Mora, of Chicago Allergy Center, and a medical expert spokesperson for the American Lung Association, spoke with HCPLive about the campaign and what specialist clinicians can do to close those gaps in their own practices.
Key Points
- COVID-19 antiviral use remains under 15%, and adult vaccination rates were only ~18% this past season
- High-risk groups (age 65+, chronic lung/heart/kidney disease, diabetes, immunocompromised) should consider a summer booster, since antibody protection lasts about 6 months
- Antiviral prophylactic treatment is available for high-risk adults and immunocompromised children 12 and older
- Specialists can help close vaccination gaps by reviewing COVID-19, flu, and RSV status at every visit
- Patients can check eligibility for the updated COVID-19 vaccine at lung.org
COVID-19 has evolved from a pandemic threat into a predictable endemic respiratory virus — one that now circulates in 2 distinct seasonal waves per year, much like influenza and RSV. That shift has direct implications for how clinicians should counsel patients about booster timing. Vaccine-induced antibody protection against severe disease typically wanes over approximately 6 months, meaning the twice-yearly pattern of circulation aligns closely with the protection window from a single vaccine dose. For high-risk patients — those aged 65 and older, and those with chronic lung disease (including asthma, COPD, interstitial lung disease, cystic fibrosis, and pulmonary hypertension), heart disease, diabetes, chronic kidney disease, or immunocompromising conditions — a summer booster is a clinically reasonable consideration even if they received the fall/winter vaccine. Adults 65 and older are now formally recommended to receive 2 doses of the 2025–26 COVID-19 vaccine at least 6 months apart.1
Beyond vaccination, the ALA campaign highlights 2 prophylactic options that remain largely unknown to patients and underutilized even among clinicians. Ensitrelvir is an oral antiviral approved for post-exposure prophylaxis in individuals aged 12 and older who have had close contact with a COVID-19-positive person. It is taken over 5 days, with 3 tablets on day 1 and 1 tablet on days 2 through 5. Pemivibart is an intravenous monoclonal antibody approved for pre-exposure prophylaxis in moderately or severely immunocompromised patients for whom vaccination is likely to be insufficient. Both options represent an underappreciated layer of protection for high-risk populations who may not mount adequate vaccine responses or who face particularly high consequences from breakthrough infection.1
For specialists — pulmonologists, allergists, rheumatologists, cardiologists, and others managing patients with the chronic conditions that confer high COVID-19 risk — Mora emphasized that every clinical encounter represents an opportunity to address vaccination status comprehensively. Reviewing COVID-19, flu, and RSV vaccination status at each visit, correcting misconceptions about whether COVID-19 vaccines are still needed, and directing patients to the ALA's eligibility checker at lung.org are all actionable steps that do not require adding time to an already compressed appointment.
Editor’s note: Mora has no relevant disclosures to report.
References
- American Lung Association. American Lung Association highlights therapeutic options available to prevent and treat COVID-19 [press release]. July 30, 2026. https://www.prnewswire.com/news-releases/american-lung-association-highlights-therapeutic-options-available-to-prevent-and-treat-covid-19-302835975.html
- American Lung Association. Prevent COVID-19. https://www.lung.org/lung-health-diseases/lung-disease-lookup/covid-19/prevention. Accessed August 6, 2026.