Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection

Abstract Neutrophils are innate immune cells involved in the elimination of pathogens and can also induce adaptive immune responses. Nα and Nβ neutrophils have been described with distinct in vitro capacity to generate antigen-specific CD8 T-cell responses. However, how these cell types exert their...

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Autores principales: Mauro Di Pilato, Miguel Palomino-Segura, Ernesto Mejías-Pérez, Carmen E. Gómez, Andrea Rubio-Ponce, Rocco D’Antuono, Diego Ulisse Pizzagalli, Patricia Pérez, Raphael Kfuri-Rubens, Alberto Benguría, Ana Dopazo, Iván Ballesteros, Carlos Oscar S. Sorzano, Andrés Hidalgo, Mariano Esteban, Santiago F. Gonzalez
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/89b84f82228e4bf9963a98f0174b37ad
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spelling oai:doaj.org-article:89b84f82228e4bf9963a98f0174b37ad2021-12-02T14:30:51ZNeutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection10.1038/s41541-021-00314-72059-0105https://doaj.org/article/89b84f82228e4bf9963a98f0174b37ad2021-04-01T00:00:00Zhttps://doi.org/10.1038/s41541-021-00314-7https://doaj.org/toc/2059-0105Abstract Neutrophils are innate immune cells involved in the elimination of pathogens and can also induce adaptive immune responses. Nα and Nβ neutrophils have been described with distinct in vitro capacity to generate antigen-specific CD8 T-cell responses. However, how these cell types exert their role in vivo and how manipulation of Nβ/Nα ratio influences vaccine-mediated immune responses are not known. In this study, we find that these neutrophil subtypes show distinct migratory and motility patterns and different ability to interact with CD8 T cells in the spleen following vaccinia virus (VACV) infection. Moreover, after analysis of adhesion, inflammatory, and migration markers, we observe that Nβ neutrophils overexpress the α4β1 integrin compared to Nα. Finally, by inhibiting α4β1 integrin, we increase the Nβ/Nα ratio and enhance CD8 T-cell responses to HIV VACV-delivered antigens. These findings provide significant advancements in the comprehension of neutrophil-based control of adaptive immune system and their relevance in vaccine design.Mauro Di PilatoMiguel Palomino-SeguraErnesto Mejías-PérezCarmen E. GómezAndrea Rubio-PonceRocco D’AntuonoDiego Ulisse PizzagalliPatricia PérezRaphael Kfuri-RubensAlberto BenguríaAna DopazoIván BallesterosCarlos Oscar S. SorzanoAndrés HidalgoMariano EstebanSantiago F. GonzalezNature PortfolioarticleImmunologic diseases. AllergyRC581-607Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Vaccines, Vol 6, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Immunologic diseases. Allergy
RC581-607
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Mauro Di Pilato
Miguel Palomino-Segura
Ernesto Mejías-Pérez
Carmen E. Gómez
Andrea Rubio-Ponce
Rocco D’Antuono
Diego Ulisse Pizzagalli
Patricia Pérez
Raphael Kfuri-Rubens
Alberto Benguría
Ana Dopazo
Iván Ballesteros
Carlos Oscar S. Sorzano
Andrés Hidalgo
Mariano Esteban
Santiago F. Gonzalez
Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection
description Abstract Neutrophils are innate immune cells involved in the elimination of pathogens and can also induce adaptive immune responses. Nα and Nβ neutrophils have been described with distinct in vitro capacity to generate antigen-specific CD8 T-cell responses. However, how these cell types exert their role in vivo and how manipulation of Nβ/Nα ratio influences vaccine-mediated immune responses are not known. In this study, we find that these neutrophil subtypes show distinct migratory and motility patterns and different ability to interact with CD8 T cells in the spleen following vaccinia virus (VACV) infection. Moreover, after analysis of adhesion, inflammatory, and migration markers, we observe that Nβ neutrophils overexpress the α4β1 integrin compared to Nα. Finally, by inhibiting α4β1 integrin, we increase the Nβ/Nα ratio and enhance CD8 T-cell responses to HIV VACV-delivered antigens. These findings provide significant advancements in the comprehension of neutrophil-based control of adaptive immune system and their relevance in vaccine design.
format article
author Mauro Di Pilato
Miguel Palomino-Segura
Ernesto Mejías-Pérez
Carmen E. Gómez
Andrea Rubio-Ponce
Rocco D’Antuono
Diego Ulisse Pizzagalli
Patricia Pérez
Raphael Kfuri-Rubens
Alberto Benguría
Ana Dopazo
Iván Ballesteros
Carlos Oscar S. Sorzano
Andrés Hidalgo
Mariano Esteban
Santiago F. Gonzalez
author_facet Mauro Di Pilato
Miguel Palomino-Segura
Ernesto Mejías-Pérez
Carmen E. Gómez
Andrea Rubio-Ponce
Rocco D’Antuono
Diego Ulisse Pizzagalli
Patricia Pérez
Raphael Kfuri-Rubens
Alberto Benguría
Ana Dopazo
Iván Ballesteros
Carlos Oscar S. Sorzano
Andrés Hidalgo
Mariano Esteban
Santiago F. Gonzalez
author_sort Mauro Di Pilato
title Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection
title_short Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection
title_full Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection
title_fullStr Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection
title_full_unstemmed Neutrophil subtypes shape HIV-specific CD8 T-cell responses after vaccinia virus infection
title_sort neutrophil subtypes shape hiv-specific cd8 t-cell responses after vaccinia virus infection
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/89b84f82228e4bf9963a98f0174b37ad
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