Results 51 to 60 of about 70,663 (209)

Chimeric Antigen Receptor T-Cell Revolution Remodeling Immunity to Conquer Autoimmune Disease

open access: yesResearch
Chimeric antigen receptor T (CAR-T) cell therapy, a groundbreaking technology in tumor immunotherapy, has demonstrated unprecedented potential in the field of autoimmune diseases in recent years.
Wenxia Shao   +3 more
doaj   +1 more source

Regions of the T cell receptor alpha and beta chains that are responsible for interactions with CD3. [PDF]

open access: yes, 1991
The T cell antigen receptor consists of the Ti alpha/beta heterodimer which recognizes antigen, and the associated CD3 chains, thought to be involved in signal transduction.
Tan, L, Turner, J, Weiss, A
core   +1 more source

Chimeric antigen receptors: “CARs” in the fast lane for rheumatology

open access: yesCurrent Opinion in Rheumatology
Purpose of review Recent advances in hematology-oncology have pioneered cell-mediated elimination of pathologic B-cell populations employing chimeric antigen receptor (CAR) T cells. In this review, we discuss recent adoption of CAR-T treatment for severe refractory autoimmune disease.
Johnson, Nathan M., Koumpouras, Fotios
openaire   +2 more sources

Recent advances in adoptive cell therapy for cancer immunotherapy

open access: yesFrontiers in Immunology
Adoptive cell therapy (ACT), a key direction in tumor immunotherapy, has achieved remarkable progress in recent years. This paper systematically reviews the current status and future trends of ACT, covering lymphokine-activated killer cells (LAK), tumor ...
Jiameng Qian   +3 more
doaj   +1 more source

Systematically optimized BCMA/CS1 bispecific CAR-T cells robustly control heterogeneous multiple myeloma

open access: yesNature Communications, 2020
One cause of relapse in cancer patients treated with chimeric antigen receptor (CAR) T cells is the loss of CAR-targeted antigens, which is particularly common in multiple myeloma (MM). Here the authors engineer a CAR recognizing two common MM-associated
Eugenia Zah   +8 more
doaj   +1 more source

Development of Chimeric Antigen Receptor (CAR) T Processes

open access: yesBiology of Blood and Marrow Transplantation, 2019
Topic Significance & Study Purpose/Background/Rationale Chimeric antigen receptor therapy (CAR-T) is an autologous genetically engineered cell that can lead to dramatic responses in patients with refractory or relapsed leukemia and lymphoma.
Theresa M. Latchford, D. Kathryn Tierney
openaire   +1 more source

Special Chimeric Antigen Receptor (CAR) Modifications of T Cells: A Review

open access: yesFrontiers in Oncology, 2022
Chimeric antigen receptor (CAR) -T cell therapy has become one of the hot topics in tumor immunity research in recent years. Although CAR-T cell therapy is highly effective in treating hematological malignancies, there are numerous obstacles that prevent CAR-T cells from having anti-tumor effects.
Lele Miao   +14 more
openaire   +3 more sources

Synthetic TRuC receptors engaging the complete T cell receptor for potent anti-tumor response

open access: yesNature Communications, 2019
Supraphysiological T cell activation by chimeric antigen receptor (CAR) contributes to T cell exhaustion and adverse events in CAR T cell therapies. Here the authors engineer a synthetic antigen receptor that integrates into the endogenous TCR complex ...
Patrick A. Baeuerle   +20 more
doaj   +1 more source

Oncologic Emergencies: Immune-Based Cancer Therapies and Complications [PDF]

open access: yes, 2020
Cancer therapies have undergone several recent advancements. Current cancer treatments include immune-based therapies comprised of checkpoint inhibitors, and adoptive immunotherapy; each treatment has the potential for complications that differ from ...
Brém, Elizabeth   +2 more
core  

The Evolving Role of CD8+CD28- Immunosenescent T Cells in Cancer Immunology [PDF]

open access: yes, 2019
Functional, tumor-specific CD8+ cytotoxic T lymphocytes drive the adaptive immune response to cancer. Thus, induction of their activity is the ultimate aim of all immunotherapies.
Dey, Mahua   +4 more
core   +1 more source

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