Clinical use of adjuvants in allergen-immunotherapy

被引:46
作者
Klimek, Ludger [1 ]
Schmidt-Weber, Carsten B. [2 ,3 ]
Kramer, Matthias F. [4 ]
Skinner, Murray A. [5 ]
Heath, Matthew D. [5 ]
机构
[1] Ctr Rhinol & Allergol, Quellen 10, D-65183 Wiesbaden, Germany
[2] Tech Univ, Ctr Allergy & Environm ZAUM, Munich, Germany
[3] Helmholtz Ctr Munich, Munich, Germany
[4] Bencard Allergie GmbH, Munich, Germany
[5] Allergy Therapeut Ltd, Worthing, England
关键词
Allergic rhinitis; adjuvant; vaccine; Monophosphoryl Lipid A; CpG-motifs; nanoparticles; microcrystalline tyrosine; subcutaneous; MONOPHOSPHORYL-LIPID-A; VIRUS-LIKE PARTICLES; PEANUT ORAL IMMUNOTHERAPY; IMMUNE-RESPONSES; DENDRITIC CELLS; STRUCTURAL BASIS; APOPTOTIC CELLS; L-TYROSINE; VACCINE; ALUMINUM;
D O I
10.1080/1744666X.2017.1292133
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Allergen-specific Immunotherapy (AIT) is the only available treatment aimed to tackle the underlying causes of allergy. The active components of subcutaneous vaccines traditionally consist of natural or modified allergen extracts which can be combined with adjuvant platforms. In recent years new targets have been further developed in an attempt to raise the safety and efficacy profile of AIT.Areas covered: In this review, we discuss the desirable attributes of adjuvants and delivery systems from empiricism to rational design, for current and future clinical applications in AIT.Expert commentary: The introduction of novel adjuvants, in combination with active targets, has been demonstrated to reduce symptoms of AIT, increase clinical efficacy of allergy treatment and reduce the number of doses. The evolution of vaccine development for AIT is entering a phase of scientific progress that challenges dogmas. Over the past century the traditional concept of immunotherapy, entailing long-course administration of native extract preparations and first generation adjuvants, has seen evolution in the past decade from proof-of-concept to clinical development pipelines encompassing the advent of second generation adjuvants and delivery systems forming essential components of modern AIT development.
引用
收藏
页码:599 / 610
页数:12
相关论文
共 103 条
[1]   Mechanisms of allergen-specific immunotherapy and immune tolerance to allergens [J].
Akdis, Cezmi A. ;
Akdis, Muebeccel .
WORLD ALLERGY ORGANIZATION JOURNAL, 2015, 8
[2]  
Alam S., 2014, Curr Treat Options Allergy, V1, P39, DOI [10.1007/s40521-013-0008-3, DOI 10.1007/S40521-013-0008-3]
[3]   Physicochemical characterization and biological activity of synthetic TLR4 agonist formulations [J].
Anderson, Ryan C. ;
Fox, Christopher B. ;
Dutill, Timothy S. ;
Shaverdian, Narek ;
Evers, Tara L. ;
Poshusta, Garrett R. ;
Chesko, James ;
Coler, Rhea N. ;
Friede, Martin ;
Reed, Steven G. ;
Vedvick, Thomas S. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 75 (01) :123-132
[4]  
[Anonymous], US PATENT, Patent No. [20030236211 A1, 20030236211]
[5]  
[Anonymous], US Patent, Patent No. [8765721 B2, 8765721]
[6]  
[Anonymous], Composition comprising phosphatidyl serine and an antigen or allergen and the use thereof, Patent No. [WO 2006059142 A1, 2006059142]
[7]  
[Anonymous], 2011, EUROPEAN PHARMACOPOE, V2537, P3690
[8]   Conformationally Constrained Lipid A Mimetics for Exploration of Structural Basis of TLR4/MD-2 Activation by Lipopolysaccharide [J].
Artner, Daniel ;
Oblak, Alja ;
Ittig, Simon ;
Garate, Jose Antonio ;
Horvat, Simon ;
Arrieumerlou, Cecile ;
Hofinger, Andreas ;
Oostenbrink, Chris ;
Jerala, Roman ;
Kosma, Paul ;
Zamyatina, Alla .
ACS CHEMICAL BIOLOGY, 2013, 8 (11) :2423-2432
[9]   Mechanisms of action of adjuvants [J].
Awate, Sunita ;
Babiuk, Lorne A. ;
Mutwiri, George .
FRONTIERS IN IMMUNOLOGY, 2013, 4
[10]   Allergen-specific immunotherapy: is it vaccination against toxins after all? [J].
Bachmann, M. F. ;
Kundig, T. M. .
ALLERGY, 2017, 72 (01) :13-23