Evidence map›Paper›PMID 26595093›Full record

ReviewExpert review of vaccines2016

Leishmania vaccine development: exploiting the host-vector-parasite interface.

S G Reed, R N Coler, D Mondal, S Kamhawi, J G Valenzuela

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of vaccines, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Interventions for American cutaneous and mucocutaneous leishmaniasis.The Cochrane database of systematic reviews · 2020
    Pooled it
  2. Safety and immunogenicity of ChAd63-KH vaccine in post-kala-azar dermal leishmaniasis patients in Sudan.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Trial
  3. Acquired tick resistance inInfection and immunity · 2025
    Article
  4. Review
  5. Tick saliva and its role in pathogen transmission.Wiener klinische Wochenschrift · 2023
    Article
  6. Review
  7. Healed Lesions of Human Cutaneous Leishmaniasis Caused ByFrontiers in cellular and infection microbiology · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Mosquito Saliva: The Hope for a Universal Arbovirus Vaccine?The Journal of infectious diseases · 2018
    Review
  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

5 authors at 4 institutions in 2 countries.

S G Reeda Infectious Disease Research Institute , Seattle WA , USA.
R N Colera Infectious Disease Research Institute , Seattle WA , USA.
D Mondalc International Center for Diarrhoeal Diseases Research, Centre for Nutrition and Food Security , Parasitology Laboratory , Dhaka , Bangladesh.
S Kamhawid Vector Molecular Biology Section, LMVR , National Institute of Allergy and Infectious Diseases, NIH , Rockville , MD , USA.
J G Valenzuelad Vector Molecular Biology Section, LMVR , National Institute of Allergy and Infectious Diseases, NIH , Rockville , MD , USA.
National Institute of Allergy and Infectious Diseases · USInfectious Disease Research Institute · USInternational Centre for Diarrhoeal Disease Research · BDUniversity of Washington · US

Funding

Molecular approaches to understand vector-host and vector-pathogen interactionsZIAAI000932 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI VALENZUELA, JESUS · 2009 to 2025
$23.1M
LEISHMANIA ANTIGENS DEFINES BY IMMUNE RESPONSESR01AI025038 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI REED, STEVEN GREGORY · 1987 to 2016
$5.6M
Intramural NIH HHS Z99 AI999999NIAID NIH HHS R01 AI025038NIAID NIH HHS R01AI025038
6 · The paper itself

Abstract

Visceral leishmaniasis (VL) is a disease transmitted by phlebotomine sand flies, fatal if untreated, and with no available human vaccine. In rodents, cellular immunity to Leishmania parasite proteins as well as salivary proteins of the sand fly is associated with protection, making them worthy targets for further exploration as vaccines. This review discusses the notion that a combination vaccine including Leishmania and vector salivary antigens may improve vaccine efficacy by targeting the parasite at its most vulnerable stage just after transmission. Furthermore, we put forward the notion that better modeling of natural transmission is needed to test efficacy of vaccines. For example, the fact that individuals living in endemic areas are exposed to sand fly bites and will mount an immune response to salivary proteins should be considered in pre-clinical and clinical evaluation of leishmaniasis vaccines. Nevertheless, despite remaining obstacles there is good reason to be optimistic that safe and effective vaccines against leishmaniasis can be developed.

Indexed as

AnimalsAntigens, ProtozoanDisease Models, AnimalDisease Transmission, InfectiousDrug DiscoveryHumansInsect ProteinsLeishmaniasis VaccinesLeishmaniasis, VisceralPsychodidaeRodentiaSalivary Proteins and PeptidesVaccines, CombinedAntigens, ProtozoanInsect ProteinsLeishmaniasis VaccinesSalivary Proteins and PeptidesVaccines, CombinedadjuvantLeishmaniasalivasand flyvaccine

Identifiers

PMID26595093
PMCPMC6019289
OpenAlexW2186899930

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.