4.7 Review

Engineered T cells: the promise and challenges of cancer immunotherapy

Journal

NATURE REVIEWS CANCER
Volume 16, Issue 9, Pages 566-581

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrc.2016.97

Keywords

-

Categories

Funding

  1. National Institutes of Health (NIH) [5T32HL007775-22]
  2. NIH grants [1RO1CA165206, P30-CA016520-35, 5R01CA120409]
  3. Leukemia and Lymphoma Society
  4. Parker Foundation

Ask authors/readers for more resources

The immune system evolved to distinguish non-self from self to protect the organism. As cancer is derived from our own cells, immune responses to dysregulated cell growth present a unique challenge. This is compounded by mechanisms of immune evasion and immunosuppression that develop in the tumour microenvironment. The modern genetic toolbox enables the adoptive transfer of engineered T cells to create enhanced anticancer immune functions where natural cancer-specific immune responses have failed. Genetically engineered T cells, so-called 'living drugs', represent a new paradigm in anticancer therapy. Recent clinical trials using T cells engineered to express chimeric antigen receptors (CARs) or engineered T cell receptors (TCRs) have produced stunning results in patients with relapsed or refractory haematological malignancies. In this Review we describe some of the most recent and promising advances in engineered T cell therapy with a particular emphasis on what the next generation of T cell therapy is likely to entail.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available