The use of sialidase therapy for respiratory viral infections

被引:38
作者
Nicholls, John M. [1 ]
Moss, Ronald B. [2 ]
Haslam, Stuart M. [3 ]
机构
[1] Univ Hong Kong, Dept Pathol, Pok Fu Lam, Hong Kong, Peoples R China
[2] Ansun BioPharma, San Diego, CA 92121 USA
[3] Univ London Imperial Coll Sci Technol & Med, Fac Nat Sci, Div Mol Biosci, London SW7 2AZ, England
关键词
Influenza; Antiviral therapy; Sialidase; Sialic acid; INFLUENZA-VIRUS INFECTION; HUMAN AIRWAY EPITHELIUM; HOST-CELL RECEPTOR; FUSION PROTEIN; STREPTOCOCCUS-PNEUMONIAE; DROPLET TRANSMISSION; ACTINOMYCES-VISCOSUS; PARAINFLUENZA VIRUS; EXPERIMENTAL DRUG; O-ACETYLATION;
D O I
10.1016/j.antiviral.2013.04.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
DAS181 is an inhaled bacterial sialidase which functions by removing sialic acid (Sia) from the surface of epithelial cells, preventing attachment and subsequent infection by respiratory viruses that utilize Sia as a receptor. DAS181 is typical of bacterial sialidases in cleaving Sia alpha 2-3 and Sia alpha 2-6 linkages, and it also has a demonstrated effect against acetylated and hydroxylated forms of Sia. The potency of the compound has been enhanced by coupling the active sialidase with an amphiregulin tag, allowing a longer duration of action and minimizing spread to the systemic circulation. DAS181 is now in Phase II development for the treatment of influenza, and it has also demonstrated activity in individual cases of parainfluenza in immunosuppressed patients. Continued evaluation of the roles and activities of bacterial sialidases is required to expand the range of successful antiviral therapies targeting Sia or its derivatives. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:401 / 409
页数:9
相关论文
共 101 条
[11]   Human rhinovirus 87 and enterovirus 68 represent a unique serotype with rhinovirus and enterovirus features [J].
Blomqvist, S ;
Savolainen, C ;
Råman, L ;
Roivainen, M ;
Hovi, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (11) :4218-4223
[12]   Cellular and molecular mechanisms of senescent erythrocyte phagocytosis by macrophages. A review [J].
Bratosin, D ;
Mazurier, J ;
Tissier, JP ;
Estaquier, J ;
Huart, JJ ;
Ameisen, JC ;
Aminoff, D ;
Montreuil, J .
BIOCHIMIE, 1998, 80 (02) :173-195
[13]   Deaths from bacterial pneumonia during 1918-19 influenza pandemic [J].
Brundage, John F. ;
Shanks, G. Dennis .
EMERGING INFECTIOUS DISEASES, 2008, 14 (08) :1193-1199
[14]   Diversity of the human erythrocyte membrane, sialic acids in relation with blood groups [J].
Bulai, T ;
Bratosin, D ;
Pons, A ;
Montreuil, J ;
Zanetta, JP .
FEBS LETTERS, 2003, 534 (1-3) :185-189
[15]   The multiple roles of amphiregulin in human cancer [J].
Busser, Benoit ;
Sancey, Lucie ;
Brambilla, Elisabeth ;
Coll, Jean-Luc ;
Hurbin, Amandine .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2011, 1816 (02) :119-131
[16]   Sialidase substrate specificity studies using chemoenzymatically synthesized sialosides containing C5-modified sialic acids [J].
Cao, Hongzhi ;
Li, Yanhong ;
Lau, Kam ;
Muthana, Saddam ;
Yu, Hai ;
Cheng, Jiansong ;
Chokhawala, Harshal A. ;
Sugiarto, Go ;
Zhang, Lei ;
Chen, Xi .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2009, 7 (24) :5137-5145
[17]   DAS181 Inhibits H5N1 Influenza Virus Infection of Human Lung Tissues [J].
Chan, Renee W. Y. ;
Chan, Michael C. W. ;
Wong, Adam C. N. ;
Karamanska, Rositsa ;
Dell, Anne ;
Haslam, Stuart M. ;
Sihoe, Alan D. L. ;
Chui, W. H. ;
Triana-Baltzer, Gallen ;
Li, Qixiang ;
Peiris, J. S. Malik ;
Fang, Fang ;
Nicholls, John M. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (09) :3935-3941
[18]   Advances in the Biology and Chemistry of Sialic Acids [J].
Chen, Xi ;
Varki, Ajit .
ACS CHEMICAL BIOLOGY, 2010, 5 (02) :163-176
[19]   Treatment of Parainfluenza 3 Infection With DAS181 in a Patient After Allogeneic Stem Cell Transplantation [J].
Chen, Yi-Bin ;
Driscoll, Jessica P. ;
McAfee, Steven L. ;
Spitzer, Thomas R. ;
Rosenberg, Eric S. ;
Sanders, Rebecca ;
Moss, Ronald B. ;
Fang, Fang ;
Marty, Francisco M. .
CLINICAL INFECTIOUS DISEASES, 2011, 53 (07) :E77-E80
[20]   THE SPECIFICITY OF VIRAL AND BACTERIAL SIALIDASES FOR ALPHA-(2-3)-LINKED AND ALPHA-(2-6)-LINKED SIALIC ACIDS IN GLYCOPROTEINS [J].
CORFIELD, AP ;
HIGA, H ;
PAULSON, JC ;
SCHAUER, R .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 744 (02) :121-126