Gene targeting as a therapeutic avenue in diseases mediated by the complement alternative pathway

被引:19
作者
Dreismann, Anna K. [1 ]
Hallam, Thomas M. [1 ]
Tam, Lawrence C. S. [1 ]
Nguyen, Calvin, V [1 ]
Hughes, Jane P. [1 ]
Ellis, Scott [1 ]
Harris, Claire L. [1 ]
机构
[1] Gyroscope Therapeut Ltd, London, England
关键词
antisense oligonucleotide; clinical trials; complement; gene therapy; preclinical models; RNAi; MEMBRANE ATTACK COMPLEX; IMMUNE-RESPONSE; ANTISENSE OLIGONUCLEOTIDES; MACULAR DEGENERATION; CHOROIDAL NEOVASCULARIZATION; AAV SEROTYPES; FACTOR-B; SIRNA; DELIVERY; ACTIVATION;
D O I
10.1111/imr.13149
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The complement alternative pathway (AP) is implicated in numerous diseases affecting many organs, ranging from the rare hematological disease paroxysmal nocturnal hemoglobinuria (PNH), to the common blinding disease age-related macular degeneration (AMD). Critically, the AP amplifies any activating trigger driving a downstream inflammatory response; thus, components of the pathway have become targets for drugs of varying modality. Recent validation from clinical trials using drug modalities such as inhibitory antibodies has paved the path for gene targeting of the AP or downstream effectors. Gene targeting in the complement field currently focuses on supplementation or suppression of complement regulators in AMD and PNH, largely because the eye and liver are highly amenable to drug delivery through local (eye) or systemic (liver) routes. Targeting the liver could facilitate treatment of numerous diseases as this organ generates most of the systemic complement pool. This review explains key concepts of RNA and DNA targeting and discusses assets in clinical development for the treatment of diseases driven by the alternative pathway, including the RNA-targeting therapeutics ALN-CC5, ARO-C3, and IONIS-FB-LRX, and the gene therapies GT005 and HMR59. These therapies are but the spearhead of potential drug candidates that might revolutionize the field in coming years.
引用
收藏
页码:402 / 419
页数:18
相关论文
共 151 条
[41]   A brief account of viral vectors and their promise for gene therapy [J].
Finer, M. ;
Glorioso, J. .
GENE THERAPY, 2017, 24 (01) :1-2
[42]   Advanced siRNA Designs Further Improve In Vivo Performance of GaINAc-siRNA Conjugates [J].
Foster, Donald J. ;
Brown, Christopher R. ;
Shaikh, Sarfraz ;
Trapp, Casey ;
Schlegel, Mark K. ;
Qian, Kun ;
Sehgal, Alfica ;
Rajeev, Kallanthottathil G. ;
Jadhav, Vasant ;
Manoharan, Muthiah ;
Kuchimanchi, Satya ;
Maier, Martin A. ;
Milstein, Stuart .
MOLECULAR THERAPY, 2018, 26 (03) :708-717
[43]   CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia [J].
Frangoul, H. ;
Altshuler, D. ;
Cappellini, M. D. ;
Chen, Y-S ;
Domm, J. ;
Eustace, B. K. ;
Foell, J. ;
de la Fuente, J. ;
Grupp, S. ;
Handgretinger, R. ;
Ho, T. W. ;
Kattamis, A. ;
Kernytsky, A. ;
Lekstrom-Himes, J. ;
Li, A. M. ;
Locatelli, F. ;
Mapara, M. Y. ;
de Montalembert, M. ;
Rondelli, D. ;
Sharma, A. ;
Sheth, S. ;
Soni, S. ;
Steinberg, M. H. ;
Wall, D. ;
Yen, A. ;
Corbacioglu, S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (03) :252-260
[44]   A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants [J].
Fritsche, Lars G. ;
Igl, Wilmar ;
Bailey, Jessica N. Cooke ;
Grassmann, Felix ;
Sengupta, Sebanti ;
Bragg-Gresham, Jennifer L. ;
Burdon, Kathryn P. ;
Hebbring, Scott J. ;
Wen, Cindy ;
Gorski, Mathias ;
Kim, Ivana K. ;
Cho, David ;
Zack, Donald ;
Souied, Eric ;
Scholl, Hendrik P. N. ;
Bala, Elisa ;
Lee, Kristine E. ;
Hunter, David J. ;
Sardell, Rebecca J. ;
Mitchell, Paul ;
Merriam, Joanna E. ;
Cipriani, Valentina ;
Hoffman, Joshua D. ;
Schick, Tina ;
Lechanteur, Yara T. E. ;
Guymer, Robyn H. ;
Johnson, Matthew P. ;
Jiang, Yingda ;
Stanton, Chloe M. ;
Buitendijk, Gabrielle H. S. ;
Zhan, Xiaowei ;
Kwong, Alan M. ;
Boleda, Alexis ;
Brooks, Matthew ;
Gieser, Linn ;
Ratnapriya, Rinki ;
Branham, Kari E. ;
Foerster, Johanna R. ;
Heckenlively, John R. ;
Othman, Mohammad I. ;
Vote, Brendan J. ;
Liang, Helena Hai ;
Souzeau, Emmanuelle ;
McAllister, Ian L. ;
Isaacs, Timothy ;
Hall, Janette ;
Lake, Stewart ;
Mackey, David A. ;
Constable, Ian J. ;
Craig, Jamie E. .
NATURE GENETICS, 2016, 48 (02) :134-143
[45]   Repair of a Site-Specific DNA Cleavage: Old-School Lessons for Cas9-Mediated Gene Editing [J].
Gallagher, Danielle N. ;
Haber, James E. .
ACS CHEMICAL BIOLOGY, 2018, 13 (02) :397-405
[46]   The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment [J].
Geerlings, Maartje J. ;
de Jong, Eiko K. ;
den Hollander, Anneke I. .
MOLECULAR IMMUNOLOGY, 2017, 84 :65-76
[47]   Contribution of animal models to the mechanistic understanding of Alternative Pathway and Amplification Loop (AP/AL)-driven Complement-mediated Diseases [J].
Gibson, Beth G. ;
Cox, Thomas E. ;
Marchbank, Kevin J. .
IMMUNOLOGICAL REVIEWS, 2023, 313 (01) :194-216
[48]   E Pluribus Unum: 50 Years of Research, Millions of Viruses, and One Goal-Tailored Acceleration of AAV Evolution [J].
Grimm, Dirk ;
Zolotukhin, Sergei .
MOLECULAR THERAPY, 2015, 23 (12) :1819-1831
[49]  
Grossman TR, 2017, MOL VIS, V23, P561
[50]   PRELP Protein Inhibits the Formation of the Complement Membrane Attack Complex [J].
Happonen, Kaisa E. ;
Furst, Camilla Melin ;
Saxne, Tore ;
Heinegard, Dick ;
Blom, Anna M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (11) :8092-8100