1. A single dose of antibody-drug conjugate cures a stage 1 model of African trypanosomiasis.
- Author
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MacGregor P, Gonzalez-Munoz AL, Jobe F, Taylor MC, Rust S, Sandercock AM, Macleod OJS, Van Bocxlaer K, Francisco AF, D'Hooge F, Tiberghien A, Barry CS, Howard P, Higgins MK, Vaughan TJ, Minter R, and Carrington M
- Subjects
- Animals, Antibodies, Monoclonal chemistry, Antiprotozoal Agents chemistry, Benzodiazepines chemistry, Female, Humans, Mice, Mice, Inbred BALB C, Pyrroles chemistry, Trypanosoma brucei brucei drug effects, Trypanosomiasis, African parasitology, Antibodies, Monoclonal administration & dosage, Antiprotozoal Agents administration & dosage, Benzodiazepines administration & dosage, Pyrroles administration & dosage, Trypanosomiasis, African drug therapy
- Abstract
Infections of humans and livestock with African trypanosomes are treated with drugs introduced decades ago that are not always fully effective and often have severe side effects. Here, the trypanosome haptoglobin-haemoglobin receptor (HpHbR) has been exploited as a route of uptake for an antibody-drug conjugate (ADC) that is completely effective against Trypanosoma brucei in the standard mouse model of infection. Recombinant human anti-HpHbR monoclonal antibodies were isolated and shown to be internalised in a receptor-dependent manner. Antibodies were conjugated to a pyrrolobenzodiazepine (PBD) toxin and killed T. brucei in vitro at picomolar concentrations. A single therapeutic dose (0.25 mg/kg) of a HpHbR antibody-PBD conjugate completely cured a T. brucei mouse infection within 2 days with no re-emergence of infection over a subsequent time course of 77 days. These experiments provide a demonstration of how ADCs can be exploited to treat protozoal diseases that desperately require new therapeutics., Competing Interests: A.L.G.M., S.R., A.M.S., T.J.V. and R.M. are employees of Medimmune. F.D., C.S.B. and P.H. are employees of Spirogen. Toxins SG3199/SG3249 and SG3552/SG3376 are subject to international patents, WO 2011/130598 A1 and WO 2014/140862 A2, respectively.
- Published
- 2019
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