Human Milk Oligosaccharides as Promising Antivirals

被引:118
作者
Morozov, Vasily [1 ]
Hansman, Grant [2 ,3 ]
Hanisch, Franz-Georg [4 ]
Schroten, Horst [1 ]
Kunz, Clemens [5 ]
机构
[1] Heidelberg Univ, Pediat Infect Dis Unit, Univ Childrens Hosp Mannheim, Heidelberg, Germany
[2] Heidelberg Univ, Schaller Res Grp, Heidelberg, Germany
[3] DKFZ, Heidelberg, Germany
[4] Univ Cologne, Fac Med, Inst Biochem 2, Cologne, Germany
[5] Justus Liebig Univ Giessen, Inst Nutr Sci, Giessen, Germany
关键词
antivirals; breast milk; human milk oligosaccharides; viral infection; BLOOD GROUP ANTIGENS; RECEPTOR-BINDING SPECIFICITY; STRUCTURAL BASIS; SIALIC-ACID; DC-SIGN; ROTAVIRUS GASTROENTERITIS; CARBOHYDRATE MICROARRAYS; NOROVIRUS INHIBITION; URINARY-EXCRETION; ESCHERICHIA-COLI;
D O I
10.1002/mnfr.201700679
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Human milk oligosaccharides (HMOs) are diverse unconjugated carbohydrates that are highly abundant in human breast milk. These glycans are investigated in the context of exhibiting multiple functions in infant growth and development. They seem to provide protection against infectious diseases, including a number of poorly manageable viral infections. Although the potential mechanism of the HMO antiviral protection is rather broad, much of the current experimental work has focused on studying of HMO antiadhesive properties. HMOs may mimic structures of viral receptors and block adherence to target cells, thus preventing infection. Still, the potential of HMOs as a source for new antiviral drugs is relatively unexploited. This can be partly attributed to the extreme complexity of the virus-carbohydrate interactions and technical difficulties in HMO isolation, characterization, and manufacturing procedures. Fortunately, we are currently entering a period of major technological advances that have enabled deeper insights into carbohydrate mediated viral entry, rational selection of HMOs as anti-entry inhibitors, and even evaluation of individual synthetic HMO structures. Here, we provide an up-to-date review on glycan binding studies for rotaviruses, noroviruses, influenza viruses, and human immunodeficiency viruses. We also discuss the preventive and therapeutic potential of HMOs as anti-entry inhibitors and address challenges on the route from fundamental studies to clinical trials.
引用
收藏
页数:14
相关论文
共 135 条
[1]   Rotavirus Entry: a Deep Journey into the Cell with Several Exits [J].
Arias, Carlos F. ;
Silva-Ayala, Daniela ;
Lopez, Susana .
JOURNAL OF VIROLOGY, 2015, 89 (02) :890-893
[2]   Physiology of Consumption of Human Milk Oligosaccharides by Infant Gut-associated Bifidobacteria [J].
Asakuma, Sadaki ;
Hatakeyama, Emi ;
Urashima, Tadasu ;
Yoshida, Erina ;
Katayama, Takane ;
Yamamoto, Kenji ;
Kumagai, Hidehiko ;
Ashida, Hisashi ;
Hirose, Junko ;
Kitaoka, Motomitsu .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (40) :34583-34592
[3]   Structural Characterization by Multistage Mass Spectrometry (MSn) of Human Milk Glycans Recognized by Human Rotaviruses [J].
Ashline, David J. ;
Yu, Ying ;
Lasanajak, Yi ;
Song, Xuezheng ;
Hu, Liya ;
Ramani, Sasirekha ;
Prasad, Venkataram ;
Estes, Mary K. ;
Cummings, Richard D. ;
Smith, David F. ;
Reinhold, Vernon N. .
MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (11) :2961-2974
[4]   Norovirus Vaccine against Experimental Human Norwalk Virus Illness [J].
Atmar, Robert L. ;
Bernstein, David I. ;
Harro, Clayton D. ;
Al-Ibrahim, Mohamed S. ;
Chen, Wilbur H. ;
Ferreira, Jennifer ;
Estes, Mary K. ;
Graham, David Y. ;
Opekun, Antone R. ;
Richardson, Charles ;
Mendelman, Paul M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (23) :2178-2187
[5]  
Bekdas M, 2014, ARCH ARGENT PEDIATR, V112, P345, DOI [10.5546/aap.2014.eng.345, 10.5546/aap.2014.345]
[6]   Structural requirements for the assembly of Norwalk virus-like particles [J].
Bertolotti-Ciarlet, A ;
White, LJ ;
Chen, R ;
Prasad, BVV ;
Estes, MK .
JOURNAL OF VIROLOGY, 2002, 76 (08) :4044-4055
[7]   High-throughput mass finger printing and Lewis blood group assignment of human milk oligosaccharides [J].
Blank, Dennis ;
Gebhardt, Sabine ;
Maass, Kai ;
Lochnit, Gunter ;
Dotz, Viktoria ;
Blank, Jennifer ;
Geyer, Rudolf ;
Kunz, Clemens .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 401 (08) :2495-2510
[8]   High-throughput X-ray crystallography for drug discovery [J].
Blundell, TL ;
Patel, S .
CURRENT OPINION IN PHARMACOLOGY, 2004, 4 (05) :490-496
[9]   Inhibition of monocyte, lymphocyte, and neutrophil adhesion to endothelial cells by human milk oligosaccharides [J].
Bode, L ;
Kunz, C ;
Muhly-Reinholz, M ;
Mayer, K ;
Seeger, W ;
Rudloff, S .
THROMBOSIS AND HAEMOSTASIS, 2004, 92 (06) :1402-1410
[10]   Human milk oligosaccharides reduce platelet-neutrophil complex formation leading to a decrease in neutrophil β2 integrin expression [J].
Bode, L ;
Rudloff, S ;
Kunz, C ;
Strobel, S ;
Klein, N .
JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 76 (04) :820-826