Therapeutic T cell engineering
By Michel Sadelain, I. Rivière, S. Riddell. Nature, 2017
769 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/8c737fe37d25757ac025573a5d5b64171031e647
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- James J. Collins
- Wilson W. Wong
- Jang-Hwan Cho
- K. High
- J. Keith Joung
- K. Ozawa
- C. Dunbar
- Michel Sadelain
In Oncology
- R. Brentjens
- S. Rafiq
- Christopher S. Hackett
- James J. Collins
- Wilson W. Wong
- Jang-Hwan Cho
- Michel Sadelain
- K. High
Citations in the corpus
- Gene therapy comes of age (2018, positive): “Recent clinical studies have found that single infusions of T cells engineered with synthetic genes encoding a chimeric antigen receptor can produce durable responses in a subset of patients (5).”
- Universal Chimeric Antigen Receptors for Multiplexed and Logical Control of T Cell Responses (2018, positive): “, 2008), regulating the activity of T cell subtypes independently may be an attractive strategy for optimizing the efficacy of CAR T cell therapy (Sadelain et al., 2017).”
- Engineering strategies to overcome the current roadblocks in CAR T cell therapy (2019, background): “…cells in patients, one promising strategy is predicated on the use of T cell populations with higher percentages of less differentiated T cell subsets that have a greater proliferative capacity, such as naive T cells, stem cell memory T (T SCM ) cells and central memory T (T CM ) cells 50,118 (Fig.”