Analysis of mucosal immune dysregulation and safety and tolerability of endoscopic topical steroid therapy for long-COVID hyposmia: randomized, double-blinded pilot study
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Background
Millions of people exhibit olfactory dysfunction years after acute SARS-CoV-2 infection. Evidence suggests unresolved olfactory epithelial inflammation may perturb function.
Here, we report (1) data from human olfactory biopsies processed for T cell studies, and (2) outcomes from a pilot clinical trial evaluating endoscopic delivery of beclomethasone to the olfactory cleft for improving olfaction in long-COVID hyposmia.
Methods
Biopsies from long-COVID hyposmia and control subjects underwent single-cell T-cell receptor (TCR) sequencing.
In a separate outpatient cohort (Duke Rhinology Clinics), we conducted a randomized, double-blind, placebo-controlled pilot trial. Eligible adults (≥18 y) had ≥3 months long-COVID smell loss confirmed by Smell Identification Test (SIT). Participants were randomized 1:1 to endoscopic delivery of saline or beclomethasone via dissolvable sponge; repeated at 2 weeks.
The primary outcome was SIT improvement ≥4 points at 1 month; secondary at 3 months. Study recruitment ran Sept 15, 2023–June 18, 2024.
Results
Biopsies show no evidence of SARS-CoV-2 or EBV/HHV-6 reactivation and demonstrate clonally expanded, pro-inflammatory T-cell subsets.
Fifteen subjects are randomized (beclomethasone n = 7, saline n = 8); 13 are analyzed (6 and 7). At 1 month, SIT improvement occurs in 66.7% (4/6) vs 28.6% (2/7) (risk difference 38.1%, 95% CI 2–97%; risk ratio 2.14, 95% CI 0.73–7.79; p = 0.28). At 3 months, rates are 66.7% vs 42.9% (RD 23.8%, 95% CI 17–80%; RR 1.74, 95% CI 0.52–6.5; p = 0.50). No adverse events are reported.
Conclusions
Human olfactory TCR-seq implicates local T-cell inflammation without local viral reservoirs. Directed, endoscopic topical steroid therapy is feasible and safe, with a non-significant trend toward improved olfaction, supporting larger trials.
Funding: NIH DC020172, American Academy of Otolaryngology–Head and Neck Surgery.
Web | DOI | PDF | Communications Medicine | Open Access
Kim, Sarah; D’Anniballe, Vincent M.; Finlay, John B.; Ko, Tiffany; Wang, Michael; Jang, David W.; Abi-Hachem, Ralph; Goldstein, Bradley J.
[Line breaks added]
Background
Millions of people exhibit olfactory dysfunction years after acute SARS-CoV-2 infection. Evidence suggests unresolved olfactory epithelial inflammation may perturb function.
Here, we report (1) data from human olfactory biopsies processed for T cell studies, and (2) outcomes from a pilot clinical trial evaluating endoscopic delivery of beclomethasone to the olfactory cleft for improving olfaction in long-COVID hyposmia.
Methods
Biopsies from long-COVID hyposmia and control subjects underwent single-cell T-cell receptor (TCR) sequencing.
In a separate outpatient cohort (Duke Rhinology Clinics), we conducted a randomized, double-blind, placebo-controlled pilot trial. Eligible adults (≥18 y) had ≥3 months long-COVID smell loss confirmed by Smell Identification Test (SIT). Participants were randomized 1:1 to endoscopic delivery of saline or beclomethasone via dissolvable sponge; repeated at 2 weeks.
The primary outcome was SIT improvement ≥4 points at 1 month; secondary at 3 months. Study recruitment ran Sept 15, 2023–June 18, 2024.
Results
Biopsies show no evidence of SARS-CoV-2 or EBV/HHV-6 reactivation and demonstrate clonally expanded, pro-inflammatory T-cell subsets.
Fifteen subjects are randomized (beclomethasone n = 7, saline n = 8); 13 are analyzed (6 and 7). At 1 month, SIT improvement occurs in 66.7% (4/6) vs 28.6% (2/7) (risk difference 38.1%, 95% CI 2–97%; risk ratio 2.14, 95% CI 0.73–7.79; p = 0.28). At 3 months, rates are 66.7% vs 42.9% (RD 23.8%, 95% CI 17–80%; RR 1.74, 95% CI 0.52–6.5; p = 0.50). No adverse events are reported.
Conclusions
Human olfactory TCR-seq implicates local T-cell inflammation without local viral reservoirs. Directed, endoscopic topical steroid therapy is feasible and safe, with a non-significant trend toward improved olfaction, supporting larger trials.
Funding: NIH DC020172, American Academy of Otolaryngology–Head and Neck Surgery.
Web | DOI | PDF | Communications Medicine | Open Access