Evidence map›Paper›PMID 42482841›Full record

ArticleTransplantation direct2026

Reactogenicity and Immunogenicity of Adjuvanted and Nonadjuvanted RSV Vaccines in Solid Organ Transplant Recipients.

Alisse Hannaford, Elene Chamberlin, Zoe Swank, Simon D van Haren, Samual Han, Sanya Thomas, Kevin Ryff, Erin M Connolly, Ella N Woehl, David J Regan and 18 more

Abstract read
In one paragraph

Article in Transplantation direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Alisse HannafordDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.ORCID https://orcid.org/0000-0002-0276-9820
Elene ChamberlinDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Zoe SwankDepartment of Pathology, Brigham and Women's Hospital, Boston, MA.
Simon D van HarenPrecision Vaccines Program, Department of Pediatrics, Boston Children's Hospital, Boston, MA.
Samual HanDepartment of Pathology, Brigham and Women's Hospital, Boston, MA.
Sanya ThomasHarvard Medical School, Boston, MA.
Kevin RyffPrecision Vaccines Program, Department of Pediatrics, Boston Children's Hospital, Boston, MA.
Erin M ConnollyDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Ella N WoehlDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
David J ReganDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Grace C ValentineDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Nicholas MorrealeDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Xiaofang LiDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Aidan EustaceDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Alexandra TongDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Zhou LanDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
David R WaltHarvard Medical School, Boston, MA.
Ofer LevyHarvard Medical School, Boston, MA.
Nicolas C IssaDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Nirmal S SharmaHarvard Medical School, Boston, MA.
Mandeep R MehraHarvard Medical School, Boston, MA.
Michael M GivertzHarvard Medical School, Boston, MA.
Stefan G TulliusHarvard Medical School, Boston, MA.
Jamil R AzziHarvard Medical School, Boston, MA.
Antonio CoppolinoHarvard Medical School, Boston, MA.
Lindsey R BadenDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Amy C ShermanDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
Ann E WoolleyDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.ORCID https://orcid.org/0000-0002-2810-1618

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
VACCINES ADJUVANT DEVELOPMENT PROGRAM IN INFECTIOUS AND IMMUNE MEDIATED DISEASES75N93023C00040 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI DOWLING, DAVID JAMES · 2023 to 2025
$4.3M
Defining vaccine immunogenicity and adoptive transfer in hematopoietic stem cell transplant recipientsK23AI185318 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Amy Caryn Sherman · 2025 to 2026
$389k
NCATS NIH HHS UL1 TR002541NIAID NIH HHS K23 AI185318NIAID NIH HHS T32 AI007061NIH HHS 75N93023C00040Wellcome Trust
6 · The paper itself

Abstract

Background: Solid organ transplant (SOT) recipients are at high risk for severe respiratory syncytial virus (RSV). While RSV vaccine immunogenicity data in transplant populations are emerging, questions remain regarding the magnitude and durability of responses, cellular immunity, and determinants of decreased response. Methods: We conducted a prospective, single-center cohort study evaluating RSV vaccine reactogenicity and immunogenicity in SOT recipients compared with healthy controls. Serum was collected pre-vaccination and at 1, 3, and 6 mo post-vaccine to measure anti-fusion glycoprotein antibodies to RSV A and B and anti-nucleocapsid antibodies as a marker of natural infection. Peripheral blood mononuclear cells were collected from a subset for RSV-fusion (F)-specific cellular analyses. Results: Forty-three SOT recipients (median age, 65) and 16 controls were enrolled (from October 2023 to January 2024). Mild reactogenicity occurred in ~25% of participants, with no severe events. In SOT recipients, anti-fusion glycoprotein IgG, RSV-F-specific CD4 Conclusions: RSV vaccination was well tolerated and immunogenic in SOT recipients. Further research should optimize vaccination strategies and ideal timing for booster doses.

Identifiers

PMID42482841
PMCPMC13387763

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.