Effects of dendritic cells from cord blood CD34+cells on human hepatocarcinoma cell line BEL-7402 in vitro and in SCID mice
Open accessAbstract
AIM: To develop a cancer vaccine of dendritic cells derived from human cord blood CD34+ cells and to investigate its cytotoxicity on human hepatocarcinoma cells in vitro and in severe combined immunodeficiency (SCID) mice. METHODS: Lymphocytes from cord blood or peripheral blood were primed by DCs, which were derived from cord blood and pulsed with whole tumor cell lysates. Nonradiative neutral red uptake assay was adopted to detect the cytotoxicity of primed lymphocytes on human hepatocarcinoma cell line BEL-7402 in vitro. The anti-tumor effect of primed lymphocytes in vivo was detected in SCID mice, including therapeutic effect and vaccination effect. RESULTS: The cytotoxicity of DC vaccine primed lymphocytes from cord blood or peripheral blood on human hepatocarcinoma cell line BEL-7402 was significantly higher than that of unprimed lymphocytes in vitro (44.09% vs 14.69%, 47.92% vs 19.44%, P<0.01). There was no significant difference between the cytotoxicity of primed lymphocytes from cord blood and peripheral blood (P>0.05). The tumor growth rate and tumor size were smaller in SCID mice treated or vaccinated with primed lymphocytes than those with unprimed lymphocytes. SCID mice vaccinated with primed lymphocytes had a lower tumor incidence (80% vs 100%, P<0.05) and delayed tumor latent period compared with mice vaccinated with unprimed lymphocytes (11 d vs 7 d, P<0.01). CONCLUSION: Vaccine of cord blood derived-DCs has an inhibitory activity on growth of human hepatocarcinoma cells in vitro and in SCID mice. The results also implicate the potential role of cord blood derived-DC vaccine in clinical tumor immunotherapy.
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Primed memory T cells may respond to subsequent infections through cross-reactions.
“These primed memory T cells may respond to subsequent infections through cross-reactions [48,52,53].”
From Evolution of the immune system in humans from infancy to old age (2015) · cites this paper as [53]
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Evolution of the immune system in humans from infancy to old age
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- Authors
- Su, Z.-J.
- Venue
- World Journal of Gastroenterology
- Publisher
- Baishideng Publishing Group Inc.
- Published
- 2005
- Volume
- 11
- Issue
- 16
- Pages
- 2502
- ISSN
- 1007-9327 (ISSN-L)
- PMC
- PMC4305643
- OpenAlex
- W2150616722
- Cited by
- 5
- References
- 26
- Citations by year
- 2023: 1 · 2015: 1
- FWCI
- 0.24
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- World Journal of Gastroenterology (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Shantou University
- Shantou University Medical College
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Cancer Research and Treatments
- Keywords
- dendritic cells, cord blood CD34+ cells, dendritic cell vaccine, hepatocellular carcinoma, BEL-7402 cells, cancer immunotherapy, cytotoxicity, tumor growth inhibition, tumor latency, tumor incidence, SCID mice, lymphocyte priming
- MeSH terms
- Animals, Dendritic Cells, Fetal Blood, Carcinoma, Hepatocellular, Humans, Liver Neoplasms, Lymphocytes, Mice, SCID, Antigens, CD34, Cancer Vaccines, Xenograft Model Antitumor Assays, Cell Line, Tumor, Mice
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