Identification of adjuvantic activity of amphotericin B in a novel, multiplexed, poly-TLR/NLR high-throughput screen

Alex C.D. Salyer, Giuseppe Caruso, Karishma K. Khetani, Lauren M. Fox, Subbalakshmi S. Malladi, Sunil A. David

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39 Scopus citations


Small-molecule agonists have been identified for TLR7, TLR8, TLR4 and TLR2 thus far, and chemotypes other than those of canonical ligands are yet to be explored for a number of innate immune receptors. The discovery of novel immunostimulatory molecules would enhance the repertoire of tools available for interrogating innate immune effector mechanisms, and provide additional venues for vaccine adjuvant development. A multiplexed, reporter gene-based high-throughput assay capable of detecting agonists of TLR2, TLR3, TLR4, TLR5, TLR7, TLR8, TLR9, NOD1 and NOD2 was utilized in screening 123,943 compounds, in which amphotericin B (AmpB) and nystatin were identified as prominent hits. The polyene antifungal agents act as TLR2- and TLR4-agonists. The TLR4-stimulatory activity of AmpB was similar to that of monophosphoryl lipid A, suggestive of TRIF-biased signaling. The adjuvantic activity of AmpB, at a dose of 100 micrograms, was comparable to several other candidate adjuvants in rabbit models of immunization. These results point to its potential applicability as a safe and effective adjuvant for human vaccines.

Original languageEnglish (US)
Article numbere0149848
JournalPloS one
Issue number2
StatePublished - Feb 2016

Bibliographical note

Funding Information:
This work was supported by National Institutes of Health/National Institute of Allergy and Infectious Diseases contract HHSN27220140056C (SD). We are grateful to Dr. Anuradha Roy, Director of the University of Kansas High Throughput Screening Laboratory, and her colleagues for assistance with plating compounds.

Publisher Copyright:
© 2016 Salyer et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


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