Chimeric antigen receptor natural killer (CAR-NK) cell design and engineering for cancer therapy

Y Gong, RGJ Klein Wolterink, J Wang, GMJ Bos… - Journal of hematology & …, 2021 - Springer
Due to their efficient recognition and lysis of malignant cells, natural killer (NK) cells are
considered as specialized immune cells that can be genetically modified to obtain capable …

Advanced microfluidic technologies for lipid nano-microsystems from synthesis to biological application

BG Carvalho, BT Ceccato, M Michelon, SW Han… - Pharmaceutics, 2022 - mdpi.com
Microfluidics is an emerging technology that can be employed as a powerful tool for
designing lipid nano-microsized structures for biological applications. Those lipid structures …

Rapid manufacturing of non-activated potent CAR T cells

S Ghassemi, JS Durgin, S Nunez-Cruz… - Nature biomedical …, 2022 - nature.com
Chimaeric antigen receptor (CAR) T cells can generate durable clinical responses in B-cell
haematologic malignancies. The manufacturing of these T cells typically involves their …

Development of a gut-on-a-chip model for high throughput disease modeling and drug discovery

C Beaurivage, E Naumovska, YX Chang… - International journal of …, 2019 - mdpi.com
A common bottleneck in any drug development process is finding sufficiently accurate
models that capture key aspects of disease development and progression. Conventional …

Lymph node subcapsular sinus microenvironment-on-a-chip modeling shear flow relevant to lymphatic metastasis and immune cell homing

KG Birmingham, MJ O'Melia, S Bordy, DR Aguilar… - Iscience, 2020 - cell.com
A lymph node sinus-on-a-chip adhesion microfluidic platform that recapitulates the
hydrodynamic microenvironment of the lymph node subcapsular sinus was engineered. This …

Expanding CAR-T cell immunotherapy horizons through microfluidics

H Kim, S Kim, H Lim, AJ Chung - Lab on a Chip, 2024 - pubs.rsc.org
Chimeric antigen receptor (CAR)-T cell therapies have revolutionized cancer treatment,
particularly in hematological malignancies. However, their application to solid tumors is …

Targeted in vivo knock-in of human alpha-1-antitrypsin cDNA using adenoviral delivery of CRISPR/Cas9

CJ Stephens, E Kashentseva, W Everett, L Kaliberova… - Gene therapy, 2018 - nature.com
Serum deficiency diseases such as alpha-1-antitrypsin deficiency are characterized by
reduced function of serum proteins, caused by deleterious genetic mutations. These …

[HTML][HTML] Concise review on optimized methods in production and transduction of lentiviral vectors in order to facilitate immunotherapy and gene therapy

HEG Ghaleh, M Bolandian, R Dorostkar, A Jafari… - Biomedicine & …, 2020 - Elsevier
Lentiviral vectors (LVs) have provided an efficient way to integrate our gene of interest into
eukaryote cells. Human immunodeficiency virus (HIV)-derived LVs have been vastly studied …

Scaffold‐mediated static transduction of T cells for CAR‐T cell therapy

P Agarwalla, EA Ogunnaike, S Ahn… - Advanced …, 2020 - Wiley Online Library
Chimeric antigen receptor T (CAR‐T) cell therapy has produced impressive clinical
responses in patients with B‐cell malignancies. Critical to the success of CAR‐T cell …

Viral Generation, Packaging, and Transduction on a Digital Microfluidic Platform

ABV Quach, SR Little, SCC Shih - Analytical Chemistry, 2022 - ACS Publications
Viral-based systems are a popular delivery method for introducing exogenous genetic
material into mammalian cells. Unfortunately, the preparation of lentiviruses containing the …