decision-making with individual patients remains 
central to RSV vaccination decisions, particularly in 
the 60-to-74 age group where the risk-benefit calcula-
tion is less clear-cut.
The ACP guidance also stops short of addressing 
immunocompromised individuals, the group for whom 
the VA study found the most pronounced reduction 
in vaccine protection over time. This gap reflects the 
broader evidence gap that veteran-focused researchers 
are now working to fill.
Implementation Challenges and VA’s Role
Despite the availability of three approved vaccines 
and clear guidance for the oldest adults, RSV vacci-
nation rates among eligible adults remain disappoint-
ingly low. By the end of the 2024–2025 respiratory 
illness season, only 48% of U.S. adults 75 and older 
and 38% of adults 60 to 74 with a high-risk condition 
reported receiving an RSV vaccine, according to the 
JAMA Internal Medicine study authors.
VA’s integrated healthcare system offers advantages 
in reaching this population with electronic health 
record prompts, centralized pharmacy infrastructure, 
and the ability to link vaccine administration directly 
to clinical care. VAMCs serve as important venues 
for catching unvaccinated older veterans at routine 
appointments and for closing immunization gaps that 
primary care in the community often misses.
The Cureus comprehensive review underscored 
that healthcare providers play a crucial role in advo-
cating for RSV vaccination and that equitable access 
to preventive solutions requires active clinical engage-
ment. For VA clinicians, that advocacy takes on added 
weight: the veteran population’s age, sex, and chronic 
disease burden collectively create one of the highest-
risk RSV populations in the country.
Safety Monitoring and Ongoing Vigilance
RSV vaccines have been associated with rare but seri-
ous adverse events that continue to be monitored in 
post-market surveillance. Guillain-Barré syndrome 
emerged as a signal in regulatory review of several 
RSV vaccine candidates.
The Cureus review identified vaccine-associated 
enhanced respiratory disease (VAERD) as an addi-
tional safety concern, as was observed in early RSV 
vaccine candidates tested decades ago. Current vac-
cines were designed with this historical lesson in mind, 
and VAERD has not emerged as a clinical problem 
with the approved products. Nonetheless, the review 
authors emphasized that “comprehensive post-market 
surveillance and ongoing pharmacovigilance are vital 
to refining vaccine strategies, ensuring safety for high-
risk groups.”1
What Comes Next
The veteran study authors concluded that veter-
ans 60 and older who received a single RSVPreF3 or 
RSVpreF vaccine dose were better protected against 
RSV illness over two respiratory illness seasons than 
unvaccinated individuals, a finding that validates cur-
rent vaccination recommendations. But they were 
equally clear that protection declined over time and 
varied meaningfully by risk group.
“The potential benefits and risks of a second vac-
cine dose in certain groups should be examined,” the 
research team stated. For immunocompromised veter-
ans and those 80 and older, the current one-dose para-
digm may need reexamination.
The development of universal RSV vaccines has 
emerged as a research priority highlighted in the 
Cureus review. The mRNA platform with its rapid 
adaptability has been cited as one of the technologies 
best positioned to contribute to next-generation RSV 
vaccine development. Whether the mRNA architec-
ture confers any durability advantage over protein-
subunit competitors across multiple seasons remains 
an open question that the VA’s data infrastructure may 
help answer in the future.
In the meantime, VA clinicians face a practical 
imperative: vaccinate eligible veterans now, document 
outcomes carefully, and remain alert for updated guid-
ance on booster dosing as the evidence base matures. 
RSV is no longer a disease for which there is no 
defense. The question now is how to make the protec-
tion last. 
1Genis D, Riaz W, Hussain A, Oz T. Current and Emerging Strategies 
for the Prevention of Respiratory Syncytial Virus (RSV) Infections: 
A Comprehensive Review of Vaccines and Antibody Therapies. 
Cureus. 2026 Jan 12. PMID: 41685002. doi:10.7759/cureus.101340.
2Bajema KL, Bui DP, Yan L, et al. Durability of Respiratory Syncytial 
Virus Vaccine Effectiveness Among US Veterans. JAMA Intern Med. 
2026 Jan 1;186(1):78–88. doi:10.1001/jamainternmed.2025.6355.
3Qiu X, Xu S, Lu Y, Luo Z, Yan Y, Wang C, Ji J. Development of 
mRNA vaccines against respiratory syncytial virus (RSV). Cyto-
kine Growth Factor Rev. 2022 Dec;68:37-53. doi: 10.1016/j.cytog-
fr.2022.10.001. Epub 2022 Oct 13. PMID: 36280532.
4Qaseem A, Obley AJ, Harrod CS, Wilt TJ, Carroll K, Humphrey LL; 
Population Health and Medical Science Committee of the American 
College of Physicians. Respiratory Syncytial Virus Vaccines in Adults 
Who Are Not Pregnant or Immunocompromised: Rapid Practice 
Points From the American College of Physicians. Ann Intern Med. 
2026 Mar 3. doi:10.7326/ANNALS-25-05485.
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