Comprehensive Analysis of the Chemokine/Cytokine Profiles in Advanced Mycosis Fungoides and Atopic Dermatitis Article Swipe
YOU?
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· 2025
· Open Access
·
· DOI: https://doi.org/10.1155/dth/6603966
Mycosis fungoides (MF) is an indolent form of cutaneous T‐cell lymphoma. Its early lesions are important to be distinguished from atopic dermatitis (AD) because of their similar immune microenvironment. We have previously demonstrated that several chemokines are involved in the pathogenesis of advanced MF. Therefore, we sought to comprehensively analyze the changes in the immune environment during the advanced phase of MF by focusing on serum cytokines and chemokines and to identify potential biomarkers for the early detection of the transition to the advanced phase of MF. Sera from 11 cases of advanced‐stage MF, 16 cases of mild AD (median EASI score = 5.75), 16 cases of severe AD (median EASI score = 28.1), and 21 healthy volunteers were analyzed using the Bio‐Plex 40 multiplex immunoassay system. The results revealed significant increases in immunosuppressive macrophage‐related factors (IL‐4, MIF, CCL3) in MF patients compared to those with AD and healthy controls. In contrast, IL‐2, CCL1, CCL7, CCL21, CCL25, and CCL26 were significantly increased in severe AD patients compared to MF patients and healthy controls. Our findings suggest that several chemokines and cytokines contribute to an immunosuppressive environment favorable for tumor growth, distinguishing MF from AD. Moreover, T‐cell proliferation and migration factors, which are mainly involved in maintaining inflammation, are elevated in severe AD compared to MF. In addition to elucidating the differences in the pathogenesis of these diseases, these factors may be important in the differential diagnosis of early MF and AD. Further studies are warranted to confirm these findings.
Related Topics
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1155/dth/6603966
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1155/dth/6603966
- OA Status
- hybrid
- Cited By
- 1
- References
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- Related Works
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- OpenAlex ID
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Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4410058093Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1155/dth/6603966Digital Object Identifier
- Title
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Comprehensive Analysis of the Chemokine/Cytokine Profiles in Advanced Mycosis Fungoides and Atopic DermatitisWork title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2025Year of publication
- Publication date
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2025-01-01Full publication date if available
- Authors
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Manami Takahashi, Taku Fujimura, Emi Yamazaki, Ryo Amagai, Kenta Oka, Yumi Kambayashi, Maki Ozawa, Tomoko Chiba, Mayuko Onodera-Amagai, Toshiya Takahashi, Yoshihide AsanoList of authors in order
- Landing page
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https://doi.org/10.1155/dth/6603966Publisher landing page
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1155/dth/6603966Direct 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
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1155/dth/6603966Direct OA link when available
- Concepts
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Medicine, Mycosis fungoides, Atopic dermatitis, Dermatology, Immunology, LymphomaTop concepts (fields/topics) attached by OpenAlex
- Cited by
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1Total citation count in OpenAlex
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2025: 1Per-year citation counts (last 5 years)
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25Number 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.lesions | 13 |
| abstract_inverted_index.results | 128 |
| abstract_inverted_index.several | 34, 177 |
| abstract_inverted_index.similar | 26 |
| abstract_inverted_index.studies | 242 |
| abstract_inverted_index.suggest | 175 |
| abstract_inverted_index.system. | 126 |
| abstract_inverted_index.(IL‐4, | 136 |
| abstract_inverted_index.T‐cell | 9, 195 |
| abstract_inverted_index.addition | 216 |
| abstract_inverted_index.advanced | 42, 58, 83 |
| abstract_inverted_index.analyzed | 119 |
| abstract_inverted_index.compared | 142, 166, 212 |
| abstract_inverted_index.elevated | 208 |
| abstract_inverted_index.factors, | 199 |
| abstract_inverted_index.findings | 174 |
| abstract_inverted_index.focusing | 63 |
| abstract_inverted_index.identify | 71 |
| abstract_inverted_index.indolent | 5 |
| abstract_inverted_index.involved | 37, 203 |
| abstract_inverted_index.patients | 141, 165, 169 |
| abstract_inverted_index.revealed | 129 |
| abstract_inverted_index.Moreover, | 194 |
| abstract_inverted_index.contrast, | 151 |
| abstract_inverted_index.controls. | 149, 172 |
| abstract_inverted_index.cutaneous | 8 |
| abstract_inverted_index.cytokines | 66, 180 |
| abstract_inverted_index.detection | 77 |
| abstract_inverted_index.diagnosis | 235 |
| abstract_inverted_index.diseases, | 226 |
| abstract_inverted_index.favorable | 186 |
| abstract_inverted_index.findings. | 248 |
| abstract_inverted_index.fungoides | 1 |
| abstract_inverted_index.important | 15, 231 |
| abstract_inverted_index.increased | 161 |
| abstract_inverted_index.increases | 131 |
| abstract_inverted_index.lymphoma. | 10 |
| abstract_inverted_index.migration | 198 |
| abstract_inverted_index.multiplex | 124 |
| abstract_inverted_index.potential | 72 |
| abstract_inverted_index.warranted | 244 |
| abstract_inverted_index.Bio‐Plex | 122 |
| abstract_inverted_index.Therefore, | 44 |
| abstract_inverted_index.biomarkers | 73 |
| abstract_inverted_index.chemokines | 35, 68, 178 |
| abstract_inverted_index.contribute | 181 |
| abstract_inverted_index.dermatitis | 21 |
| abstract_inverted_index.previously | 31 |
| abstract_inverted_index.transition | 80 |
| abstract_inverted_index.volunteers | 117 |
| abstract_inverted_index.differences | 220 |
| abstract_inverted_index.elucidating | 218 |
| abstract_inverted_index.environment | 55, 185 |
| abstract_inverted_index.immunoassay | 125 |
| abstract_inverted_index.maintaining | 205 |
| abstract_inverted_index.significant | 130 |
| abstract_inverted_index.demonstrated | 32 |
| abstract_inverted_index.differential | 234 |
| abstract_inverted_index.pathogenesis | 40, 223 |
| abstract_inverted_index.distinguished | 18 |
| abstract_inverted_index.inflammation, | 206 |
| abstract_inverted_index.proliferation | 196 |
| abstract_inverted_index.significantly | 160 |
| abstract_inverted_index.distinguishing | 190 |
| abstract_inverted_index.comprehensively | 48 |
| abstract_inverted_index.advanced‐stage | 92 |
| abstract_inverted_index.immunosuppressive | 133, 184 |
| abstract_inverted_index.microenvironment. | 28 |
| abstract_inverted_index.macrophage‐related | 134 |
| cited_by_percentile_year.max | 95 |
| cited_by_percentile_year.min | 91 |
| countries_distinct_count | 0 |
| institutions_distinct_count | 11 |
| citation_normalized_percentile.value | 0.89746243 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | True |