Glycoconjugate vaccines: current approaches towards faster vaccine design

被引:108
作者
Micoli, Francesca [1 ]
Del Bino, Linda [2 ]
Alfini, Renzo [1 ]
Carboni, Filippo [2 ]
Romano, Maria Rosaria [2 ]
Adamo, Roberto [2 ]
机构
[1] GSK Vaccines Inst Global Hlth Srl, Technol Platform, Siena, Italy
[2] GSK, Res Ctr, Siena, Italy
关键词
Carbohydrates; glycoconjugates; glycoengineering; liposomes; outer membrane vesicles; synthetic oligosaccharides; vaccines; SOLID-PHASE SYNTHESIS; PNEUMOCOCCAL POLYSACCHARIDE VACCINE; NEISSERIA-MENINGITIDIS SEROGROUP; OUTER-MEMBRANE VESICLES; CANDIDATE BIOCONJUGATE VACCINE; VI-CAPSULAR POLYSACCHARIDE; N-LINKED GLYCOSYLATION; CONJUGATE VACCINE; GENERALIZED MODULES; CHEMOENZYMATIC SYNTHESIS;
D O I
10.1080/14760584.2019.1657012
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: Over the last decades, glycoconjugate vaccines have been proven to be a successful strategy to prevent infectious diseases. Many diseases remain to be controlled, especially in developing countries, and emerging antibiotic-resistant bacteria present an alarming public-health threat. The increasing complexity of future vaccines, and the need to accelerate development processes have triggered the development of faster approaches to glycoconjugate vaccines design. Areas covered: This review provides an overview of recent progress in glycoconjugation technologies toward faster vaccine design. Expert opinion: Among the different emerging approaches, glycoengineering has the potential to combine glycan assembly and conjugation to carrier systems (such as proteins or outer membrane vesicles) in one step, resulting in a simplified manufacturing process and fewer analytical controls. Chemical and enzymatic strategies, and their automation can facilitate glycoepitope identification for vaccine design. Other approaches, such as the liposomal encapsulation of polysaccharides, potentially enable fast and easy combination of numerous antigens in the same formulation. Additional progress is envisaged in the near future, and some of these systems still need to be further validated in humans. In parallel, new strategies are needed to accelerate the vaccine development process, including the associated clinical trials, up to vaccine release onto the market.
引用
收藏
页码:881 / 895
页数:15
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