Evidence map›Paper›PMID 34862075›Full record

ArticleVaccine2021

Tick immunity using mRNA, DNA and protein-based Salp14 delivery strategies.

Jaqueline Matias, Cheyne Kurokawa, Andaleeb Sajid, Sukanya Narasimhan, Gunjan Arora, Husrev Diktas, Geoffrey E Lynn, Kathleen DePonte, Norbert Pardi, Jesus G Valenzuela and 2 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.1field-weighted citation impact, top 3% of its field
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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Immunization with mRNA-LNPs EncodingPathogens (Basel, Switzerland) · 2025
    Article
  3. Borrelia surface proteins: new horizons in Lyme disease diagnosis.Applied microbiology and biotechnology · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
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  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Development of an mRNA-lipid nanoparticle vaccine against Lyme disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  20. Article
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

12 authors at 3 institutions in 1 country.

Jaqueline MatiasSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Cheyne KurokawaSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Andaleeb SajidSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Sukanya NarasimhanSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Gunjan AroraSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Husrev DiktasSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Geoffrey E LynnSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Kathleen DePonteSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Norbert PardiDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Jesus G ValenzuelaVector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Disease, National Institutes of Health, 12735 Twinbrook Parkway, Rockville, MD 20852, USA.
Drew WeissmanDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Erol FikrigSection of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA. Electronic address: erol.fikrig@yale.edu.
Yale University · USUniversity of Pennsylvania · USNational Institutes of Health · US

Funding

Tick Resources CoreP01AI138949 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI Erol Fikrig · 2018 to 2026
$13.5M
IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
Investigations of Lyme spirochete transmission as a complex network of microbial and ecological interactionsR01GM148992 · NIGMS · UNIVERSITY OF RHODE ISLAND · PI COURET, JANNELLE, LORD, CYNTHIA C · 2022 to 2025
$2.3M
The role of tick gut microbiota in Borrelia burgdorferi transmission to miceR01AI126033 · NIAID · YALE UNIVERSITY · PI FIKRIG, EROL, NARASIMHAN, SUKANYA · 2017 to 2020
$1.7M
Targets of Acquired Tick-Resistance As Anti-Tick VaccinesR41AI145778 · NIAID · L2 DIAGNOSTICS, LLC · PI NARASIMHAN, SUKANYA · 2019 to 2020
$597k
NHLBI NIH HHS T32 HL007974NIAID NIH HHS P01 AI138949NIAID NIH HHS R01 AI126033NIAID NIH HHS R41 AI145778NIGMS NIH HHS R01 GM148992
6 · The paper itself

Abstract

Guinea pigs exposed to multiple infestations with Ixodes scapularis ticks develop acquired resistance to ticks, which is also known as tick immunity. The I. scapularis salivary components that contribute to tick immunity are likely multifactorial. An anticoagulant that inhibits factor Xa, named Salp14, is present in tick saliva and is associated with partial tick immunity. A tick bite naturally releases tick saliva proteins into the vertebrate host for several days, which suggests that the mode of antigen delivery may influence the genesis of tick immunity. We therefore utilized Salp14 as a model antigen to examine tick immunity using mRNA lipid nanoparticles (LNPs), plasmid DNA, or recombinant protein platforms. salp14 containing mRNA-LNPs vaccination elicited erythema at the tick bite site after tick challenge that occurred earlier, and that was more pronounced, compared with DNA or protein immunizations. Humoral and cellular responses associated with tick immunity were directed towards a 25 amino acid region of Salp14 at the carboxy terminus of the protein, as determined by antibody responses and skin-testing assays. This study demonstrates that the model of antigen delivery, also known as the vaccine platform, can influence the genesis of tick immunity in guinea pigs. mRNA-LNPs may be useful in helping to elicit erythema at the tick bite site, one of the most important early hallmarks of acquired tick resistance. mRNA-LNPs containing tick genes is a useful platform for the development of vaccines that can potentially prevent selected tick-borne diseases.

Indexed as

IxodesAnimalsDNAGuinea PigsLiposomesNanoparticlesRNA, MessengerSalivary Proteins and PeptidesVaccinesDNALipid NanoparticlesLiposomesRNA, Messengersalivary protein 14, Ixodes scapularisSalivary Proteins and PeptidesVaccinesAcquired tick resistanceIxodes scapularisNucleic acid vaccineTick saliva proteinsVaccine

Identifiers

PMID34862075
PMCPMC8671329
OpenAlexW3216062253

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.