«That's one of the big goals: to
engineer these cells from patients and then use them to study those patients» diseases.»
Recently, scientists have
engineered cells from a patient's own immune system to fight blood cancers.
Not exact matches
«We concluded that stem
cells used in cardiac therapy should be drawn
from healthy donors or be better genetically
engineered for the
patient.»
To manufacture CAR T
cells, scientists extract bone marrow
from a
patient, introduce genetic instructions for a CAR into the T
cells, and then infuse those
engineered immune
cells back into the person's bloodstream.
CAR T
cells are T
cells that are removed
from a
patient, genetically
engineered to grow a protein «sensor» that targets them to tumor
cells, and then re-injected into the
patient.
Since the 1970s tissue
engineers have been figuring out how to grow skin, bone, cartilage, and even parts of vital organs using
cells harvested directly
from patients.
The researchers, led by University of California, San Diego neuroscientist Mark Tuszynski, took skin
cells from the
patients, grew them up in a culture dish and genetically
engineered them to make human nerve growth factor (NGF).
Over the past two years, investigators
from the Perelman School of Medicine at the University of Pennsylvania have reported results
from a human trial in GBM using chimeric antigen receptor (CAR) T
cell therapy, through which
patients» own T
cells were
engineered to track down and kill cancer
cells that express a tumor - specific protein known as EGFRvIII.
If some of those
cells could be removed
from a person with AIDS, genetically
engineered to be resistant, and then returned to the
patient, they might spawn an immune system that is completely resistant to the disease.
T
cells are collected
from the
patient's blood and genetically
engineered to express
cell - surface proteins called CARs, which recognize specific molecules found on the surface of cancer
cells.
In the new work, the researchers added serum
from Finnish narcolepsy
patients who had received Pandemrix to
cells that were
engineered to display human hypo cretin receptor 2 on their surface.
A chip developed by mechanical
engineers at Worcester Polytechnic Institute (WPI) can trap and identify metastatic cancer
cells in a small amount of blood drawn
from a cancer
patient.
«Circulating tumor
cells —
cells from a tumor that have escaped into the bloodstream with the potential to spread into other tissues — are extremely useful for assessing a
patient's disease in order to select the most appropriate treatment,» said UBC mechanical
engineering professor Hongshen Ma, the lead researcher.
Lead researcher Dr Gordana Vunjak - Novakovic said: «The availability of personalised bone grafts
engineered from the
patient's own stem
cells would revolutionise the way we currently treat these defects.»
Dr. Sonntag studies this concept on the molecular and cellular level using a translational research approach that integrates the analysis of human material, such as postmortem brains, primary
cell systems, and neural
cell populations generated
from patients» - or healthy individuals» - derived induced pluripotent stem
cells (iPSC), or induced neurons (iNs), in combination with molecular, biochemistry, and lentivirus - mediated gene -
engineering technologies.
Now,
patients with pancreatic cancer desperate for new treatment options will potentially benefit
from a powerful new technology that uses genetic
engineering to turn their own immune
cells into «specially trained assassins» capable of finding, attacking, and eliminating pancreatic cancer tumors.
These drugs free a
patient's immune system
from cancer - induced suppression, while others
engineer a
patient's own white blood
cells to attack cancer.
For the other adult
patients that might still benefit
from a cord blood donor, either two cord blood units are combined for a single transplant, or more recently, there are some exciting new graft
engineering technologies that are emerging to expand stem or progenitor
cells in the laboratory before infusion or modify the
cells in some way to make them more potent at the time of transplant.
In addition to growing new skin for burn victims,
cells from hair follicles could potentially be used to
engineer vascular grafts and possibly regenerate cardiac tissues for
patients with heart problems.
In the long run, scientists hope to use organoids and induced pluripotent stem
cells to
engineer tissue replacements in
patients suffering
from diseases that currently are treated with direct transplants of fetal tissue.
«As the only
engineer in the U.S. Senate,» Sununu said, «I've been proud to protect funding for the National Science Foundation
from political manipulation and fully support funding for adult and amniotic stem
cell research — which has already resulted in a number of treatments that have proven to be successful in
patient trials.»
CAR - T
cell therapy is a specific form of adoptive T
cell transfer in which T
cells are removed
from the
patient, genetically
engineered in the lab to recognize a cancer antigen, expanded to billions of copies, and then returned to the
patient.
Other researchers are using CRISPR to
engineer the genomes of heart
cells created
from the iPS
cells of
patients with cardiovascular disorders to study the genetic causes of the cardiomyopathies and congenital heart defects.
Stem
Cells Translational Medicine welcomes original articles and concise reviews describing the clinically relevant translational aspects of stem cells and progenitor cells for cell - based therapy, tissue engineering and regenerative medicine from the bench to patient
Cells Translational Medicine welcomes original articles and concise reviews describing the clinically relevant translational aspects of stem
cells and progenitor cells for cell - based therapy, tissue engineering and regenerative medicine from the bench to patient
cells and progenitor
cells for cell - based therapy, tissue engineering and regenerative medicine from the bench to patient
cells for
cell - based therapy, tissue
engineering and regenerative medicine
from the bench to
patient care.
A team of chemical and biomedical
engineers from the Cockrell School of Engineering at The University of Texas at Austin, in collaboration with researchers
from the University of Pennsylvania, have discovered that HIV - infected
patients experience a dysfunction in a certain type of immune
cell: the follicular helper T (Tfh)
cell.
Staff at the clinic will take these immune
cells from a
patient, have the
cells specially
engineered in a nearby Hutch
cell - processing facility, and then re-infuse them to attack the
patient's cancer.
His gene therapy — delivering nanoparticles could transform
patients into their own T -
cell engineering labs, allowing them to be treated with reprogrammed T
cells almost
from the moment of diagnosis, skipping the waiting period and high cost of current approaches.
As noted above, existing cancer vaccines that use dendritic
cells require extracting
cells from a
patient's blood, treating them with an
engineered protein or nucleic acid that combines tumor antigens with immune - stimulating molecules, and returning the activated dendritic
cells to the
patient.
Tactiva's lead platform is a unique approach to adoptive
cell transfer (ACT), a form of immunotherapy in which a
patient's own immune
cells are drawn
from blood, genetically
engineered, multiplied and injected back into the
patient in order to launch a powerful attack against cancer.