​Another outstanding educational event brought to you by the ITAE Group.  

Copyright 2020.

We are GDPR compliant, to view our privacy policy and how we handle your data please click here.


How long does the VIVIT dissection last?

The post mortem experience is 5 hours long, split into 2 parts.

How many people can participate in one VIVIT dissection?

There is 150 tickets available for each session. This is a comfortable number that can engage with the experience given the AV equipment installed.

Is the anatomy human?

No. The anatomy is of swine origin. Identical in size and structure -once harvested the samples are moved into VIVIT. VIVIT is a life size synthetic cadaver which is dissected for the audience to teach the structure and function of the human body.


Anatomy Lab.png

Tickets purchased directly from us are sold subject to our terms and conditions. All tickets purchased are non-refundable and non-transferable. Download terms and conditions here.

Some event content may vary from the guideline programmes and content descriptions are for guideline purposes only. Right to amend or change content before/during the experience reserved.

In the news this week … CJD

In the news this week, doctors have been given permission to give a British man with CJD a pioneering treatment. There is currently no treatment for this fatal condition. The treatment being offered to this patient is known as PRN100.

Creutzfeldt-Jakob disease (CJD) is a disorder that affects the brain and is fatal. It is caused by a protein, called a prion. These are misfolded proteins that are infectious, and they cause the misfolding of other proteins leading to their dysfunction. The majority of cases are spontaneous, whereas there are a few cases that have been inherited in an autosomal dominant fashion. Infection can occur through exposure to infected brain or spinal tissue as these proteins reside in the CNS. CJD has much greater occurrences in populations that practice cannibalism, this is known as kuru disease, found primarily amongst the Fore people in Papua New Guinea.

Accumulation of these misfolded proteins within the neural tissue eventually leads to neuronal degeneration and therefore the clinical onset of the disease. The classic symptoms of CJD are rapidly progressing dementia and myoclonus (spasmodic jerky contractions of muscles). Conformational change of proteins occurs which leads condensation centres of protein accumulation, plaque formation occurs which results in neuronal cell death progressing to spongiform encephalopathy. Initially there us a latency period which varies greatly but is on average about 10 years, but can be greater than 30years.

The PRN100 treatment that a patient in London is receiving is a manmade antibody therapy. Due to the nature of the disease causing misfolding of the body’s own proteins, the immune system doesn’t recognise these as foreign and therefore doesn’t produce antibodies to them in order to attack them. PRN100 is an antibody designed to attach tightly to normal proteins in order to prevent them from combining with the prions which would try and misfold the protein. Therefore, this antibody would stop the chain reaction of more proteins becoming misfolded however would not regress the disease. Despite the lack of knowledge about this treatment and the potential challenges it may face, researchers, patients and relatives are keen to start delivering this therapy to rapidly progressing cases due to the lack of alternative treatment available.