SUPLEXA immunotherapeutic cells are derived by activation, differentiation, and expansion of cancer patient peripheral blood mononuclear cells (PBMCs) by an ‘training’ melanoma tumor cell line that has been engineered to express multiple immunomodulatory factors.
This article offers an important example of how growth factors used during ex vivo manufacturing can critically influence the functional characteristics of NK, NKT-like and CD8 T cells. PMID: 33537030
This article reviews the known biologic role of NKT cells, cells that are positioned at the interface of the innate and adaptive immune systems. PMID: 30158927
This article documents the impact of NK and NKT cells on myeloid-derived suppressor cells, a key immunosuppressive element present in the tumor microenvironment. PMID: 21670315
This review article documents the further application of synthetic biologic to NK cells that extends beyond chimeric antigen receptor (CAR) technology. PMID: 28668320
This review article documents the application of synthetic biologic exemplified by chimeric antigen receptor (CAR) technology to a key innate immune cell, the NK cell. PMID: 30075127
This article reviews the potential role of NK cells in oncology. PMID: 31478911
This article reviews the application of synthetic biology approached to gd T cells. PMID: 29997614
This article reviews the potential role of γδ T cells in oncology. PMID: 29937769
This article reviews the known foundational concepts underlying synthetic biology approached to T cells engineering exemplified by chimeric antigen receptor (CAR) technology. PMID: 30680780
This article reviews the concept of TILS in the era of ubiquitous checkpoint inhibition therapy. PMID: 31187421
This review article demonstrates that in an ex vivo setting, an antigen presenting cells line can expand NK cells with strong anti-tumor activity. Link to PubMed PMID: 24204673
This review article demonstrates that in a vaccine setting, a tumor cell line engineered with a single immunomodulator can influence the host immune system to become activated against that tumor type. PMID: 26161414