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PMID: 20693839 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Chemoimmunotherapy.

Cancer journal (Sudbury, Mass.) ·Vol. 16 ·No. 4 ·2010-00-00 ·Pages 295-303

Emens LA

Abstract

Cancer chemotherapy drugs are historically regarded as detrimental to immunity because of their myelosuppressive effects. However, accumulating data suggest that the antitumor activity of conventional cancer chemotherapy results in part from its ability to harness the innate and adaptive immune systems by inducing immunologically active tumor cell death. Additional data broaden the immunologic effect of cancer chemotherapy drugs, demonstrating that some drugs have the ability to disrupt pathways of immune suppression and immune tolerance in a manner that depends on the drug dose, and the timing of its administration in relation to immunotherapy. Understanding the cellular and molecular basis of the interactions between chemotherapy drugs and the immune system will facilitate the strategic development of chemoimmunotherapy treatment regimens that both maximize tumor regression and the antitumor immune response for the long-term clinical benefit of cancer patients.

MeSH Terms
Animals Antineoplastic Agents/administration & dosage,therapeutic use Antineoplastic Combined Chemotherapy Protocols/therapeutic use Combined Modality Therapy Humans Immunotherapy/methods Neoplasms/drug therapy,immunology,therapy
Chemicals
Antineoplastic Agents
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Emens Leisha A
Department of Oncology, The Johns Hopkins University, 1650 Orleans St, Room 409, Bunting Blaustein Cancer Research Building, Baltimore, MD 21231-1000, USA. [email protected]
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Article Info
Journal
Cancer journal (Sudbury, Mass.)
Abbr.
Cancer J
ISSN
1540-336X
Published
2010-00-00
Pages
295-303
Language
English
Region
United States
NLM ID
100931981
PMCID
PMC2919833
Subset
IM
Grants
NCI NIH HHS · P50 CA088843 · United States
NCI NIH HHS · K23 CA098498-01 · United States
NCI NIH HHS · K23 CA098498 · United States
NCI NIH HHS · P50 CA88843 · United States
NCI NIH HHS · P50 CA088843-08 · United States
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