Preclinical development of plant‐based oral immune modulatory therapy for haemophilia B

dc.contributor.authorSrinivasan, Aparajitha
dc.contributor.authorHerzog, Roland W.
dc.contributor.authorKhan, Imran
dc.contributor.authorSherman, Alexandra
dc.contributor.authorBertolini, Thais
dc.contributor.authorWynn, Tung
dc.contributor.authorDaniell, Henry
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2023-03-20T16:40:55Z
dc.date.available2023-03-20T16:40:55Z
dc.date.issued2021-10
dc.description.abstractAnti‐drug antibody (ADA) formation is a major complication in treatment of the X‐linked bleeding disorder haemophilia B (deficiency in coagulation factor IX, FIX). Current clinical immune tolerance protocols are often not effective due to complications such as anaphylactic reactions against FIX. Plant‐based oral tolerance induction may address this problem, as illustrated by the recent first regulatory approval of orally delivered plant cells to treat peanut allergy. Our previous studies showed that oral delivery of plant cells expressing FIX fused to the transmucosal carrier CTB (cholera toxin subunit B) in chloroplasts suppressed ADA in animals with haemophilia B. We report here creation of the first lettuce transplastomic lines expressing a coagulation factor, in the absence of antibiotic resistance gene. Stable integration of the CTB‐FIX gene and homoplasmy (transformation of ˜10 000 copies in each cell) were maintained in both T1 and T2 generation marker‐free plants. CTB‐FIX expression in lyophilized leaves of T1 and T2 marker‐free plants was 1.0–1.5 mg/g dry weight, confirming that the marker excision did not affect antigen levels. Oral administration of CTB‐FIX to Sprague Dawley rats at 0.25, 1 or 2.5 mg/kg did not produce overt adverse effects or toxicity. The no‐observed‐adverse‐effect level (NOAEL) is at least 2.5 mg/kg for a single oral administration in rats. Oral administration of CTB‐FIX at 0.3 or 1.47 mg/kg either mixed in food or as an oral suspension to Beagle dogs did not produce any observable toxicity. These toxicology studies should facilitate filing of regulatory approval documents and evaluation in haemophilia B patients.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationSrinivasan A, Herzog RW, Khan I, et al. Preclinical development of plant-based oral immune modulatory therapy for haemophilia B. Plant Biotechnol J. 2021;19(10):1952-1966. doi:10.1111/pbi.13608en_US
dc.identifier.urihttps://hdl.handle.net/1805/31972
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1111/pbi.13608en_US
dc.relation.journalPlant Biotechnology Journalen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourcePMCen_US
dc.subjectAntibiotic resistance free plantsen_US
dc.subjectAnaphylaxisen_US
dc.subjectOral protein drug deliveryen_US
dc.subjectTolerance inductionen_US
dc.subjectToxicologyen_US
dc.subjectRegulatory approvalen_US
dc.titlePreclinical development of plant‐based oral immune modulatory therapy for haemophilia Ben_US
dc.typeArticleen_US
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
PBI-19-1952.pdf
Size:
1.02 MB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.99 KB
Format:
Item-specific license agreed upon to submission
Description: