Source:http://linkedlifedata.com/resource/pubmed/id/12150448
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2002-8-1
|
pubmed:abstractText |
The development of delayed-type hypersensitivity (DTH) response to recall antigens has long been utilized as a measure of immune competence. It is assumed that because patients with advanced stage cancers exhibit multiple immune system defects they may not be responsive to immunization. We pre-selected patients with advanced HER-2/neu (HER2) overexpressing breast and ovarian cancers for enrolment into a phase I trial designed to evaluate the immunogenicity of a HER2 peptide vaccine based on the patient's immune competence as assessed by DTH skin testing to common recall antigens (Multitest CMI, Institut Merieux, Lyon, France). At the time of a positive DTH response to tetanus toxoid (tt) peripheral blood was obtained to measure T cell responses to tt. Of 53 patients evaluated, 38 (72%) were not anergic. Among the 15 (28%) who were, seven patients with advanced stage breast cancer were re-tested a median of 26 days (range 12-150 days) after receiving a tt bopster vaccination. Five of the seven had positive DTH responses when re-challenged with tt and six had peripheral blood tetanus specific T cell response with stimulation index >2.0. Thus, the majority of patients studied with advanced stage breast or ovarian cancer were able to mount a DTH response to common recall antigens. Moreover, a negative response by DTH testing to a battery of common recall antigens was not a reflection of the breast cancer patient's ability to mount a cell-mediated immune response to a vaccinated antigen, tt.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0167-6806
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
74
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
17-23
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:12150448-Adult,
pubmed-meshheading:12150448-Aged,
pubmed-meshheading:12150448-Aged, 80 and over,
pubmed-meshheading:12150448-Antigens,
pubmed-meshheading:12150448-Breast Neoplasms,
pubmed-meshheading:12150448-Cancer Vaccines,
pubmed-meshheading:12150448-Female,
pubmed-meshheading:12150448-Genes, erbB-2,
pubmed-meshheading:12150448-Humans,
pubmed-meshheading:12150448-Hypersensitivity, Delayed,
pubmed-meshheading:12150448-Immune Tolerance,
pubmed-meshheading:12150448-Middle Aged,
pubmed-meshheading:12150448-T-Lymphocytes,
pubmed-meshheading:12150448-Tetanus Toxoid,
pubmed-meshheading:12150448-Vaccination
|
pubmed:year |
2002
|
pubmed:articleTitle |
Delayed type hypersensitivity response to recall antigens does not accurately reflect immune competence in advanced stage breast cancer patients.
|
pubmed:affiliation |
Tumor Vaccine Group, University of Washington, Seattle 98195-6527, USA. kschiff@u.washington.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|