Bone metabolism in Langerhans cell histiocytosis
Langerhans cell histiocytosis (LCH) is a rare disease of not well-defined etiology that involves immune cell activation and frequently affects the skeleton. Bone involvement in LCH usually presents in the form of osteolytic lesions along with low bone mineral density. Various molecules involved in b...
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Published in | Endocrine Connections Vol. 7; no. 7; pp. R246 - R253 |
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Language | English |
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01.07.2018
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Abstract | Langerhans cell histiocytosis (LCH) is a rare disease of not well-defined etiology that involves immune cell activation and frequently affects the skeleton. Bone involvement in LCH usually presents in the form of osteolytic lesions along with low bone mineral density. Various molecules involved in bone metabolism are implicated in the pathogenesis of LCH or may be affected during the course of the disease, including interleukins (ILs), tumor necrosis factor α, receptor activator of NF-κB (RANK) and its soluble ligand RANKL, osteoprotegerin (OPG), periostin and sclerostin. Among them IL-17A, periostin and RANKL have been proposed as potential serum biomarkers for LCH, particularly as the interaction between RANK, RANKL and OPG not only regulates bone homeostasis through its effects on the osteoclasts but also affects the activation and survival of immune cells. Significant changes in circulating and lesional RANKL levels have been observed in LCH patients irrespective of bone involvement. Standard LCH management includes local or systematic administration of corticosteroids and chemotherapy. Given the implication of RANK, RANKL and OPG in the pathogenesis of the disease and the osteolytic nature of bone lesions, agents aiming at inhibiting the RANKL pathway and/or osteoclastic activation, such as bisphosphonates and denosumab, may have a role in the therapeutic approach of LCH although further clinical investigation is warranted. |
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AbstractList | Langerhans cell histiocytosis (LCH) is a rare disease of not well-defined etiology that involves immune cell activation and frequently affects the skeleton. Bone involvement in LCH usually presents in the form of osteolytic lesions along with low bone mineral density. Various molecules involved in bone metabolism are implicated in the pathogenesis of LCH or may be affected during the course of the disease, including interleukins (ILs), tumor necrosis factor α, receptor activator of NF-κB (RANK) and its soluble ligand RANKL, osteoprotegerin (OPG), periostin and sclerostin. Among them IL-17A, periostin and RANKL have been proposed as potential serum biomarkers for LCH, particularly as the interaction between RANK, RANKL and OPG not only regulates bone homeostasis through its effects on the osteoclasts but also affects the activation and survival of immune cells. Significant changes in circulating and lesional RANKL levels have been observed in LCH patients irrespective of bone involvement. Standard LCH management includes local or systematic administration of corticosteroids and chemotherapy. Given the implication of RANK, RANKL and OPG in the pathogenesis of the disease and the osteolytic nature of bone lesions, agents aiming at inhibiting the RANKL pathway and/or osteoclastic activation, such as bisphosphonates and denosumab, may have a role in the therapeutic approach of LCH although further clinical investigation is warranted. |
Author | Tsoli, Marina Anastasilakis, Athanasios D Kaltsas, Gregory Makras, Polyzois |
AuthorAffiliation | 1st Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece Department of Endocrinology, 424 General Military Hospital, Thessaloniki, Greece Department of Endocrinology and Diabetes, 251 Hellenic Air Force & VA General Hospital, Athens, Greece |
AuthorAffiliation_xml | – name: Department of Endocrinology, 424 General Military Hospital, Thessaloniki, Greece – name: 1st Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece – name: Department of Endocrinology and Diabetes, 251 Hellenic Air Force & VA General Hospital, Athens, Greece |
Author_xml | – sequence: 1 givenname: Athanasios D surname: Anastasilakis fullname: Anastasilakis, Athanasios D email: a.anastasilakis@gmail.com organization: Department of Endocrinology, 424 General Military Hospital, Thessaloniki, Greece – sequence: 2 givenname: Marina surname: Tsoli fullname: Tsoli, Marina organization: 1st Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece – sequence: 3 givenname: Gregory surname: Kaltsas fullname: Kaltsas, Gregory organization: 1st Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece – sequence: 4 givenname: Polyzois surname: Makras fullname: Makras, Polyzois organization: Department of Endocrinology and Diabetes, 251 Hellenic Air Force & VA General Hospital, Athens, Greece |
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Snippet | Langerhans cell histiocytosis (LCH) is a rare disease of not well-defined etiology that involves immune cell activation and frequently affects the skeleton.... |
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SubjectTerms | bisphosphonates denosumab Langerhans cell histiocytosis (LCH) osteoporosis receptor activator of NF-κB ligand (RANKL) Review |
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Title | Bone metabolism in Langerhans cell histiocytosis |
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