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Paving the way towards an effective treatment for multiple sclerosis: advances in cell therapy

作     者:M.J.Mansilla S.Presas-Rodríguez A.Teniente-Serra I.González-Larreategui B.Quirant-Sánchez F.Fondelli N.Djedovic D.Iwaszkiewicz-Grześ K.Chwojnicki D.Miljković PTrzonkowski C.Ramo-Tello E.M.Martínez-Cáceres 

作者机构:Division of ImmunologyLCMNGermans Trias i Pujol University Hospital and Research InstituteBarcelonaSpain Department of Cellular BiologyPhysiology and ImmunologyUniversitat Autònoma de BarcelonaBellaterraSpain Multiple Sclerosis UnitDepartment of NeurosciencesGermans Trias i Pujol University HospitalBarcelonaSpain Department of MedicineUniversitat Autònoma de BarcelonaBellaterraSpain View author publications Department of ImmunologyInstitute for Biological Research“Siniša Stanković”-National Institute of Republic of SerbiaUniversity of BelgradeBelgradeSerbia Department of Medical ImmunologyMedical University of GdańskGdańskPoland Poltreg S.A.GdańskPoland Department of Anaesthesiology&Intensive CareMedical University of GdańskGdańskPoland 

出 版 物:《Cellular & Molecular Immunology》 (中国免疫学杂志(英文版))

年 卷 期:2021年第18卷第6期

页      面:1353-1374页

核心收录:

学科分类:1002[医学-临床医学] 1010[医学-医学技术(可授医学、理学学位)] 100215[医学-康复医学与理疗学] 10[医学] 

基  金:funding from the European Union's Horizon 2020 research and innovation program under grant agreement 779316(RESTORE) the support of project PI17/01521 and PI20/01313,integrated in the Plan Nacional de I+D+1 and cosupported by the ISCIII-Subdireccidn General de Evaluacion and the Fondo Europeo de Desarrollo Regional(FEDER) and the support of National Centre for Research and Development,Poland(grant n°STRATEGMED1/233368/1/NCBR/2014).MJ.M.is beneficiary of a Sara Borrell contract from the ISCIII and the FEDER.N.D.and D.M.are supported by MPNTR Republika Srbija,grant n°451-03-68/2020-14/200007 

主  题:multiple sclerosis cell-based therapy tolerance neuroprotection autoimmunity 

摘      要:Multiple sclerosis(MS)is a leading cause of chronic neurological disability in young to middle-aged adults,affecting~2.5 million people ***,most therapeutics for MS are systemic immunosuppressive or immunomodulatory drugs,but these drugs are unable to halt or reverse the disease and have the potential to cause serious adverse ***,there is an urgent need for the development of next-generation treatments that,alone or in combination,stop the undesired autoimmune response and contribute to the restoration of *** review analyzes current MS treatments as well as different cell-based therapies that have been proposed to restore homeostasis in MS patients(tolerogenic dendritic cells,regulatory T cells,mesenchymal stem cells,and vaccination with T cells).Data collected from preclinical studies performed in the experimental autoimmune encephalomyelitis(EAE)model of MS in animals,in vitro cultures of cells from MS patients and the initial results of phase I/II clinical trials are analyzed to better understand which parameters are relevant for obtaining an efficient cell-based therapy for MS.

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