Academy of Sciences
ID : 25690
Organisme : FWF Austrian Science Fund
ID : T923-B26
Organisme : Oesterreichische Nationalbank
ID : 18517

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Auteurs

Katrin Pansy (K)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Barbara Uhl (B)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Jelena Krstic (J)

Division of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Medical University of Graz, Neue Stiftingtalstraße 6/II, 8010 Graz, Austria.

Marta Szmyra (M)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Karoline Fechter (K)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Ana Santiso (A)

Division of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Universitätsplatz 4, 8010 Graz, Austria.

Lea Thüminger (L)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Hildegard Greinix (H)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Julia Kargl (J)

Division of Pharmacology, Otto Loewi Research Center, Medical University of Graz, Universitätsplatz 4, 8010 Graz, Austria.

Katharina Prochazka (K)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

Julia Feichtinger (J)

Division of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Medical University of Graz, Neue Stiftingtalstraße 6/II, 8010 Graz, Austria.

Alexander Ja Deutsch (AJ)

Division of Hematology, Medical University of Graz, Auenbruggerplatz 38, 8036 Graz, Austria.

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