Evidence map›Paper›PMID 33499143›Full record

ReviewPharmaceutics2021

TLR Agonists as Vaccine Adjuvants Targeting Cancer and Infectious Diseases.

Marina Luchner, Sören Reinke, Anita Milicic

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 159 papers.

0numbers the graph read from it
0cells of the map it votes in
159citing papers in PubMed
15.7field-weighted citation impact, top 1% 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

159 citing papers in PubMed, 274 citations in OpenAlex.

  1. Review
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  5. In Vitro and Embryonic Evaluation of RecombinantPathogens (Basel, Switzerland) · 2026
    Article
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99 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Marina LuchnerDepartment of Biochemistry, Magdalen College Oxford, University of Oxford, Oxford OX1 4AU, UK.ORCID 0000-0003-2461-3541
Sören ReinkeThe Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7DQ, UK.ORCID 0000-0003-2412-385X
Anita MilicicThe Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7DQ, UK.ORCID 0000-0002-7984-1317
University of Oxford · GB

Funding

Medical Research Council MC_PC_13069Medical Research Council MC_PC_15029Medical Research Council MC_PC_16056Medical Research Council MC_PC_17167
6 · The paper itself

Abstract

Modern vaccines have largely shifted from using whole, killed or attenuated pathogens to being based on subunit components. Since this diminishes immunogenicity, vaccine adjuvants that enhance the immune response to purified antigens are critically needed. Further advantages of adjuvants include dose sparing, increased vaccine efficacy in immunocompromised individuals and the potential to protect against highly variable pathogens by broadening the immune response. Due to their ability to link the innate with the adaptive immune response, Toll-like receptor (TLR) agonists are highly promising as adjuvants in vaccines against life-threatening and complex diseases such as cancer, AIDS and malaria. TLRs are transmembrane receptors, which are predominantly expressed by innate immune cells. They can be classified into cell surface (TLR1, TLR2, TLR4, TLR5, TLR6) and intracellular TLRs (TLR3, TLR7, TLR8, TLR9), expressed on endosomal membranes. Besides a transmembrane domain, each TLR possesses a leucine-rich repeat (LRR) segment that mediates PAMP/DAMP recognition and a TIR domain that delivers the downstream signal transduction and initiates an inflammatory response. Thus, TLRs are excellent targets for adjuvants to provide a "danger" signal to induce an effective immune response that leads to long-lasting protection. The present review will elaborate on applications of TLR ligands as vaccine adjuvants and immunotherapeutic agents, with a focus on clinically relevant adjuvants.

Indexed as

adjuvantcancerimmunogenicityimmunotherapyMyD88NF-κBToll-like receptorstype I interferonvaccine

Identifiers

PMID33499143
PMCPMC7911620
OpenAlexW3122174179

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.