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Printable Handouts
Navigable Slide Index
- Introduction
- Outline
- Cytomegalovirus is a herpesvirus
- Cytomegaloviruses are everywhere
- Historical prospective
- HCMV-associated diseases
- Congenital cytomegalovirus (cCMV) infection
- Congenital CMV
- CMV-associated cancers
- Anti-cytomegalovirus drugs
- Anti-virals in development
- Biologicals targeting CMV
- CMV vaccine development
- Human cytomegalovirus (HCMV)
- HCMV model
- Known entry factors of CMV
- Different mechanisms dependent on cell type
- HCMV life cycle
- CMV latency/reactivation
- The CMV latency-reactivation cycle
- Regulatory factors involved in CMV latency
- CMV is an opportunistic and successful virus
- Immune system-simplified
- MHC class I antigen presentation
- Down-regulation of class I molecules by mutant HCMV
- Other viruses also evade MHC class I
- Natural killer cells
- Cytomegalovirus evasion of NK responses
- CMV factors that limit NK cell activation
- Cellular targets of HCMV miRNA
- CMV genes that mediate cellular functions
- Outstanding topics
Topics Covered
- Introduction to human cytomegalovirus (CMV)
- Diseases associated with CMV
- Therapeutics targeting CMV
- Development of CMV vaccines
- CMV entry factors
- CMV life cycle
- CMV latency and reactivation cycle
- CMV immune evasion strategies including evasion of NK cells
Links
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Talk Citation
Tortorella, D. (2020, April 29). Cytomegalovirus biology [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/ATTX3152.Export Citation (RIS)
Publication History
Financial Disclosures
- There are no commercial/financial matters to disclose.
A selection of talks on Immunology
Transcript
Please wait while the transcript is being prepared...
0:00
My name is Domenico Tortorella.
I'm a professor in the Department of Microbiology at
the Icahn School of Medicine at Mount Sinai in New York City.
Today, I'm going to discuss some of the highlights of the importance of cytomegalovirus and cytomegalovirus entry.
0:17
The outline of the presentation will include an introduction to herpes viruses,
cytomegalovirus prevalence and disease,
current anti-viral agents and some vaccine trials.
Basically, the importance of,
and for you to recognize the complication of, the CMV life-cycle;
and one aspect is viral entry,
viral latency and one important aspect of the virus is its ability to
persist in their host and we're going to
discuss the important immune evasion strategies of the virus.
0:50
Cytomegalovirus is a herpes virus, and
herpesviruses are basically in three different categories-
considered Alpha, Beta, and Gamma.
The Alpha herpesviruses consist of
herpes simplex virus 1 and 2 and varicella-zoster virus.
You can see in all cases these are
neurotropic viruses and they have a relatively large genome size.
The Beta herpesviruses, a small category, includes
cytomegalovirus, human herpesvirus 6,
human herpesvirus 7,
and they cause wide tissue tropism,
but they're very species-specific.
Recently, HHV 6 and 7 have been associated with Alzheimer's disease
and a recent publication in Immunity shows
that these viruses can affect multiple cell types as well
as potentially cause different various diseases and we're going to
discuss more about the different aspects of all the different diseases
that is associated with the proliferation of human cytomegalovirus.
Note that human cytomegalovirus is the largest genome,
which is over 230 kilobases and we'll see at
the end how a lot of that genome is dedicated to all viral invasion.
The last group is the Gamma herpesviruses,
they usually infect lymph cells and they're considered lymphotropic.
They're associated with cancer,
and these include the Epstein-Barr virus and the Gamma as well as
the Kaposi's sarcoma herpes virus that was more or less discovered,
caused lots of disease in HIV infected individuals and in all cases,
these are viruses that after a primary infection,
in most cases, they cause permanent latent infection,
which usually means they're latent in different reservoirs
of the host and they reactivate at different times
that are based on immunocompromised or inflammatory responses of the host.