<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Advances in Molecular Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Advances in Molecular Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Успехи молекулярной онкологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-805X</issn><issn publication-format="electronic">2413-3787</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">849</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2026-13-2-26-36</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">The immune microenvironment and promising strategies for neuroblastoma therapy</article-title><trans-title-group xml:lang="ru"><trans-title>Иммунное микроокружение и перспективные стратегии терапии нейробластомы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0001-3534-2911</contrib-id><name-alternatives><name xml:lang="en"><surname>Karpov</surname><given-names>Gleb A.</given-names></name><name xml:lang="ru"><surname>Карпов</surname><given-names>Глеб Андреевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>gleb13.karpov@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1308-8622</contrib-id><name-alternatives><name xml:lang="en"><surname>Druy</surname><given-names>A. E.</given-names></name><name xml:lang="ru"><surname>Друй</surname><given-names>А. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>gleb13.karpov@gmail.com</email><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГАОУ ВО «Российский национальный исследовательский медицинский университет им. Н.И. Пирогова» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center Of Pediatric Hematology, Oncology and Immunology, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Dr. Sergey Berezin Medical Institute</institution></aff><aff><institution xml:lang="ru">Международный институт биологических систем им. Сергея Березина</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2026-06-19" publication-format="electronic"><day>19</day><month>06</month><year>2026</year></pub-date><volume>13</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>26</fpage><lpage>36</lpage><history><date date-type="received" iso-8601-date="2026-02-10"><day>10</day><month>02</month><year>2026</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2026, ABV-Press</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2026, АБВ-пресс</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="en">ABV-Press</copyright-holder><copyright-holder xml:lang="ru">АБВ-пресс</copyright-holder><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://umo.abvpress.ru/jour/about/editorialPolicies</ali:license_ref></license></permissions><self-uri xlink:href="https://umo.abvpress.ru/jour/article/view/849">https://umo.abvpress.ru/jour/article/view/849</self-uri><abstract xml:lang="en"><p>Neuroblastoma is a malignant tumor found in children and characterized by exceptional heterogeneity and complex microenvironment which plays a key role in disease progression and response to therapy. The review summarizes the modern data on cell composition of neuroblastoma microenvironment and its effect on prognosis promoting formation of promising treatment strategies. Modulation of tumor microenvironment can become the key approach to development of effective targeted therapy and immunotherapy for various types of neuroblastoma.</p></abstract><trans-abstract xml:lang="ru"><p>Нейробластома – злокачественная опухоль детского возраста, характеризующаяся исключительной гетерогенностью и сложным микроокружением, которое играет определяющую роль в прогрессировании заболевания и ответе на терапию. В обзоре систематизированы современные данные о клеточном составе микроокружения нейробластомы и его влиянии на прогноз, способствующие формированию перспективных стратегий лечения. Модуляция микроокружения этой опухоли может быть ключевым направлением для разработки эффективной таргетной терапии и иммунотерапии при разных типах нейробластомы.</p></trans-abstract><kwd-group xml:lang="en"><kwd>tumor microenvironment</kwd><kwd>immunotherapy</kwd><kwd>prognosis</kwd><kwd>neuroblastoma</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>опухолевое микроокружение</kwd><kwd>иммунотерапия</kwd><kwd>прогноз</kwd><kwd>нейробластома</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Cheung N.V., Dyer M.A. Neuroblastoma: developmental biology, cancer genomics and immunotherapy. Nat Rev Cancer 2013;13(6):397–411. DOI: 10.1038/nrc3526</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Blavier L., Yang R., DeClerck Y.A. The tumor microenvironment in neuroblastoma: new players, new mechanisms of interaction and new perspectives Cancers (Basel) 2020;12(10):2912. DOI: 10.3390/cancers12102912</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Gunaydin G. CAFs interacting with TAMs in tumor microenvironment to enhance tumorigenesis and immune evasion. Front Oncol 2021;11:668349. DOI: 10.3389/fonc.2021.668349</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Sahai E., Astsaturov I., Cukierman E. et al. A framework for advancing our understanding of cancer-associated fibroblasts. Nat Rev Cancer 2020;20(3):174–86. DOI: 10.1038/s41568-019-0238-1</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Hashimoto O., Yoshida M., Koma Y. et al. Collaboration of cancer-associated fibroblasts and tumour-associated macrophages for neuroblastoma development. J Pathol 2016;240(2):211–23. DOI: 10.1002/path.4769</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Mosser D.M., Edwards J P. Exploring the full spectrum of macrophage activation. Nat Rev Immunol 2008;8(12):958–69. DOI: 10.1038/nri2448</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>DeNardo D.G., Barreto J.B., Andreu P. et al. CD4(+) T cells regulate pulmonary metastasis of mammary carcinomas by enhancing protumor properties of macrophages. Cancer Cell 2009;16(2):91–102. DOI: 10.1016/j.ccr.2009.06.018</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Ganesan A.P., Johansson M., Ruffell B. et al. Tumor-infiltrating regulatory T cells inhibit endogenous cytotoxic T cell responses to lung adenocarcinoma. J Immunol 2013;191(4):2009–17. DOI: 10.4049/jimmunol.1301317</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Purwar R., Schlapbach C., Xiao S. et al. Robust tumor immunity to melanoma mediated by interleukin-9-producing T cells. Nat Med 2012;18(8):1248–53. DOI: 10.1038/nm.2856</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Sun Y., Xu S. Tumor-associated CD204-positive macrophage is a prognostic marker in clinical stage I lung adenocarcinoma. Biomed Res Int 2018;2018:8459193. DOI: 10.1155/2018/8459193</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Asgharzadeh S., Salo J.A., Ji L. et al. Clinical significance of tumor-associated inflammatory cells in metastatic neuroblastoma. J Clin Oncol 2012;30(28):3525–32. DOI: 10.1200/jco.2011.40.9169</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Zhang P., Wu X., Basu M. et al. MYCN amplification is associated with repressed cellular immunity in neuroblastoma: an in silico immunological analysis of TARGET database. Front Immunol 2017;8:1473. DOI: 10.3389/fimmu.2017.01473</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Mina M., Boldrini R., Citti A. et al. Tumor-infiltrating T lymphocytes improve clinical outcome of therapy-resistant neuroblastoma. OncoImmunology 2015;4(9):e1019981. DOI: 10.1080/2162402x.2015.1019981</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Zhong X., Zhang Y., Wang L. et al. Cellular components in tumor microenvironment of neuroblastoma and the prognostic value. Peer J 2019;7:e8017. DOI: 10.7717/peerj.8017</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Morandi F., Pozzi S., Barco S. et al. CD4+CD25hiCD127− Treg and CD4+CD45R0+CD49b+LAG3+ Tr1 cells in bone marrow and peripheral blood samples from children with neuroblastoma. OncoImmunology 2016;5(12):e1249553. DOI: 10.1080/2162402x.2016.1249553</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Schaafsma E., Jiang C., Cheng C. B cell infiltration is highly associated with prognosis and an immune-infiltrated tumor microenvironment in neuroblastoma. J Cancer Metastasis Treat 2021;7(34):10.20517/2394-4722.2021.72. DOI: 10.20517/2394-4722.2021.72</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Mei S., Alchahin A.M., Embaie B.T. et al. Single-cell analyses of metastatic bone marrow in human neuroblastoma reveals microenvironmental remodeling and metastatic signature. JCI Insight 2024;9(6):e173337. DOI: 10.1172/jci.insight.173337</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Wei J.S., Kuznetsov I.B., Zhang S. et al. Clinically relevant cytotoxic immune cell signatures and clonal expansion of T-cell receptors in HIGH-RISK MYCN-not-amplified human neuroblastoma. Clin Cancer Res 2018;24(22):5673–84. DOI: 10.1158/1078-0432.ccr-18-0599</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Layer J.P., Kronmüller M.T., Quast T. et al. Amplification of N-Myc is associated with a T-cell-poor microenvironment in metastatic neuroblastoma restraining interferon pathway activity and chemokine expression. OncoImmunology 2017;6(6):e1320626. DOI: 10.1080/2162402x.2017.1320626</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Raffaghello L., Prigione I., Airoldi I. et al. Downregulation and/or release of NKG2D ligands as immune evasion strategy of human neuroblastoma. Neoplasia 2004;6(5):558–68. DOI: 10.1593/neo.04316</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Wienke J., Visser L.L., Kholosy W.M. et al. Integrative analysis of neuroblastoma by single-cell RNA sequencing identifies the NECTIN2-TIGIT axis as a target for immunotherapy. Cancer Cell 2024;42(2):283–300.e8. DOI: 10.1016/j.ccell.2023.12.008</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Vanichapol T., Chutipongtanate S., Anurathapan U., Hongeng S. Immune escape mechanisms and future prospects for immunotherapy in neuroblastoma. Biomed Res Int 2018;2018:1812535. DOI: 10.1155/2018/1812535</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Castriconi R., Cantoni C., Della Chiesa M. et al. Transforming growth factor β1 inhibits expression of NKp30 and NKG2D receptors: Consequences for the NK-mediated killing of dendritic cells. Proc Natl Acad Sci USA 2003;100(7):4120–5. DOI: 10.1073/pnas.0730640100</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Park Y.P., Choi S., Kiesler P. et al. Complex regulation of human NKG2D-DAP10 cell surface expression: opposing roles of the γc cytokines and TGF-β1. Blood 2011;118(11):3019–27. DOI: 10.1182/blood-2011-04-346825</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Gao Y., Souza-Fonseca-Guimaraes F., Bald T. et al. Tumor immunoevasion by the conversion of effector NK cells into type 1 innate lymphoid cells. Nat Immunol 2017;18(9):1004–15. DOI: 10.1038/ni.3800</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Zhen Z., Guo X., Liao R. et al. Involvement of IL-10 and TGF-β in HLA-E-mediated neuroblastoma migration and invasion. Oncotarget 2016;7(28):44340–9. DOI: 10.18632/oncotarget.10041</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Morandi F., Levreri I., Bocca P. et al. Human neuroblastoma cells trigger an immunosuppressive program in monocytes by stimulating soluble HLA-G release. Cancer Res 2007;67(13):6433–41. DOI: 10.1158/0008-5472.can-06-4588</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Bergers G., Brekken R., McMahon G. et al. Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis. Nat Cell Biol 2000;2(10):737–44. DOI: 10.1038/35036374</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Itatani Y., Yamamoto T., Zhong C. et al. Suppressing neutrophil-dependent angiogenesis abrogates resistance to anti-VEGF antibody in a genetic model of colorectal cancer. Proc Natl Acad Sci USA 2020;117(35):21598–608. DOI: 10.1073/pnas.2008112117</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Condamine T., Dominguez G.A., Youn J.I. et al. Lectin-type oxidized LDL receptor-1 distinguishes population of human polymorphonuclear myeloid-derived suppressor cells in cancer patients. Sci Immunol 2016;1(2):aaf8943. DOI: 10.1126/sciimmunol.aaf8943</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Chao T., Furth E.E., Vonderheide R.H. CXCR2-dependent accumulation of tumor-associated neutrophils regulates T-cell immunity in pancreatic ductal adenocarcinoma. Cancer Immunol Res 2016;4(11):968–82. DOI: 10.1158/2326-6066.CIR-16-0188</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Morandi F., Barco S., Stigliani S. et al. Altered erythropoiesis and decreased number of erythrocytes in children with neuroblastoma. Oncotarget 2017;8(32):53194–209. DOI: 10.18632/oncotarget.18285</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Zeng L., Liu X.-Y., Chen K. et al. Phosphoserine phosphatase as an indicator for survival through potentially influencing the infiltration levels of immune cells in neuroblastoma. Front Cell Dev Bio 2022;10:873710. DOI: 10.3389/fcell.2022.873710</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Zhang Y., Zhang C., Ma Y. et al. Prediction to the prognosis of children with neuroblastoma by nomogram based on the first-diagnosed inflammatory markers. Pediatr Surg Int 2022;39(1):17. DOI: 10.1007/s00383-022-05302-z</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Erbe A.K., Diccianni M.B., Mody R. et al. KIR/KIR-ligand genotypes and clinical outcomes following chemoimmunotherapy in patients with relapsed or refractory neuroblastoma: a report from the Children’s Oncology Group. J Immunother Cancer 2023;11(2):e006530. DOI: 10.1136/jitc-2022-006530</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Fultang L., Gamble L.D., Gneo L. et al. Macrophage-derived IL1beta and TNFalpha regulate arginine metabolism in neuroblastoma. Cancer Res 2019;79(3):611–24. DOI: 10.1158/0008-5472.CAN-18-2139</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Stip M.C., Teeuwen L., Dierselhuis M.P. et al. Targeting the myeloid microenvironment in neuroblastoma. J Exp Clin Cancer Res 2023;42(1):337. DOI: 10.1186/s13046-023-02913-9</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Facciabene A., Motz G.T., Coukos G. T-regulatory cells: key players in tumor immune escape and angiogenesis. Cancer Res 2012;72(9):2162–71. DOI: 10.1158/0008-5472.can-11-3687</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Matthay K.K., Blaes F., Hero B. et al. Opsoclonus myoclonus syndrome in neuroblastoma a report from a workshop on the dancing eyes syndrome at the advances in neuroblastoma meeting in Genoa, Italy, 2004. Cancer Letters 2005;228(1–2):275–82. DOI: 10.1016/j.canlet.2005.01.051</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Ding X., Yang W., Ren Q. et al. Serum IgG-induced microglial activation enhances neuronal cytolysis via the NO/sGC/PKG pathway in children with opsoclonus-myoclonus syndrome and neuroblastoma. J Neuroinflammation 2020;17(1):190. DOI: 10.1186/s12974-020-01839-9</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Rudnick E., Khakoo Y., Antunes N.L. et al. Opsoclonus-myoclonus-ataxia syndrome in neuroblastoma: Clinical outcome and antineuronal antibodies – a report from the Children’s cancer group study. Med Pediatr Oncol 2001;36(6):612–22. DOI: 10.1002/mpo.1138</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Gambini C., Conte M., Bernini G. et al. Neuroblastic tumors associated with opsoclonus-myoclonus syndrome: histological, immunohistochemical and molecular features of 15 Italian cases. Virch Arch 2003;442(6):555–62. DOI: 10.1007/s00428-002-0747-1</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Fukushima H., Inoue T., Takama Y. et al. Clinicopathological features of neuroblastic tumors with opsoclonus-myoclonus-ataxia syndrome: follicular structure predicts a better neurological outcome. Pathol Int 2017;67(10):503–9. DOI: 10.1111/pin.12591</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Fühlhuber V., Bick S., Kirsten A. et al. Elevated B-cell activating factor BAFF, but not APRIL, correlates with CSF cerebellar autoantibodies in pediatric opsoclonus-myoclonus syndrome. J Neuroimmunol 2009;210(1–2):87–91. DOI: 10.1016/j.jneuroim.2009.03.006</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Amini A., Lang B., Heaney D., Irani S.R. Multiple sequential antibody-associated syndromes with a recurrent mutated neuroblastoma. Neurology 2016;87(6):634–6. DOI: 10.1212/wnl.0000000000002945</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Olgun N., Arayici M.E., Kızmazoglu D., Cecen R.E. Assessment of chemo-immunotherapy regimens in patients with refractory or relapsed neuroblastoma: a systematic review with meta-analysis of critical oncological outcomes. J Clin Med 2025;14(3):934. DOI: 10.3390/jcm14030934</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Philippova J., Shevchenko J., Sennikov S. GD2-targeting therapy: a comparative analysis of approaches and promising directions. Front Immunol 2004;15:1371345. DOI: 10.3389/fimmu.2024.1371345</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Theruvath J., Menard M., Smith B.A.H. et al. Anti-GD2 synergizes with CD47 blockade to mediate tumor eradication. Nat Med 2022;28(2):333–44. DOI: 10.1038/s41591-021-01625-x</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Coronado E., Yañez Y., Vidal E. et al. Intratumoral immunosuppression profiles in 11q-deleted neuroblastomas provide new potential therapeutic targets. Mol Oncol 2021;15(2):364–80. DOI: 10.1002/1878-0261.12868</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Liu X., Wills C.A., Chen L. et al. Tipifarnib inhibits the secretion of tumor-derived small extracellular vesicles and enhances the immunotherapeutic efficacy of dinutuximab in neuroblastoma. Cancer Res 2022;82(Suppl 12):4216. DOI: 10.1158/1538-7445.am2022-4216</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Liu X., Wills C.A., Chen L. et al. Small extracellular vesicles induce resistance to anti-GD2 immunotherapy unveiling tipifarnib as an adjunct to neuroblastoma immunotherapy. J Immunother Cancer 2022;10(4):e004399. DOI: 10.1136/jitc-2021-004399</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Rowshanrava B., Halliday N., Sansom D.M. CTLA-4: a moving target in immunotherapy. Blood 2017;131(1):58–67. DOI: 10.1182/blood-2017-06-741033</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Mao C., Poimenidou M., Craig B.T. Current knowledge and perspectives of immunotherapies for neuroblastoma. Cancers 2024;16(16):2865. DOI: 10.3390/cancers16162865</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Shirinbak S., Chan R.Y., Shahani S. et al. Combined immune checkpoint blockade increases CD8+CD28+PD-1+ effector T cells and provides a therapeutic strategy for patients with neuroblastoma. OncoImmunology 2021;10(1):1838140. DOI: 10.1080/2162402x.2020.1838140</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Majzner R.G., Simon J.S., Grosso J.F. et al. Assessment of programmed death-ligand 1 expression and tumor-associated immune cells in pediatric cancer tissues. Cancer 2017;123(19):3807–15. DOI: 10.1002/cncr.30724</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Alborzinia H., Chen Z., Yildiz U. et al. LRP8-mediated selenocysteine uptake is a targetable vulnerability in MYCN-amplified neuroblastoma. EMBO Mol Med 2023;15(8):e18014. DOI: 10.15252/emmm.202318014</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Nomura M., Ueno A., Saga K. et al. Accumulation of cytosolic calcium induces necroptotic cell death in human neuroblastoma. Cancer Res 2013;74(4):1056–66. DOI: 10.1158/0008-5472.can-13-1283</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Galluzzi L., Kepp O., Hett E. et al. Immunogenic cell death in cancer: concept and therapeutic implications. J Transl Med 2023;21(1):162. DOI: 10.1186/s12967-023-04017-6</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Mussai F., Egan S., Hunter S. et al. Neuroblastoma arginase activity creates an immunosuppressive microenvironment that impairs autologous and engineered immunity. Cancer Res 2015;75(15):3043–53. DOI: 10.1158/0008-5472.can-14-3443</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Yau T., Cheng P.N., Chan P. et al. Preliminary efficacy, safety, pharmacokinetics, pharmacodynamics and quality of life study of pegylated recombinant human arginase 1 in patients with advanced hepatocellular carcinoma. Invest New Drugs 2015;33(2):496–504. DOI: 10.1007/s10637-014-0200-8</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Locatelli F., Pagliara D., De Ioris M.A. et al. GD2-targeting CAR T cells in high-risk neuroblastoma: a phase 1/2 trial. Nat Med 2025;31(11):3689–99. DOI: 10.1038/s41591-025-03874-6</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Li C., Sharma S., Heczey A.A. et al. Long-term outcomes of GD2-directed CAR-T cell therapy in patients with neuroblastoma. Nat Med 2025;31(4):1125–9. DOI: 10.1038/s41591-025-03513-0</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Bosse K.R., Raman P., Zhu Z. et al. Identification of GPC2 as an oncoprotein and candidate immunotherapeutic target in high-risk neuroblastoma. Cancer Cell 2017;32(3):295–309:e12. DOI: 10.1016/j.ccell.2017.08.003</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Li N., Fu H., Hewitt S.M. et al. Therapeutically targeting glypican-2 via single-domain antibody-based chimeric antigen receptors and immunotoxins in neuroblastoma. Proc Natl Acad Sci USA 2017;114(32):E6623–31. DOI: 10.1073/pnas.1706055114</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Moog-Lutz C., Degoutin J., Gouzi J.Y. et al. Activation and inhibition of anaplastic lymphoma kinase receptor tyrosine kinase by monoclonal antibodies and absence of agonist activity of pleiotrophin. J Biol Chem 2005;280(28):26039–48. DOI: 10.1074/jbc.m501972200</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Walker A.J., Majzner R.G., Zhang L. et al. Tumor antigen and receptor densities regulate efficacy of a chimeric antigen receptor targeting anaplastic lymphoma kinase. Mol Ther 2017;25(9):2189–201. DOI: 10.1016/j.ymthe.2017.06.008</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Okada R., Reyes-González J.M., Rodriguez C. et al. GPC2-targeted CAR T cells engineered with NFAT-inducible membrane-tethered IL15/IL21 exhibit enhanced activity against neuroblastoma. Cancer Immunol Res 2025;13(9):1363–73. DOI: 10.1158/2326-6066.cir-24-0975</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Giudice A.M., Roth S.L., Matlaga S. et al. Reprogramming the neuroblastoma tumor immune microenvironment to enhance GPC2 CAR T cells. Mol Ther 2025;33(9):4552–69. DOI: 10.1016/j.ymthe.2025.05.025</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Zeromski J., Nyczak E., Dyszkiewicz W. Significance of cell adhesion molecules, CD56/NCAM in particular, in human tumor growth and spreading. Folia Histochem Cytobiol 2001;39(Suppl. 2):36–7.</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Crossland D.L., Denning W.L., Ang S. et al. Antitumor activity of CD56-chimeric antigen receptor T cells in neuroblastoma and SCLC models. Oncogene 2018;37(27):3686–97. DOI: 10.1038/s41388-018-0187-2</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Bodden M., Häcker A., Röder J. et al. Co-expression of an IL-15 superagonist facilitates self-enrichment of GD2-targeted CAR-NK cells and mediates potent cell killing in the absence of IL-2. Cancers 2023;15(17):4310. DOI: 10.3390/cancers15174310</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Moghimi B., Muthugounder S., Jambon S. et al. Preclinical assessment of the efficacy and specificity of GD2-B7H3 SynNotch CAR-T in metastatic neuroblastoma. Nat Commun 2021;12(1):511. DOI: 10.1038/s41467-020-20785-x</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Suurs F.V., Hooge M.N.L., De Vries E.G. et al. A review of bispecific antibodies and antibody constructs in oncology and clinical challenges. Pharmacol Ther 2019;201:103–19. DOI: 10.1016/j.pharmthera.2019.04.006</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Kitidee K., Amonyingcharoen S., Preedagasamzin S. et al. Combining CD3/GD2 bispecific T cell engager with human Vγ9Vδ2 T cells facilitates neuroblastoma cell targeting and killing in vitro. PLoS One 2025;20(6):e0325389. DOI: 10.1371/journal.pone.0325389</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Muthukutty P., Yoo S.Y. Oncolytic virus engineering and utilizations: cancer immunotherapy perspective. Viruses 2023;15(8):1645. DOI: 10.3390/v15081645</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Chu Y., Tian M., Saini U. et al. Combinatorial immunotherapy with anti-ROR1 CAR NK cells and an IL-21 secreting oncolytic virus against neuroblastoma. Mol Ther Oncol 2024;33(1):200927. DOI: 10.1016/j.omton.2024.200927</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Wing A., Fajardo C.A., Posey A.D. et al. Improving CART-cell therapy of solid tumors with oncolytic virus-driven production of a bispecific T-cell engager. Cancer Immunol Res 2018;6(5):605–16. DOI: 10.1158/2326-6066.cir-17-0314</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Caescu C.I., Guo X., Tesfa L. et al. Colony stimulating factor-1 receptor signaling networks inhibit mouse macrophage inflammatory responses by induction of microRNA-21. Blood 2015;125(8):e1–13. DOI: 10.1182/blood-2014-10-608000</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Mao Y., Eissler N., Blanc K.L. et al. Targeting suppressive myeloid cells potentiates checkpoint inhibitors to control spontaneous neuroblastoma. Clin Cancer Res 2016;22(15):3849–59. DOI: 10.1158/1078-0432.ccr-15-1912</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Wu H., Sheard M.A., Malvar J. et al. Anti-CD105 antibody eliminates tumor microenvironment cells and enhances anti-GD2 antibody immunotherapy of neuroblastoma with activated natural killer cells. Clin Cancer Res 2019;25(15):4761–74. DOI: 10.1158/1078-0432.ccr-18-3358</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Rohila D., Park I.H., Pham T.V. et al. Targeting macrophage Syk enhances responses to immune checkpoint blockade and radiotherapy in high-risk neuroblastoma. Front Immunol 2023;14:1148317. DOI: 10.3389/fimmu.2023.1148317</mixed-citation></ref></ref-list></back></article>
