New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus

被引:6
|
作者
Diethelm-Varela, Benjamin [1 ]
Soto, Jorge A. [1 ,2 ]
Riedel, Claudia A. [2 ]
Bueno, Susan M. [1 ]
Kalergis, Alexis M. [1 ,3 ]
机构
[1] Pontificia Univ Catolica Chile, Millennium Inst Immunol & Immunotherapy, Fac Ciencias Biol, Dept Genet Mol & Microbiol, Santiago, Chile
[2] Univ Andres Bello, Millennium Inst Immunol & Immunotherapy, Fac Ciencias Vida, Dept Ciencias Biol, Santiago, Chile
[3] Pontificia Univ Catolica Chile, Fac Med, Dept Endocrinol, Santiago, Chile
来源
关键词
prevention; treatment; antibodies; respiratory syncytial virus; HUMANIZED MONOCLONAL-ANTIBODY; CELL-MEDIATED CYTOTOXICITY; PRETERM INFANTS; FC-RECEPTORS; HIGH-RISK; THERAPEUTIC ANTIBODIES; NUCLEOCAPSID PROTEIN; VACCINE CANDIDATE; DNA IMMUNIZATION; IMMUNE-RESPONSE;
D O I
10.2147/IDR.S379660
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Since the discovery of the human respiratory syncytial virus (hRSV), multiple research efforts have been conducted to develop vaccines and treatments capable of reducing the risk of severe disease, hospitalization, long-term sequelae, and death from this pathogen in susceptible populations. In this sense, therapies specifically directed against hRSV are mainly based on monoclonal and polyclonal antibodies such as intravenous IgG (IVIG)-RSV and the monoclonal antibody palivizumab. However, these therapies are associated with significant limitations, including the need for the recruitment of a high number of convalescent volunteers who donate blood to procure IVIG-RSV and the costs associated with the need for repeated administrations of palivizumab. These limitations render this product not cost-effective for populations other than high-risk patients. These problems have underscored that it is still necessary to identify new safe and effective therapies for human use. However, these new therapies must benefit from a comparatively cheap production cost and the opportunity to be available to the high-risk population and anyone who requires treatment. Here, we review the different antibodies used to prevent the pathology caused by hRSV infection, highlighting therapies currently approved for human use and their clinical value. Also, the new, most promising candidates based on preclinical studies and clinical trial results are revised.
引用
收藏
页码:2061 / 2074
页数:14
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