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      Nerve growth factor antibody for the treatment of osteoarthritis pain and chronic low-back pain: mechanism of action in the context of efficacy and safety

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          Abstract

          Chronic pain continues to be a significant global burden despite the availability of a variety of nonpharmacologic and pharmacologic treatment options. Thus, there is a need for new analgesics with novel mechanisms of action. In this regard, antibodies directed against nerve growth factor (NGF-Abs) are a new class of agents in development for the treatment of chronic pain conditions such as osteoarthritis and chronic low-back pain. This comprehensive narrative review summarizes evidence supporting pronociceptive functions for NGF that include contributing to peripheral and central sensitization through tropomyosin receptor kinase A activation and stimulation of local neuronal sprouting. The potential role of NGF in osteoarthritis and chronic low-back pain signaling is also examined to provide a mechanistic basis for the observed efficacy of NGF-Abs in clinical trials of these particular pain states. Finally, the safety profile of NGF-Abs in terms of common adverse events, joint safety, and nerve structure/function is discussed.

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          Most cited references100

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          Nerve growth factor expression and innervation of the painful intervertebral disc.

          Following a previous description of nociceptive nerve fibre growth into usually aneural inner parts of painful intervertebral disc (IVD), this study has investigated whether nociceptive nerve ingrowth into painful IVD is stimulated by local production of neurotrophins. Immunohistochemistry and in situ hybridization have been used to investigate expression of the candidate neurotrophin, nerve growth factor (NGF), and its high- and low-affinity receptors trk-A and p75, respectively, in painful IVD excised for the management of low back pain. IVD from patients with back pain were of two types: those that when examined by discography reproduced the patient symptoms (pain level IVD) and those that did not (non-pain level IVD). Microvascular blood vessels accompanied nerve fibres growing into pain level IVD and these expressed NGF. The adjacent nerves expressed the high-affinity NGF receptor trk-A. These vessels entered the normally avascular IVD through the discal end plates. NGF expression was not identified in non-pain level or control IVD. Some non-pain level IVD had vessels within them, which entered through the annulus fibrosus. These did not express NGF nor did nerves accompany them. These findings show that nociceptive nerve ingrowth into painful IVD is causally linked with NGF production by blood vessels growing into the IVD, from adjacent vertebral bodies. Copyright 2002 John Wiley & Sons, Ltd.
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            Antagonism of nerve growth factor-TrkA signaling and the relief of pain.

            Nerve growth factor (NGF) was originally discovered as a neurotrophic factor essential for the survival of sensory and sympathetic neurons during development. However, in the adult NGF has been found to play an important role in nociceptor sensitization after tissue injury. The authors outline mechanisms by which NGF activation of its cognate receptor, tropomyosin-related kinase A receptor, regulates a host of ion channels, receptors, and signaling molecules to enhance acute and chronic pain. The authors also document that peripherally restricted antagonism of NGF-tropomyosin-related kinase A receptor signaling is effective for controlling human pain while appearing to maintain normal nociceptor function. Understanding whether there are any unexpected adverse events and how humans may change their behavior and use of the injured/degenerating tissue after significant pain relief without sedation will be required to fully appreciate the patient populations that may benefit from these therapies targeting NGF.
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              Osteoarthritis joint pain: the cytokine connection.

              Osteoarthritis is a chronic and painful disease of synovial joints. Chondrocytes, synovial cells and other cells in the joint can express and respond to cytokines and chemokines, and all of these molecules can also be detected in synovial fluid of patients with osteoarthritis. The presence of inflammatory cytokines in the osteoarthritic joint raises the question whether they may directly participate in pain generation by acting on innervating joint nociceptors. Here, we first provide a systematic discussion of the known proalgesic effects of cytokines and chemokines that have been detected in osteoarthritic joints, including TNF-α, IL-1, IL-6, IL-15, IL-10, and the chemokines, MCP-1 and fractalkine. Subsequently, we discuss what is known about their contribution to joint pain based on studies in animal models. Finally, we briefly discuss limited data available from clinical studies in human osteoarthritis.
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                Author and article information

                Journal
                Pain
                Pain
                JPAIN
                Pain
                JOP
                Pain
                Wolters Kluwer (Philadelphia, PA )
                0304-3959
                1872-6623
                22 May 2019
                October 2019
                : 160
                : 10
                : 2210-2220
                Affiliations
                [a ]Department of Experimental Pain Research Mannheim, University of Heidelberg, Heidelberg, Germany
                [b ]Department of Pharmacology, Cancer Center, University of Arizona, Tucson, AZ, United States
                [c ]Department of Internal Medicine, Division of Rheumatology, Rush University, Chicago, IL, United States
                [d ]Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA, United States
                [e ]Department of Anesthesiology and Pharmacology, University of California at San Diego, La Jolla, CA, United States
                [f ]Medical Affairs, Pfizer, New York, NY, United States
                [g ]Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States
                Author notes
                [* ]Corresponding author. Address: Lilly Research Laboratories, Eli Lilly and Company, DC 1546, 88/4, Lilly Corporate Center, Indianapolis, IN 46285. Tel.: 317-652-4947; fax: 317-433-4901. E-mail address: viktrup_lars@ 123456lilly.com (L. Viktrup).
                Article
                PAIN-D-18-01284 00006
                10.1097/j.pain.0000000000001625
                6756297
                31145219
                934671c7-521f-46f3-a271-1c308fa34b2b
                Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain.

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

                History
                : 27 December 2018
                : 09 May 2019
                : 13 May 2019
                Categories
                Comprehensive Review
                Custom metadata
                TRUE

                Anesthesiology & Pain management
                nerve growth factor,mechanism of action,chronic pain,osteoarthritis,chronic low-back pain

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