A Novel, Orally Delivered Antibody Therapy and Its Potential to PreventClostridioides difficileInfection in Pre-clinical Models

被引:12
作者
Roberts, April K. [1 ]
Harris, Hannah C. [2 ]
Smith, Michael [1 ]
Giles, Joanna [3 ]
Polak, Oktawia [3 ]
Buckley, Anthony M. [2 ]
Clark, Emma [2 ]
Ewin, Duncan [2 ]
Moura, Ines B. [2 ]
Spitall, William [2 ]
Shone, Clifford C. [1 ]
Wilcox, Mark [2 ,4 ]
Chilton, Caroline [2 ]
Donev, Rossen [3 ]
机构
[1] Publ Hlth England, Natl Infect Serv, Toxins Grp, Porton Down, England
[2] Univ Leeds, Leeds Inst Med Res, Fac Med & Hlth, Leeds, W Yorkshire, England
[3] MicroPharm Ltd, Newcastle Emlyn, Wales
[4] Leeds Gen Infirm, Leeds Teaching Hosp NHS Trust, Dept Microbiol, Leeds, W Yorkshire, England
来源
FRONTIERS IN MICROBIOLOGY | 2020年 / 11卷
基金
“创新英国”项目;
关键词
Clostridioides difficileinfection (CDI); immunotherapy of CDI; oral antibodies; formulation protecting antibodies from digestion; inactivation; in vivohamster model of CDI; in vitrohuman gut model of CDI; CLOSTRIDIUM-DIFFICILE; TOXIN-B; IN-VITRO; OVINE ANTIBODY; BOWMAN-BIRK; GUT MODEL; INFECTION; VANCOMYCIN; DISEASE; PREVENT;
D O I
10.3389/fmicb.2020.578903
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Clostridioides difficileinfection (CDI) is a toxin-mediated infection in the gut and a major burden on healthcare facilities worldwide. We rationalized that it would be beneficial to design an antibody therapy that is delivered to, and is active at the site of toxin production, rather than neutralizing the circulating and luminal toxins after significant damage of the layers of the intestines has occurred. Here we describe a highly potent therapeutic, OraCAb, with high antibody titers and a formulation that protects the antibodies from digestion/inactivation in the gastrointestinal tract. The potential of OraCAb to prevent CDI in anin vivohamster model and anin vitrohuman colon model was assessed. In the hamster model we optimized the ratio of the antibodies against each of the toxins produced byC. difficile(Toxins A and B). The concentration of immunoglobulins that is effective in a hamster model of CDI was determined. A highly significant difference in animal survival for those given an optimized OraCAb formulation versus an untreated control group was observed. This is the first study testing the effect of oral antibodies for treatment of CDI in anin vitrogut model seeded with a human fecal inoculum. Treatment with OraCAb successfully neutralized toxin production and did not interfere with the colonic microbiota in this model. Also, treatment with a combination of vancomycin and OraCAb prevented simulated CDI recurrence, unlike vancomycin therapy alone. These data demonstrate the efficacy of OraCAb formulation for the treatment of CDI in pre-clinical models.
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页数:16
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