| Literature DB >> 33431825 |
Helen Ashwin1, Jovana Sadlova2, Barbora Vojtkova2, Tomas Becvar2, Patrick Lypaczewski3, Eli Schwartz4, Elizabeth Greensted1, Katrien Van Bocxlaer1, Marion Pasin5, Kai S Lipinski5, Vivak Parkash1, Greg Matlashewski3, Alison M Layton1, Charles J Lacey1, Charles L Jaffe6, Petr Volf7, Paul M Kaye8.
Abstract
Leishmaniasis is widely regarded as a vaccine-preventable disease, but the costs required to reach pivotal Phase 3 studies and uncertainty about which candidate vaccines should be progressed into human studies significantly limits progress in vaccine development for this neglected tropical disease. Controlled human infection models (CHIMs) provide a pathway for accelerating vaccine development and to more fully understand disease pathogenesis and correlates of protection. Here, we describe the isolation, characterization and GMP manufacture of a new clinical strain of Leishmania major. Two fresh strains of L. major from Israel were initially compared by genome sequencing, in vivo infectivity and drug sensitivity in mice, and development and transmission competence in sand flies, allowing one to be selected for GMP production. This study addresses a major roadblock in the development of vaccines for leishmaniasis, providing a key resource for CHIM studies of sand fly transmitted cutaneous leishmaniasis.Entities:
Year: 2021 PMID: 33431825 DOI: 10.1038/s41467-020-20569-3
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919