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| Content Provider | PubMed Central |
|---|---|
| Author | Dudda, Jan C. Salaun, Bruno Ji, Yun Palmer, Douglas C. Monnot, Gwennaelle C. Merck, Estelle Caroline, Boudousquie Utzschneider, Daniel T. Escobar, Thelma M. Perret, Rachel A., Muljo Stefan Hebeisen, Michael Rufer, Nathalie Dietmar, Zehn Donda, Alena Restifo, Nicholas P. Held, Werner Luca, Gattinoni Romero, Pedro |
| Abstract | MicroRNAs regulate the function of several immune cells but their role in promoting CD8+ T-cell immunity remains unknown. Here we report that miR-155 is required for CD8+ T-cell responses to both virus and cancer. In the absence of miR-155, accumulation of effector CD8+ T cells was severely reduced during acute and chronic viral infections and control of virus replication was impaired. Similarly, Mir155-/- CD8+ T cells were in effective at controlling tumor growth, whereas miR-155 overexpression enhanced the antitumor response. miR-155 deficiency resulted in accumulation of SOCS-1 causing defective cytokine signaling through STAT5. Consistently, enforced expression of SOCS-1 in CD8+ T cells phenocopied the miR-155 deficiency, whereas SOCS-1 silencing augmented tumor destruction. These findings identify miR-155 and its target SOCS-1 as key regulators of effector CD8+ T cells that can be modulated to potentiate immunotherapies for infectious diseases and cancer. |
| Related Links | http://dx.doi.org/10.1016/j.immuni.2012.12.006 |
| Ending Page | 753 |
| Page Count | 12 |
| Starting Page | 742 |
| File Format | |
| ISSN | 10747613 |
| e-ISSN | 10974180 |
| Journal | Immunity |
| Issue Number | 4 |
| Volume Number | 38 |
| Language | English |
| Publisher Date | 2013-04-01 |
| Access Restriction | Open |
| Subject Keyword | Immunology Immunology and Allergy Infectious Diseases Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Infectious Diseases Immunology and Allergy Immunology |
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