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Adjuvant AS01 activates human monocytes for costimulation and systemic inflammation. | LitMetric

Adjuvant AS01 activates human monocytes for costimulation and systemic inflammation.

Vaccine

Case Western Reserve University School of Medicine, Cleveland, OH, USA; Geriatric Research, Education, and Clinical Center, Louis Stokes VA Northeast Ohio Healthcare System, Cleveland, OH, USA. Electronic address:

Published: January 2024

AI Article Synopsis

  • The recombinant zoster vaccine (RZV) is highly effective, even in those over 80, due in part to its adjuvant AS01, although studies on how AS01 activates human immune cells are limited.
  • Researchers stimulated peripheral blood mononuclear cells (PBMC) with AS01 and used advanced techniques like flow cytometry and RNA sequencing to analyze the effects.
  • The study found that AS01 primarily activates monocytes, leading to the increased production of inflammatory cytokines, and highlights potential pathways to improve vaccine responses in older adults.

Article Abstract

Background: The adjuvanted recombinant zoster vaccine (RZV) is highly effective even in adults over 80 years old. The high efficacy of RZV is attributed to its highly reactogenic adjuvant, AS01, but limited studies have been done on AS01's activation of human immune cells.

Methods: We stimulated peripheral blood mononuclear cells (PBMC) with AS01 and used flow cytometry and RNA Sequencing (RNAseq) to analyze the impacts on human primary cells.

Results: We found that incubation of PBMC with AS01 activated monocytes to a greater extent than any other cell population, including dendritic cells. Both classical and non-classical monocytes demonstrated this activation. RNASeq showed that TNF-ɑ and IL1R pathways were highly upregulated in response to AS01 exposure, even in older adults.

Conclusions: In a PBMC co-culture, AS01 strongly activates human monocytes to upregulate costimulation markers and induce cytokines that mediate systemic inflammation. Understanding AS01's impacts on human cells opens possibilities to further address the reduced vaccine response associated with aging.

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Source
http://dx.doi.org/10.1016/j.vaccine.2023.12.010DOI Listing

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