Evidence map›Paper›PMID 42213280›Full record

ReviewMolecular biology reports2026

TLR ligands as immunomodulators: mechanistic insights and therapeutic potential in infectious and inflammatory diseases.

Divya Verma, Sarthak Dhar, Takhellambam Malemnganba, Sanyukta Sharma, Sramona Kar, Vijay Kumar Prajapati

Abstract readReview
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In one paragraph

Review in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Divya VermaDepartment of Biochemistry, University of Delhi South Campus, Dhaula Kuan, New Delhi, India.
Sarthak DharDepartment of Biochemistry, University of Delhi South Campus, Dhaula Kuan, New Delhi, India.
Takhellambam MalemnganbaDepartment of Biochemistry, University of Delhi South Campus, Dhaula Kuan, New Delhi, India.
Sanyukta SharmaDepartment of Biochemistry, University of Delhi South Campus, Dhaula Kuan, New Delhi, India.
Sramona KarDepartment of Biochemistry, University of Delhi South Campus, Dhaula Kuan, New Delhi, India.
Vijay Kumar PrajapatiDepartment of Biochemistry, University of Delhi South Campus, Dhaula Kuan, New Delhi, India. vkp@south.du.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are central sentinels of innate immunity that bridge early pathogen recognition to long-term adaptive responses. They act as receptors recognizing pathogen-associated molecular patterns (PAMPs-highly conserved molecular motifs) and damage-associated molecular patterns (DAMPs- allow the innate immune system to distinguish "non-self" from "self"), making them critical players in the context of protective host defence and autoimmune disorders, thus regulating inflammation. This review provides a comprehensive summary of TLR ligands as immunomodulators, with an emphasis on their mechanistic underpinnings and translational potential in infectious disease, vaccine design, and autoimmunity. The article begins with outlining the structural features and signalling pathways of TLRs, explaining both MyD88-dependent and TRIF-dependent cascades that culminate in cytokine, chemokine, and type I interferon production. These pathways orchestrate a wide range of effector responses, from macrophage activation to T and B cell differentiation, highlighting TLRs as master regulators of immune response. Importantly, the review underscores the dualistic nature of TLR signalling: while TLR agonists can serve as potent vaccine adjuvants, chronic or dysregulated TLR activation can drive autoimmune pathology. The article highlights preclinical and clinical evidence for TLR ligands as vaccine adjuvants or therapeutic agents for autoimmune conditions, aiming to suppress pathophysiology. Collectively, this review highlights TLR ligands as versatile immunomodulatory tools with diverse applications and immense clinical potential. The detailed mechanistic insights, along with critical shortcomings in light of safety guidelines, provide a balanced perspective on TLR-targeted therapies. This can serve as a roadmap for harnessing TLR pathways, enabling researchers and clinicians to design next-generation vaccines, manage infectious diseases, and develop autoimmune therapies.

Indexed as

Communicable DiseasesImmunologic FactorsImmunomodulating AgentsInflammationToll-Like ReceptorsAnimalsAutoimmune DiseasesAutoimmunityHumansImmunity, InnateInnate Immunity RecognitionLigandsSignal TransductionToll-Like Receptor AgonistsImmunologic FactorsImmunomodulating AgentsLigandsToll-Like Receptor AgonistsToll-Like ReceptorsAutoimmune diseasesImmunomodulationInfectious diseasesTLR signalling

Identifiers

What OpenQuestion holds

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Registered trials

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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.