Autoimmune encephalitis with negative anti-neuronal antibodies – clinical characteristics and available methods of antibody detection
Authors:
H. Mojžíšová 1; M. Elišák 1; ; J. Hanzalová 1,2; M. Petržalka 1; P. Marusič 1
Authors place of work:
Neurologická klinika, 2. LF UK a FN Motol, Praha
1; Ústav imunologie, 2. LF UK a FN Motol, Praha
2
Published in the journal:
Cesk Slov Neurol N 2020; 83/116(3): 251-256
Category:
Review Article
doi:
https://doi.org/10.14735/amcsnn2020251
Summary
Autoimmune encephalitis is a relatively recently recognized clinical unit. Diagnosis is based on clinical manifestations of the disease, and can be further confirmed by positivity of specific anti-neuronal antibodies. In spite of the fact that there are new types of antibodies discovered almost every year, there are still patients who manifest with clinical signs of autoimmune encephalitis, and yet do not test positive on anti-neuronal antibody assay testing. The reasons for this can be as follows: 1) specific antibodies for these cases might not have been discovered yet; 2) methods used for their detection are not sensitive enough; or 3) humoral immunity does not play a major role in the autoimmune response in a particular case. The absence of anti-neuronal antibodies to confirm the diagnosis of autoimmune encephalitis complicates clinical diagnosis. Recognition and early identification of the group of patients with negativity of anti-neuronal antibodies is crucial, because prompt initiation of immunotherapy is associated with a better outcome.
Keywords:
autoimmune encephalitis – anti-neuronal antibodies – limbic encephalitis
Zdroje
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Štítky
Paediatric neurology Neurosurgery NeurologyČlánok vyšiel v časopise
Czech and Slovak Neurology and Neurosurgery
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