Back to Search Start Over

Pharmacodynamics of ATI-2307 in a rabbit model of cryptococcal meningoencephalitis.

Authors :
Giamberardino CD
Tenor JL
Toffaletti DL
Palmucci JR
Schell W
Boua J-VK
Marius C
Stott KE
Steele SL
Hope W
Cilla D
Perfect JR
Source :
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2023 Oct 18; Vol. 67 (10), pp. e0081823. Date of Electronic Publication: 2023 Sep 20.
Publication Year :
2023

Abstract

Cryptococcal meningoencephalitis (CM) is a devastating fungal disease with high morbidity and mortality. The current regimen that is standard-of-care involves a combination of three different drugs administered for up to one year. There is a critical need for new therapies due to both toxicity and inadequate fungicidal activity of the currently available antifungal drugs. ATI-2307 is a novel aryl amidine that disrupts the mitochondrial membrane potential and inhibits the respiratory chain complexes of fungi-it thus represents a new mechanism for direct antifungal action. Furthermore, ATI-2307 selectively targets fungal mitochondria via a fungal-specific transporter that is not present in mammalian cells. It has very potent in vitro anticryptococcal activity. In this study, the efficacy of ATI-2307 was tested in a rabbit model of CM. ATI-2307 demonstrated significant fungicidal activity at dosages between 1 and 2 mg/kg/d, and these results were superior to fluconazole and similar to amphotericin B treatment. When ATI-2307 was combined with fluconazole, the antifungal effect was greater than either therapy alone. While ATI-2307 has potent anticryptococcal activity in the subarachnoid space, its ability to reduce yeasts in the brain parenchyma was relatively less over the same study period. This new drug, with its unique mechanism of fungicidal action and ability to positively interact with an azole, has demonstrated sufficient anticryptococcal potential in this experimental setting to be further evaluated in clinical studies.<br />Competing Interests: J.R.P. receives grants/consulting support from Appili, Pfizer, Matinas, Cidara, Scynexis, and F2G. C.D.G. has received salary support on projects funded by Amplyx, Appili, Pfizer, Astellas, Minnetronix, Sfunga, and Interventional Analgesix and owns less than $5,000 of stock in GSK, Bristol-Meyers Squibb, Affimed, Nkarta, Actinium. William Hope holds or has recently held research grants with UKRI, F2G, Spero Therapeutics, Antabio, Pfizer, Bugworks, Phico Therapeutics, BioVersys, GARDP, and NAEJA-RGM. He is (or has recently been) a consultant for Appili Therapeutics, F2G, Spero Therapeutics, NAEJA-RGM, Centauri, Pfizer, Phico Therapeutics, and VenatoRx. He is a member of the Specialist Advisory Committee for GARDP and the Specialty National Co-lead for Infectious Diseases for the National Institute of Health Research (NIHR).

Details

Language :
English
ISSN :
1098-6596
Volume :
67
Issue :
10
Database :
MEDLINE
Journal :
Antimicrobial agents and chemotherapy
Publication Type :
Academic Journal
Accession number :
37728934
Full Text :
https://doi.org/10.1128/aac.00818-23