Both mucosal-associated invariant and natural killer T-cell deficiency in multiple myeloma can be countered by PD-1 inhibition Article Swipe
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· 2017
· Open Access
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· DOI: https://doi.org/10.3324/haematol.2017.163758
Both mucosal-associated invariant and natural killer T-cell deficiency in multiple myeloma can be countered by PD-1 inhibitionMucosal associated invariant T (MAIT) cells primarily contribute to immune defense against infectious pathogens and regulate pathogenesis of various inflammatory diseases. 1They are innate-like T lymphocytes expressing an invariant TCR Vα7.2-Jα33 chain in humans and displaying high expression levels of CD161 and IL-18R.They are primarily localized in mucosal tissue and respond to vitamin B2 metabolites in an MHC class 1b (MR1)-dependent manner. 1 Despite a different ontogeny, MAIT cells share a close lineage relationship with invariant natural killer T (iNKT) cells, another invariant T-cell subset recognizing glycolipids and important for anti-tumor immunity. 1,2Moreover, it has been suggested that they share a common niche and could therefore be functionally redundant. 3Recently, MAIT cells have been implicated in cancer and were shown to support antitumor immunity; 4 however, their exact role has not been well explored.Until now, most reports on involvement of MAIT cells in cancer have been limited to mucosaassociated cancers. 5Recently, however, Wallace et al. reported MAIT cell deficiency in chronic lymphocyte leukemia (CLL), suggesting a possible involvement of MAIT cells in hematologic malignancies as well. 4Further investigation of MAIT cell functionality in cancer patients beyond mucosa-associated malignancies is, therefore, warranted.In multiple myeloma (MM), invariant T cells such as iNKT cells have been reported by us and others to be deficient. 6This has not yet been investigated for MAIT cells and whether they prove to be haematologica 2017;
Related Topics
- Type
- letter
- Language
- en
- Landing Page
- https://doi.org/10.3324/haematol.2017.163758
- http://www.haematologica.org/content/haematol/102/7/e266.full.pdf
- OA Status
- gold
- Cited By
- 35
- References
- 16
- Related Works
- 10
- OpenAlex ID
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Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W2604599595Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.3324/haematol.2017.163758Digital Object Identifier
- Title
-
Both mucosal-associated invariant and natural killer T-cell deficiency in multiple myeloma can be countered by PD-1 inhibitionWork title
- Type
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letterOpenAlex work type
- Language
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enPrimary language
- Publication year
-
2017Year of publication
- Publication date
-
2017-04-06Full publication date if available
- Authors
-
Mérédis Favreau, Koen Venken, Sylvia Faict, Ken Maes, Kim De Veirman, Elke De Bruyne, Xavier Leleu, Louis Boon, Dirk Elewaut, Karin Vanderkerken, Eline MenuList of authors in order
- Landing page
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https://doi.org/10.3324/haematol.2017.163758Publisher landing page
- PDF URL
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https://www.haematologica.org/content/haematol/102/7/e266.full.pdfDirect link to full text PDF
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YesWhether a free full text is available
- OA status
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goldOpen access status per OpenAlex
- OA URL
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https://www.haematologica.org/content/haematol/102/7/e266.full.pdfDirect OA link when available
- Concepts
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Immunology, Pathogenesis, Immune system, T-cell receptor, Multiple myeloma, Innate immune system, Biology, Natural killer T cell, T cellTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
35Total citation count in OpenAlex
- Citations by year (recent)
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2025: 6, 2024: 2, 2023: 3, 2022: 10, 2021: 4Per-year citation counts (last 5 years)
- References (count)
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16Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.with | 90 |
| abstract_inverted_index.(MM), | 209 |
| abstract_inverted_index.1They | 37 |
| abstract_inverted_index.2017; | 243 |
| abstract_inverted_index.6This | 227 |
| abstract_inverted_index.CD161 | 56 |
| abstract_inverted_index.cells | 21, 84, 127, 157, 186, 212, 216, 235 |
| abstract_inverted_index.chain | 47 |
| abstract_inverted_index.class | 74 |
| abstract_inverted_index.close | 87 |
| abstract_inverted_index.could | 120 |
| abstract_inverted_index.exact | 143 |
| abstract_inverted_index.niche | 118 |
| abstract_inverted_index.prove | 239 |
| abstract_inverted_index.share | 85, 115 |
| abstract_inverted_index.shown | 135 |
| abstract_inverted_index.their | 142 |
| abstract_inverted_index.well. | 191 |
| abstract_inverted_index.(CLL), | 179 |
| abstract_inverted_index.(MAIT) | 20 |
| abstract_inverted_index.(iNKT) | 95 |
| abstract_inverted_index.T-cell | 6, 99 |
| abstract_inverted_index.beyond | 201 |
| abstract_inverted_index.cancer | 132, 159, 199 |
| abstract_inverted_index.cells, | 96 |
| abstract_inverted_index.common | 117 |
| abstract_inverted_index.humans | 49 |
| abstract_inverted_index.immune | 25 |
| abstract_inverted_index.killer | 5, 93 |
| abstract_inverted_index.levels | 54 |
| abstract_inverted_index.others | 223 |
| abstract_inverted_index.subset | 100 |
| abstract_inverted_index.tissue | 64 |
| abstract_inverted_index.Despite | 79 |
| abstract_inverted_index.Wallace | 168 |
| abstract_inverted_index.against | 27 |
| abstract_inverted_index.another | 97 |
| abstract_inverted_index.chronic | 176 |
| abstract_inverted_index.defense | 26 |
| abstract_inverted_index.limited | 162 |
| abstract_inverted_index.lineage | 88 |
| abstract_inverted_index.manner. | 77 |
| abstract_inverted_index.mucosal | 63 |
| abstract_inverted_index.myeloma | 10, 208 |
| abstract_inverted_index.natural | 4, 92 |
| abstract_inverted_index.reports | 152 |
| abstract_inverted_index.respond | 66 |
| abstract_inverted_index.support | 137 |
| abstract_inverted_index.various | 34 |
| abstract_inverted_index.vitamin | 68 |
| abstract_inverted_index.whether | 237 |
| abstract_inverted_index.4Further | 192 |
| abstract_inverted_index.cancers. | 165 |
| abstract_inverted_index.however, | 141, 167 |
| abstract_inverted_index.leukemia | 178 |
| abstract_inverted_index.multiple | 9, 207 |
| abstract_inverted_index.patients | 200 |
| abstract_inverted_index.possible | 182 |
| abstract_inverted_index.regulate | 31 |
| abstract_inverted_index.reported | 171, 219 |
| abstract_inverted_index.antitumor | 138 |
| abstract_inverted_index.countered | 13 |
| abstract_inverted_index.different | 81 |
| abstract_inverted_index.diseases. | 36 |
| abstract_inverted_index.immunity. | 107 |
| abstract_inverted_index.immunity; | 139 |
| abstract_inverted_index.important | 104 |
| abstract_inverted_index.invariant | 2, 18, 44, 91, 98, 210 |
| abstract_inverted_index.localized | 61 |
| abstract_inverted_index.ontogeny, | 82 |
| abstract_inverted_index.pathogens | 29 |
| abstract_inverted_index.primarily | 22, 60 |
| abstract_inverted_index.suggested | 112 |
| abstract_inverted_index.therefore | 121 |
| abstract_inverted_index.3Recently, | 125 |
| abstract_inverted_index.5Recently, | 166 |
| abstract_inverted_index.anti-tumor | 106 |
| abstract_inverted_index.associated | 17 |
| abstract_inverted_index.contribute | 23 |
| abstract_inverted_index.deficiency | 7, 174 |
| abstract_inverted_index.deficient. | 226 |
| abstract_inverted_index.displaying | 51 |
| abstract_inverted_index.expressing | 42 |
| abstract_inverted_index.expression | 53 |
| abstract_inverted_index.implicated | 130 |
| abstract_inverted_index.infectious | 28 |
| abstract_inverted_index.lymphocyte | 177 |
| abstract_inverted_index.redundant. | 124 |
| abstract_inverted_index.suggesting | 180 |
| abstract_inverted_index.therefore, | 205 |
| abstract_inverted_index.IL-18R.They | 58 |
| abstract_inverted_index.glycolipids | 102 |
| abstract_inverted_index.hematologic | 188 |
| abstract_inverted_index.innate-like | 39 |
| abstract_inverted_index.involvement | 154, 183 |
| abstract_inverted_index.lymphocytes | 41 |
| abstract_inverted_index.metabolites | 70 |
| abstract_inverted_index.recognizing | 101 |
| abstract_inverted_index.1,2Moreover, | 108 |
| abstract_inverted_index.Vα7.2-Jα33 | 46 |
| abstract_inverted_index.functionally | 123 |
| abstract_inverted_index.inflammatory | 35 |
| abstract_inverted_index.investigated | 232 |
| abstract_inverted_index.malignancies | 189, 203 |
| abstract_inverted_index.pathogenesis | 32 |
| abstract_inverted_index.relationship | 89 |
| abstract_inverted_index.warranted.In | 206 |
| abstract_inverted_index.functionality | 197 |
| abstract_inverted_index.haematologica | 242 |
| abstract_inverted_index.investigation | 193 |
| abstract_inverted_index.explored.Until | 149 |
| abstract_inverted_index.(MR1)-dependent | 76 |
| abstract_inverted_index.mucosaassociated | 164 |
| abstract_inverted_index.inhibitionMucosal | 16 |
| abstract_inverted_index.mucosa-associated | 202 |
| abstract_inverted_index.mucosal-associated | 1 |
| cited_by_percentile_year.max | 99 |
| cited_by_percentile_year.min | 94 |
| countries_distinct_count | 2 |
| institutions_distinct_count | 11 |
| citation_normalized_percentile.value | 0.74659915 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |