Delicate Role of PD-L1/PD-1 Axis in Blood Vessel Inflammatory Diseases: Current Insight and Future Significance.


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:
31 Oct 2020
Historique:
received: 30 09 2020
revised: 25 10 2020
accepted: 28 10 2020
entrez: 4 11 2020
pubmed: 5 11 2020
medline: 26 3 2021
Statut: epublish

Résumé

Immune checkpoint molecules are the antigen-independent generator of secondary signals that aid in maintaining the homeostasis of the immune system. The programmed death ligand-1 (PD-L1)/PD-1 axis is one among the most extensively studied immune-inhibitory checkpoint molecules, which delivers a negative signal for T cell activation by binding to the PD-1 receptor. The general attributes of PD-L1's immune-suppressive qualities and novel mechanisms on the barrier functions of vascular endothelium to regulate blood vessel-related inflammatory diseases are concisely reviewed. Though targeting the PD-1/PD-L1 axis has received immense recognition-the Nobel Prize in clinical oncology was awarded in the year 2018 for this discovery-the use of therapeutic modulating strategies for the PD-L1/PD-1 pathway in chronic inflammatory blood vessel diseases is still limited to experimental models. However, studies using clinical specimens that support the role of PD-1 and PD-L1 in patients with underlying atherosclerosis are also detailed. Of note, delicate balances in the expression levels of PD-L1 that are needed to preserve T cell immunity and to curtail acute as well as chronic infections in underlying blood vessel diseases are discussed. A significant link exists between altered lipid and glucose metabolism in different cells and the expression of PD-1/PD-L1 molecules, and its possible implications on vascular inflammation are justified. This review summarizes the most recent insights concerning the role of the PD-L1/PD-1 axis in vascular inflammation and, in addition, provides an overview exploring the novel therapeutic approaches and challenges of manipulating these immune checkpoint proteins, PD-1 and PD-L1, for suppressing blood vessel inflammation.

Identifiants

pubmed: 33142805
pii: ijms21218159
doi: 10.3390/ijms21218159
pmc: PMC7663405
pii:
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0
Immune Checkpoint Inhibitors 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Priya Veluswamy (P)

Heart Surgery Research, Department of Cardiothoracic Surgery, Faculty of Medicine, Otto-von Guericke University, D-39120 Magdeburg, Germany.

Max Wacker (M)

Heart Surgery Research, Department of Cardiothoracic Surgery, Faculty of Medicine, Otto-von Guericke University, D-39120 Magdeburg, Germany.

Maximilian Scherner (M)

Heart Surgery Research, Department of Cardiothoracic Surgery, Faculty of Medicine, Otto-von Guericke University, D-39120 Magdeburg, Germany.

Jens Wippermann (J)

Heart Surgery Research, Department of Cardiothoracic Surgery, Faculty of Medicine, Otto-von Guericke University, D-39120 Magdeburg, Germany.

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