Emerging infectious diseases, vaccines and Guillain–Barré syndrome
Corresponding Author
Haruki Koike
Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence
Haruki Koike, Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466-8550 Japan.
Email: [email protected]
Search for more papers by this authorMasahisa Katsuno
Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Search for more papers by this authorCorresponding Author
Haruki Koike
Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Correspondence
Haruki Koike, Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466-8550 Japan.
Email: [email protected]
Search for more papers by this authorMasahisa Katsuno
Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
Search for more papers by this author[Correction added on 19 July 2021, after first online publication: In Abstract, the word “COVID-19” has been inserted at the end of this sentence “…encoding the spike protein of SARS-CoV-2, against.” so it should read as “…encoding the spike protein of SARS-CoV-2, against COVID-19.”]
Abstract
The recent outbreak of Zika virus infection increased the incidence of Guillain–Barré syndrome (GBS). Following the first reported case of GBS after Zika virus infection in 2013, there has been a considerable increase in the incidence of GBS in endemic countries, such as French Polynesia and Latin American countries. The association between coronavirus disease 2019 (COVID-19), caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and GBS is another emerging research hotspot. Electrophysiological studies have suggested that GBS patients associated with Zika virus infection or COVID-19 tend to manifest acute inflammatory demyelinating polyneuropathy, rather than acute motor axonal neuropathy (AMAN). Causative autoantibodies, such as anti-ganglioside antibodies in AMAN associated with Campylobacter jejuni infection, have not been identified in GBS associated with these emerging infectious diseases. Nevertheless, recent studies suggested molecular mimicry between these viruses and human proteins related to GBS. Recent studies have shown the efficacy of new vaccines, containing artificial messenger RNA encoding the spike protein of SARS-CoV-2, against COVID-19. These vaccines are now available in many countries and massive vaccination campaigns are currently ongoing. Although there are long-standing concerns about the increased risk of GBS after inoculation of conventional vaccines, the risk of GBS is not considered a legitimate reason to limit administration of currently available vaccines, because the benefits outweigh the risks.
DISCLOSURE
Conflict of interest: The authors declare no conflict of interest.
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