Adoptive T cell therapy: points to consider. (April 2018)
- Record Type:
- Journal Article
- Title:
- Adoptive T cell therapy: points to consider. (April 2018)
- Main Title:
- Adoptive T cell therapy: points to consider
- Authors:
- Yee, Cassian
- Abstract:
- Highlights: Adoptive cellular therapy is represented by 3 major modalities: tumor-infiltrating lymphocyte therapy, CAR/TCR-engineered cell therapy and endogenous T cell therapy. CAR T cell therapy directed to CD19 demonstrated remarkable efficacy and long-lasting benefit for patients with B cell malignancies. The in vivo persistence of transferred T cells and development of multivalent responses are associated with a favorable clinical response. Combination strategies to enhance ACT will use other modalities such as immune checkpoint blockade, agonist antibodies, vaccines and other immune based approaches. Abstract : Adoptive Cell Therapy (ACT) has enjoyed a revival in recent years with the approval of CAR T cells for the treatment of patients with B cell malignancies. Advancing the use of adoptively transferred T cells for the treatment of patients with solid tumor and other hematologic malignancies however, will require addressing numerous effector cell intrinsic as well as tumor micro environmental hurdles and exploiting a broader ACT platform that includes not only engineered CAR-T cells, but also other forms of ACT including Endogenous T Cell (ETC) and Tumor-infiltrating Lymphocyte (TIL) therapy. In this review, we open this discussion with some 'points to consider' as a starting point for envisioning more effective strategies that are now feasible because of recent discoveries In immune resistance and the development of enabling technologies to harness the power ofHighlights: Adoptive cellular therapy is represented by 3 major modalities: tumor-infiltrating lymphocyte therapy, CAR/TCR-engineered cell therapy and endogenous T cell therapy. CAR T cell therapy directed to CD19 demonstrated remarkable efficacy and long-lasting benefit for patients with B cell malignancies. The in vivo persistence of transferred T cells and development of multivalent responses are associated with a favorable clinical response. Combination strategies to enhance ACT will use other modalities such as immune checkpoint blockade, agonist antibodies, vaccines and other immune based approaches. Abstract : Adoptive Cell Therapy (ACT) has enjoyed a revival in recent years with the approval of CAR T cells for the treatment of patients with B cell malignancies. Advancing the use of adoptively transferred T cells for the treatment of patients with solid tumor and other hematologic malignancies however, will require addressing numerous effector cell intrinsic as well as tumor micro environmental hurdles and exploiting a broader ACT platform that includes not only engineered CAR-T cells, but also other forms of ACT including Endogenous T Cell (ETC) and Tumor-infiltrating Lymphocyte (TIL) therapy. In this review, we open this discussion with some 'points to consider' as a starting point for envisioning more effective strategies that are now feasible because of recent discoveries In immune resistance and the development of enabling technologies to harness the power of tumor - reactive T cells for adoptive cell therapy. … (more)
- Is Part Of:
- Current opinion in immunology. Volume 51(2018)
- Journal:
- Current opinion in immunology
- Issue:
- Volume 51(2018)
- Issue Display:
- Volume 51, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 51
- Issue:
- 2018
- Issue Sort Value:
- 2018-0051-2018-0000
- Page Start:
- 197
- Page End:
- 203
- Publication Date:
- 2018-04
- Subjects:
- Immunology -- Periodicals
Allergy -- Periodicals
Immunology -- Abstracts -- Periodicals
Allergy -- Abstracts -- Periodicals
616.079 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09527915 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.coi.2018.04.007 ↗
- Languages:
- English
- ISSNs:
- 0952-7915
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.775300
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11607.xml