Tissue‐Resident Memory and Follicular/Peripheral Helper PD‐1 + T Cells Infiltrate Lesional Skin in Atopic Dermatitis Article Swipe
Heena Mehta
,
Léane Pellerin
,
Manuel Rubio
,
Catherine Maari
,
Étienne Saint‐Cyr Proulx
,
Sharan Nischal
,
Vaishali R. Moulton
,
Monica Leung
,
Robert Bissonnette
,
Marika Sarfati
·
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1002/eji.202551820
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1002/eji.202551820
Atopic dermatitis (AD) is primarily driven by Th2 cells. Although CD3 + T cells and CD11c + cells predominate in lesional (L) over nonlesional (NL) skin, both sites harbor epidermal dysregulation and a type 2 profile relative to healthy skin. Therapeutics focusing on Th2‐mediated pathways partially fill an unmet medical need, highlighting the importance of further characterizing the adaptive and innate immune landscape in L versus NL skin. Paired L and NL biopsies and matched blood samples were collected from 10 patients. The immunophenotype and cytokine profile of immune cells were examined at the single‐cell level using multiparameter flow cytometry and unsupervised analysis. L compared with NL skin was predominantly infiltrated by CD4 + CD103 + PD‐1 + tissue‐resident memory T cells (TRMs) that positively correlated with disease severity (EASI). CD4 + CD103 + PD‐1 + TRMs coexpressed CD25 and ICOS. Frequencies of skin‐resident CD4 + CD103 − PD‐1 + CXCR5 + CCR5 +/− follicular/peripheral helper T cells (Tfh/Tph) were also augmented in L skin. CCR5 − Tfh/Tph coexpressed ICOS, OX40, and IFN‐γ along with IL‐4 or CD120b while CCR5 + Tfh/Tph coexpressed IL‐4Rα. Furthermore, inflammatory monocytes and monocyte‐derived dendritic cells (Mo‐DCs) positively correlated with CD4 + CD103 + PD‐1 + TRMs and EASI in L skin. These findings enhance our knowledge of AD's innate and adaptive immune profile which may facilitate the discovery of novel therapeutic targets.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1002/eji.202551820
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/eji.202551820
- OA Status
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- References
- 52
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4411458385
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4411458385Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1002/eji.202551820Digital Object Identifier
- Title
-
Tissue‐Resident Memory and Follicular/Peripheral Helper PD‐1 + T Cells Infiltrate Lesional Skin in Atopic DermatitisWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2025Year of publication
- Publication date
-
2025-06-01Full publication date if available
- Authors
-
Heena Mehta, Léane Pellerin, Manuel Rubio, Catherine Maari, Étienne Saint‐Cyr Proulx, Sharan Nischal, Vaishali R. Moulton, Monica Leung, Robert Bissonnette, Marika SarfatiList of authors in order
- Landing page
-
https://doi.org/10.1002/eji.202551820Publisher landing page
- PDF URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/eji.202551820Direct link to full text PDF
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YesWhether a free full text is available
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-
hybridOpen access status per OpenAlex
- OA URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/eji.202551820Direct OA link when available
- Concepts
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Immunophenotyping, Immunology, Flow cytometry, CD11c, Immune system, Atopic dermatitis, Biology, IL-2 receptor, T cell, Acquired immune system, Innate immune system, Phenotype, Gene, BiochemistryTop concepts (fields/topics) attached by OpenAlex
- Cited by
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0Total citation count in OpenAlex
- References (count)
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52Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.(TRMs) | 123 |
| abstract_inverted_index.Atopic | 1 |
| abstract_inverted_index.CD120b | 178 |
| abstract_inverted_index.IL‐4 | 176 |
| abstract_inverted_index.PD‐1 | 117, 135, 149, 200 |
| abstract_inverted_index.Paired | 69 |
| abstract_inverted_index.cells. | 9 |
| abstract_inverted_index.driven | 6 |
| abstract_inverted_index.harbor | 29 |
| abstract_inverted_index.helper | 156 |
| abstract_inverted_index.immune | 62, 89, 218 |
| abstract_inverted_index.innate | 61, 215 |
| abstract_inverted_index.memory | 120 |
| abstract_inverted_index.versus | 66 |
| abstract_inverted_index.(EASI). | 130 |
| abstract_inverted_index.Tfh/Tph | 168, 182 |
| abstract_inverted_index.disease | 128 |
| abstract_inverted_index.enhance | 210 |
| abstract_inverted_index.further | 56 |
| abstract_inverted_index.healthy | 39 |
| abstract_inverted_index.matched | 75 |
| abstract_inverted_index.medical | 50 |
| abstract_inverted_index.profile | 36, 87, 219 |
| abstract_inverted_index.samples | 77 |
| abstract_inverted_index.ABSTRACT | 0 |
| abstract_inverted_index.Although | 10 |
| abstract_inverted_index.IFN‐γ | 173 |
| abstract_inverted_index.adaptive | 59, 217 |
| abstract_inverted_index.biopsies | 73 |
| abstract_inverted_index.compared | 105 |
| abstract_inverted_index.cytokine | 86 |
| abstract_inverted_index.examined | 92 |
| abstract_inverted_index.findings | 209 |
| abstract_inverted_index.focusing | 42 |
| abstract_inverted_index.lesional | 21 |
| abstract_inverted_index.pathways | 45 |
| abstract_inverted_index.relative | 37 |
| abstract_inverted_index.severity | 129 |
| abstract_inverted_index.targets. | 228 |
| abstract_inverted_index.(Tfh/Tph) | 159 |
| abstract_inverted_index.analysis. | 103 |
| abstract_inverted_index.augmented | 162 |
| abstract_inverted_index.collected | 79 |
| abstract_inverted_index.cytometry | 100 |
| abstract_inverted_index.dendritic | 190 |
| abstract_inverted_index.discovery | 224 |
| abstract_inverted_index.epidermal | 30 |
| abstract_inverted_index.knowledge | 212 |
| abstract_inverted_index.landscape | 63 |
| abstract_inverted_index.monocytes | 187 |
| abstract_inverted_index.partially | 46 |
| abstract_inverted_index.patients. | 82 |
| abstract_inverted_index.primarily | 5 |
| abstract_inverted_index.(Mo‐DCs) | 192 |
| abstract_inverted_index.IL‐4Rα. | 184 |
| abstract_inverted_index.correlated | 126, 194 |
| abstract_inverted_index.dermatitis | 2 |
| abstract_inverted_index.facilitate | 222 |
| abstract_inverted_index.importance | 54 |
| abstract_inverted_index.positively | 125, 193 |
| abstract_inverted_index.Frequencies | 142 |
| abstract_inverted_index.coexpressed | 138, 169, 183 |
| abstract_inverted_index.infiltrated | 111 |
| abstract_inverted_index.nonlesional | 24 |
| abstract_inverted_index.predominate | 19 |
| abstract_inverted_index.therapeutic | 227 |
| abstract_inverted_index.Furthermore, | 185 |
| abstract_inverted_index.Therapeutics | 41 |
| abstract_inverted_index.highlighting | 52 |
| abstract_inverted_index.inflammatory | 186 |
| abstract_inverted_index.unsupervised | 102 |
| abstract_inverted_index.dysregulation | 31 |
| abstract_inverted_index.predominantly | 110 |
| abstract_inverted_index.single‐cell | 95 |
| abstract_inverted_index.Th2‐mediated | 44 |
| abstract_inverted_index.characterizing | 57 |
| abstract_inverted_index.multiparameter | 98 |
| abstract_inverted_index.immunophenotype | 84 |
| abstract_inverted_index.skin‐resident | 144 |
| abstract_inverted_index.tissue‐resident | 119 |
| abstract_inverted_index.monocyte‐derived | 189 |
| abstract_inverted_index.follicular/peripheral | 155 |
| cited_by_percentile_year | |
| countries_distinct_count | 2 |
| institutions_distinct_count | 10 |
| sustainable_development_goals[0].id | https://metadata.un.org/sdg/3 |
| sustainable_development_goals[0].score | 0.6299999952316284 |
| sustainable_development_goals[0].display_name | Good health and well-being |
| citation_normalized_percentile.value | 0.37166069 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | True |