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bioRxiv · 10.1101/2021.06.30.450486

TAILORED DC INDUCE PROTECTIVE HIV-1 SPECIFIC POLYFUNCTIONAL CD8+ T CELLS IN THE LYMPHOID TISSUE FROM HUMANIZED BLT MICE

Calvet-Mirabent, M.·Claiborne, D. T.·Deruaz, M.·Tanno, S.·Serra, C.·Delgado-Arevalo, C.·Sanchez-Cerrillo, I.·Santos, I.·Sanz, J.·Garcia-Fraile, L.·Sanchez-Madrid, F.·Alfranca, A.·Munoz-Fernandez, M. A.·Allen, T. M.·Buzon, M. J.·Balazs, A. B.·Vrbanac, V.·Martin-Gayo, E.
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Abstract

Effective function of CD8+ T cells and enhanced innate activation of dendritic cells (DC) in response to HIV-1 is linked to protective antiviral immunity in controllers. Manipulation of DC targeting the master regulator TANK-binding Kinase 1 (TBK1) might be useful to acquire controller-like properties. Here, we evaluated the impact of TBK1-primed DC inducing protective CD8+ T cell responses in lymphoid tissue and peripheral blood and their association with reduced HIV-1 disease progression in vivo in the humanized bone marrow, liver and thymus (hBLT) mouse model. A higher proportion of hBLT-mice vaccinated with TBK1-primed DC exhibited less severe CD4+ T cell depletion following HIV-1 infection compared to control groups. This was associated with infiltration of CD8+ T cells in the white pulp from the spleen, reduced spread of infected p24+ cells to secondary lymphoid organs and with preserved abilities of CD8+ T cells from the spleen and blood of vaccinated animals to induce specific polyfunctional responses upon antigen stimulation. Therefore, TBK1-primed DC might be an useful tool for subsequent vaccine studies. Author summaryEmulating protective immunological characteristics from individuals capable of spontaneously controlling HIV-1 infection might be useful for the development of a protective vaccine. Enhanced function of dendritic cells (DC) in these HIV-1 controllers depends on the activation of TANK-binding Kinase 1 (TBK1) and might associate with protective T cells. Our study evaluated the ability of DCs trained through TBK1 activation inducing protective adaptive immune responses against HIV-1 and reducing disease progression in vivo, using a humanized mouse model. Our data indicate that mice vaccinated with tailored DC exhibit delayed disease progression, increased induction of protective CD8+ T lymphocyte subsets in the lymphoid tissue and blood upon antigen recognition. Therefore, trained-DC might be an useful tool for future HIV-1 vaccine designs.

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Calvet-Mirabent, M., Claiborne, D. T., Deruaz, M., Tanno, S., Serra, C., Delgado-Arevalo, C., Sanchez-Cerrillo, I., Santos, I., Sanz, J., Garcia-Fraile, L., Sanchez-Madrid, F., Alfranca, A., Munoz-Fernandez, M. A., Allen, T. M., Buzon, M. J., Balazs, A. B., Vrbanac, V., Martin-Gayo, E.. 2021-06-30. TAILORED DC INDUCE PROTECTIVE HIV-1 SPECIFIC POLYFUNCTIONAL CD8+ T CELLS IN THE LYMPHOID TISSUE FROM HUMANIZED BLT MICE. https://doi.org/10.1101/2021.06.30.450486

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