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Single-cell analysis of myeloid cells in HPV+ tonsillar cancer

Jimenez, David Gomez LU ; Altunbulakli, Can LU orcid ; Swoboda, Sabine LU orcid ; Sobti, Aastha LU ; Askmyr, David LU ; Ali, Ashfaq LU orcid ; Greiff, Lennart LU and Lindstedt, Malin LU (2023) In Frontiers in Immunology 13.
Abstract

The incidence of human papillomavirus-positive (HPV+) tonsillar cancer has been sharply rising during the last decades. Myeloid cells represent an appropriate therapeutic target due to their proximity to virus-infected tumor cells, and their ability to orchestrate antigen-specific immunity, within the tonsil. However, the interrelationship of steady-state and inflammatory myeloid cell subsets, and their impact on patient survival remains unexplored. Here, we used single-cell RNA-sequencing to map the myeloid compartment in HPV+ tonsillar cancer. We observed an expansion of the myeloid compartment in HPV+ tonsillar cancer, accompanied by interferon-induced cellular responses both in dendritic cells (DCs)... (More)

The incidence of human papillomavirus-positive (HPV+) tonsillar cancer has been sharply rising during the last decades. Myeloid cells represent an appropriate therapeutic target due to their proximity to virus-infected tumor cells, and their ability to orchestrate antigen-specific immunity, within the tonsil. However, the interrelationship of steady-state and inflammatory myeloid cell subsets, and their impact on patient survival remains unexplored. Here, we used single-cell RNA-sequencing to map the myeloid compartment in HPV+ tonsillar cancer. We observed an expansion of the myeloid compartment in HPV+ tonsillar cancer, accompanied by interferon-induced cellular responses both in dendritic cells (DCs) and monocyte-macrophages. Our analysis unveiled the existence of four DC lineages, two macrophage polarization processes, and their sequential maturation profiles. Within the DC lineages, we described a balance shift in the frequency of progenitor and mature cDC favoring the cDC1 lineage in detriment of cDC2s. Furthermore, we observed that all DC lineages apart from DC5s matured into a common activated DC transcriptional program involving upregulation of interferon-inducible genes. In turn, the monocyte-macrophage lineage was subjected to early monocyte polarization events, which give rise to either interferon-activated or CXCL-producing macrophages, the latter enriched in advanced tumor stages. We validated the existence of most of the single-cell RNA-seq clusters using 26-plex flow cytometry, and described a positive impact of cDC1 and interferon-activated DCs and macrophages on patient survival using gene signature scoring. The current study contributes to the understanding of myeloid ontogeny and dynamics in HPV-driven tonsillar cancer, and highlights myeloid biomarkers that can be used to assess patient prognosis.

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author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
dendritic cell, human papilloma virus, macrophage, myeloid cell, single-cell RNA-sequencing, tonsillar cancer
in
Frontiers in Immunology
volume
13
article number
1087843
publisher
Frontiers Media S. A.
external identifiers
  • scopus:85147267106
  • pmid:36741389
ISSN
1664-3224
DOI
10.3389/fimmu.2022.1087843
language
English
LU publication?
yes
id
55e0f553-93ed-433d-999c-0344ebabf01e
date added to LUP
2023-02-23 14:50:10
date last changed
2024-06-14 00:13:17
@article{55e0f553-93ed-433d-999c-0344ebabf01e,
  abstract     = {{<p>The incidence of human papillomavirus-positive (HPV<sup>+</sup>) tonsillar cancer has been sharply rising during the last decades. Myeloid cells represent an appropriate therapeutic target due to their proximity to virus-infected tumor cells, and their ability to orchestrate antigen-specific immunity, within the tonsil. However, the interrelationship of steady-state and inflammatory myeloid cell subsets, and their impact on patient survival remains unexplored. Here, we used single-cell RNA-sequencing to map the myeloid compartment in HPV<sup>+</sup> tonsillar cancer. We observed an expansion of the myeloid compartment in HPV<sup>+</sup> tonsillar cancer, accompanied by interferon-induced cellular responses both in dendritic cells (DCs) and monocyte-macrophages. Our analysis unveiled the existence of four DC lineages, two macrophage polarization processes, and their sequential maturation profiles. Within the DC lineages, we described a balance shift in the frequency of progenitor and mature cDC favoring the cDC1 lineage in detriment of cDC2s. Furthermore, we observed that all DC lineages apart from DC5s matured into a common activated DC transcriptional program involving upregulation of interferon-inducible genes. In turn, the monocyte-macrophage lineage was subjected to early monocyte polarization events, which give rise to either interferon-activated or CXCL-producing macrophages, the latter enriched in advanced tumor stages. We validated the existence of most of the single-cell RNA-seq clusters using 26-plex flow cytometry, and described a positive impact of cDC1 and interferon-activated DCs and macrophages on patient survival using gene signature scoring. The current study contributes to the understanding of myeloid ontogeny and dynamics in HPV-driven tonsillar cancer, and highlights myeloid biomarkers that can be used to assess patient prognosis.</p>}},
  author       = {{Jimenez, David Gomez and Altunbulakli, Can and Swoboda, Sabine and Sobti, Aastha and Askmyr, David and Ali, Ashfaq and Greiff, Lennart and Lindstedt, Malin}},
  issn         = {{1664-3224}},
  keywords     = {{dendritic cell; human papilloma virus; macrophage; myeloid cell; single-cell RNA-sequencing; tonsillar cancer}},
  language     = {{eng}},
  month        = {{01}},
  publisher    = {{Frontiers Media S. A.}},
  series       = {{Frontiers in Immunology}},
  title        = {{Single-cell analysis of myeloid cells in HPV<sup>+</sup> tonsillar cancer}},
  url          = {{http://dx.doi.org/10.3389/fimmu.2022.1087843}},
  doi          = {{10.3389/fimmu.2022.1087843}},
  volume       = {{13}},
  year         = {{2023}},
}