Q3 2022

Chimeric Antigen Receptor Structure and Manufacturing of Clinical Grade CAR Engineered Cells using Different Bioreactors

Farhatullah Syed · Riad El Fakih · Ali D. Alahmari · Ahmed S. Osman Ali · Mahmoud Aljurf
10.56875/2589-0646.1048 390 المشاهدات 16 الاقتباسات
16
الاقتباسات
390
المشاهدات
الملخص



Increasing success of adaptive cell therapy (ACT), such as genetically engineered T cells to express chimeric antigen receptors (CARs) proven to be highly significant technological advancements and impressive clinical outcomes in selected haematological malignancies, with promising efficacy. The evolution of CAR designs beyond the conventional structures is necessary to address some of the limitations of conventional CAR therapy and to expand the use of CAR T cells to a wider range of malignancies. There are various obstacles with a wide range of engineering strategies in order to improve the safety, efficacy and applicability of this therapeutic modality. Here we describe details of modular CAR structure with all the necessary domains and what is known about proximal CAR signalling in T cells. Furthermore, the global need for adoptive cell therapy is expanding very rapidly, and there is an urgent increasing demand for fully automated manufacturing methods that can produce large scale clinical grade high quality CAR engineered immune cells. Despite the advances in automation for the production of clinical grade CAR engineered cells, the manufacturing process is costly, consistent and involves multiple steps, including selection, activation, transduction, and Ex-Vivo expansion. Among these complex manufacturing phases, the choice of culture system to generate a high number of functional cells needs to be evaluated and optimized. Here we list the most advance fully automated to semi-automated bioreactor platforms can be used for the production of clinical grade CAR engineered cells for clinical trials but are far from being standardized. New processing options are available and a systematic effort seeking automation, standardization and the increase of production scale, would certainly help to bring the costs down and ultimately democratise this personalized therapy. In this review, we describe in detail different CAR engineered T cell platforms available and can be used in future for clinical-grade CAR engineered ATMP production.

الاستشهاد بهذا المقال (APA)
Farhatullah, S., Riad, E. F., Ali, D. A., Ahmed, S. O. A., Mahmoud, A. (2022). Chimeric Antigen Receptor Structure and Manufacturing of Clinical Grade CAR Engineered Cells using Different Bioreactors. Hematology/Oncology and Stem Cell Therapy. https://doi.org/10.56875/2589-0646.1048
أبحاث ذات صلة
The Risk and Prognosis of COVID-19 Infection in Cancer Patients
Ghada M. ElGohary; Shahrukh Hashmi; Jan Styczynski; Mohamed A. Kharfan-Dabaja; R · 2022
80
استشهاد
396
Molecular mediators of breast cancer metastasis
Ragini Yeeravalli; Amitava Das · 2021
39
استشهاد
386
Venetoclax and decitabine for treatment of relapsed T-cell acute lymphoblastic leukemia
Nosha Farhadfar; Ying Li; William S. May; Carolyn Brooke Adams · 2021
38
استشهاد
389
Acute upper limb ischemia in a patient with COVID-19
Parminder Kaur; Firas Qaqa; Amr Ramahi; Yezin Shamoon; Monisha Singhal; Fayez Sh · 2021
35
استشهاد
387
26
استشهاد
388
الوصول
عرض النص الكامل عبر DOI
نُشر في
الرقم الدولي ISSN 1658-3876
الربعية Q3
درجة المؤشر القياس العربي 72
التخصص Medicine & Health Sciences
الناشر Elsevier / King Faisal Specialist H
الدولة 🇸🇦 Saudi Arabia
عرض ملف المجلة →
المؤلفون
تفاصيل النشر
السنة 2022
اللغة English
أُضيف في 28 Jul 2026