PD‐1/PD‐L1 pathway: Basic biology and role in cancer immunotherapy
Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the most efficient strategy to raise beneficial antitumo...
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Published in | Journal of cellular physiology Vol. 234; no. 10; pp. 16824 - 16837 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.10.2019
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Subjects | |
Online Access | Get full text |
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Abstract | Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the most efficient strategy to raise beneficial antitumor immune responses. Programmed cell death protein 1 (PD‐1) plays an important role in subsiding immune responses and promoting self‐tolerance through suppressing the activity of T cells and promoting differentiation of regulatory T cells. PD‐1 is considered as an immune checkpoint and protects against autoimmune responses through both induction of apoptosis in antigen‐specific T cells and inhibiting apoptosis in regulatory T cells. Several clinical trials exerting PD‐1 monoclonal antibodies as well as other immune‐checkpoint blockades have had prosperous outcomes and opened new horizons in tumor immunotherapy. Nonetheless, a bulk of patients have failed to respond to these newly emerging immune‐based approach and the survival rate was not satisfying. Additional strategies, especially combination therapies, has been initiated and been further promising. Attempts to identify novel and well‐suited predictive biomarkers are also sensed. In this review, the promotion of cancer immunotherapy targeting PD‐1 immunoinhibitory pathway is discussed.
In this review, the promotion of cancer immunotherapy targeting programmed cell death protein 1 immunoinhibitory pathway is discussed. |
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AbstractList | Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the most efficient strategy to raise beneficial antitumor immune responses. Programmed cell death protein 1 (PD‐1) plays an important role in subsiding immune responses and promoting self‐tolerance through suppressing the activity of T cells and promoting differentiation of regulatory T cells. PD‐1 is considered as an immune checkpoint and protects against autoimmune responses through both induction of apoptosis in antigen‐specific T cells and inhibiting apoptosis in regulatory T cells. Several clinical trials exerting PD‐1 monoclonal antibodies as well as other immune‐checkpoint blockades have had prosperous outcomes and opened new horizons in tumor immunotherapy. Nonetheless, a bulk of patients have failed to respond to these newly emerging immune‐based approach and the survival rate was not satisfying. Additional strategies, especially combination therapies, has been initiated and been further promising. Attempts to identify novel and well‐suited predictive biomarkers are also sensed. In this review, the promotion of cancer immunotherapy targeting PD‐1 immunoinhibitory pathway is discussed.
In this review, the promotion of cancer immunotherapy targeting programmed cell death protein 1 immunoinhibitory pathway is discussed. Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the most efficient strategy to raise beneficial antitumor immune responses. Programmed cell death protein 1 (PD-1) plays an important role in subsiding immune responses and promoting self-tolerance through suppressing the activity of T cells and promoting differentiation of regulatory T cells. PD-1 is considered as an immune checkpoint and protects against autoimmune responses through both induction of apoptosis in antigen-specific T cells and inhibiting apoptosis in regulatory T cells. Several clinical trials exerting PD-1 monoclonal antibodies as well as other immune-checkpoint blockades have had prosperous outcomes and opened new horizons in tumor immunotherapy. Nonetheless, a bulk of patients have failed to respond to these newly emerging immune-based approach and the survival rate was not satisfying. Additional strategies, especially combination therapies, has been initiated and been further promising. Attempts to identify novel and well-suited predictive biomarkers are also sensed. In this review, the promotion of cancer immunotherapy targeting PD-1 immunoinhibitory pathway is discussed. Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the most efficient strategy to raise beneficial antitumor immune responses. Programmed cell death protein 1 (PD-1) plays an important role in subsiding immune responses and promoting self-tolerance through suppressing the activity of T cells and promoting differentiation of regulatory T cells. PD-1 is considered as an immune checkpoint and protects against autoimmune responses through both induction of apoptosis in antigen-specific T cells and inhibiting apoptosis in regulatory T cells. Several clinical trials exerting PD-1 monoclonal antibodies as well as other immune-checkpoint blockades have had prosperous outcomes and opened new horizons in tumor immunotherapy. Nonetheless, a bulk of patients have failed to respond to these newly emerging immune-based approach and the survival rate was not satisfying. Additional strategies, especially combination therapies, has been initiated and been further promising. Attempts to identify novel and well-suited predictive biomarkers are also sensed. In this review, the promotion of cancer immunotherapy targeting PD-1 immunoinhibitory pathway is discussed.Over the course of past few years, cancer immunotherapy has been accompanied with promising results. However, preliminary investigations with respect to immunotherapy concentrated mostly on targeting the immune checkpoints, nowadays, emerge as the most efficient strategy to raise beneficial antitumor immune responses. Programmed cell death protein 1 (PD-1) plays an important role in subsiding immune responses and promoting self-tolerance through suppressing the activity of T cells and promoting differentiation of regulatory T cells. PD-1 is considered as an immune checkpoint and protects against autoimmune responses through both induction of apoptosis in antigen-specific T cells and inhibiting apoptosis in regulatory T cells. Several clinical trials exerting PD-1 monoclonal antibodies as well as other immune-checkpoint blockades have had prosperous outcomes and opened new horizons in tumor immunotherapy. Nonetheless, a bulk of patients have failed to respond to these newly emerging immune-based approach and the survival rate was not satisfying. Additional strategies, especially combination therapies, has been initiated and been further promising. Attempts to identify novel and well-suited predictive biomarkers are also sensed. In this review, the promotion of cancer immunotherapy targeting PD-1 immunoinhibitory pathway is discussed. |
Author | Aslani, Saeed Salmaninejad, Arash Alimardani, Malihe Valilou, Saeed Farajzadeh Pasdar, Alireza Sahebkar, Amirhossein Shabgah, Arezoo Gowhari |
Author_xml | – sequence: 1 givenname: Arash orcidid: 0000-0001-6141-3915 surname: Salmaninejad fullname: Salmaninejad, Arash organization: Faculty of Medicine, Mashhad University of Medical Sciences – sequence: 2 givenname: Saeed Farajzadeh surname: Valilou fullname: Valilou, Saeed Farajzadeh organization: Universal Scientific Education and Research Network (USERN) – sequence: 3 givenname: Arezoo Gowhari surname: Shabgah fullname: Shabgah, Arezoo Gowhari organization: Mashhad University of Medical Sciences – sequence: 4 givenname: Saeed surname: Aslani fullname: Aslani, Saeed organization: Tehran University of Medical Sciences – sequence: 5 givenname: Malihe surname: Alimardani fullname: Alimardani, Malihe organization: Faculty of Medicine, Mashhad University of Medical Sciences – sequence: 6 givenname: Alireza surname: Pasdar fullname: Pasdar, Alireza organization: Medical School, University of Aberdeen – sequence: 7 givenname: Amirhossein surname: Sahebkar fullname: Sahebkar, Amirhossein email: sahebkara@mums.ac.ir organization: School of Pharmacy, Mashhad University of Medical Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30784085$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Antigens Antitumor activity Apoptosis B7-H1 Antigen - genetics B7-H1 Antigen - metabolism Biomarkers Cancer Cancer immunotherapy cancer therapy Cell death Clinical trials Gene Expression Regulation, Neoplastic Humans Immune checkpoint Immunological tolerance Immunoregulation Immunotherapy Lymphocytes Lymphocytes T Medical research Monoclonal antibodies monoclonal antibody Neoplasms - therapy PD-L1 protein PD‐1 PD‐L‐1 Programmed Cell Death 1 Receptor - genetics Programmed Cell Death 1 Receptor - metabolism Survival |
Title | PD‐1/PD‐L1 pathway: Basic biology and role in cancer immunotherapy |
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