For many illnesses, researchers would like to study
the diseased cells from a patient in the lab; their ultimate hope is that they can also fix those cells by modifying them genetically and then inject them back into the patient.
Not exact matches
Lab - grown tissues derived
from patients» stem
cells may also allow researchers to screen drugs and test their effectiveness on
diseases like cancer.
Skin
cells are easy to collect
from patients and share the same genetic blueprint — and
disease - causing mutations — as brain
cells.
«In theory, we could model progression of the
disease by reprogramming skin
cells from patients at a range of ages, including before symptoms begin.
To develop their «
disease in a dish» model, the team took skin
cells from patients with Allan - Herndon - Dudley syndrome and reprogrammed them into induced pluripotent stem
cells, which then can be developed into any type of tissue in the body.
They isolated blood
cells from HIV - positive
patients on antiretroviral therapy and at different stages of
disease progression, as well as
cells from non-infected individuals.
Creating a whole set of miniature new livers might take as little as obtaining liver
cells from healthy donors and placing them inside the lymph nodes of
patients suffering
from liver
disease.
In preclinical studies using
cell models that mimicked liver
cells of
patients with the rare
disease Friedreich's ataxia (FA), a widely used cholesterol - lowering drug increased a precursor of HDL (high - density lipoprotein), the «good cholesterol,» according to new research published in PLOS ONE
from the Perelman School of Medicine at the University of Pennsylvania.
The Porteus team started with human stem
cells from the blood of
patients with sickle
cell disease, corrected the gene mutation using CRISPR and then concentrated the human stem
cells so that 90 percent carried the corrected sickle
cell gene.
«Cardiac stem
cells from heart
disease patients may be harmful: Researchers discover molecular pathway involved in toxic interaction between host
cells and immune system.»
Mice transplanted with
cells grown
from a
patient suffering
from Huntington's
disease (HD) develop the clinical features and brain pathology of that
patient, suggests a study published in the latest issue of Acta Neuropathologica by CHA University in Korea, in collaboration with researchers at Université Laval in Québec City, Canada.
The new findings build on prior research
from the Dhodapkar lab demonstrating that
patients with Gaucher
disease, an inherited lipid storage disorder, have a significant increased risk for developing myeloma; and the discovery of a subset of lipid - reactive immune
cells, called type II NKT - TFH, that promote the development of plasma
cells.
Scientists
from the University of Cambridge's Institute for Medical Research obtained skin
cells from 10
patients — seven who had various forms of inherited liver
disease, and three healthy controls.
These techniques include: human tissue created by reprogramming
cells from people with the relevant
disease (dubbed «
patient in a dish»); «body on a chip» devices, where human tissue samples on a silicon chip are linked by a circulating blood substitute; many computer modelling approaches, such as virtual organs, virtual
patients and virtual clinical trials; and microdosing studies, where tiny doses of drugs given to volunteers allow scientists to study their metabolism in humans, safely and with unsurpassed accuracy.
In addition to helping understand
disease by providing more powerful study models, «what this technology would allow you to do is reprogram a skin
cell, for example,
from a Parkinson's
patient... into a pluripotent
cell and then in a petri dish redirect that
cell into... a neuron» to treat that
patient.
The
cells were derived
from eggs that had been injected with DNA
from the
patients, so they could eventually be transplanted back to replace or correct the
patient's
diseased cells without fear of immune rejection.
Diabetes researchers are considering various replacements for insulin injections: Transplanting new pancreatic islet
cells that make insulin, coaxing the
patient's own islets to regenerate, or treating diabetics early in the
disease with immune - suppressing therapies to prevent their body
from destroying the rest of their pancreatic islets.
In the next phase of the study, researchers will genetically sequence tumor
cells from at least 500
patients and follow the course of their
disease.
The new technique can also be used to grow muscle
cells from iPS
cells from patients with neuromuscular
diseases like ALS, spinal muscular atrophy and muscular dystrophy.
In new research, scientists reprogrammed skin
cells from patients with rare blood disorders into iPSCs, highlighting the great promise of these
cells in advancing understanding of those challenging
diseases — and eventually in treating them.
Researchers can create iPSCs
from a
patient's blood or skin
cells, and use these
patient - specific
cells to study
diseases or even create new tissues that could be transplanted back into the
patient as therapy.
Another key finding of the research was that the impact of vitamin D on inflammatory
disease can not be predicted using
cells from healthy individuals or even
from the blood of
patients with inflammation as
cells from the
disease tissue are very different.
In this study, researchers took
cells from patients with blood cancer MDS and turned them into stem
cells to study the deletions of human chromosome 7 often associated with this
disease.
Labs could rejuvenate
cells from patients and perhaps then grow them into new tissue that could repair parts worn out by old age or
disease.
Last week, scientists at Harvard University and Columbia University announced that they had proved the viability of a new way to study a
disease — amyotrophic lateral sclerosis — by reprogramming
cells from a
patient to become pluripotent stem
cells, which can then become any type of
cell or tissue.
Zheng, together with Leah Boyer, then a researcher in Gage's lab and now director of Salk's Stem
Cell Core, generated
diseased neurons by taking skin
cells from patients with Leigh syndrome, reprogramming them into stem
cells in culture and then coaxing them to develop into brain
cells in a dish.
It has been understood for several years that, in
patients suffering
from this
disease, immune
cells attack the aquaporin - 4 water channel of the brain
cells.
Desgrosellier said the team will follow up with mouse models containing tumor fragments
from patients to better reflect the diversity of
cell types present in human
disease.
Hwang claimed to have perfected somatic
cell nuclear transplant, a procedure in which genetic material is removed
from a donated egg and replaced with DNA
from the
patient to create cloned
cells that could regenerate
diseased tissues or organs.
In the longer term, these methods could hasten progress toward replacing a damaged or
diseased kidney with tissue derived
from a
patient's own
cells.
Plus, hopes for therapeutic cloning rest on the ability to produce embryonic stem
cells from cells harvested
from diseased patients.
Dr Leonardo Guasti added: «It represents an entirely new concept for the study of the adrenal gland as the ability to generate donor - specific and functional adrenal - like
cells will facilitate the next generation of
cell - based treatments for adrenal insufficiency, the modelling of adrenal specific
diseases, and the testing of personalised interventions on
cells derived
from patients.»
And it suggests that stem
cells derived
from embryos should remain the primary reference for iPS
cells when researchers want to compare how
cells from diseased patients behave, says Nissim Benvenisty of Hebrew University of Jerusalem, who has studied differences between ES
cells and iPS
cells derived
from carriers of fragile X syndrome.
The capsule creates the biotechnical condition for it, because it separates the donator's
cells from the body of the receiver and transfers the hormones which are important for the metabolism exclusively «In the eyes of Dresden scientists this kind of transplantation will be suitable for
patients with adrenal insufficiency but also with congenital
diseases such as the lack of 21 - hydroxylase.
The
disease model, described in a new study by a UC San Francisco - led team, involves taking skin
cells from patients with the bone
disease, reprogramming them in a lab dish to their embryonic state, and deriving stem
cells from them.
Researchers have developed a new way to study bone disorders and bone growth, using stem
cells from patients afflicted with a rare, genetic bone
disease.
The day after his disciplinary dismissal
from University of Tokyo for «damaging the university's honor or credibility,» Hisashi Moriguchi maintained in an interview with ScienceInsider that he really did participate in a groundbreaking experiment to treat a heart
disease patient with cardiac muscle
cells derived
from the
patient's own induced pluripotent stem (iPS)
cells.
Patients could benefit
from having their own
cells reprogrammed into ones that could help treat
disease, potentially eliminating the prospect of immune rejection.
The researchers
from UC Berkeley, UC San Francisco Benioff Children's Hospital Oakland Research Institute (CHORI) and the University of Utah School of Medicine hope to re-infuse
patients with the edited stem
cells and alleviate symptoms of the
disease, which primarily afflicts those of African descent and leads to anemia, painful blood blockages and early death.
Researchers in Keele University's Research Institute for Science and Technology in Medicine and at the Haywood Rheumatology Centre, in Staffordshire, UK, and the University Hospitals of North Midlands NHS Trust, have for the first time identified
disease - associated changes to the DNA epigenome in joint fluid
cells from patients with rheumatoid arthritis.
Scientists want to be able to clone early human embryos, using
cells from patients with various
diseases, so they can study the
diseases in the lab and develop new treatments for them.
«They continue to have the gene and they produce VEGF - A, but it's like the
patient's
cells don't realize they could be more protected or suffer
from the
disease much less if the
cells produce more of this particular protective factor.»
And by creating personalized organoids
from the reprogrammed
cells of
patients, scientists could study
disease in a very individualized way — or maybe even use organoid structures to replace certain damaged tissues, such as in the liver or spinal cord.
«This study represents our progress towards making airway spheres
from any
patient with a lung disorder and learning about that
patient's
disease from those
cells.
In a new study published in Molecular Psychiatry the researchers describe how
cells from patients with the severe developmental
disease lissencephaly differ
from healthy
cells.
«That's one of the big goals: to engineer these
cells from patients and then use them to study those
patients»
diseases.»
These vulnerable
patients, whose immune defenses have taken a dramatic double hit
from both their original
disease and the treatments required to repopulate their immune system with donor
cells, are especially susceptible to a wide range of infections that typically don't cause major problems in healthy people.
«Alzheimer's in a dish: Stem
cells from patients offer model and drug - discovery platform for early onset form of
disease.»
Although treatment for sickle -
cell disease with marrow
from related donors is now accepted as a standard of care, treatment with marrow taken
from an unrelated donor is still evolving, reserved for only the most seriously sick
patients.
«We see this mild increase in Aβ42 in
cells from patients with Alzheimer's
disease, which seems to be enough to trigger
disease processes,» said Young - Pearse, a Harvard Stem
Cell Institute - affiliated faculty member at Brigham and Women's Hospital.