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Erschienen in: Cancer Immunology, Immunotherapy 2/2008

01.02.2008 | Commentary

Tumor stromal barriers to the success of adoptive T cell therapy

verfasst von: Vy Phan, Mary L. Disis

Erschienen in: Cancer Immunology, Immunotherapy | Ausgabe 2/2008

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Excerpt

Adoptive transfer of tumor competent T cells has long been studied as a therapeutic modality that may result in complete tumor eradication [1]. Indeed, T cells have the potential to home to all sites of metastatic disease no matter where the location and induce antigen-specific cell destruction. Theoretically, local clonal expansion of T cells in response to antigen will allow persistent killing over time until every cancer cell has been eradicated. No chemotherapeutic or biologic therapy developed to date has the ability to result in a persistent long lived anti-tumor effect. Unfortunately, the road to developing successful adoptive T cell therapy as a standard treatment for solid tumors has been littered with roadblocks. …
Literatur
1.
Zurück zum Zitat Cheever MA, Chen W (1997) Therapy with cultured T cells: principles revisited. Immunol Rev 157:177–194PubMedCrossRef Cheever MA, Chen W (1997) Therapy with cultured T cells: principles revisited. Immunol Rev 157:177–194PubMedCrossRef
2.
Zurück zum Zitat Leen AM, Rooney CM, Foster AE (2007) Improving T cell therapy for cancer. Annu Rev Immunol 25:243–265PubMedCrossRef Leen AM, Rooney CM, Foster AE (2007) Improving T cell therapy for cancer. Annu Rev Immunol 25:243–265PubMedCrossRef
3.
Zurück zum Zitat Hori S, Nomura T, Sakaguchi S (2003) Control of regulatory T cell development by the transcription factor Foxp3. Science 299(5609):1057–1061PubMedCrossRef Hori S, Nomura T, Sakaguchi S (2003) Control of regulatory T cell development by the transcription factor Foxp3. Science 299(5609):1057–1061PubMedCrossRef
4.
Zurück zum Zitat Chen A et al (2007) Depleting intratumoral CD4+CD25+ regulatory T cells via FasL protein transfer enhances the therapeutic efficacy of adoptive T cell transfer. Cancer Res 67(3):1291–1298PubMedCrossRef Chen A et al (2007) Depleting intratumoral CD4+CD25+ regulatory T cells via FasL protein transfer enhances the therapeutic efficacy of adoptive T cell transfer. Cancer Res 67(3):1291–1298PubMedCrossRef
5.
Zurück zum Zitat Yee C et al (2002) Adoptive T cell therapy using antigen-specific CD8+ T cell clones for the treatment of patients with metastatic melanoma: in vivo persistence, migration, and antitumor effect of transferred T cells. Proc Natl Acad Sci USA 99(25):16168–16173PubMedCrossRef Yee C et al (2002) Adoptive T cell therapy using antigen-specific CD8+ T cell clones for the treatment of patients with metastatic melanoma: in vivo persistence, migration, and antitumor effect of transferred T cells. Proc Natl Acad Sci USA 99(25):16168–16173PubMedCrossRef
6.
Zurück zum Zitat Dudley ME et al (2005) Adoptive cell transfer therapy following non-myeloablative but lymphodepleting chemotherapy for the treatment of patients with refractory metastatic melanoma. J Clin Oncol 23(10):2346–2457PubMedCrossRef Dudley ME et al (2005) Adoptive cell transfer therapy following non-myeloablative but lymphodepleting chemotherapy for the treatment of patients with refractory metastatic melanoma. J Clin Oncol 23(10):2346–2457PubMedCrossRef
7.
Zurück zum Zitat Morgan RA et al (2006) Cancer regression in patients after transfer of genetically engineered lymphocytes. Science 314(5796):126–129PubMedCrossRef Morgan RA et al (2006) Cancer regression in patients after transfer of genetically engineered lymphocytes. Science 314(5796):126–129PubMedCrossRef
8.
Zurück zum Zitat Bernhard H, et al (2007) Adoptive transfer of autologous, HER-specific, cytotoxic T lymphocytes for the treatment of HER2-overexpressing breast cancer. Cancer Immunol Immunother (in press) Bernhard H, et al (2007) Adoptive transfer of autologous, HER-specific, cytotoxic T lymphocytes for the treatment of HER2-overexpressing breast cancer. Cancer Immunol Immunother (in press)
9.
Zurück zum Zitat Blankenstein T (2005) The role of tumor stroma in the interaction between tumor and immune system. Curr Opin Immunol 17(2):180–186PubMedCrossRef Blankenstein T (2005) The role of tumor stroma in the interaction between tumor and immune system. Curr Opin Immunol 17(2):180–186PubMedCrossRef
10.
Zurück zum Zitat Ho WY et al (2003) Adoptive immunotherapy: engineering T cell responses as biologic weapons for tumor mass destruction. Cancer Cell 3(5):431–437PubMedCrossRef Ho WY et al (2003) Adoptive immunotherapy: engineering T cell responses as biologic weapons for tumor mass destruction. Cancer Cell 3(5):431–437PubMedCrossRef
11.
Zurück zum Zitat Thanarajasingam U, et al (2007) Delivery of CCL21 to metastatic disease improves the efficacy of adoptive T-cell therapy. Cancer Res 67(1):300–308PubMedCrossRef Thanarajasingam U, et al (2007) Delivery of CCL21 to metastatic disease improves the efficacy of adoptive T-cell therapy. Cancer Res 67(1):300–308PubMedCrossRef
12.
Zurück zum Zitat Spiotto MT, Rowley DA, Schreiber H (2004) Bystander elimination of antigen loss variants in established tumors. Nat Med 10(3):294–298PubMedCrossRef Spiotto MT, Rowley DA, Schreiber H (2004) Bystander elimination of antigen loss variants in established tumors. Nat Med 10(3):294–298PubMedCrossRef
13.
Zurück zum Zitat Dunn GP et al (2005) A critical function for type I interferons in cancer immunoediting. Nat Immunol 6(7):722–729PubMedCrossRef Dunn GP et al (2005) A critical function for type I interferons in cancer immunoediting. Nat Immunol 6(7):722–729PubMedCrossRef
14.
Zurück zum Zitat Pages F et al (2005) Effector memory T cells, early metastasis, and survival in colorectal cancer. N Engl J Med 353(25):2654–2666PubMedCrossRef Pages F et al (2005) Effector memory T cells, early metastasis, and survival in colorectal cancer. N Engl J Med 353(25):2654–2666PubMedCrossRef
15.
Zurück zum Zitat Galon J et al (2006) Type, density, and location of immune cells within human colorectal tumors predict clinical outcome. Science 313(5795):1960–1964PubMedCrossRef Galon J et al (2006) Type, density, and location of immune cells within human colorectal tumors predict clinical outcome. Science 313(5795):1960–1964PubMedCrossRef
16.
Zurück zum Zitat Zhang L et al (2003) Intratumoral T cells, recurrence, and survival in epithelial ovarian cancer. N Engl J Med 348(3):203–213PubMedCrossRef Zhang L et al (2003) Intratumoral T cells, recurrence, and survival in epithelial ovarian cancer. N Engl J Med 348(3):203–213PubMedCrossRef
17.
Zurück zum Zitat Chen Q et al (2006) Fever-range thermal stress promotes lymphocyte trafficking across high endothelial venules via an interleukin 6 trans-signaling mechanism. Nat Immunol 7(12):1299–1308PubMedCrossRef Chen Q et al (2006) Fever-range thermal stress promotes lymphocyte trafficking across high endothelial venules via an interleukin 6 trans-signaling mechanism. Nat Immunol 7(12):1299–1308PubMedCrossRef
18.
Zurück zum Zitat Skitzki J, Chen Q, Fisher D, Muhitch J, Wang W, Repasky E, Evans S (2007) Systemic thermal therapy improves effector cell trafficking to sites of tumor and clinical outcome. Abstract, STM Annual Meeting Skitzki J, Chen Q, Fisher D, Muhitch J, Wang W, Repasky E, Evans S (2007) Systemic thermal therapy improves effector cell trafficking to sites of tumor and clinical outcome. Abstract, STM Annual Meeting
19.
Zurück zum Zitat Zhang B et al (2007) Induced sensitization of tumor stroma leads to eradication of established cancer by T cells. J Exp Med 204(1):49–55PubMedCrossRef Zhang B et al (2007) Induced sensitization of tumor stroma leads to eradication of established cancer by T cells. J Exp Med 204(1):49–55PubMedCrossRef
20.
Zurück zum Zitat Marijt WA et al (2003) Hematopoiesis-restricted minor histocompatibility antigens HA-1- or HA-2-specific T cells can induce complete remissions of relapsed leukemia. Proc Natl Acad Sci USA 100(5):2742–2747PubMedCrossRef Marijt WA et al (2003) Hematopoiesis-restricted minor histocompatibility antigens HA-1- or HA-2-specific T cells can induce complete remissions of relapsed leukemia. Proc Natl Acad Sci USA 100(5):2742–2747PubMedCrossRef
21.
Zurück zum Zitat Bollard CM et al (2004) Cytotoxic T lymphocyte therapy for Epstein-Barr virus+ Hodgkin’s disease. J Exp Med 200(12):1623–1633PubMedCrossRef Bollard CM et al (2004) Cytotoxic T lymphocyte therapy for Epstein-Barr virus+ Hodgkin’s disease. J Exp Med 200(12):1623–1633PubMedCrossRef
Metadaten
Titel
Tumor stromal barriers to the success of adoptive T cell therapy
verfasst von
Vy Phan
Mary L. Disis
Publikationsdatum
01.02.2008
Verlag
Springer-Verlag
Erschienen in
Cancer Immunology, Immunotherapy / Ausgabe 2/2008
Print ISSN: 0340-7004
Elektronische ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-007-0356-6

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