Anti-TGF-β Antibody Combined with Dendritic Cells Produce Antitumor Effects in Osteosarcoma
Open accessAbstract
BACKGROUND: We previously reported the combination of tumor cryotreatment with dendritic cells to promote antitumor immunity. The effect of the combination treatment with dendritic cells and antitransforming growth factor-β (anti-TGF-β) antibody on the elimination of regulatory T cells and the inhibition of tumor growth was investigated. QUESTIONS/PURPOSES: The effects of the combination treatment with dendritic cells and anti-TGF-β antibody on the enhancement of systemic immune responses and inhibition of metastatic tumor growth were investigated in a murine osteosarcoma (LM8) model. MATERIALS AND METHODS: To evaluate activation of the immune response, we established the following three groups of C3H mice (60 mice total): (1) excision only; (2) tumor excision and administration of anti-TGF-β antibody; and (3) tumor excision and administration of dendritic cells exposed to cryotreated tumor lysates with anti-TGF-β antibody. RESULTS: The mice that received dendritic cells exposed to cryotreated tumor lysates with anti-TGF-β antibody showed increased numbers of CD8(+) T lymphocytes, reduced regulatory T lymphocytes in the metastatic lesion, and inhibition of metastatic growth. The combined therapy group showed reduced numbers of regulatory T lymphocytes in the spleen and high serum interferon γ level. CONCLUSIONS: The control of the inhibitory condition induced by regulatory T cells is important to improve the suppression of the cytotoxic lymphocytes. Combining dendritic cells with anti-TGF-β antibody enhanced the systemic immune response. CLINICAL RELEVANCE: We suggest that our immunotherapy could be developed further to improve the treatment of osteosarcoma.
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Combined DCs and anti-TGF-β antibodies enhanced systemic immune responses in mice models.
“Kawano et al. suggested that combined DCs and anti-TGF-β antibodies to treat osteosarcoma and detected enhanced systematic immune responses in mice models [149].”
From Advances on immunotherapy for osteosarcoma (2024) · cites this paper as [149]
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Rosenberg, S. A., Yang, J. C., Sherry, R. M., Kammula, U. S., Hughes, M. S., Phan, G. Q., Citrin, D. E., Restifo, N. P., Robbins, P. F., Wunderlich, J. R., et al. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-0116 · Cited by 2,145 · see citing works
Viguier, M. A., Lemaı̂tre, F., VEROLA, O., Cho, M.-S., Gorochov, G., Dubertret, L., Bachelez, H., Kourilsky, P., & Ferradini, L. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.2.1444 · Cited by 686 · see citing works
Liang, B., Workman, C., Lee, J., Chew, C., Dale, B. M., Colonna, L., Flores, M., Li, N., Schweighoffer, E., Greenberg, S., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.9.5916 · Cited by 566 · see citing works
Laouar, Y., Sutterwala, F. S., Gorelik, L., & Flavell, R. A. (2005) · Nature Immunology · doi:10.1038/ni1197 · Cited by 452 · see citing works
Huber, S., Schramm, C., Lehr, H. A., Mann, A., Schmitt, S., Becker, C., Protschka, M., Galle, P. R., Neurath, M. F., & Blessing, M. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.11.6526 · Cited by 390 · see citing works
Biswas, S., Guix, M., Rinehart, C., Dugger, T. C., Chytil, A. M., Moses, H. L., Freeman, M. L., & Arteaga, C. L. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30740 · Cited by 346 · see citing works
Stiller, C. A., Bielack, S., Jundt, G., & Steliarova‐Foucher, E. (2006) · European Journal of Cancer · doi:10.1016/j.ejca.2006.05.015 · Cited by 283 · see citing works
Bacci, G., Briccoli, A., Rocca, M., Ferrari, S., Donati, D. M., Longhi, A., Bertoni, F., Bacchini, P., Giacomini, S., Forni, C., et al. (2003) · Annals of Oncology · doi:10.1093/annonc/mdg286 · Cited by 187 · see citing works
Zhong, Z., Carroll, K. D., Policarpio, D., Osborn, C., Gregory, M., Bassi, R., Jimenez, X., Prewett, M., Liebisch, G., Persaud, K., et al. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-1634 · Cited by 123 · see citing works
Terabe, M., Ambrosino, E., Takaku, S., O’Konek, J. J., Venzon, D. J., Lonning, S. M., McPherson, J. M., & Berzofsky, J. A. (2009) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-1066 · Cited by 112 · see citing works
Squamous cell carcinoma of the skin and lip in renal homograft recipients
Mullen, D. L., Silverberg, S. G., Penn, I., & Hammond, W. S. (1976) · Cancer · doi:10.1002/1097-0142(197602)37:2 · Cited by 98 · see citing works
Dendritic Cell‐Based Immunotherapy for Prostate Cancer
Jähnisch, H., Fuessel, S., Kießling, A., Wehner, R., Zastrow, S., Bachmann, M. P., Rieber, E. P., Wirth, M. P., & Schmitz, M. (2010) · Journal of Immunology Research · doi:10.1155/2010/517493 · Cited by 92 · see citing works
Tumor angiogenesis as a prognostic factor in ovarian carcinoma
Schoell, W., Pieber, D., Reich, O., LAHOUSEN, M., Janicek, M. F., Güçer, F., & Winter, R. (1997) · Cancer · doi:10.1002/(sici)1097-0142(19971215)80:12 · Cited by 88 · see citing works
Hawinkels, L. J. A. C., Verspaget, H. W., van Duijn, W., Zon, J. M. V. D., Zuidwijk, K., Kubben, F. J. G. M., Verheijen, J. H., Hommes, D. W., Lamers, C. B. H. W., & Sier, C. F. M. (2007) · British Journal of Cancer · doi:10.1038/sj.bjc.6603877 · Cited by 86 · see citing works
Blockade of TGF‐β enhances tumor vaccine efficacy mediated by CD8+ T cells
Takaku, S., Terabe, M., Ambrosino, E., Peng, J., Lonning, S. M., McPherson, J. M., & Berzofsky, J. A. (2009) · International Journal of Cancer · doi:10.1002/ijc.24961 · Cited by 82 · see citing works
Gil‐Guerrero, L., Dotor, J., Huibregtse, I. L., Casares, N., López-Vázquez, A. B., Rudilla, F., Riezu‐Boj, J. I., López‐Sagaseta, J., Hermida, J., van Deventer, S. J. H., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.1.126 · Cited by 68 · see citing works
Osteosarcoma in very young children
Kager, L., Zoubek, A., Dominkus, M., Lang, S., Bodmer, N., Jundt, G., Klingebiel, T., Jürgens, H., Gadner, H., Bielack, S., et al. (2010) · Cancer · doi:10.1002/cncr.25287 · Cited by 65 · see citing works
Lutz, M. B., & Rößner, S. (2007) · Immunobiology · doi:10.1016/j.imbio.2007.09.001 · Cited by 48 · see citing works
Nishida, H., Tsuchiya, H., & Tomita, K. (2008) · Journal of Bone and Joint Surgery - British Volume · doi:10.1302/0301-620x.90b9.20671 · Cited by 47 · see citing works
Self-citationSoleimani, A. H., Berntsen, A., Svane, I. M., & Pedersen, A. E. (2009) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2009.02322.x · Cited by 40 · see citing works
Cryoimmunologic Antitumor Effects Enhanced by Dendritic Cells in Osteosarcoma
Kawano, M., Nishida, H., Nakamoto, Y., Tsumura, H., & Tsuchiya, H. (2010) · Clinical Orthopaedics and Related Research · doi:10.1007/s11999-010-1302-z · Cited by 32 · see citing works
Self-citationImmunologic Aspects of Osteosarcoma and Their Application to Therapy
Marsh, B., FLYNN, L., & Enneking, W. F. (1972) · Journal of Bone and Joint Surgery · doi:10.2106/00004623-197254070-00001 · Cited by 29 · see citing works
Immunologic aspects of osteosarcoma and their application to therapy. A preliminary report.
Marsh, B., Flynn, L., & Enneking, W. F. (1972) · PubMed · Cited by 28 · see citing works
Marcove, R. C., Southam, C. M., LEVIN, A. G., Mike, M., & Huvos, A. G. (1971) · PubMed · Cited by 20 · see citing works
An MHC-linked locus modulates thymic differentiation of CD4+CD25+Foxp3+ regulatory T lymphocytes
Tellier, J., van Meerwijk, J. P. M., & Romagnoli, P. (2006) · International Immunology · doi:10.1093/intimm/dxl084 · Cited by 14 · see citing works
Proceedings: Clinical trial of autogenous tumor vaccine for treatment of osteogenic sarcoma.
Southam, C. M., Marcove, R. C., LEVIN, A. G., Buchsbaum, H. J., & Mike, M. (1972) · PubMed · Cited by 9 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Immunotherapy for osteosarcoma: Fundamental mechanism, rationale, and recent breakthroughs
Chen, C., Xie, L., Ren, T., Huang, Y., Xu, J. H., & Guo, W. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.12.024 · Cited by 573 · see citing works
Yang, Z., Qi, Y., Lai, N., Zhang, J., Chen, Z., Liu, M., Zhang, W., Luo, R., & Kang, S. (2018) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-017-0664-4 · Cited by 307 · see citing works
Advances on immunotherapy for osteosarcoma
Yu, S., & Yao, X. (2024) · Molecular Cancer · doi:10.1186/s12943-024-02105-9 · Cited by 270 · see citing works
Heymann, M.-F., Lézot, F., & Heymann, D. (2019) · Cellular Immunology · doi:10.1016/j.cellimm.2017.10.011 · Cited by 233 · see citing works
Bone microenvironment signals in osteosarcoma development
Alfranca, A., Martínez-Cruzado, L., Tornín, J., Abarrategi, A., Amaral, A. T., de Álava, E., Menéndez, P. R., Garcı́a-Castro, J., & Rodrı́guez, R. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1918-y · Cited by 224 · see citing works
Osteosarcoma: Cells‐of‐Origin, Cancer Stem Cells, and Targeted Therapies
Abarrategi, A., Tornín, J., Martínez-Cruzado, L., Hamilton, A., Martínez‐Campos, E., Rodrigo, J. P., González, M. V., Baldini, N., Garcı́a-Castro, J., & Rodrı́guez, R. (2016) · Stem Cells International · doi:10.1155/2016/3631764 · Cited by 211 · see citing works
Sheng, G., Gao, Y., Yong, Y., & Wu, H. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.780264 · Cited by 202 · see citing works
Immunotherapy for osteosarcoma: Where do we go from here?
Wedekind, M. F., Wagner, L. M., & Cripe, T. P. (2018) · Pediatric Blood & Cancer · doi:10.1002/pbc.27227 · Cited by 153 · see citing works
TGF-β Signaling in Bone Remodeling and Osteosarcoma Progression
Lamora, A., Talbot, J., Mullard, M., Royer, B. B.-L., Rédiní, F., & Verrecchia, F. (2016) · Journal of Clinical Medicine · doi:10.3390/jcm5110096 · Cited by 131 · see citing works
Zhu, T., Han, J., Liu, Y., Cai, Z., Sun, W. Y., Hua, Y., & Xu, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.907550 · Cited by 113 · see citing works
Novel molecular insights and new therapeutic strategies in osteosarcoma
Otoukesh, B., Boddouhi, B., Moghtadaei, M., Kaghazian, P., & Kaghazian, M. (2018) · Cancer Cell International · doi:10.1186/s12935-018-0654-4 · Cited by 94 · see citing works
An overview of resistance to chemotherapy in osteosarcoma and future perspectives
García-Ortega, D. Y., Cabrera-Nieto, S. A., Caro-Sánchez, C. H. S., & Cruz‐Ramos, M. (2022) · Cancer Drug Resistance · doi:10.20517/cdr.2022.18 · Cited by 86 · see citing works
Innate Immune Cells: A Potential and Promising Cell Population for Treating Osteosarcoma
Wang, Z., Wang, Z., Li, B., Wang, S., Chen, T., & Ye, Z. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01114 · Cited by 76 · see citing works
Kawano, M., Tanaka, K., Itonaga, I., Iwasaki, T., Miyazaki, M., Ikeda, S., & Tsumura, H. (2016) · Oncology Letters · doi:10.3892/ol.2016.4175 · Cited by 67 · see citing works
Self-citationImmunotherapy in soft tissue and bone sarcoma: unraveling the barriers to effectiveness
Panagi, M., Pilavaki, P., Constantinidou, A., & Stylianopoulos, T. (2022) · Theranostics · doi:10.7150/thno.72800 · Cited by 55 · see citing works
Tu, S., Xu, L., Qiu, J., Zhou, J., Wang, H., Hu, S., Yao, Y., Wang, Y., Deng, Y., Zhou, Y., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.650105 · Cited by 51 · see citing works
Decoding the Impact of Tumor Microenvironment in Osteosarcoma Progression and Metastasis
Nirala, B. K., Yamamichi, T., Petrescu, D. I., Shafin, T. N., & Yustein, J. T. (2023) · Cancers · doi:10.3390/cancers15205108 · Cited by 51 · see citing works
Ehnman, M., Chaabane, W., Haglund, F., & Tsagkozis, P. (2019) · Current Oncology Reports · doi:10.1007/s11912-019-0839-6 · Cited by 43 · see citing works
Dendritic cells combined with anti-GITR antibody produce antitumor effects in osteosarcoma
KAWANO, M., TANAKA, K., ITONAGA, I., IWASAKI, T., MIYAZAKI, M., IKEDA, S., & TSUMURA, H. (2015) · Oncology Reports · doi:10.3892/or.2015.4161 · Cited by 38 · see citing works
Self-citationTsai, Y., Chen, Y., Cheng, P.-C., Tsai, H., Shiau, A., Tzai, T., & Wu, C. (2013) · Small · doi:10.1002/smll.201202755 · Cited by 38 · see citing works
Targeting transforming growth factor beta signaling in metastatic osteosarcoma
Ge, R., & Huang, G. M. (2023) · Journal of bone oncology · doi:10.1016/j.jbo.2023.100513 · Cited by 37 · see citing works
Role of extracellular vesicles in osteosarcoma
Yang, Q., Liu, J., Wu, B., Wang, X., Jiang, Y., & Zhu, D. (2022) · International Journal of Medical Sciences · doi:10.7150/ijms.74137 · Cited by 30 · see citing works
Liang, H., Cui, M., Tu, J., & Chen, X. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1394339 · Cited by 30 · see citing works
Targeting metastasis in paediatric bone sarcomas
Bull, E. C., Singh, A., Harden, A. M., Soanes, K., Habash, H., Toracchio, L., Carrabotta, M., Schreck, C., Shah, K. M., Riestra, P. V., et al. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02365-z · Cited by 30 · see citing works
Ying, H., Li, Z., Li, M.-P., & Liu, W. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1217669 · Cited by 26 · see citing works
Gao, X., Han, D. K., & Fan, W. (2016) · Experimental Cell Research · doi:10.1016/j.yexcr.2016.10.019 · Cited by 23 · see citing works
Bozorgi, A., & Sabouri, L. (2021) · Cancer Treatment and Research Communications · doi:10.1016/j.ctarc.2021.100324 · Cited by 22 · see citing works
Lan, M., Zhu, X.-P., Cao, Z.-Y., Liu, J.-M., Lin, Q., & Liu, Z.-L. (2018) · Journal of Bone Oncology · doi:10.1016/j.jbo.2018.07.010 · Cited by 19 · see citing works
Osteosarcoma immune microenvironment: cellular struggle and novel therapeutic insights
Zhang, Y., Jiang, S., Lv, J., Feng, W., Yu, Y., & Zhao, H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1584450 · Cited by 22 · see citing works
Liao, Z., Li, M., Wen, G., Wang, K., Yao, D., Chen, E., Liang, Y., Xing, T., Su, K., Liang, C., et al. (2023) · npj Precision Oncology · doi:10.1038/s41698-023-00415-7 · Cited by 17 · see citing works
miRNA in Machine-learning-based Diagnostics of Cancers
Kang, W., Kouznetsova, V. L., & Tsigelny, I. F. (2022) · Cancer Screening and Prevention · doi:10.14218/csp.2021.00001 · Cited by 16 · see citing works
Osteosarcoma from the unknown to the use of exosomes as a versatile and dynamic therapeutic approach
Paiva‐Santos, A. C., Domingues, C., Jarak, I., Veiga, F., & Figueiras, A. (2021) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2021.12.003 · Cited by 16 · see citing works
Pu, F., Chen, F., Zhang, Z., Liu, J., & Shao, Z. (2020) · OncoTargets and Therapy · doi:10.2147/ott.s266835 · Cited by 14 · see citing works
Strategies to Overcome Resistance to Immune-Based Therapies in Osteosarcoma
Hattinger, C. M., Salaroglio, I. C., Fantoni, L., Godel, M., Casotti, C., Kopecka, J., Scotlandi, K., Ibrahim, T., Riganti, C., & Serra, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24010799 · Cited by 13 · see citing works
Identification of the shared gene signatures in retinoblastoma and osteosarcoma by machine learning
Ye, R., Yuan, Q., You, W., Huang, Y., Lin, Z., Tang, H., & Zeng, R. (2024) · Scientific Reports · doi:10.1038/s41598-024-82789-7 · Cited by 16 · see citing works
Sun, C., MA, X., ZHOU, C., Zhang, Z., & GUO, J. (2023) · Anticancer Research · doi:10.21873/anticanres.16514 · Cited by 10 · see citing works
Osteoimmunology in bone malignancies: a symphony with evil
Song, C., Tong, T., Dai, B., Zhu, Y., Chen, E., Zhang, M., & Zhang, W. (2024) · Journal of the National Cancer Center · doi:10.1016/j.jncc.2024.09.001 · Cited by 9 · see citing works
Wang, X., Luo, C., & Zhang, D. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1621521 · Cited by 8 · see citing works
Wang, H., Zhu, T., Yang, K., Xu, C., Zhang, Z., Liu, G., & Ren, H. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1702219 · Cited by 7 · see citing works
Jia, X., Shi, Y., Su, J., Zhou, Y., Li, W., Li, Y., Di, B., An, F., & Yan, C. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115876 · Cited by 6 · see citing works
Sergi, C. M. (2024) · Discover Oncology · doi:10.1007/s12672-024-01240-5 · Cited by 5 · see citing works
Role of tumor-derived exosomes and immune cells in osteosarcoma progression and targeted therapy
Wang, J., & Shi, K. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1658358 · Cited by 5 · see citing works
Lai, G., Zhao, X., Chen, Y., Xie, T., Su, Z., Lin, J., Chen, K., & Chen, K. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114260 · Cited by 4 · see citing works
Novel anthracyclines with enhanced immunogenic effects against drug resistant osteosarcoma cells
Gazzano, E., Kopecka, J., Castella, B., Buondonno, I., Costamagna, C., & Riganti, C. (2018) · Journal of Molecular and Clinical Medicine · doi:10.31083/j.jmcm.2018.04.325001 · Cited by 4 · see citing works
Protein-bound polysaccharide-K reduces the proportion of regulatory T cells in vitro and in vivo
Aoki, R., Iijima, H., Kato, M., Uchida, M., Wada, T., Murata, M., OGAWA, K., Naritaka, Y., & Yoshimatsu, K. (2013) · Oncology Reports · doi:10.3892/or.2013.2834 · Cited by 3 · see citing works
Paediatric therapeutic development workshop on osteosarcoma
Baxter, J. S., Montiel-Equihua, C., Molenaar, J. J., Berlanga, P., Bishop, M. W., Blanc, P., Campbell-Hewson, Q., Casanova, M., Cortés‐Ciriano, I., Crompton, B. D., et al. (2026) · British Journal of Cancer · doi:10.1038/s41416-026-03572-1 · Cited by 1 · see citing works
Zhao, G., Pu, N., Nuerxiati, A., Yin, H.-L., Zhang, L., Lou, W., & Wu, W. (2022) · Cancer Screening and Prevention · doi:10.14218/csp.2022.00001 · Cited by 1 · see citing works
Cancer Immunotherapy Confers a Global Benefit
Aryan, Z., Keshavarz‐Fathi, M., Mellstedt, H., & Rezaei, N. (2020) · Springer eBooks · doi:10.1007/978-3-030-57949-4_1 · Cited by 1 · see citing works
Cancer Immunotherapy Confers a Global Benefit
Aryan, Z., Mellstedt, H., & Rezaei, N. (2015) · Springer eBooks · doi:10.1007/978-3-662-46410-6_1
Sun, R., Pei, Y., Li, C., Lu, H., & Liu, Y. (2026) · Bulletin of Mathematical Biology · doi:10.1007/s11538-026-01616-4
Metabolic–immune crosstalk in osteosarcoma: mechanisms and therapeutic opportunities
Wan, X., He, W., He, B., & Chen, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1818745
- Authors
- Kawano, M., Itonaga, I., Iwasaki, T., Tsuchiya, H., & Tsumura, H.
- Affiliations
- Oita University (JP)
- Kanazawa University (JP)
- Corresponding author
- Kawano, Masanori
- Venue
- Clinical Orthopaedics & Related Research
- Published
- 2012-08
- Volume
- 470
- Issue
- 8
- Pages
- 2288-2294
- ISSN
- 0009-921X (ISSN-L)
- PMC
- PMC3392369
- OpenAlex
- W1999506915
- Cited by
- 51
- References
- 26
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 5 · 2023: 6 · 2022: 6 · 2021: 4 · 2020: 3 · 2019: 2 · 2018: 5 · 2017: 1 · 2016: 4 · 2015: 3 · 2013: 2
- FWCI
- 0.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Clinical Orthopaedics and Related Research (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- osteosarcoma, anti-TGF-beta antibody, dendritic cells, cancer immunotherapy, regulatory T cells, CD8+ T cells, interferon-gamma, tumor lysate, metastasis suppression
- MeSH terms
- Animals, Antibodies, Monoclonal, Bone Neoplasms, Combined Modality Therapy, Dendritic Cells, Female, Mice, Inbred C3H, Osteosarcoma, Tumor Cells, Cultured, Transforming Growth Factor beta, Treatment Outcome, CD8-Positive T-Lymphocytes, Cancer Vaccines, Xenograft Model Antitumor Assays, Mice
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