Increased vaccine tolerability and protection via NF-κB modulation.
B A MoserRachel C SteinhardtY Escalante-BuendiaD A BoltzK M BarkerB J CassaidyMatthew G RosenbergerStan YooB G McGonnigalAaron P Esser KahnPublished in: Science advances (2020)
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.
Keyphrases
- nuclear factor
- toll like receptor
- inflammatory response
- oxidative stress
- signaling pathway
- lps induced
- early stage
- hiv positive
- antiretroviral therapy
- hiv infected
- zika virus
- drug delivery
- human immunodeficiency virus
- hepatitis c virus
- clinical trial
- lipopolysaccharide induced
- hiv aids
- dendritic cells
- open label
- dengue virus
- men who have sex with men
- double blind