Evidence map›Paper›PMID 25156362›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Characterization of cross-protection by genetically modified live-attenuated Leishmania donovani parasites against Leishmania mexicana.

Ranadhir Dey, Gayathri Natarajan, Parna Bhattacharya, Hannah Cummings, Pradeep K Dagur, César Terrazas, Angamuthu Selvapandiyan, John P McCoy, Robert Duncan, Abhay R Satoskar and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 57 citations in OpenAlex.

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  9. Anti-Tumor Effect of Parasitic Protozoans.Bioengineering (Basel, Switzerland) · 2022
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  10. The History of Live AttenuatedPathogens (Basel, Switzerland) · 2022
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  14. Inoculation of theMicroorganisms · 2021
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  15. Review
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  19. Nanoparticulate drug delivery systems for the treatment of neglected tropical protozoan diseases.The journal of venomous animals and toxins including tropical diseases · 2019
    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

11 authors at 6 institutions in 2 countries.

Ranadhir DeyDivision of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD 20993;
Gayathri NatarajanDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 42310;
Parna BhattacharyaDivision of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD 20993;
Hannah CummingsDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 42310;
Pradeep K DagurNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892; and.
César TerrazasDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 42310;
Angamuthu SelvapandiyanInstitute of Molecular Medicine, New Delhi 110020, India.
John P McCoyNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892; and.
Robert DuncanDivision of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD 20993;
Abhay R SatoskarDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 42310; Hira.Nakhasi@fda.hhs.gov Abhay.Satoskar@osumc.edu.
Hira L NakhasiDivision of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD 20993; Hira.Nakhasi@fda.hhs.gov Abhay.Satoskar@osumc.edu.
The Ohio State University Wexner Medical Center · USCenter for Biologics Evaluation and Research · USInstitute of Molecular Medicine · INNational Heart Lung and Blood Institute · USNational Institutes of Health · USUnited States Food and Drug Administration · US

Funding

Flow Cytometry Core FacilityZICHL005905 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DAGUR, PRADEEP · 2009 to 2025
$32.3M
Intramural NIH HHS ZIC HL005905
6 · The paper itself

Abstract

Previously, we showed that genetically modified live-attenuated Leishmania donovani parasite cell lines (LdCen(-/-) and Ldp27(-/-)) induce a strong cellular immunity and provide protection against visceral leishmaniasis in mice. In this study, we explored the mechanism of cross-protection against cutaneous lesion-causing Leishmania mexicana. Upon challenge with wild-type L. mexicana, mice immunized either for short or long periods showed significant protection. Immunohistochemical analysis of ears from immunized/challenged mice exhibited significant influx of macrophages, as well as cells expressing MHC class II and inducible NO synthase, suggesting an induction of potent host-protective proinflammatory responses. In contrast, substantial inhibition of IL-10, IL-4, and IL-13 expression and the absence of degranulated mast cells and less influx of eosinophils within the ears of immunized/challenged mice suggested a controlled anti-inflammatory response. L. mexicana Ag-stimulated lymph node cell culture from the immunized/challenged mice revealed induction of IFN-γ secretion by the CD4 and CD8 T cells compared with non-immunized/challenged mice. We also observed suppression of Th2 cytokines in the culture supernatants of immunized/challenged lymph nodes compared with non-immunized/challenged mice. Adoptively transferred total T cells from immunized mice conferred strong protection in recipient mice against L. mexicana infection, suggesting that attenuated L. donovani can provide protection against heterologous L. mexicana parasites by induction of a strong T cell response. Furthermore, bone marrow-derived dendritic cells infected with LdCen(-/-) and Ldp27(-/-) parasites were capable of inducing a strong proinflammatory response leading to the proliferation of Th1 cells. These studies demonstrate the potential of live-attenuated L. donovani parasites as pan-Leishmania species vaccines.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCross ReactionsCytokinesHistocompatibility Antigens Class IIImmunity, CellularLeishmania donovaniLeishmania mexicanaLeishmaniasis, CutaneousLeishmaniasis VaccinesMacrophagesMiceMice, Inbred BALB CVaccines, AttenuatedCytokinesHistocompatibility Antigens Class IILeishmaniasis VaccinesVaccines, Attenuated

Identifiers

PMID25156362
PMCPMC6480318
OpenAlexW2161130214

What OpenQuestion holds

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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.