Not exact matches
Nadeau stumbled upon one study, in mice, describing how environmental factors can tag Foxp3 with chemical markers that tell
T -
cell precursors to switch the gene on or off.
In PLAT - 02, the CAR
T cells are reprogrammed to recognize and target the CD19 protein that is expressed by most
precursor B acute lymphoblastic leukemia
cells.
Here, Patil et al. have carried out single RNA - seq and sequenced the
T cell receptors (TCRs) of CD4 +
T cells from human blood to identify
precursors that give rise to CD4 - CTLs.
A detailed comparison of gene expression signatures between ETP ALL tumors and and normal human hematopoietic progenitor
cells revealed a somewhat surprising finding: ETP - ALL expression patterns were less consistent with early
T -
cell precursors, as might have been expected, but more similar to the expression profile of normal hematopoietic stem
cells and granulocyte macrophage
precursors.
Although similar numbers of total splenic gp33 - LCMV — specific
T cells were observed between genotypes (Fig. 5B), the distribution of gp33 - LCMV — specific CD8 +
T cell effector and memory subsets were altered, such that there was a significantly lower percentage of short - term effector
T cells and reciprocal changes in memory
precursor cells among gp33 - specifc CD8 +
T cells in WT relative to DKO mice (Fig. 5C), with a trend in changes in absolute
cell numbers, consistent with temporal data from peripheral blood (Fig. 5A).
Six weeks postinfection, splenocytes were analyzed for gp33 - LCMV — specific total CD8 +
T cells (B) or short - lived effector
cells and memory
precursor effector
cells (C).
Consistent with prior reports on effector
cells (35), we observed that, among CD8 +
T cells specific for the dominant epitope of LCMV (GP33), the percentages of short - lived effector
cells (KLRG1 + CD127 −) were increased, and the percentages of memory
precursor cells (KLRG1 + CD127 +) were decreased in the peripheral blood of DGKζ − / −, Cbl - b − / −, and DKO mice relative to WT mice after acute infection (Fig. 5A).
Schallenberg S, Tsai PY, Riewaldt J, Kretschmer K. Identification of an immediate Foxp3 −
precursor population to Foxp3 + regulatory
T cells in peripheral lymphoid organs of non-manipulated mice.
The genetic basis of early
T -
cell precursor acute lymphoblastic leukaemia Nature, 481 (7380), 157 - 163 DOI: 10.1038 / nature10725
In terms of mechanism, the authors found that the presence of H. hepaticus, even as it triggers inflammation via Th17
cells, also indirectly turns on genes that instruct immature
precursor T cells to become Tregs.
Other CAR
T -
cell therapies approved in 2017 include tisagenlecleucel for the treatment of children and young adults up to 25 years of age with relapsed or refractory B -
cell precursor acute lymphoblastic leukemia and axicabtagene ciloleucil (aci - cel; Yescarta) for adults with relapsed or refractory DLBCL.
CD8 (+) cytotoxic and CD4 (+) helper / inducer
T cells develop from common thymocyte
precursors that express both CD4 and CD8 molecules.
In their latest study, researchers at La Jolla Institute for Allergy and Immunology (LJI) used single -
cell transcriptome analysis to identify a hitherto unknown
precursor for a poorly understood subgroup of killer
T cells that is primarily found in humans with chronic viral infections.
Single
cell analysis identifies new immune
cell precursor; reveals surprising heterogeneity in a poorly understood subgroup of antiviral
T lymphocytes
Precursors of human CD4 + cytotoxic
T lymphocytes identified by single -
cell transcriptome analysis.
A phase I / II trial of KTE - C19 (anti-CD19 CAR
T cells) for pediatric and adolescent subjects with relapsed / refractory B -
precursor acute lymphoblastic leukemia -LRB-
New CFSE - based assay to determine susceptibility to lysis by cytotoxic
T cells of leukemic
precursor cells within a heterogeneous target
cell population.
Second, the aging thymus gland, where
precursor stem
cells are transformed into effective
T -
cells, slowly shrinks with age, losing the
cells that are responsible for educating emerging immunological warriors.
CpG stimulation of
precursor B lineage acute lymphoblastic leukemia induces a distinct change in costimulatory molecule expression and shifts allogeneic
T cells towards a Th1 response.
IL - 6 has been shown to be involved in diverse physiological processes such as
T -
cell activation, induction of immunoglobulin secretion, initiation of hepatic acute phase protein synthesis, and stimulation of hematopoietic
precursor cell proliferation and differentiation.
The DC then process the RNA into a protein, splits the protein and presents the protein fragments outside the
cell to neighboring CD8
T cells, which are
precursors to CTLs.