Abstract
Adjuvants have been used in vaccines for over a century, however, the search for safe and effective vaccine adjuvants continues. In recent decades toll-like-receptor (TLR) agonists have been investigated as potential vaccine adjuvants. In this regard, the majority of the currently investigated TLR agonists are non-protein microbial components such as lipopolysaccharides, oligonucleotides, and lipopeptides. On the other hand, a growing number of studies reveal that TLR signaling and immune responses can be activated by numerous bacterial proteins. However, their potential roles as adjuvants have been somewhat overlooked. Herein, we discuss several such bacterial proteins which exhibit adjuvant properties, including the activation of TLR signaling, antigen presenting cell maturation, pro-inflammatory cytokine production and adaptive immune response. The protein nature of these TLR agonists presents several unique features not shared by non-protein TLR agonists. These properties include the amenability for modifying the structure and function as necessary for optimal immunogenicity and minimal toxicity. Protein adjuvants can be genetically fused to protein antigens which ensure the co-delivery of adjuvant-antigen not only into the same cell but also in the same endocytic cargo, leading to more effective activation of innate and adaptive immune response.
Highlights
Vaccine and AdjuvantsSince its discovery more than a century ago vaccines continue to save millions of lives and prevent many more from the debilitating effects of numerous infectious diseases each year [1]
Following Edward Jenner’s successful use of a Cowpox virus to protect humans from Smallpox [2, 3], several live attenuated vaccines have been developed such as measles, mumps, rubella, rotavirus, influenza, tuberculosis, cholera, and typhoid [4]
Live attenuated vaccines are comprised of weakened forms of pathogenic microbes which cause limited infections, but induce long-lasting protection [3]
Summary
Vaccine and AdjuvantsSince its discovery more than a century ago vaccines continue to save millions of lives and prevent many more from the debilitating effects of numerous infectious diseases each year [1]. Adjuvants induce recruitment of various innate immune cells including neutrophils, macrophages and DCs [7,8,9,10]. It is well recognized that cytokines secreted by activated APCs are required to overcome peripheral-tolerance controlled by CD4+CD25+ Treg cells, which limits the adaptive immune responses to antigens [17].
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