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Abstract Details

Post-vaccine Myelitis: A Rare Event Often Overemphasized
Autoimmune Neurology
P3 - Poster Session 3 (5:00 PM-6:00 PM)
2-012
To describe clinical and imaging characteristics of myelitis associated with vaccination.
Vaccination has been perceived as a common cause of myelitis. Understanding the demographic, clinical, and paraclinical features of these cases may help avoid misdiagnosis.

We conducted a retrospective review of 1,448 patients evaluated at our Myelitis and Myelopathy Center (2003-2025). Patients were included if they developed myelitis within 2 months following vaccination and did not meet 2017 McDonald criteria for multiple sclerosis at first clinic visit. Demographic, clinical, and paraclinical data were obtained. 

Eleven patients were included (55% male, 64% white) with majority (64%) having subacute symptom onset. Vaccines included pneumococcal (n=1), influenza (n=2), yellow fever (n=2), and COVID-19 (n=6). The median time from vaccination to symptom onset was 14 days (IQR 12-21). At symptom nadir, median modified Rankin Scale was 4 (range 1–4): five (45%) were wheelchair-dependent. Bladder dysfunction occurred in eight (73%) and severe constipation in six (55%). The majority had cerebrospinal fluid (CSF) pleocytosis and elevated protein. Oligoclonal bands were absent in nine (82%), while one showed CSF-restricted and one mirror band(s). All infectious PCRs were negative. All patients were negative for AQP4 antibodies, and MOG antibodies were negative in all nine patients tested. On initial spinal cord MRI, eight patients (73%) had a monofocal longitudinally extensive lesion, with a median length of 5 vertebral segments (IQR 1-10). The central cord was most often affected (55%), and enhancement occurred in four patients (36%) with root enhancement in two (18%).  Over a median follow-up of 2.9 years (IQR 1.5–3.9), there were no changes in diagnosis.

Post-vaccination myelitis is rare and accounts for only a small proportion of all myelitis cases. Careful evaluation and longitudinal follow-up are essential to exclude other causes and unmasking of relapsing conditions.

Authors/Disclosures
Daniela Riveros Acosta, MD
PRESENTER
Dr. Riveros Acosta has nothing to disclose.
David Acero-Garces, MD Dr. Acero-Garces has nothing to disclose.
Asli Buyukkurt, MD Dr. Buyukkurt has nothing to disclose.
Clare M. Lambert, MD Dr. Lambert has nothing to disclose.
Scott D. Newsome, DO, FAAN (Johns Hopkins Hospital) Dr. Newsome has received personal compensation in the range of $10,000-$49,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Genentech. Dr. Newsome has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Newsome has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for TG Therapeutics. The institution of Dr. Newsome has received research support from Biogen. The institution of Dr. Newsome has received research support from Genentech/Roche. The institution of Dr. Newsome has received research support from Department of Defense. The institution of Dr. Newsome has received research support from Patient Centered Outcomes Research Institute. The institution of Dr. Newsome has received research support from National MS Society. The institution of Dr. Newsome has received research support from Lundbeck. The institution of Dr. Newsome has received research support from Sanofi. The institution of Dr. Newsome has received research support from Kyverna Therapeutics. Dr. Newsome has received personal compensation in the range of $10,000-$49,999 for serving as a Lead PI for Clinical Trial with Roche.
Carlos A. Pardo-Villamizar, MD (Johns Hopkins U, Med Dept of Neurology) The institution of Dr. Pardo-Villamizar has received research support from National Institutes of Health. The institution of Dr. Pardo-Villamizar has received research support from Bart McLean Fund for Neuroimmunology Research .