Source:http://linkedlifedata.com/resource/pubmed/id/18616968
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
36
|
pubmed:dateCreated |
2008-8-11
|
pubmed:abstractText |
We have previously established a cancer vaccine using autologous DCs, generated by in vitro stimulation with IL-4 and GM-CSF, and pulsed with six HLA-A*0201 binding wild-type p53 derived peptides. This vaccine was used in combination with low-dose interleukin-2 in a recently published clinical Phase II trial where 26 HLA-A2+ patients with progressive late-stage metastatic breast cancer (BC) were included. Almost 1/3rd of the patients obtained stable disease or minor regression during treatment with a positive correlation to tumour over-expression of p53. In the present study, we performed a comprehensive analysis of the effector stage of the p53-specific CD8+ T cells by the use of Dextramer Technology and multicolour FACS. Pre- and post-treatment blood samples from eight BC patients were analysed. Independent of clinical outcome p53-specific T cells were phenotypic distinctly antigen experienced (CD44high, CCR-7low and CD62Llow). Furthermore, fresh blood from 18 cancer patients included in the vaccination trial were prospectively examined for more general treatment associated quantitative and qualitative changes in T cell subpopulations. We found that the frequency of CD4+ CD25high regulatory T cells was almost doubled after only 4 weeks of weekly vaccination and low-dose IL-2. In addition, a decrease in the percentage of CD27highCCR-7high CD4/CD8 naïve T cells was measured particularly in patients with progressive disease during vaccination. Finally, prior to immunotherapy a higher percentage of both CD28 and CD27 positive CD8naïve/early effector memory T cells were present in chemotherapy-treated patients.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0264-410X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
26
|
pubmed:volume |
26
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4716-24
|
pubmed:meshHeading |
pubmed-meshheading:18616968-Adjuvants, Immunologic,
pubmed-meshheading:18616968-Breast Neoplasms,
pubmed-meshheading:18616968-CD4-Positive T-Lymphocytes,
pubmed-meshheading:18616968-CD8-Positive T-Lymphocytes,
pubmed-meshheading:18616968-Cancer Vaccines,
pubmed-meshheading:18616968-Dendritic Cells,
pubmed-meshheading:18616968-Female,
pubmed-meshheading:18616968-Flow Cytometry,
pubmed-meshheading:18616968-Humans,
pubmed-meshheading:18616968-Interleukin-2,
pubmed-meshheading:18616968-Leukocytes, Mononuclear,
pubmed-meshheading:18616968-Lymphocyte Subsets,
pubmed-meshheading:18616968-T-Lymphocytes, Regulatory,
pubmed-meshheading:18616968-Tumor Suppressor Protein p53,
pubmed-meshheading:18616968-Vaccination
|
pubmed:year |
2008
|
pubmed:articleTitle |
Alterations in p53-specific T cells and other lymphocyte subsets in breast cancer patients during vaccination with p53-peptide loaded dendritic cells and low-dose interleukin-2.
|
pubmed:affiliation |
Department of Oncology, Center for Cancer Immune Therapy, Copenhagen University Hospital at Herlev, Denmark. inge.m.svane@dadlnet.dk
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Clinical Trial, Phase II
|