Evidence map›Paper›PMID 32709117›Full record

ReviewMicroorganisms2020

Can We Harness Immune Responses to Improve Drug Treatment in Leishmaniasis?

Raphael Taiwo Aruleba, Katharine C Carter, Frank Brombacher, Ramona Hurdayal

Open access · goldAbstract readReview
In one paragraph

Review in Microorganisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

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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

4 authors at 3 institutions in 2 countries.

Raphael Taiwo ArulebaDepartment of Molecular and Cell Biology, University of Cape Town, Cape Town 7925, South Africa.ORCID 0000-0003-0879-344X
Katharine C CarterStrathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0NR, UK.ORCID 0000-0003-2507-1844
Frank BrombacherInternational Centre for Genetic Engineering and Biotechnology, Cape Town Component, Cape Town 7925, South Africa.ORCID 0000-0001-8881-6781
Ramona HurdayalDepartment of Molecular and Cell Biology, University of Cape Town, Cape Town 7925, South Africa.ORCID 0000-0001-7758-521X
South African Medical Research Council · ZAUniversity of Cape Town · ZAUniversity of Strathclyde · GB

Funding

Poliomyelitis Research Foundation grant numbers: 113446 and 120407Poliomyelitis Research Foundation and University of Cape Town Science Faculty PhD fellowship grant number: 19/70University of Cape Town 2019 Enabling Grant Seeker Excellence Award
6 · The paper itself

Abstract

Leishmaniasis is a vector-borne parasitic disease that has been neglected in priority for control and eradication of malaria, tuberculosis, and HIV/AIDS. Collectively, over one seventh of the world's population is at risk of being infected with 0.7-1.2 million new infections reported annually. Clinical manifestations range from self-healing cutaneous lesions to fatal visceral disease. The first anti-leishmanial drugs were introduced in the 1950's and, despite several shortcomings, remain the mainstay for treatment. Regardless of this and the steady increase in infections over the years, particularly among populations of low economic status, research on leishmaniasis remains under funded. This review looks at the drugs currently in clinical use and how they interact with the host immune response. Employing chemoimmunotherapeutic approaches may be one viable alternative to improve the efficacy of novel/existing drugs and extend their lifespan in clinical use.

Indexed as

chemotherapyhost directed therapyimmunityimmunochemotherapyleishmaniasis

Identifiers

PMID32709117
PMCPMC7409143
OpenAlexW3043412581

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.