Immune correlates underlying small fiber neuropathy presenting as vaccine-associated post-acute SARS- coronavirus syndrome

TL;DR

Some people develop small fiber neuropathy after SARS-CoV-2 vaccination, showing immune imbalances similar to post-acute SARS-CoV-2 syndrome.

Contribution

Identifies immune correlates in vaccine-associated post-acute SARS-CoV-2 syndrome with small fiber neuropathy.

Findings

Patients showed increased NKG2D+CD8+ and NKG2D+DNAM-1+CD4+ T-cells.

Reduced small fiber density was observed in most biopsies.

Anti-ACE-2 and NRP-1 antibodies were not significantly elevated in patients.

Abstract

A spectrum of adverse events overlapping with Post-acute Sequelae of SARS-CoV-2 infection (PASC) occurs in some patients following SARS-CoV-2 vaccination including small fiber neuropathy (SFN) and cognitive symptoms.

Accruing information regarding disease course and immune response imbalances in these patients.

We studied 71 previously healthy patients with neurological symptoms following SARS-CoV-vaccination. All had negative neurological workup for central/peripheral involvement (MR, EMG/EN). Cutaneous biopsy (21pts.) and peripheral blood sampling (20pts) were performed for anti-idiotype Ab analysis (ACE-2,NRP-1) (ELISA, IF) and for Flowcytometric analysis.

Paresthesia, cognitive impairment and autonomic symptoms agreed with SFN international definition. Comparative differences included abrupt onset, presence of simultaneous diverse paresthesia across multiple body regions frequently affecting the facial and cervical regions (44%) and the trunk (26%), associated to dysautonomia. Median time from vaccination to symptom manifestation was 3 days (mean ± SD: 8.76 ± 17.4 days). Symptom severity was still high (5.9 ± 1.9 mean+SD) at the time of evaluation and sampling, (382 ± 133 days from onset. Reduced small fiber density was observed in 19/21 biopsies. Anti-ACE-2 antibodies in 9/71pts. (12%) and 4/19 (21%) vaccinated HD sera and NRP-1 reactivity in 14/71 (20%) patient and 1/19 (5%) HD sera were not significantly increased. Peripheral NKG2D+CD8+ and NKG2D+DNAM-1+CD4+ T-cells were increased. Circulating inflammatory CD34+ cells were increased and generated in vitro a prevalence of NKG2D+DNAM-1+ T-cells.

PASC-vac SFN is associated with persistent immune imbalances common to other immune-mediated diseases. Additional effort to identify immune mechanisms unleashing PASC-vac SFN will contribute to modulate future early interventions for these patients and refine vaccine design.

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