Controlling Rotavirus-associated diarrhea: Could single-domain antibody fragments make the difference?

被引:19
作者
Maffey, Lucia [1 ]
Vega, Celina G. [1 ]
Parreno, Viviana [1 ]
Garaicoechea, Lorena [1 ]
机构
[1] INTA Castelar, Ctr Invest Ciencias Vet & Agron, Inst Virol, Buenos Aires, DF, Argentina
来源
REVISTA ARGENTINA DE MICROBIOLOGIA | 2015年 / 47卷 / 04期
关键词
Rotavirus; Neonatal diarrhea; VHHs; Single domain antibody fragments; Nanobodies; SACCHAROMYCES-BOULARDII; DOUBLE-BLIND; IN-VITRO; CONFER PROTECTION; IMMUNE-RESPONSES; CONTROLLED-TRIAL; VACCINE; CHILDREN; EFFICACY; PIG;
D O I
10.1016/j.ram.2015.09.005
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Group A Rotavirus (RVA) remains a leading cause of severe diarrhea and child mortality. The variable domain of camelid heavy chain antibodies (VHH) display potent antigen-binding capacity, have low production costs and are suitable for oral therapies. Two sets of anti-RVA VHHs have been developed: ARP1-ARP3; 2KD1-3B2. Here, we explore the potential of both sets as a prevention strategy complementary to vaccination and a treatment option against RVA-associated diarrhea in endangered populations. Both sets have been expressed in multiple production systems, showing extensive neutralizing capacity against strains of RVA in vitro. They were also tested in the neonatal mouse model with various degrees of success in preventing or treating RVA-induced diarrhea. Interestingly, mitigation of the symptoms was also achieved with freeze-dried ARP1, so that it could be applied in areas where cold chains are difficult to maintain. 3B2 was tested in a pre-clinical trial involving gnotobiotic piglets where it conferred complete protection against RVA-induced diarrhea. ARP1 was used in the first clinical trial for anti-RVA VHHs, successfully reducing stool output in infants with RVA diarrhea, with no detected side effects. (C) 2015 Asociacion Argentina de Microbiologia. Published by Elsevier Espana, S.L.U.
引用
收藏
页码:368 / 379
页数:12
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