The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.
Murine dendritic cells pulsed with whole tumor lysates mediate potent antitumor immune responses in vitro and in vivo
Open accessAbstract
The highly efficient nature of dendritic cells (DC) as antigen-presenting cells raises the possibility of uncovering in tumor-bearing hosts very low levels of T cell reactivity to poorly immunogenic tumors that are virtually undetectable by other means. Here, we demonstrate the in vitro and in vivo capacities of murine bone marrow-derived, cytokine-driven DC to elicit potent and specific anti-tumor responses when pulsed with whole tumor lysates. Stimulation of naive spleen-derived T cells by tumor lysate-pulsed DC generated tumor-specific proliferative cytokine release and cytolytic reactivities in vitro. In addition, in two separate strains of mice with histologically distinct tumors, s.c. injections of DC pulsed with whole tumor lysates effectively primed these animals to reject subsequent lethal challenges with viable parental tumor cells and, important to note, also mediated significant reductions in the number of metastases established in the lungs. Tumor rejection depended on host-derived CD8+T cells and, to a lesser extent, CD4+T cells. Spleens from mice that had rejected their tumors contained specific precursor cytotoxic T lymphocytes. The use of whole tumor lysates as a source of tumor-associated antigen(s) for pulsing of DC circumvents several limitations encountered with other methods as well as provides certain distinct advantages, which are discussed. These data serve as rationale for our recent initiation of a phase I clinical trial of immunization with autologous tumor lysate-pulsed DC in adult and pediatric cancer patients.
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Cited by
Antigen Presentation and T Cell Stimulation by Dendritic Cells
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Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming
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Tumor-infiltrating T lymphocytes: Friends or foes?
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Whole Tumor Antigen Vaccines: Where Are We?
Chiang, C., Coukos, G., & Kandalaft, L. (2015) · Vaccines · doi:10.3390/vaccines3020344 · Cited by 269
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Metadata
- Authors
- Fields, R. C., Shimizu, K., & Mulé, J. J.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 1998-08-04
- Volume
- 95
- Issue
- 16
- Pages
- 9482-9487
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2129980000
- Cited by
- 454
- References
- 25
- FWCI
- 10.15
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Fields, R. C., Shimizu, K., & Mulé, J. J. (1998). Murine dendritic cells pulsed with whole tumor lysates mediate potent antitumor immune responses in vitro and in vivo. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.95.16.9482
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