Source:http://linkedlifedata.com/resource/pubmed/id/11956096
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2002-4-16
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pubmed:abstractText |
Most cytotoxic drugs have gross effects on the immune system, such as neutropenia and lymphopenia. However, their effects on tumor-specific immune responses are unknown. Gemcitabine is a nucleoside analogue that is frequently used to treat non-small cell lung cancer. It is also active in other malignancies, either alone or in combination with cisplatin. Here, we investigate its effects on antigen-specific antitumor immunity using a murine tumor cell line transfected to express influenza virus hemagglutinin (HA). CD4(+), CD8(+), and B220(+) lymphocyte numbers all decreased during chemotherapy (120 microg/g, i.p., every third day for five doses), but B cells were selectively depleted. Gemcitabine induced a profound suppression of the IgG antibody response to HA, and this was unrelated to tumor size. In contrast, in vitro T-lymphocyte recall responses to the class I- and class II-restricted dominant peptide epitopes of HA were enhanced in tumor-bearing, gemcitabine-treated mice. We found that gemcitabine was >2-fold more potent in its ability to inhibit B-lymphocyte proliferation compared with T-lymphocyte proliferation. Thus, gemcitabine does not appear to be detrimental to specific antitumor cellular immunity and may be useful in combination chemo-immunotherapy protocols. In contrast, vaccination protocols requiring a humoral immune response for maximal efficacy may be compromised in patients treated with gemcitabine.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/Antimetabolites, Antineoplastic,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxycytidine,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes, B-Lymphocyte,
http://linkedlifedata.com/resource/pubmed/chemical/Immunosuppressive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/gemcitabine
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0008-5472
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2353-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11956096-Animals,
pubmed-meshheading:11956096-Antibodies, Neoplasm,
pubmed-meshheading:11956096-Antimetabolites, Antineoplastic,
pubmed-meshheading:11956096-B-Lymphocyte Subsets,
pubmed-meshheading:11956096-B-Lymphocytes,
pubmed-meshheading:11956096-Combined Modality Therapy,
pubmed-meshheading:11956096-Deoxycytidine,
pubmed-meshheading:11956096-Epitopes, B-Lymphocyte,
pubmed-meshheading:11956096-Immunosuppressive Agents,
pubmed-meshheading:11956096-Immunotherapy,
pubmed-meshheading:11956096-Lymphocyte Activation,
pubmed-meshheading:11956096-Mice,
pubmed-meshheading:11956096-Mice, Inbred BALB C,
pubmed-meshheading:11956096-Mice, Transgenic,
pubmed-meshheading:11956096-Spleen
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pubmed:year |
2002
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pubmed:articleTitle |
Gemcitabine exerts a selective effect on the humoral immune response: implications for combination chemo-immunotherapy.
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pubmed:affiliation |
Western Australian Institute for Medical Research, University Department of Medicine, Queen Elizabeth II Medical Centre, 4th Floor, G Block, Nedlands, Perth, Western Australia 6009.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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