TY - JOUR
T1 - Nasal Immunization With Small Molecule Mast Cell Activators Enhance Immunity to Co-Administered Subunit Immunogens
AU - Johnson-Weaver, Brandi T.
AU - Choi, Hae Woong
AU - Yang, Hang
AU - Granek, Josh A.
AU - Chan, Cliburn
AU - Abraham, Soman N.
AU - Staats, Herman F.
N1 - Funding Information:
This work was funded by the National Institute of Allergy and Infectious Diseases (NIAID) Adjuvant Discovery Contract #HHSN272201400054C.
Funding Information:
Fang Wang assisted with performing the in vitro cytokine and viability assays. The Duke Small Molecule Synthesis Facility (SMSF) synthesized the small molecule mast cell activators for use in the described studies. WNV challenge studies were performed under the management of Dr. Charles McGee and multiplexed immunoassays were performed under the management of Dr. Andrew N. Macintyre under the direction of Dr. Gregory D. Sempowski in the Duke Regional Biocontainment Laboratory, which received partial support for construction from the National Institutes of Health, National Institute of Allergy and Infectious Diseases (UC6-AI058607).
Publisher Copyright:
© Copyright © 2021 Johnson-Weaver, Choi, Yang, Granek, Chan, Abraham and Staats.
PY - 2021/9/10
Y1 - 2021/9/10
N2 - Mast cell activators are a novel class of mucosal vaccine adjuvants. The polymeric compound, Compound 48/80 (C48/80), and cationic peptide, Mastoparan 7 (M7) are mast cell activators that provide adjuvant activity when administered by the nasal route. However, small molecule mast cell activators may be a more cost-efficient adjuvant alternative that is easily synthesized with high purity compared to M7 or C48/80. To identify novel mast cell activating compounds that could be evaluated for mucosal vaccine adjuvant activity, we employed high-throughput screening to assess over 55,000 small molecules for mast cell degranulation activity. Fifteen mast cell activating compounds were down-selected to five compounds based on in vitro immune activation activities including cytokine production and cellular cytotoxicity, synthesis feasibility, and selection for functional diversity. These small molecule mast cell activators were evaluated for in vivo adjuvant activity and induction of protective immunity against West Nile Virus infection in BALB/c mice when combined with West Nile Virus envelope domain III (EDIII) protein in a nasal vaccine. We found that three of the five mast cell activators, ST101036, ST048871, and R529877, evoked high levels of EDIII-specific antibody and conferred comparable levels of protection against WNV challenge. The level of protection provided by these small molecule mast cell activators was comparable to the protection evoked by M7 (67%) but markedly higher than the levels seen with mice immunized with EDIII alone (no adjuvant 33%). Thus, novel small molecule mast cell activators identified by high throughput screening are as efficacious as previously described mast cell activators when used as nasal vaccine adjuvants and represent next-generation mast cell activators for evaluation in mucosal vaccine studies.
AB - Mast cell activators are a novel class of mucosal vaccine adjuvants. The polymeric compound, Compound 48/80 (C48/80), and cationic peptide, Mastoparan 7 (M7) are mast cell activators that provide adjuvant activity when administered by the nasal route. However, small molecule mast cell activators may be a more cost-efficient adjuvant alternative that is easily synthesized with high purity compared to M7 or C48/80. To identify novel mast cell activating compounds that could be evaluated for mucosal vaccine adjuvant activity, we employed high-throughput screening to assess over 55,000 small molecules for mast cell degranulation activity. Fifteen mast cell activating compounds were down-selected to five compounds based on in vitro immune activation activities including cytokine production and cellular cytotoxicity, synthesis feasibility, and selection for functional diversity. These small molecule mast cell activators were evaluated for in vivo adjuvant activity and induction of protective immunity against West Nile Virus infection in BALB/c mice when combined with West Nile Virus envelope domain III (EDIII) protein in a nasal vaccine. We found that three of the five mast cell activators, ST101036, ST048871, and R529877, evoked high levels of EDIII-specific antibody and conferred comparable levels of protection against WNV challenge. The level of protection provided by these small molecule mast cell activators was comparable to the protection evoked by M7 (67%) but markedly higher than the levels seen with mice immunized with EDIII alone (no adjuvant 33%). Thus, novel small molecule mast cell activators identified by high throughput screening are as efficacious as previously described mast cell activators when used as nasal vaccine adjuvants and represent next-generation mast cell activators for evaluation in mucosal vaccine studies.
KW - adjuvant discovery
KW - mast cells
KW - nasal vaccine
KW - small molecule adjuvants
KW - vaccine adjuvants
UR - http://www.scopus.com/inward/record.url?scp=85115726408&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2021.730346
DO - 10.3389/fimmu.2021.730346
M3 - Article
C2 - 34566991
AN - SCOPUS:85115726408
SN - 1664-3224
VL - 12
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 730346
ER -