Literature DB >> 25943068

Programmed cell death-1 inhibition in lymphoma.

Eliza A Hawkes1, Andrew Grigg2, Geoff Chong3.   

Abstract

Cancers can evade the host immune system by inducing upregulation of immune inhibitory signals. Anti-programmed cell death-1 (PD-1) monoclonal antibodies block these inhibitory signals allowing the host to mount an immune response against malignant cells. This class of drugs is active in solid tumours, where upregulation of cell-surface PD-1 ligand proteins is nearly uniform. Because lymphoma is a malignancy of immune system cells, the role of the PD-1 pathway in these neoplasms is more complex. However, early clinical trials using PD-1 inhibitors have shown significant clinical activity in various subtypes of relapsed lymphoma. In this Review, we assess the scientific literature on the role of the PD-1 pathway in lymphoma, the relevant clinical data for PD-1 inhibition, and future strategies for this next generation of anticancer agents.
Copyright © 2015 Elsevier Ltd. All rights reserved.

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Year:  2015        PMID: 25943068     DOI: 10.1016/S1470-2045(15)70103-8

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  16 in total

1.  Immunomodulatory antibodies for the treatment of lymphoma: Report on the CALYM Workshop.

Authors:  Roch Houot; Philippe Gaulard; Robert Schreiber; Ira Mellman; Olivier Lambotte; Pierre G Coulie; Thierry Fest; Alan Korman; Ronald Levy; Margaret Shipp; Karin Tarte; Holbrook Kohrt; Aurélien Marabelle; Stephen Ansell; Hervé Watier; Andrea van Elsas; Arun Balakumaran; Frederick Arce Vargas; Sergio A Quezada; Gilles Salles; Daniel Olive
Journal:  Oncoimmunology       Date:  2016-05-19       Impact factor: 8.110

2.  The role of novel immunotherapies in non-Hodgkin lymphoma.

Authors:  Allyson Pishko; Sunita D Nasta
Journal:  Transl Cancer Res       Date:  2017-02       Impact factor: 1.241

Review 3.  Targeting Triple Negative Breast Cancer With Oncolytic Adenoviruses.

Authors:  Gabriela Green-Tripp; Callum Nattress; Gunnel Halldén
Journal:  Front Mol Biosci       Date:  2022-06-24

4.  Structure of the Complex of Human Programmed Death 1, PD-1, and Its Ligand PD-L1.

Authors:  Krzysztof M Zak; Radoslaw Kitel; Sara Przetocka; Przemyslaw Golik; Katarzyna Guzik; Bogdan Musielak; Alexander Dömling; Grzegorz Dubin; Tad A Holak
Journal:  Structure       Date:  2015-10-22       Impact factor: 5.006

Review 5.  Immunotherapy of cancer: from monoclonal to oligoclonal cocktails of anti-cancer antibodies: IUPHAR Review 18.

Authors:  Silvia Carvalho; Francesca Levi-Schaffer; Michael Sela; Yosef Yarden
Journal:  Br J Pharmacol       Date:  2016-03-14       Impact factor: 8.739

Review 6.  Improvement of the anticancer efficacy of PD-1/PD-L1 blockade via combination therapy and PD-L1 regulation.

Authors:  Mengling Wu; Qianrui Huang; Yao Xie; Xuyi Wu; Hongbo Ma; Yiwen Zhang; Yong Xia
Journal:  J Hematol Oncol       Date:  2022-03-12       Impact factor: 17.388

Review 7.  Targets, Toxins, and T Cells--a Review of New Monoclonal Antibodies in the Treatment of Peripheral T Cell Lymphomas.

Authors:  Jonathan Hebb; Holbrook Kohrt
Journal:  Curr Hematol Malig Rep       Date:  2015-12       Impact factor: 4.213

Review 8.  Nivolumab as Programmed Death-1 (PD-1) Inhibitor for Targeted Immunotherapy in Tumor.

Authors:  Liting Guo; Haijun Zhang; Baoan Chen
Journal:  J Cancer       Date:  2017-02-10       Impact factor: 4.207

9.  PD-L1 Nanobody Competitively Inhibits the Formation of the PD-1/PD-L1 Complex: Comparative Molecular Dynamics Simulations.

Authors:  Xin Sun; Xiao Yan; Wei Zhuo; Jinke Gu; Ke Zuo; Wei Liu; Li Liang; Ya Gan; Gang He; Hua Wan; Xiaojun Gou; Hubing Shi; Jianping Hu
Journal:  Int J Mol Sci       Date:  2018-07-07       Impact factor: 5.923

10.  Evaluation of the C-Terminal Fragment of Entamoeba histolytica Gal/GalNAc Lectin Intermediate Subunit as a Vaccine Candidate against Amebic Liver Abscess.

Authors:  Xiangyang Min; Meng Feng; Yue Guan; Suqin Man; Yongfeng Fu; Xunjia Cheng; Hiroshi Tachibana
Journal:  PLoS Negl Trop Dis       Date:  2016-01-29
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