«Ultimately, we have to get
a human model for human diseases so that we can expand human experimental biology in an ethical way and ensure that better, safer drugs get to patients faster,» he says.
Not exact matches
The Dr Hadwen Trust
for Humane Research claims that «in some instances, reliance on inaccurate animal «
models» of
human disease have undoubtedly delayed medical progress.»
Gene therapy delivered to a specific part of the brain reverses symptoms of depression in a mouse
model of the
disease — potentially laying the groundwork
for a new approach to treating severe cases of
human depression in which drugs are ineffective.
To better understand their findings, the team examined the animal
model for APS1 (i.e. mice with the same genetic defect as
human patients with the syndrome) and found that male mice spontaneously developed an inflammatory
disease in their prostate glands — a so - called prostatitis — and reacted to transglutaminase 4.
Human tissue grown in the laboratory offers a critical
model for understanding the
disease process.
Reductions in biodiversity from illegal wildlife trade can have other substantial negative
human health impacts, including the loss of potential sources of pharmaceuticals, experimental
models for studying
disease, crop pollination and micronutrients
for humans lacking alternative sources of protein.
With our
human gut - on - a-chip, we can not only culture the normal gut microbiome
for extended times, but we can also analyze contributions of pathogens, immune cells, and vascular and lymphatic endothelium, as well as
model specific
diseases to understand complex pathophysiological responses of the intestinal tract.»
Scientists study VSV, which causes acute
disease in livestock but typically does not lead to illness in people, as a
model for viruses that are harmful to
humans.
«The study results elucidate the molecular mechanisms underlying
disease progression in multiple sclerosis
models, providing a basis
for future clinical trials to determine safety and efficacy of these chemical agents in
humans with demyelinating disorders,» says Patrizia Casaccia, MD, PhD, Professor of Neuroscience, Genetics and Genomic Sciences at Mount Sinai and senior author of the study.
And the enrichments may make the animals better at what they do: serving as important
models for human disease.
This proof - of - principle study shows «
for the first time... that
human iPS cells can be used to
model a diverse range of inherited
diseases in adult cells,» the authors wrote in their paper, published online in The Journal of Clinical Investigation August 25.
For example, rats are often good models for humans in disease research, but they aren't when it comes to pooping because rats are pellet poope
For example, rats are often good
models for humans in disease research, but they aren't when it comes to pooping because rats are pellet poope
for humans in
disease research, but they aren't when it comes to pooping because rats are pellet poopers.
Additionally, work in a mouse
model revealed similar cells, indicating that the progenitors are conserved from mouse to
human, and therefore, they must be «important cells with promising potential
for cell therapy in treating liver
disease,» explained Dr. Gouon - Evans.
More recently, researchers have induced stem cells from
diseased human somatic cells, which may serve as new
model systems
for various illnesses.
«New gene editing technique turns
human pluripotent stem cells into a
model system
for polycystic kidney
disease.»
These observations and others have convinced the researchers that their CRISPR / Cas9 and hPSC system produces a stable, biologically accurate
human model for a common genetic
disease where new understanding and new therapies are desperately needed.
Most animal studies of the
disease are conducted with laboratory mice that have been genetically engineered and bred to
model ALS, but
for this research, investigators used rats with ALS because they more accurately portray the
disease's variable course in
humans.
In recent years, songbirds» similarities to
human vocal learning have piqued researchers» interests in using them as a functional animal
model to study the neurological basis
for Huntington's
disease.
«Finches offer researchers a new tool with which to study Huntington's
disease: Like
humans, songbirds learn their vocalizations, suggesting they could be useful as
models for certain disorders.»
Like
humans, songbirds such as zebra finches (above) can learn vocalizations, and this similarity suggests they could serve as
models for research on Huntington's
disease and other neurodegenerative disorders that affect speech and vocalization.
«Investigators create complex kidney structures from
human stem cells derived from adults: New technique offers
model for studying
disease, progress toward cell therapy.»
Mini-organ
models promise enormous advantages
for understanding basic
human biology, teasing apart
human disease processes, and offering an accurate testing ground
for finding or vetting drug therapies.
Mardinoglu says the team's network
modeling approach, which relied on data from the Sweden - based
Human Protein Atlas project and The Genotype - Tissue Expression (GTEx) project consortia, can be used in the identification of drug targets and eventually in the development of efficient strategies
for treating a number of chronic liver
diseases.
«The mouse
models don't recapitulate the
human disease,» said Ravi Basavappa of the National Institutes of Health, which gave Fine one of its 12 Pioneer Awards
for «unusually bold,» high - risk, and potentially high - impact research.
«Using the fruit fly as a
model [
for a
human disease] is extremely exciting,» he adds.
Because of the similarities in ocular anatomy, canine
models contribute significantly to the understanding of retinal
disease mechanisms and the development of new therapies
for human patients.
«We found many examples in which an entire species should have a serious genetic ailment, but instead were healthy,» said Nicholas Katsanis, Ph.D., director of the Center
for Human Disease Modeling and professor cell biology and pediatrics at Duke.
Using a recently developed genome - editing technique called CRISPR, a Chinese team has successfully altered two target genes in cynomolgus monkeys, paving the way
for the development of monkey
models that mimic
human diseases.
This research is all aimed at tissue repair strategies, but it also may provide new in vitro
models for human disease.
The researchers hope their new cell lines will be a useful resource
for studying the cellular and molecular intricacies of Huntington's further, and suggest they may provide a
model for examining other
diseases of the brain that are specific to
humans.
One of the most promising avenues
for developing a cure, however, is through gene therapy, and to create those therapies requires animal
models of
disease that closely replicate the
human condition.
The investigators used the nanoparticle plus the iRGD to deliver irinotecan in a robust animal
model for pancreatic cancer that closely mimics
human disease.
«We think that
for the first time, we have a mouse
model of anorexia that closely resembles the conditions leading up to the
disease in
humans,» said study leader Lori Zeltser, PhD, associate professor of pathology & cell biology and a researcher in the Naomi Berrie Diabetes Center.
Though mutations that cause
human cancer have traditionally been thought to originate from heredity or environmental sources, these results — grounded in a novel mathematical
model based on data from around the world — support a role
for so - called «R» or random mutations in driving the
disease.
Critics charge that rabbits are not good animal
models for human brain
diseases and note that the dialysis patients suffered from dialysis encephalopathy, or «dialysis dementia,» not Alzheimer's
disease.
«There are
human diseases for which we have dog
models,» she says.
«The dog is an invaluable
model for exploring hereditary copper - storage
diseases, and observations made in this study will benefit both canine and
human patient populations.»
«These are strong evidence that cave fish could be a good
model for human psychiatric
disease.»
«
For example, there is a huge amount of interest and excitement globally in growing cerebral organoids» — miniature brain - like organs that can be studied in laboratory experiments — «from stem cells to
model human brain development and
disease mechanisms.
«Large animal
models of
human disease, like cats, are really helpful
for determining what's going to happen in a child when you're treating them,» Vite said.
Overall, this work illustrates that better understanding the basic biology of the immune system in preclinical
models may open up a window
for the development of novel treatments
for human autoimmune
disease.
The researchers hope their study leads to better measures
for modeling and predicting infectious
disease transmission, but there are still open questions about the
human - wildlife interface of
disease.
Colorado State University biologists say this sporadic ebb and flow of prairie dog plague is an ideal
model for the study of rare infectious zoonotic
disease —
disease that can jump from wildlife to
humans — like MERS (Middle East Respiratory Syndrome) and Ebola.
Given the rapid succession of generations in yeast, we can use it as a
model organism — and study the mechanisms of aneuploidy in much greater detail to find out whether we can derive from it new approaches
for diagnosing and treating
human diseases.»
Findings from mouse
models suggest that eye examination could be used as a noninvasive screening tool
for human brain
diseases.
«Previous studies of cardiac microtissues primarily used harvested rat cardiomyocytes, which is an imperfect
model for human disease.»
But Franklin and others suspect that in their zeal to clean up, facilities may have wiped out some of the microbial complexity that makes mice useful
models for human disease.
It's now possible to not only
model disease using the cells, but also to compare iPSCs from
humans to those of our closest living relatives --- great apes, with which we share a majority of genes ---
for insight into what molecular and cellular features make us
human.
Thank you
for airing Joseph Garner's views on the futility of trying to cure mouse «
models» of
human diseases (29...
«If the mouse
models are indicative of
human disease, the combination therapy can increase the proportion of patients who respond to therapy without additional adverse side effects and can improve the quality of life
for cancer patients.»