Abstract

The leishmanin skin test was used for almost a century to detect exposure and immunity to Leishmania, the causative agent of leishmaniasis, a major neglected tropical disease. Due to a lack of antigen used for the intradermal injection, the leishmanin skin test is no longer available. As leishmaniasis control programs are advancing and new vaccines are entering clinical trials, it is essential to re-introduce the leishmanin skin test. Here we establish a Leishmania donovani strain and describe the production, under Good Laboratory Practice conditions, of leishmanin soluble antigen used to induce the leishmanin skin test in animal models of infection and vaccination. Using a mouse model of cutaneous leishmaniasis and a hamster model of visceral leishmaniasis, soluble antigen induces a leishmanin skin test response following infection and vaccination with live attenuated Leishmania major (LmCen-/-). Both the CD4+ and CD8+ T-cells are necessary for the leishmanin skin test response. This study demonstrates the feasibility of large-scale production of leishmanin antigen addressing a major bottleneck for performing the leishmanin skin test in future surveillance and vaccine clinical trials.

As leishmaniasis control programs and new vaccines are advancing, it is necessary to re-introduce the leishmanin skin test to monitor transmission and immunity. This study describes the generation and validation of a new leishmanin skin test antigen for future re-introduction into endemic countries.

Details

Title
Production of leishmanin skin test antigen from Leishmania donovani for future reintroduction in the field
Author
Dey, Ranadhir 1   VIAFID ORCID Logo  ; Alshaweesh, Jalal 2 ; Singh, Kamaleshwar P. 3 ; Lypaczewski, Patrick 4   VIAFID ORCID Logo  ; Karmakar, Subir 3 ; Klenow, Laura 1 ; Paulini, Kayla 4   VIAFID ORCID Logo  ; Kaviraj, Swarnendu 3 ; Kamhawi, Shaden 5   VIAFID ORCID Logo  ; Valenzuela, Jesus G. 5   VIAFID ORCID Logo  ; Singh, Sanjay 3 ; Hamano, Shinjiro 2   VIAFID ORCID Logo  ; Satoskar, Abhay R. 6   VIAFID ORCID Logo  ; Gannavaram, Sreenivas 1   VIAFID ORCID Logo  ; Nakhasi, Hira L. 1   VIAFID ORCID Logo  ; Matlashewski, Greg 4   VIAFID ORCID Logo 

 Division of Emerging and Transfusion Transmitted Diseases, CBER, FDA, Silver Spring, USA (GRID:grid.290496.0) (ISNI:0000 0001 1945 2072) 
 Nagasaki University, Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273); Nagasaki University, The Joint Usage/Research Center on Tropical Disease, Institute of Tropical Medicine (NEKKEN), Nagasaki, Japan (GRID:grid.174567.6) (ISNI:0000 0000 8902 2273) 
 Gennova Biopharmaceuticals, Hinjawadi Phase II, Pune, India (GRID:grid.464807.9) (ISNI:0000 0004 1767 0246) 
 McGill University, Department of Microbiology and Immunology, Montreal, Canada (GRID:grid.14709.3b) (ISNI:0000 0004 1936 8649) 
 Vector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, NIH, Rockville, USA (GRID:grid.419681.3) (ISNI:0000 0001 2164 9667) 
 Ohio State University, Department of Pathology and Microbiology, Columbus, USA (GRID:grid.261331.4) (ISNI:0000 0001 2285 7943) 
Pages
7028
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2885386653
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.