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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Anti-Cancer Agents in Medicinal Chemistry</journal-id><journal-title-group><journal-title xml:lang="en">Anti-Cancer Agents in Medicinal Chemistry</journal-title><trans-title-group xml:lang="ru"><trans-title>Anti-Cancer Agents in Medicinal Chemistry</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1871-5206</issn><issn publication-format="electronic">1875-5992</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">644066</article-id><article-id pub-id-type="doi">10.2174/0118715206321574240821112747</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Oncology</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Immunomodulatory Roles of IL-15 in Immune Cells and its Potential for Cancer Immunotherapy</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Youhan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Ma</surname><given-names>Wen</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Tian</surname><given-names>Xuewen</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Qinglu</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Lu</surname><given-names>Xin</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Luo</surname><given-names>Ying</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Xu</surname><given-names>Jun</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Graduate School of Education, Shandong Sport University</institution></aff><aff id="aff2"><institution>Department of Clinical laboratory, Central Hospital of Zibo</institution></aff><pub-date date-type="pub" iso-8601-date="2024-10-15" publication-format="electronic"><day>15</day><month>10</month><year>2024</year></pub-date><volume>24</volume><issue>20</issue><issue-title xml:lang="ru"/><fpage>1457</fpage><lpage>1466</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/1871-5206/article/view/644066">https://journals.eco-vector.com/1871-5206/article/view/644066</self-uri><abstract xml:lang="en"><p id="idm46041443468480">:Interleukin-15 (IL-15) was identified in 1994 as a T-cell growth factor with the capability to mimic the functions of IL-2. IL-15 engages with the IL-15Rα subunit expressed on the surface of antigen-presenting cells (APCs) and, through a trans-presentation mechanism, activates the IL-2/IL-15Rβγ complex receptor on the surface of natural killer (NK) cells and CD8+ T cells. This interaction initiates a cascade of downstream signaling pathways, playing a pivotal role in the activation, proliferation, and anti-apoptotic processes in NK cells, CD8+ T cells, and B cells. It provides a substantial theoretical foundation and potential therapeutic targets for tumor immunotherapy. Whether through active or passive immunotherapeutic strategies, IL-15 has emerged as a critical molecule for stimulating anti-tumor cell proliferation.</p></abstract><kwd-group xml:lang="en"><kwd>Tumor</kwd><kwd>NK</kwd><kwd>CD8+T</kwd><kwd>B cell</kwd><kwd>IL-15</kwd><kwd>natural killer.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Liu, Z.; Han, C.; Fu, Y.X. Targeting innate sensing in the tumor microenvironment to improve immunotherapy. Cell. Mol. Immunol., 2020, 17(1), 13-26. doi: 10.1038/s41423-019-0341-y PMID: 31844141</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Takatsu, K.; Nakajima, H. IL-5 and eosinophilia. Curr. Opin. Immunol., 2008, 20(3), 288-294. doi: 10.1016/j.coi.2008.04.001 PMID: 18511250</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Weng, N.P.; Liu, K.; Catalfamo, M.; Li, Y.; Henkart, P.A. IL-15 is a growth factor and an activator of CD8 memory T cells. Ann. N. Y. Acad. Sci., 2002, 975(1), 46-56. doi: 10.1111/j.1749-6632.2002.tb05940.x PMID: 12538153</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Giri, J.G.; Anderson, D.M.; Kumaki, S.; Park, L.S.; Grabstein, K.H.; Cosman, D. IL-15, a novel T cell growth factor that shares activities and receptor components with IL-2. J. Leukoc. Biol., 1995, 57(5), 763-766. doi: 10.1002/jlb.57.5.763 PMID: 7759955</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Fehniger, T.A. Mystery solved: IL-15. J. Immunol., 2019, 202(11), 3125-3126. doi: 10.4049/jimmunol.1900419 PMID: 31109944</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Yang, Y.; Lundqvist, A. Immunomodulatory effects of IL-2 and IL-15; implications for cancer immunotherapy. Cancers (Basel), 2020, 12(12), 3586. doi: 10.3390/cancers12123586 PMID: 33266177</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Bilotta, M.T.; Antignani, A.; Fitzgerald, D.J. Managing the TME to improve the efficacy of cancer therapy. Front. Immunol., 2022, 13, 954992. doi: 10.3389/fimmu.2022.954992 PMID: 36341428</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Becker, J.C.; Andersen, M.H.; Schrama, D.; thor Straten, P. Immune-suppressive properties of the tumor microenvironment. Cancer Immunol. Immunother., 2013, 62(7), 1137-1148. doi: 10.1007/s00262-013-1434-6 PMID: 23666510</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Hanahan, D.; Coussens, L.M. Accessories to the crime: functions of cells recruited to the tumor microenvironment. Cancer Cell, 2012, 21(3), 309-322. doi: 10.1016/j.ccr.2012.02.022 PMID: 22439926</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Mannino, M.H.; Zhu, Z.; Xiao, H.; Bai, Q.; Wakefield, M.R.; Fang, Y. The paradoxical role of IL-10 in immunity and cancer. Cancer Lett., 2015, 367(2), 103-107. doi: 10.1016/j.canlet.2015.07.009 PMID: 26188281</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Larson, C.; Oronsky, B.; Carter, C.A.; Oronsky, A.; Knox, S.J.; Sher, D.; Reid, T.R. TGF-beta: a master immune regulator. Expert Opin. Ther. Targets, 2020, 24(5), 427-438. doi: 10.1080/14728222.2020.1744568 PMID: 32228232</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Vaupel, P.; Multhoff, G. Accomplices of the hypoxic tumor microenvironment compromising antitumor immunity: Adenosine, lactate, acidosis, vascular endothelial growth factor, potassium ions, and phosphatidylserine. Front. Immunol., 2017, 8, 1887. doi: 10.3389/fimmu.2017.01887 PMID: 29312351</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Madden, M.Z.; Rathmell, J.C. The complex integration of T-cell metabolism and immunotherapy. Cancer Discov., 2021, 11(7), 1636-1643. doi: 10.1158/2159-8290.CD-20-0569 PMID: 33795235</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Yan, J.; Smyth, M.J.; Teng, M.W.L. Interleukin (IL)-12 and IL-23 and their conflicting roles in cancer. Cold Spring Harb. Perspect. Biol., 2018, 10(7), a028530. doi: 10.1101/cshperspect.a028530 PMID: 28716888</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Takaki, S.; Kanazawa, H.; Shiiba, M.; Takatsu, K. A critical cytoplasmic domain of the interleukin-5 (IL-5) receptor alpha chain and its function in IL-5-mediated growth signal transduction. Mol. Cell. Biol., 1994, 14(11), 7404-7413. doi: 10.1128/MCB.14.11.7404 PMID: 7935454</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Mlecnik, B.; Bindea, G.; Angell, H.K.; Sasso, M.S.; Obenauf, A.C.; Fredriksen, T.; Lafontaine, L.; Bilocq, A.M.; Kirilovsky, A.; Tosolini, M.; Waldner, M.; Berger, A.; Fridman, W.H.; Rafii, A.; Valge-Archer, V.; Pagès, F.; Speicher, M.R.; Galon, J. Functional network pipeline reveals genetic determinants associated with in situ lymphocyte proliferation and survival of cancer patients. Sci. Transl. Med., 2014, 6(228), 228ra37. doi: 10.1126/scitranslmed.3007240 PMID: 24648340</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Mac Cheever, M.A. Twelve immunotherapy drugs that could cure cancers. Immunol. Rev., 2008, 222(1), 357-368. doi: 10.1111/j.1600-065X.2008.00604.x PMID: 18364014</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Giri, J.G.; Kumaki, S.; Ahdieh, M.; Friend, D.J.; Loomis, A.; Shanebeck, K.; DuBose, R.; Cosman, D.; Park, L.S.; Anderson, D.M. Identification and cloning of a novel IL-15 binding protein that is structurally related to the alpha chain of the IL-2 receptor. EMBO J., 1995, 14(15), 3654-3663. doi: 10.1002/j.1460-2075.1995.tb00035.x PMID: 7641685</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Badoual, C.; Bouchaud, G.; Agueznay, N.E.H.; Mortier, E.; Hans, S.; Gey, A.; Fernani, F.; Peyrard, S.; -Puig, P.L.; Bruneval, P.; Sastre, X.; Plet, A.; Garrigue-Antar, L.; Quintin-Colonna, F.; Fridman, W.H.; Brasnu, D.; Jacques, Y.; Tartour, E. The soluble alpha chain of interleukin-15 receptor: a proinflammatory molecule associated with tumor progression in head and neck cancer. Cancer Res., 2008, 68(10), 3907-3914. doi: 10.1158/0008-5472.CAN-07-6842 PMID: 18483276</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Zhang, N.; Bevan, M.J. CD8(+) T cells: foot soldiers of the immune system. Immunity, 2011, 35(2), 161-168. doi: 10.1016/j.immuni.2011.07.010 PMID: 21867926</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Reiser, J.; Banerjee, A. Effector, memory, and dysfunctional CD8 + T cell fates in the antitumor immune response. J. Immunol. Res., 2016, 2016, 1-14. doi: 10.1155/2016/8941260 PMID: 27314056</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Klebanoff, C.A.; Gattinoni, L.; Palmer, D.C.; Muranski, P.; Ji, Y.; Hinrichs, C.S.; Borman, Z.A.; Kerkar, S.P.; Scott, C.D.; Finkelstein, S.E.; Rosenberg, S.A.; Restifo, N.P. Determinants of successful CD8+ T-cell adoptive immunotherapy for large established tumors in mice. Clin. Cancer Res., 2011, 17(16), 5343-5352. doi: 10.1158/1078-0432.CCR-11-0503 PMID: 21737507</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Gao, S.; Liang, X.; Wang, H.; Bao, B.; Zhang, K.; Zhu, Y.; Shao, Q. Stem cell-like memory T cells: A perspective from the dark side. Cell. Immunol., 2021, 361, 104273. doi: 10.1016/j.cellimm.2020.104273 PMID: 33422699</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Germain, R.N. T-cell development and the CD4CD8 lineage decision. Nat. Rev. Immunol., 2002, 2(5), 309-322. doi: 10.1038/nri798 PMID: 12033737</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Lu, C.; Liu, Y.; Ali, N.M.; Zhang, B.; Cui, X. The role of innate immune cells in the tumor microenvironment and research progress in anti-tumor therapy. Front. Immunol., 2023, 13, 1039260. doi: 10.3389/fimmu.2022.1039260 PMID: 36741415</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Kucuksezer, U.C.; Aktas Cetin, E.; Esen, F.; Tahrali, I.; Akdeniz, N.; Gelmez, M.Y.; Deniz, G. The role of natural killer cells in autoimmune diseases. Front. Immunol., 2021, 12, 622306. doi: 10.3389/fimmu.2021.622306 PMID: 33717125</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Nolz, J.C.; Richer, M.J. Control of memory CD8+ T cell longevity and effector functions by IL-15. Mol. Immunol., 2020, 117, 180-188. doi: 10.1016/j.molimm.2019.11.011 PMID: 31816491</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Blank, C.U.; Haining, W.N.; Held, W.; Hogan, P.G.; Kallies, A.; Lugli, E.; Lynn, R.C.; Philip, M.; Rao, A.; Restifo, N.P.; Schietinger, A.; Schumacher, T.N.; Schwartzberg, P.L.; Sharpe, A.H.; Speiser, D.E.; Wherry, E.J.; Youngblood, B.A.; Zehn, D. Defining T cell exhaustion. Nat. Rev. Immunol., 2019, 19(11), 665-674. doi: 10.1038/s41577-019-0221-9 PMID: 31570879</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Lee, J.; Lee, K.; Bae, H.; Lee, K.; Lee, S.; Ma, J.; Jo, K.; Kim, I.; Jee, B.; Kang, M.; Im, S.J. IL-15 promotes self-renewal of progenitor exhausted CD8 T cells during persistent antigenic stimulation. Front. Immunol., 2023, 14, 1117092. doi: 10.3389/fimmu.2023.1117092 PMID: 37409128</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>OSullivan, D.; van der Windt, G.J.W.; Huang, S.C.C.; Curtis, J.D.; Chang, C.H.; Buck, M.D.; Qiu, J.; Smith, A.M.; Lam, W.Y.; DiPlato, L.M.; Hsu, F.F.; Birnbaum, M.J.; Pearce, E.J.; Pearce, E.L. Memory CD8+ T cells use cell-intrinsic lipolysis to support the metabolic programming necessary for development. Immunity, 2018, 49(2), 375-376. doi: 10.1016/j.immuni.2018.07.018 PMID: 30134202</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Kurtulus, S.; Tripathi, P.; Moreno-Fernandez, M.E.; Sholl, A.; Katz, J.D.; Grimes, H.L.; Hildeman, D.A. Bcl-2 allows effector and memory CD8+ T cells to tolerate higher expression of Bim. J. Immunol., 2011, 186(10), 5729-5737. doi: 10.4049/jimmunol.1100102 PMID: 21451108</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Waldmann, T.A.; Miljkovic, M.D.; Conlon, K.C. Interleukin-15 (dys)regulation of lymphoid homeostasis: Implications for therapy of autoimmunity and cancer. J. Exp. Med., 2020, 217(1), e20191062. doi: 10.1084/jem.20191062 PMID: 31821442</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Goldrath, A.W.; Sivakumar, P.V.; Glaccum, M.; Kennedy, M.K.; Bevan, M.J.; Benoist, C.; Mathis, D.; Butz, E.A. Cytokine requirements for acute and Basal homeostatic proliferation of naive and memory CD8+ T cells. J. Exp. Med., 2002, 195(12), 1515-1522. doi: 10.1084/jem.20020033 PMID: 12070279</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Schluns, K.S.; Williams, K.; Ma, A.; Zheng, X.X.; Lefrançois, L. Cutting edge: requirement for IL-15 in the generation of primary and memory antigen-specific CD8 T cells. J. Immunol., 2002, 168(10), 4827-4831. doi: 10.4049/jimmunol.168.10.4827 PMID: 11994430</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Tan, J.T.; Ernst, B.; Kieper, W.C.; LeRoy, E.; Sprent, J.; Surh, C.D. Interleukin (IL)-15 and IL-7 jointly regulate homeostatic proliferation of memory phenotype CD8+ cells but are not required for memory phenotype CD4+ cells. J. Exp. Med., 2002, 195(12), 1523-1532. doi: 10.1084/jem.20020066 PMID: 12070280</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Kurz, E.; Hirsch, C.A.; Dalton, T.; Shadaloey, S.A.; Khodadadi-Jamayran, A.; Miller, G.; Pareek, S.; Rajaei, H.; Mohindroo, C.; Baydogan, S.; Ngo-Huang, A.; Parker, N.; Katz, M.H.G.; Petzel, M.; Vucic, E.; McAllister, F.; Schadler, K.; Winograd, R.; Bar-Sagi, D. Exercise-induced engagement of the IL-15/IL-15Rα axis promotes anti-tumor immunity in pancreatic cancer. Cancer Cell, 2022, 40(7), 720-737.e5. doi: 10.1016/j.ccell.2022.05.006 PMID: 35660135</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Ali, A.K.; Nandagopal, N.; Lee, S.H. IL-15PI3KAKTmTOR: A critical pathway in the life journey of natural killer cells. Front. Immunol., 2015, 6, 355. doi: 10.3389/fimmu.2015.00355 PMID: 26257729</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Cheuk, S.; Schlums, H.; Gallais Sérézal, I.; Martini, E.; Chiang, S.C.; Marquardt, N.; Gibbs, A.; Detlofsson, E.; Introini, A.; Forkel, M.; Höög, C.; Tjernlund, A.; Michaëlsson, J.; Folkersen, L.; Mjösberg, J.; Blomqvist, L.; Ehrström, M.; Ståhle, M.; Bryceson, Y.T.; Eidsmo, L. CD49a expression defines tissue-resident CD8+ T cells poised for cytotoxic function in human skin. Immunity, 2017, 46(2), 287-300. doi: 10.1016/j.immuni.2017.01.009 PMID: 28214226</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Zhou, X.; Yu, J.; Cheng, X.; Zhao, B.; Manyam, G.C.; Zhang, L.; Schluns, K.; Li, P.; Wang, J.; Sun, S.C. The deubiquitinase Otub1 controls the activation of CD8+ T cells and NK cells by regulating IL-15-mediated priming. Nat. Immunol., 2019, 20(7), 879-889. doi: 10.1038/s41590-019-0405-2 PMID: 31182807</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Raulet, D.H.; Vance, R.E. Self-tolerance of natural killer cells. Nat. Rev. Immunol., 2006, 6(7), 520-531. doi: 10.1038/nri1863 PMID: 16799471</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Soelistyoningsih, D.; Susianti, H.; Kalim, H.; Handono, K. The phenotype of CD3CD56bright and CD3CD56dim natural killer cells in systemic lupus erythematosus patients and its relation to disease activity. Reumatologia, 2022, 60(4), 258-265. doi: 10.5114/reum.2022.119042 PMID: 36186836</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Poznanski, S.M.; Ashkar, A.A. Shining light on the significance of NK cell CD56 brightness. Cell. Mol. Immunol., 2018, 15(12), 1071-1073. doi: 10.1038/s41423-018-0163-3 PMID: 30275534</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Michel, T.; Poli, A.; Cuapio, A.; Briquemont, B.; Iserentant, G.; Ollert, M.; Zimmer, J. Human CD56 bright NK cells: An update. J. Immunol., 2016, 196(7), 2923-2931. doi: 10.4049/jimmunol.1502570 PMID: 26994304</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Koch, J.; Steinle, A.; Watzl, C.; Mandelboim, O. Activating natural cytotoxicity receptors of natural killer cells in cancer and infection. Trends Immunol., 2013, 34(4), 182-191. doi: 10.1016/j.it.2013.01.003 PMID: 23414611</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Terrén, I.; Orrantia, A.; Vitallé, J.; Astarloa-Pando, G.; Zenarruzabeitia, O.; Borrego, F. Modulating NK cell metabolism for cancer immunotherapy. Semin. Hematol., 2020, 57(4), 213-224. doi: 10.1053/j.seminhematol.2020.10.003 PMID: 33256914</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Correia, A.L.; Guimaraes, J.C.; Auf der Maur, P.; De Silva, D.; Trefny, M.P.; Okamoto, R.; Bruno, S.; Schmidt, A.; Mertz, K.; Volkmann, K.; Terracciano, L.; Zippelius, A.; Vetter, M.; Kurzeder, C.; Weber, W.P.; Bentires-Alj, M. Hepatic stellate cells suppress NK cell-sustained breast cancer dormancy. Nature, 2021, 594(7864), 566-571. doi: 10.1038/s41586-021-03614-z PMID: 34079127</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Castillo, E.F.; Schluns, K.S. Regulating the immune system via IL-15 transpresentation. Cytokine, 2012, 59(3), 479-490. doi: 10.1016/j.cyto.2012.06.017 PMID: 22795955</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Balsamo, M.; Scordamaglia, F.; Pietra, G.; Manzini, C.; Cantoni, C.; Boitano, M.; Queirolo, P.; Vermi, W.; Facchetti, F.; Moretta, A.; Moretta, L.; Mingari, M.C.; Vitale, M. Melanoma-associated fibroblasts modulate NK cell phenotype and antitumor cytotoxicity. Proc. Natl. Acad. Sci. USA, 2009, 106(49), 20847-20852. doi: 10.1073/pnas.0906481106 PMID: 19934056</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Ma, S.; Caligiuri, M.A.; Yu, J. Harnessing IL-15 signaling to potentiate NK cell-mediated cancer immunotherapy. Trends Immunol., 2022, 43(10), 833-847. doi: 10.1016/j.it.2022.08.004 PMID: 36058806</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Dean, I.; Lee, C.Y.C.; Tuong, Z.K.; Li, Z.; Tibbitt, C.A.; Willis, C.; Gaspal, F.; Kennedy, B.C.; Matei-Rascu, V.; Fiancette, R.; Nordenvall, C.; Lindforss, U.; Baker, S.M.; Stockmann, C.; Sexl, V.; Hammond, S.A.; Dovedi, S.J.; Mjösberg, J.; Hepworth, M.R.; Carlesso, G.; Clatworthy, M.R.; Withers, D.R. Rapid functional impairment of natural killer cells following tumor entry limits anti-tumor immunity. Nat. Commun., 2024, 15(1), 683. doi: 10.1038/s41467-024-44789-z PMID: 38267402</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Mishra, H.K.; Dixon, K.J.; Pore, N.; Felices, M.; Miller, J.S.; Walcheck, B. Activation of ADAM17 by IL-15 limits human NK cell proliferation. Front. Immunol., 2021, 12, 711621. doi: 10.3389/fimmu.2021.711621 PMID: 34367174</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Watkinson, F.; Nayar, S.K.; Rani, A.; Sakellariou, C.A.; Elhage, O.; Papaevangelou, E.; Dasgupta, P.; Galustian, C. IL-15 upregulates telomerase expression and potently increases proliferative capacity of NK, NKT-like, and CD8 T cells. Front. Immunol., 2021, 11, 594620. doi: 10.3389/fimmu.2020.594620 PMID: 33537030</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Ghosh, A.K.; Sinha, D.; Biswas, R.; Biswas, T. IL-15 stimulates NKG2D while promoting IgM expression of B-1a cells. Cytokine, 2017, 95, 43-50. doi: 10.1016/j.cyto.2017.02.014 PMID: 28235675</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Zhang, C.; Zhang, J.; Niu, J.; Zhang, J.; Tian, Z. Interleukin-15 improves cytotoxicity of natural killer cells via up-regulating NKG2D and cytotoxic effector molecule expression as well as STAT1 and ERK1/2 phosphorylation. Cytokine, 2008, 42(1), 128-136. doi: 10.1016/j.cyto.2008.01.003 PMID: 18280748</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Khameneh, H.J.; Fonta, N.; Zenobi, A.; Niogret, C.; Ventura, P.; Guerra, C.; Kwee, I.; Rinaldi, A.; Pecoraro, M.; Geiger, R.; Cavalli, A.; Bertoni, F.; Vivier, E.; Trumpp, A.; Guarda, G. Myc controls NK cell development, IL-15-driven expansion, and translational machinery. Life Sci. Alliance, 2023, 6(7), e202302069. doi: 10.26508/lsa.202302069 PMID: 37105715</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Wang, X.; Zhao, X.Y. Transcription factors associated with IL-15 cytokine signaling during NK cell development. Front. Immunol., 2021, 12, 610789. doi: 10.3389/fimmu.2021.610789 PMID: 33815365</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Carson, W.E.; Fehniger, T.A.; Haldar, S.; Eckhert, K.; Lindemann, M.J.; Lai, C.F.; Croce, C.M.; Baumann, H.; Caligiuri, M.A. A potential role for interleukin-15 in the regulation of human natural killer cell survival. J. Clin. Invest., 1997, 99(5), 937-943. doi: 10.1172/JCI119258 PMID: 9062351</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Huntington, N.D.; Puthalakath, H.; Gunn, P.; Naik, E.; Michalak, E.M.; Smyth, M.J.; Tabarias, H.; Degli-Esposti, M.A.; Dewson, G.; Willis, S.N.; Motoyama, N.; Huang, D.C.S.; Nutt, S.L.; Tarlinton, D.M.; Strasser, A. Interleukin 15mediated survival of natural killer cells is determined by interactions among Bim, Noxa and Mcl-1. Nat. Immunol., 2007, 8(8), 856-863. doi: 10.1038/ni1487 PMID: 17618288</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Koka, R.; Burkett, P.R.; Chien, M.; Chai, S.; Chan, F.; Lodolce, J.P.; Boone, D.L.; Ma, A. Interleukin (IL)-15Ralpha-deficient natural killer cells survive in normal but not IL-15Ralpha-deficient mice. J. Exp. Med., 2003, 197(8), 977-984. doi: 10.1084/jem.20021836 PMID: 12695489</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Oberoi, P.; Kamenjarin, K.; Villena Ossa, J.F.; Uherek, B.; Bönig, H.; Wels, W.S. Directed differentiation of mobilized hematopoietic stem and progenitor cells into functional NK cells with enhanced antitumor activity. Cells, 2020, 9(4), 811. doi: 10.3390/cells9040811 PMID: 32230942</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Wang, Y.; Zhang, Y.; Yi, P.; Dong, W.; Nalin, A.P.; Zhang, J.; Zhu, Z.; Chen, L.; Benson, D.M.; Mundy-Bosse, B.L.; Freud, A.G.; Caligiuri, M.A.; Yu, J. The IL-15AKTXBP1s signaling pathway contributes to effector functions and survival in human NK cells. Nat. Immunol., 2019, 20(1), 10-17. doi: 10.1038/s41590-018-0265-1 PMID: 30538328</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Ma, S.; Han, J.; Li, Z.; Xiao, S.; Zhang, J.; Yan, J.; Tang, T.; Barr, T.; Kraft, A.S.; Caligiuri, M.A.; Yu, J. An XBP1sPIM-2 positive feedback loop controls IL-15mediated survival of natural killer cells. Sci. Immunol., 2023, 8(81), eabn7993. doi: 10.1126/sciimmunol.abn7993 PMID: 36897958</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Roy, K.; Chakraborty, M.; Kumar, A.; Manna, A.K.; Roy, N.S. The NFκB signaling system in the generation of B-cell subsets: from germinal center B cells to memory B cells and plasma cells. Front. Immunol., 2023, 14, 1185597. doi: 10.3389/fimmu.2023.1185597 PMID: 38169968</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Cargill, T.; Culver, E.L. The role of B cells and B cell therapies in immune-mediated liver diseases. Front. Immunol., 2021, 12, 661196. doi: 10.3389/fimmu.2021.661196 PMID: 33936097</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Wang, Y.; Liu, J.; Burrows, P.D.; Wang, J.Y. B cell development and maturation. Adv. Exp. Med. Biol., 2020, 1254, 1-22. doi: 10.1007/978-981-15-3532-1_1 PMID: 32323265</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Yoshimoto, M. The ontogeny of murine B-1a cells. Int. J. Hematol., 2020, 111(5), 622-627. doi: 10.1007/s12185-019-02787-8 PMID: 31802412</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Sabatino, J.J., Jr; Pröbstel, A.K.; Zamvil, S.S. B cells in autoimmune and neurodegenerative central nervous system diseases. Nat. Rev. Neurosci., 2019, 20(12), 728-745. doi: 10.1038/s41583-019-0233-2 PMID: 31712781</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Anderson, N.M.; Simon, M.C. The tumor microenvironment. Curr. Biol., 2020, 30(16), R921-R925. doi: 10.1016/j.cub.2020.06.081 PMID: 32810447</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Chandnani, N.; Gupta, I.; Mandal, A.; Sarkar, K. Participation of B cell in immunotherapy of cancer. Pathol. Res. Pract., 2024, 255, 155169. doi: 10.1016/j.prp.2024.155169 PMID: 38330617</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Rastogi, I.; Jeon, D.; Moseman, J.E.; Muralidhar, A.; Potluri, H.K.; McNeel, D.G. Role of B cells as antigen presenting cells. Front. Immunol., 2022, 13, 954936. doi: 10.3389/fimmu.2022.954936 PMID: 36159874</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Laumont, C.M.; Nelson, B.H. B cells in the tumor microenvironment: Multi-faceted organizers, regulators, and effectors of anti-tumor immunity. Cancer Cell, 2023, 41(3), 466-489. doi: 10.1016/j.ccell.2023.02.017 PMID: 36917951</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Armitage, R.J.; Macduff, B.M.; Eisenman, J.; Paxton, R.; Grabstein, K.H. IL-15 has stimulatory activity for the induction of B cell proliferation and differentiation. J. Immunol., 1995, 154(2), 483-490. doi: 10.4049/jimmunol.154.2.483 PMID: 7814861</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Kanti Ghosh, A.; Sinha, D.; Mukherjee, S.; Biswas, R.; Biswas, T. IL-15 temporally reorients IL-10 biased B-1a cells toward IL-12 expression. Cell. Mol. Immunol., 2016, 13(2), 229-239. doi: 10.1038/cmi.2015.08 PMID: 25748019</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Gill, N.; Paltser, G.; Ashkar, A.A. Interleukin-15 expression affects homeostasis and function of B cells through NK cell-derived interferon-γ. Cell. Immunol., 2009, 258(1), 59-64. doi: 10.1016/j.cellimm.2009.03.010 PMID: 19361783</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Waldmann, T.; Dubois, S.; Tagaya, Y. Contrasting roles of IL-2 and IL-15 in the life and death of lymphocytes: implications for immunotherapy. Immunity, 2001, 14(2), 105-110. doi: 10.1016/S1074-7613(09)00091-0 PMID: 11239443</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Nagy, É.; Mocsár, G.; Sebestyén, V.; Volkó, J.; Papp, F.; Tóth, K.; Damjanovich, S.; Panyi, G.; Waldmann, T.A.; Bodnár, A.; Vámosi, G. Membrane Potential Distinctly Modulates Mobility and Signaling of IL-2 and IL-15 Receptors in T Cells. Biophys. J., 2018, 114(10), 2473-2482. doi: 10.1016/j.bpj.2018.04.038 PMID: 29754714</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Hilton, L.R.; Rätsep, M.T.; VandenBroek, M.M.; Jafri, S.; Laverty, K.J.; Mitchell, M.; Theilmann, A.L.; Smart, J.A.; Hawke, L.G.; Moore, S.D.; Renaud, S.J.; Soares, M.J.; Morrell, N.W.; Ormiston, M.L. Impaired interleukin-15 signaling via BMPR2 loss drives natural killer cell deficiency and pulmonary hypertension. Hypertension, 2022, 79(11), 2493-2504. doi: 10.1161/HYPERTENSIONAHA.122.19178 PMID: 36043416</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Choi, Y.J.; Lee, H.; Kim, J.H.; Kim, S.Y.; Koh, J.Y.; Sa, M.; Park, S.H.; Shin, E.C. CD5 suppresses IL-15induced proliferation of human memory CD8+ T cells by inhibiting mTOR pathways. J. Immunol., 2022, 209(6), 1108-1117. doi: 10.4049/jimmunol.2100854 PMID: 36002232</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Ma, S.; Tang, T.; Wu, X.; Mansour, A.G.; Lu, T.; Zhang, J.; Wang, L.S.; Caligiuri, M.A.; Yu, J. PDGF-D−PDGFRβ signaling enhances IL-15mediated human natural killer cell survival. Proc. Natl. Acad. Sci. USA, 2022, 119(3), e2114134119. doi: 10.1073/pnas.2114134119 PMID: 35027451</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Raeber, M.E.; Sahin, D.; Boyman, O. Interleukin-2based therapies in cancer. Sci. Transl. Med., 2022, 14(670), eabo5409. doi: 10.1126/scitranslmed.abo5409 PMID: 36350987</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Reardon, S. How to supercharge cancer-fighting cells: give them stem-cell skills. Nature, 2024, 628(8008), 486. doi: 10.1038/d41586-024-01043-2 PMID: 38600202</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Chapoval, A.I.; Fuller, J.A.; Kremlev, S.G.; Kamdar, S.J.; Evans, R. Combination chemotherapy and IL-15 administration induce permanent tumor regression in a mouse lung tumor model: NK and T cell-mediated effects antagonized by B cells. J. Immunol., 1998, 161(12), 6977-6984. doi: 10.4049/jimmunol.161.12.6977 PMID: 9862733</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Van Belle, T.; Grooten, J. IL-15 and IL-15Ralpha in CD4+T cell immunity. Arch. Immunol. Ther. Exp. (Warsz.), 2005, 53(2), 115-126. PMID: 15928580</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Bergamaschi, C.; Pandit, H.; Nagy, B.A.; Stellas, D.; Jensen, S.M.; Bear, J.; Cam, M.; Valentin, A.; Fox, B.A.; Felber, B.K.; Pavlakis, G.N. Heterodimeric IL-15 delays tumor growth and promotes intratumoral CTL and dendritic cell accumulation by a cytokine network involving XCL1, IFN-γ, CXCL9 and CXCL10. J. Immunother. Cancer, 2020, 8(1), e000599. doi: 10.1136/jitc-2020-000599 PMID: 32461349</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Rubinstein, M.P.; Kovar, M.; Purton, J.F.; Cho, J.H.; Boyman, O.; Surh, C.D.; Sprent, J. Converting IL-15 to a superagonist by binding to soluble IL-15Rα. Proc. Natl. Acad. Sci. USA, 2006, 103(24), 9166-9171. doi: 10.1073/pnas.0600240103 PMID: 16757567</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Zhu, X.; Marcus, W.D.; Xu, W.; Lee, H.; Han, K.; Egan, J.O.; Yovandich, J.L.; Rhode, P.R.; Wong, H.C. Novel human interleukin-15 agonists. J. Immunol., 2009, 183(6), 3598-3607. doi: 10.4049/jimmunol.0901244 PMID: 19710453</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Waldmann, T.A.; Dubois, S.; Miljkovic, M.D.; Conlon, K.C. IL-15 in the combination immunotherapy of cancer. Front. Immunol., 2020, 11, 868. doi: 10.3389/fimmu.2020.00868 PMID: 32508818</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Shen, J.; Zou, Z.; Guo, J.; Cai, Y.; Xue, D.; Liang, Y.; Wang, W.; Peng, H.; Fu, Y.X. An engineered concealed IL-15-R elicits tumor-specific CD8+T cell responses through PD-1-cis delivery. J. Exp. Med., 2022, 219(12), e20220745. doi: 10.1084/jem.20220745 PMID: 36165896</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Hirayama, A.V.; Chou, C.K.; Miyazaki, T.; Steinmetz, R.N.; Di, H.A.; Fraessle, S.P.; Gauthier, J.; Fiorenza, S.; Hawkins, R.M.; Overwijk, W.W.; Riddell, S.R.; Marcondes, M.Q.; Turtle, C.J. A novel polymer-conjugated human IL-15 improves efficacy of CD19-targeted CAR T-cell immunotherapy. Blood Adv., 2023, 7(11), 2479-2493. doi: 10.1182/bloodadvances.2022008697 PMID: 36332004</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Mujib, S.; Jones, R.B.; Lo, C.; Aidarus, N.; Clayton, K.; Sakhdari, A.; Benko, E.; Kovacs, C.; Ostrowski, M.A. Antigen-independent induction of Tim-3 expression on human T cells by the common γ-chain cytokines IL-2, IL-7, IL-15, and IL-21 is associated with proliferation and is dependent on the phosphoinositide 3-kinase pathway. J. Immunol., 2012, 188(8), 3745-3756. doi: 10.4049/jimmunol.1102609 PMID: 22422881</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Conlon, K.C.; Lugli, E.; Welles, H.C.; Rosenberg, S.A.; Fojo, A.T.; Morris, J.C.; Fleisher, T.A.; Dubois, S.P.; Perera, L.P.; Stewart, D.M.; Goldman, C.K.; Bryant, B.R.; Decker, J.M.; Chen, J.; Worthy, T.Y.A.; Figg, W.D., Sr; Peer, C.J.; Sneller, M.C.; Lane, H.C.; Yovandich, J.L.; Creekmore, S.P.; Roederer, M.; Waldmann, T.A. Redistribution, hyperproliferation, activation of natural killer cells and CD8 T cells, and cytokine production during first-in-human clinical trial of recombinant human interleukin-15 in patients with cancer. J. Clin. Oncol., 2015, 33(1), 74-82. doi: 10.1200/JCO.2014.57.3329 PMID: 25403209</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Romee, R.; Cooley, S.; Berrien-Elliott, M.M.; Westervelt, P.; Verneris, M.R.; Wagner, J.E.; Weisdorf, D.J.; Blazar, B.R.; Ustun, C.; DeFor, T.E.; Vivek, S.; Peck, L.; DiPersio, J.F.; Cashen, A.F.; Kyllo, R.; Musiek, A.; Schaffer, A.; Anadkat, M.J.; Rosman, I.; Miller, D.; Egan, J.O.; Jeng, E.K.; Rock, A.; Wong, H.C.; Fehniger, T.A.; Miller, J.S. First-in-human phase 1 clinical study of the IL-15 superagonist complex ALT-803 to treat relapse after transplantation. Blood, 2018, 131(23), 2515-2527. doi: 10.1182/blood-2017-12-823757 PMID: 29463563</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Liu, R.B.; Engels, B.; Schreiber, K.; Ciszewski, C.; Schietinger, A.; Schreiber, H.; Jabri, B. IL-15 in tumor microenvironment causes rejection of large established tumors by T cells in a noncognate T cell receptor-dependent manner. Proc. Natl. Acad. Sci. USA, 2013, 110(20), 8158-8163. doi: 10.1073/pnas.1301022110 PMID: 23637340</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Di Matteo, S.; Munari, E.; Fiore, P.F.; Santopolo, S.; Sampaoli, C.; Pelosi, A.; Chouaib, S.; Tumino, N.; Vacca, P.; Mariotti, F.R.; Ebert, S.; Machwirth, M.; Haas, D.; Pezzullo, M.; Pietra, G.; Grottoli, M.; Buart, S.; Mortier, E.; Maggi, E.; Moretta, L.; Caruana, I.; Azzarone, B. The roles of different forms of IL-15 in human melanoma progression. Front. Immunol., 2023, 14, 1183668. doi: 10.3389/fimmu.2023.1183668 PMID: 37334356</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Fehniger, T.A.; Caligiuri, M.A. Interleukin 15: biology and relevance to human disease. Blood, 2001, 97(1), 14-32. doi: 10.1182/blood.V97.1.14 PMID: 11133738</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Yuan, H.; Meng, X.; Guo, W.; Cai, P.; Li, W.; Li, Q.; Wang, W.; Sun, Y.; Xu, Q.; Gu, Y. Transmembrane-bound IL-15promoted epithelial-mesenchymal transition in renal cancer cells requires the Src-dependent Akt/GSK-3β/β-catenin pathway. Neoplasia, 2015, 17(5), 410-420. doi: 10.1016/j.neo.2015.04.002 PMID: 26025664</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Azzi, S.; Gallerne, C.; Romei, C.; Le Coz, V.; Gangemi, R.; Khawam, K.; Devocelle, A.; Gu, Y.; Bruno, S.; Ferrini, S.; Chouaib, S.; Eid, P.; Azzarone, B.; Giron-Michel, J. Human renal normal, tumoral, and cancer stem cells express membrane-bound interleukin-15 isoforms displaying different functions. Neoplasia, 2015, 17(6), 509-517. doi: 10.1016/j.neo.2015.06.002 PMID: 26152359</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Guo, J.; Liang, Y.; Xue, D.; Shen, J.; Cai, Y.; Zhu, J.; Fu, Y.X.; Peng, H. Tumor-conditional IL-15 pro-cytokine reactivates anti-tumor immunity with limited toxicity. Cell Res., 2021, 31(11), 1190-1198. doi: 10.1038/s41422-021-00543-4 PMID: 34376814</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Wrangle, J.M.; Velcheti, V.; Patel, M.R.; Garrett-Mayer, E.; Hill, E.G.; Ravenel, J.G.; Miller, J.S.; Farhad, M.; Anderton, K.; Lindsey, K.; Taffaro-Neskey, M.; Sherman, C.; Suriano, S.; Swiderska-Syn, M.; Sion, A.; Harris, J.; Edwards, A.R.; Rytlewski, J.A.; Sanders, C.M.; Yusko, E.C.; Robinson, M.D.; Krieg, C.; Redmond, W.L.; Egan, J.O.; Rhode, P.R.; Jeng, E.K.; Rock, A.D.; Wong, H.C.; Rubinstein, M.P. ALT-803, an IL-15 superagonist, in combination with nivolumab in patients with metastatic non-small cell lung cancer: a non-randomised, open-label, phase 1b trial. Lancet Oncol., 2018, 19(5), 694-704. doi: 10.1016/S1470-2045(18)30148-7 PMID: 29628312</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Brammer, J.E.; Ballen, K.; Sokol, L.; Querfeld, C.; Nakamura, R.; Mishra, A.; McLaughlin, E.M.; Feith, D.; Azimi, N.; Waldmann, T.A.; Tagaya, Y.; Loughran, T. Effective treatment with the selective cytokine inhibitor BNZ-1 reveals the cytokine dependency of T-LGL leukemia. Blood, 2023, 142(15), 1271-1280. doi: 10.1182/blood.2022017643 PMID: 37352612</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Slavuljica, I.; Krmpotić, A.; Jonjić, S. Manipulation of NKG2D ligands by cytomegaloviruses: impact on innate and adaptive immune response. Front. Immunol., 2011, 2, 85. PMID: 22566874</mixed-citation></ref></ref-list></back></article>
