Rational Combination Immunotherapy: Understand the Biology.
Identifieur interne : 000C97 ( Main/Exploration ); précédent : 000C96; suivant : 000C98Rational Combination Immunotherapy: Understand the Biology.
Auteurs : Howard L. Kaufman [États-Unis]Source :
- Cancer immunology research [ 2326-6074 ] ; 2017.
Descripteurs français
- KwdFr :
- MESH :
- immunologie : Carcinome pulmonaire non à petites cellules, Tumeurs du poumon.
- usage thérapeutique : Chloroquine.
- Animaux, Association de médicaments, Autophagie, Carcinome pulmonaire non à petites cellules, Humains, Immunothérapie, Tumeurs du poumon.
English descriptors
- KwdEn :
- Animals, Antineoplastic Agents, Immunological (therapeutic use), Autophagy (drug effects), CD47 Antigen (antagonists & inhibitors), CD47 Antigen (immunology), Carcinoma, Non-Small-Cell Lung (immunology), Carcinoma, Non-Small-Cell Lung (therapy), Chloroquine (therapeutic use), Drug Therapy, Combination, Humans, Immunotherapy, Lung Neoplasms (immunology), Lung Neoplasms (therapy).
- MESH :
- chemical , antagonists & inhibitors : CD47 Antigen.
- chemical , immunology : CD47 Antigen.
- chemical , therapeutic use : Antineoplastic Agents, Immunological, Chloroquine.
- drug effects : Autophagy.
- immunology : Carcinoma, Non-Small-Cell Lung, Lung Neoplasms.
- therapy : Carcinoma, Non-Small-Cell Lung, Lung Neoplasms.
- Animals, Drug Therapy, Combination, Humans, Immunotherapy.
Abstract
Selecting rational treatment combinations remains a major challenge for improving immunotherapy outcomes. In this issue of Cancer Immunology Research, Zhang and colleagues reduced tumors by inhibiting CD47 in a lung carcinoma model, a treatment that inadvertently induced autophagy through inhibition of the Akt/mTOR pathway. By also targeting autophagy, the therapeutic response improved, highlighting the importance of understanding the biology beneath antitumor immunity. Cancer Immunol Res; 5(5); 355-6. ©2017 AACRSee article by Zhang et al., p. 363.
DOI: 10.1158/2326-6066.CIR-17-0128
PubMed: 28465453
Affiliations:
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Le document en format XML
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<term>Autophagy (drug effects)</term>
<term>CD47 Antigen (antagonists & inhibitors)</term>
<term>CD47 Antigen (immunology)</term>
<term>Carcinoma, Non-Small-Cell Lung (immunology)</term>
<term>Carcinoma, Non-Small-Cell Lung (therapy)</term>
<term>Chloroquine (therapeutic use)</term>
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<term>Immunothérapie</term>
<term>Tumeurs du poumon ()</term>
<term>Tumeurs du poumon (immunologie)</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Antineoplastic Agents, Immunological</term>
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<front><div type="abstract" xml:lang="en">Selecting rational treatment combinations remains a major challenge for improving immunotherapy outcomes. In this issue of <i>Cancer Immunology Research</i>
, Zhang and colleagues reduced tumors by inhibiting CD47 in a lung carcinoma model, a treatment that inadvertently induced autophagy through inhibition of the Akt/mTOR pathway. By also targeting autophagy, the therapeutic response improved, highlighting the importance of understanding the biology beneath antitumor immunity. <i>Cancer Immunol Res; 5(5); 355-6. ©2017 AACR</i>
<i>See article by Zhang et al., p. 363.</i>
</div>
</front>
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