The next frontier in vaccine design: blending immune correlates of protection into rational vaccine design

ElsevierVolume 78, October 2022, 102234Current Opinion in ImmunologyHighlights•

Vaccine development during the COVID-19 pandemic lacked thorough insight of CoPs.

CoPs must go beyond simple quantitative antibody blocking.

Interplay between innate, adaptive and tissue-resident immunity determines protection.

Understanding mechanistic CoPs provides a path for the rational design of vaccines.

Despite the extraordinary speed and success in SARS-Cov-2 vaccine development, the emergence of variants of concern perplexed the vaccine development community. Neutralizing antibodies waned antibodies waned and were evaded by viral variants, despite the preservation of protection against severe disease and death across vaccinated populations. Similar to other vaccine design efforts, the lack of mechanistic correlates of immunity against Coronavirus Disease 2019, raised questions related to the need for vaccine redesign and boosting. Hence, our limited understanding of mechanistic correlates of immunity – across pathogens - remains a major obstacle in vaccine development. The identification and incorporation of mechanistic correlates of immunity are key to the accelerated design of highly impactful globally relevant vaccines. Systems-biology tools can be applied strategically to define a complete understanding of mechanistic correlates of immunity. Embedding immunological dissection and target immune profile identification, beyond canonical antibody binding and neutralization, may accelerate the design and success of durable protective vaccines.

© 2022 The Authors. Published by Elsevier Ltd.

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