Career Goals: I plan to pursue a career in scientific research focused on
understanding the human immune response to various infectious agents for diagnostic and vaccine design purpose.
Not exact matches
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.»
The UNC research team, led by Lemon and Jason Whitmire, Ph.D., Associate Professor in UNC's Department of Genetics, is now poised to investigate the complicated interplay of nonspecific «innate» and specific «adaptive»
immune responses that ultimately control the infection and eliminate HAV from the host — processes that are not well
understood for any of the five
human hepatitis viruses.
«These data provide the basis for
understanding the
immune response to filovirus infections in
humans,» said Bukreyev.
Hypothesis driven approaches to vaccinology can utilise the knowledge gained from mechanistic mouse models and our molecular
understanding of intrinsic defects to
human cells.5 However, caution is required when extrapolating data from murine models, as there are substantial differences between
immune ageing in mice and
humans.6 Nevertheless, model systems and ex vivo analyses of molecular alterations in aged
human cells have identified multiple changes in the vaccination
response with age and the aged
immune system in general.
For
understanding the biology of gene - gene, gene - drug and gene - microenvironment interactions, a considerably broader range of in vitro and in vivo model systems is required — we are generating 1,000 organoid cultures from
human cancers, characterising their genomes, functional dependencies and drug
response, and we are expanding our in vivo models to study the interface between cancer and the
immune system and microenvironment.
She continued describing
human history with pathogens, showing how signals of ancient, pathogen - driven selection can be used to
understand immune response.
It is based on the scientific
understanding and high - throughput analyses of
human immune responses to disease - related proteins in selected populations including elderly with the capability to stay healthy during the aging process.
In the proposed partnership between Addis Ababa University (AAU) and J. Craig Venter Institute (JCVI), the objective is to build genomics capacity at AAU and to apply newly developed skills towards
understanding the relationships of active TB disease with Mtb strain type diversity and host components such as the
human respiratory microbiome and protein - based analysis of
immune responses in the respiratory tract.
Using gene - targeted mice and
human cells that lack specific components of the
immune system, a better
understanding of the
immune response to DENV and ZIKV is critical for developing much - needed vaccines and antivirals.
As current therapeutics are limited, it is essential to define the
immune evasion strategies of these fungal pathogens which cause life - threatening infections and at the same time to
understand the
immune response of the
human host to these fungal pathogens.