Is There a Place for Chimeric Antigen Receptor-T Cells in the Treatment of Chronic Autoimmune Rheumatic Diseases?

被引:45
作者
Orvain, Cindy [1 ]
Boulch, Morgane [2 ]
Bousso, Philippe [3 ]
Allanore, Yannick [4 ,5 ]
Avouac, Jerome [4 ,5 ]
机构
[1] CNRS UMR8104, INSERM U1016, Inst Cochin, Paris, France
[2] Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
[3] Inst Pasteur, INSERM U1223, Equipe Labellisee Ligue Canc, Dynam Immune Responses Unit, Paris, France
[4] Univ Paris 05, Inst Cochin, CNRS UMR8104, INSERM U1016, Paris, France
[5] Hop Cochin, AP HP, Serv Rhumatol, Paris, France
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; LOW-DOSE IL-2; DOUBLE-BLIND; TARGETED THERAPY; DENDRITIC CELLS; IN-VITRO; RITUXIMAB; EFFICACY; AUTOANTIBODIES; ARTHRITIS;
D O I
10.1002/art.41812
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chimeric antigen receptor-T (CAR-T) cell therapy is based on specific targeting of tumor antigens, leading to lysis and destruction of tumor cells. The high potency of CAR-T cells in the management of B cell malignancies has been demonstrated. Following the success of this therapeutic strategy, new CAR-T cell-derived constructs that have the ability to eradicate pathogenic B cells or restore tolerance have been developed. The present review discusses how the knowledge and technology generated by the use of CAR-T cells may be translated and integrated into ongoing therapeutic strategies for autoimmune rheumatic diseases. To this end, we describe the details of CAR-T cell technology, as well as the meaningful achievements attained with the use of CAR-T cells in onco-hematology. In addition, we review the preliminary data obtained with CAR-T cells and their derivative constructs in experimental models of autoimmune diseases. Finally, we focus on how CAR-T cell engineering interferes with the pathogenesis of 3 chronic autoimmune rheumatic diseases-rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis-and discuss whether these constructs might yield greater efficacy and be associated with fewer adverse events compared to current treatment strategies.
引用
收藏
页码:1954 / 1965
页数:12
相关论文
共 82 条
[1]   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-+
[2]   Function of Novel Anti-CD19 Chimeric Antigen Receptors with Human Variable Regions Is Affected by Hinge and Transmembrane Domains [J].
Alabanza, Leah ;
Pegues, Melissa ;
Geldres, Claudia ;
Shi, Victoria ;
Wiltzius, Jed J. W. ;
Sievers, Stuart A. ;
Yang, Shicheng ;
Kochenderfer, James N. .
MOLECULAR THERAPY, 2017, 25 (11) :2452-2465
[3]   De Novo-Induced Self-Antigen-Specific Foxp3+ Regulatory T Cells Impair the Accumulation of Inflammatory Dendritic Cells in Draining Lymph Nodes [J].
Alissafi, Themis ;
Hatzioannou, Aikaterini ;
Ioannou, Marianna ;
Sparwasser, Tim ;
Gruen, Joachim R. ;
Gruetzkau, Andreas ;
Verginis, Panayotis .
JOURNAL OF IMMUNOLOGY, 2015, 194 (12) :5812-5824
[4]   B lymphocyte signaling established by the CD19/CD22 loop regulates autoimmunity in the tight-skin mouse [J].
Asano, N ;
Fujimoto, M ;
Yazawa, N ;
Shirasawa, S ;
Hasegawa, M ;
Okochi, H ;
Tamaki, K ;
Tedder, TF ;
Sato, S .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 165 (02) :641-650
[5]   Persistence of long-lived plasma cells and humoral immunity in individuals responding to CD19-directed CAR T-cell therapy [J].
Bhoj, Vijay G. ;
Arhontoulis, Dimitrios ;
Wertheim, Gerald ;
Capobianchi, James ;
Callahan, Colleen A. ;
Ellebrecht, Christoph T. ;
Obstfeld, Amrom E. ;
Lacey, Simon F. ;
Melenhorst, Jan J. ;
Nazimuddin, Farzana ;
Hwang, Wei-Ting ;
Maude, Shannon L. ;
Wasik, Mariusz A. ;
Bagg, Adam ;
Schuster, Stephen ;
Feldman, Michael D. ;
Porter, David L. ;
Grupp, Stephen A. ;
June, Carl H. ;
Milone, Michael C. .
BLOOD, 2016, 128 (03) :360-370
[6]   SAR3419: An Anti-CD19-Maytansinoid Immunoconjugate for the Treatment of B-Cell Malignancies [J].
Blanc, Veronique ;
Bousseau, Anne ;
Caron, Anne ;
Carrez, Chantal ;
Lutz, Robert J. ;
Lambert, John M. .
CLINICAL CANCER RESEARCH, 2011, 17 (20) :6448-6458
[7]   Suppression of Murine Colitis and its Associated Cancer by Carcinoembryonic Antigen-Specific Regulatory T Cells [J].
Blat, Dan ;
Zigmond, Ehud ;
Alteber, Zoya ;
Waks, Tova ;
Eshhar, Zelig .
MOLECULAR THERAPY, 2014, 22 (05) :1018-1028
[8]   Type 1 diabetes immunotherapy using polyclonal regulatory T cells [J].
Bluestone, Jeffrey A. ;
Buckner, Jane H. ;
Fitch, Mark ;
Gitelman, Stephen E. ;
Gupta, Shipra ;
Hellerstein, Marc K. ;
Herold, Kevan C. ;
Lares, Angela ;
Lee, Michael R. ;
Li, Kelvin ;
Liu, Weihong ;
Long, S. Alice ;
Masiello, Lisa M. ;
Vinh Nguyen ;
Putnam, Amy L. ;
Rieck, Mary ;
Sayre, Peter H. ;
Tang, Qizhi .
SCIENCE TRANSLATIONAL MEDICINE, 2015, 7 (315)
[9]   Characterization of inflammatory cell infiltrate of scleroderma skin: B cells and skin score progression [J].
Bosello, Silvia ;
Angelucci, Cristiana ;
Lama, Gina ;
Alivernini, Stefano ;
Proietti, Gabriella ;
Tolusso, Barbara ;
Sica, Gigliola ;
Gremese, Elisa ;
Ferraccioli, Gianfranco .
ARTHRITIS RESEARCH & THERAPY, 2018, 20
[10]   Eradication of systemic B-cell tumors by genetically targeted human T lymphocytes co-stimulated by CD80 and interleukin-15 [J].
Brentjens, RJ ;
Latouche, JB ;
Santos, E ;
Marti, F ;
Gong, MC ;
Lyddane, C ;
King, PD ;
Larson, S ;
Weiss, M ;
Rivière, I ;
Sadelain, M .
NATURE MEDICINE, 2003, 9 (03) :279-286