Tuesday, 1 July 2014

EAE is not a useful model for demyelinating disease

Peter O. Behan PO & Chaudhuri A. EAE is not a useful model for demyelinating disease DOI: 10.1016/j.msard.2014.06.003

Experimental allergic encephalomyelitis (EAE) is the commonest, readily induced, organspecific, autoimmune disorder of laboratory animals of its kind. It is an artificial disorder brought about by the immunization of susceptible animals with brain antigens in complete Freund's adjuvant (CFA). Variations can be induced by altering the nature of the antigen and the conditions involving immunization. Whilst it is often described as a demyelinating disease, in strict terms it is not, since the primary pathologic process is not demyelination but rather an encephalomyelitis that is immunologically induced. Rather, the prototype demyelinating disease is multiple sclerosis and its variants. In this paper, the central question we ask is whether the data gleaned from the EAE model contributes to our understanding of the pathological events in MS. Towards answering this, we describe the historical development of EAE and its hyperacute form, and discuss the findings studied extensively in the non-human primate which show that ordinary EAE is an exact model for ADEM in the human, and that the hyperacute form of EAE is represented by AHLE in the human. Additionally, we shall comment on the latest research on new variants of EAE, and explain our opinion regarding the use of EAE models in research aiming to understand the pathogenesis of multiple sclerosis.
This is the counter story or in fact the driver to our paper


Experimental autoimmune encephalomyelitis is a good model of multiple sclerosis if used wisely

Rather than try and take this paper apart, EAEers need to read and embrace some of the comments as collectively EAEers need to up their game. 

They also need to find the realities verses the fiction of some EAE studies. This is a useful paper, if read wisely

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