Published September 9, 2020 | Version v1
Journal article Open

Increased vaccine tolerability and protection via NF-kB modulation

  • 1. University of Chicago
  • 2. Illinois Institute of Technology
  • 3. University of California, Irvine

Description

Improving adjuvant responses is a promising pathway to develop vaccines against some pathogens (e.g., HIV or dengue). One challenge in adjuvant development is modulating the inflammatory response, which can cause excess side effects, while maintaining immune activation and protection. No approved adjuvants yet have the capability to independently modulate inflammation and protection. Here, we demonstrate a method to limit inflammation while retaining and often increasing the protective responses. To accomplish this goal, we combined a partial selective nuclear factor kappa B (NF-kB) inhibitor with several current adjuvants. The resulting vaccines reduce systemic inflammation and boost protective responses. In an influenza challenge model, we demonstrate that this approach enhances protection. This method was tested across a broad range of adjuvants and antigens. We anticipate these studies will lead to an alternative approach to vaccine formulation design that may prove broadly applicable to a wide range of adjuvants and vaccines.

Data availability

All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary Materials. Additional data related to this paper may be requested from the authors.

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Additional details

Identifiers

DOI
10.1126/sciadv.aaz8700
Other
oai:uchicago.tind.io:11004

Funding

National Science Foundation
DGE-1321846
National Institutes of Health
1U01Al124286-01
National Institutes of Health
1DP2Al112194-01
National Institutes of Health
GM099594
Defense Threat Reduction Agency
HDTRA11810052

UChicago Information

Division(s)
Pritzker School of Molecular Engineering