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Published on: October 22, 2013
Campylobacter jejuni O:19 serotype-associated Guillain-Barré syndrome in a child: the first case reported from Greece
S Chatzipanagiotou1, K Kilidireas, G Trimis
1Department of Clinical Microbiology, Aeginition Hospital, Medical School of Athens, Vass. Sophias av. 72-4, 115 28 Athens, Greece. chatlouk@hotmail.com
Insights
This study reports a child with Guillain-Barré syndrome (GBS) after Campylobacter jejuni infection. The findings link C. jejuni to GBS through specific antibodies and genetic markers.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Guillain-Barré syndrome (GBS) is an autoimmune disorder affecting the peripheral nervous system.
- Campylobacter jejuni infections are a known trigger for GBS, particularly in certain populations.
- Understanding the specific serotypes and genetic predispositions is crucial for GBS research.
Observation:
- A pediatric case of GBS following infection with Campylobacter jejuni HS serotype O:19 is presented.
- The patient exhibited positive antibodies against C. jejuni and autoantibodies targeting peripheral nerve ganglioside GM1.
- The patient was positive for HLA-B35 and HLA-DR8 antigens, genetic markers associated with C. jejuni-triggered GBS.
Findings:
- The presence of anti-C. jejuni and anti-GM1 antibodies strongly correlates with the diagnosis of GBS.
- The identified HLA antigens (HLA-B35, HLA-DR8) in the patient align with previously observed genetic associations in C. jejuni-related GBS.
- This case represents the first documented instance of C. jejuni-associated GBS in Greece.
Implications:
- This case highlights the importance of recognizing C. jejuni as a potential cause of GBS in pediatric patients.
- Further epidemiological and clinical studies are needed to confirm the association and prevalence of C. jejuni-associated GBS in Greece.
- Identifying specific triggers and host factors can improve GBS diagnosis and potentially inform future treatment strategies.
Abstract:
We present a case of Guillain-Barré syndrome (GBS) following Campylobacter jejuni HS serotype O:19 infection in a child. Antibodies against C. jejuni and autoantibodies to the peripheral nerve gangliosides GM1 were positive, a pattern correlating well with the existence of an inflammatory neuropathy like GBS. The patient shared the HLA-B35 and HLA-DR8 antigens, which have been found to be increased in GBS patients with previous C. jejuni infection. As this is the first diagnosed C. jejuni-associated GBS case reported from Greece, further clinical and epidemiologic investigations are warranted.
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