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American Association of Immunologists, ImmunoHorizons, 1(2), p. 1-11, 2018

DOI: 10.4049/immunohorizons.1700054

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IL-27p28 Production by XCR1 + Dendritic Cells and Monocytes Effectively Predicts Adjuvant-Elicited CD8 + T Cell Responses

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Abstract It is well accepted that the innate response is a necessary prerequisite to the formation of the adaptive response. This is true for T cell responses against infections or adjuvanted subunit vaccination. However, specific innate parameters with predictive value for the magnitude of an adjuvant-elicited T cell response have yet to be identified. We previously reported how T cell responses induced by subunit vaccination were dependent on the cytokine IL-27. These findings were unexpected, given that T cell responses to an infection typically increase in the absence of IL-27. Using a novel IL-27p28–eGFP reporter mouse, we now show that the degree to which an adjuvant induces IL-27p28 production from dendritic cells and monocytes directly predicts the magnitude of the T cell response elicited. To our knowledge, these data are the first to identify a concrete innate correlate of vaccine-elicited cellular immunity, and they have significant practical and mechanistic implications for subunit vaccine biology.