Rocking bioreactors automate media exchange and transduction to reduce labor intensity and contamination risks in cell therapy manufacturing.
Adoptive transfer of primed B cells bypasses pre-existing antibody interference to boost specific cell counts.
Vx-001 vaccine overcomes non-immunogenic tumor resistance by using optimized cryptic TERT peptides to induce cytotoxic T lymphocyte responses.
Plant-derived mitogens stimulate NK and T cell expansion while removing zoonotic infection risks from animal proteins.
Fixed ratio ex vivo activated lymphocytic subsets enhance targeting specificity in personalized cancer therapies.
A protocol generates cortical organoids from human pluripotent stem cells that produce low-frequency electrical oscillations.
Separating hematopoietic progenitor cells via specific marker profiles to produce CD4/CD8 double positive cells.
An in-vitro cell cluster maintains functional lymphoid organization to produce antigen-specific antibodies and simulate adaptive immunity.
Enzymatic degradation of a porous 3D matrix releases viable target cells, enabling early detection without complex diagnostic infrastructure.
Enriched regulatory T cell composition with naive and central memory subsets improves lineage stability.
Segmenting differentiation into stages with BMP4 and VEGF overcomes low purity and efficiency bottlenecks.
A cell-based flow cytometry method detects neutralizing factors in patient fluids using receptor-expressing cells.
Surface-bound cytokines on magnetic carriers replace K562 feeder cells to proliferate natural killer cells while eliminating immune rejection risks.
Replacing IL-2 with IL-21 and IL-7 prevents terminal differentiation, sustaining expansion without sacrificing long-term survival.
A method generates T regulatory cells by exposing pluripotent stem cells to thymic medullary epithelial cells.
Suppressing PI3Kα activity in avian B cells overcomes immune tolerance barriers to generate high-affinity antibodies.
Exogenous transcription factors reverse myeloid lineage potential to generate patient-specific immune cells.