Novel therapeutic strategies for autoimmune and inflammatory rheumatic diseases

被引:15
作者
Felten, Renaud [1 ,2 ,3 ]
Mertz, Philippe [3 ]
Sebbag, Eden [3 ]
Scherlinger, Marc [3 ,4 ]
Arnaud, Laurent [3 ,4 ]
机构
[1] Hop Univ Strasbourg, Ctr Invest Clin, Inserm 1434, Strasbourg, France
[2] IBMC, Immunopathol & Chim Therapeut, CNRS UPR 3572, Strasbourg, France
[3] Hop Univ Strasbourg, Ctr Natl Reference Malad Autoimmunes RESO, Serv Rhumatol, Strasbourg, France
[4] Inst Natl Sante & Rech Med INSERM, Lab ImmunoRhumatol Mol, UMR S 1109, Strasbourg, France
关键词
biological products; molecular targeted therapy; immunomodulating agents; review; inflammatory disease; SYSTEMIC-LUPUS-ERYTHEMATOSUS; STEM-CELL TRANSPLANTATION; PULSE CYCLOPHOSPHAMIDE; RNA INTERFERENCE; T-CELLS; ARTHRITIS; ANTIBODY; NANOPARTICLES; ETANERCEPT; SCLEROSIS;
D O I
10.1016/j.drudis.2023.103612
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drugs of unknown mechanisms of action are no longer being developed because we have largely capitalized on our improved understanding of the immunopathogenesis of immune-mediated inflammatory diseases (IMIDs) to develop therapeutic monoclonal antibodies (mAbs) and targeted treatments. These therapies have profoundly revolutionized the care of IMIDs. However, because of the heterogeneity of IMIDs and the redundancy of the targeted molecular pathways, some patients with IMIDs might not respond to a specific targeted drug or their disease might relapse secondarily. Therefore, there is much at stake in the development of new therapeutic strategies, which include combinations of mAbs or bispecific mAbs (BsMAbs), nanobodies and nanoparticles (NPs), therapeutic vaccines, small interfering RNA (siRNA) interference, autologous hematopoietic stem cell transplan-tation (aHSCT), or chimeric antigen receptor (CAR)-T cells. With the broad pipeline of targeted treatments in clinical development, the therapeutic paradigm is rapidly evolving from whether new drugs will be available to the complex selection of the most adequate targeted treatment (or treatment combination) at the patient level. This paradigm change highlights the need to better characterize the heterogeneous immunological spectrum of these diseases. Only then will these novel therapeutic strategies be able to fully demonstrate their potential to treat IMIDs.
引用
收藏
页数:9
相关论文
共 74 条
[1]   Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis [J].
Adams, D. ;
Gonzalez-Duarte, A. ;
O'Riordan, W. D. ;
Yang, C. -C. ;
Ueda, M. ;
Kristen, A. V. ;
Tournev, I. ;
Schmidt, H. H. ;
Coelho, T. ;
Berk, J. L. ;
Lin, K. -P. ;
Vita, G. ;
Attarian, S. ;
Plante-Bordeneuve, V. ;
Mezei, M. M. ;
Campistol, J. M. ;
Buades, J. ;
Brannagan, T. H., III ;
Kim, B. J. ;
Oh, J. ;
Parman, Y. ;
Sekijima, Y. ;
Hawkins, P. N. ;
Solomon, S. D. ;
Polydefkis, M. ;
Dyck, P. J. ;
Gandhi, P. J. ;
Goyal, S. ;
Chen, J. ;
Strahs, A. L. ;
Nochur, S. V. ;
Sweetser, M. T. ;
Garg, P. P. ;
Vaishnaw, A. K. ;
Gollob, J. A. ;
Suhr, O. B. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (01) :11-21
[2]   Targeting cardiac fibrosis with engineered T cells [J].
Aghajanian, Haig ;
Kimura, Toru ;
Rurik, Joel G. ;
Hancock, Aidan S. ;
Leibowitz, Michael S. ;
Li, Li ;
Scholler, John ;
Monslow, James ;
Lo, Albert ;
Han, Wei ;
Wang, Tao ;
Bedi, Kenneth ;
Morley, Michael P. ;
Saldana, Ricardo A. Linares ;
Bolar, Nikhita A. ;
McDaid, Kendra ;
Assenmacher, Charles-Antoine ;
Smith, Cheryl L. ;
Wirth, Dagmar ;
June, Carl H. ;
Margulies, Kenneth B. ;
Jain, Rajan ;
Pure, Ellen ;
Albelda, Steven M. ;
Epstein, Jonathan A. .
NATURE, 2019, 573 (7774) :430-+
[3]  
[Anonymous], 2010, Drug Discov Today Technol, V7, pe95, DOI 10.1016/j.ddtec.2010.03.002
[4]  
[Anonymous], EFFICACY SAFETY SUBC
[5]  
[Anonymous], ClinicalTrials
[6]   Modulation of Anti-Tumor Necrosis Factor Alpha (TNF-α) Antibody Secretion in Mice Immunized with TNF-α Kinoid [J].
Assier, Eric ;
Semerano, Luca ;
Duvallet, Emilie ;
Delavallee, Laure ;
Bernier, Emilie ;
Laborie, Marion ;
Grouard-Vogel, Geraldine ;
Larcier, Patrick ;
Bessis, Natacha ;
Boissier, Marie-Christophe .
CLINICAL AND VACCINE IMMUNOLOGY, 2012, 19 (05) :699-703
[7]   Tumor Necrosis Factor-Alpha Targeting Can Protect against Arthritis with Low Sensitization to Infection [J].
Belmellat, Nadia ;
Semerano, Luca ;
Segueni, Noria ;
Damotte, Diane ;
Decker, Patrice ;
Ryffel, Bernhard ;
Quesniaux, Valerie ;
Boissier, Marie-Christophe ;
Assier, Eric .
FRONTIERS IN IMMUNOLOGY, 2017, 8
[8]   Safety of combination therapy with two bDMARDs in patients with rheumatoid arthritis: A systematic review and meta-analysis [J].
Boleto, Goncalo ;
Kanagaratnam, Lukshe ;
Drame, Moustapha ;
Salmon, Jean-Hugues .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2019, 49 (01) :35-42
[9]   Autologous non-myeloablative haemopoietic stem-cell transplantation compared with pulse cyclophosphamide once per month for systemic sclerosis (ASSIST): an open-label, randomised phase 2 trial [J].
Burt, Richard K. ;
Shah, Sanjiv J. ;
Dill, Karin ;
Grant, Thomas ;
Gheorghiade, Mihai ;
Schroeder, James ;
Craig, Robert ;
Hirano, Ikuo ;
Marshall, Karin ;
Ruderman, Eric ;
Jovanovic, Borko ;
Milanetti, Francesca ;
Jain, Sandeep ;
Boyce, Kristin ;
Morgan, Amy ;
Carr, James ;
Barr, Walter .
LANCET, 2011, 378 (9790) :498-506
[10]   Efficacy and Safety of ABBV-3373, a Novel Anti-Tumor Necrosis Factor Glucocorticoid Receptor Modulator Antibody-Drug Conjugate, in Adults with Moderate-to-Severe Rheumatoid Arthritis Despite Methotrexate Therapy: A Randomized, Double-Blind, Active-Controlled Proof-of-Concept Phase IIa Trial [J].
Buttgereit, Frank ;
Aelion, Jacob ;
Rojkovich, Bernadette ;
Zubrzycka-Sienkiewicz, Anna ;
Chen, Su ;
Yang, Yang ;
Arikan, Dilek ;
D'Cunha, Ronilda ;
Pang, Yinuo ;
Kupper, Hartmut ;
Radstake, Timothy ;
Amital, Howard .
ARTHRITIS & RHEUMATOLOGY, 2023, 75 (06) :879-889