Evidence map›Paper›PMID 40279312›Full record

ReviewAnnual review of immunology2025

Bidirectional Communication Between the Innate and Adaptive Immune Systems.

Kathrynne A Warrick, Charles N Vallez, Hannah E Meibers, Chandrashekhar Pasare

Abstract readReview
In one paragraph

Review in Annual review of immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Review
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  6. Immunometabolic Remodeling in Ischemic and Non-Ischemic Heart Failure.Journal of cardiovascular translational research · 2026
    Review
  7. Review
  8. Review
  9. Article
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  12. Article
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  17. Review
  18. The spleen-brain axis in Alzheimer's disease and related dementias: Integrating immune and metabolic regulation.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  19. Review
  20. Review
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.

Kathrynne A WarrickDivision of Immunobiology and Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA ; email: chandrashekhar.pasare@cchmc.org.
Charles N VallezDivision of Immunobiology and Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA ; email: chandrashekhar.pasare@cchmc.org.
Hannah E MeibersDivision of Immunobiology and Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA ; email: chandrashekhar.pasare@cchmc.org.
Chandrashekhar PasareDivision of Immunobiology and Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA ; email: chandrashekhar.pasare@cchmc.org.

Funding

Innate mechanisms of regulation of Th17 responsesR01AI123176 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Chandrashekhar Pasare · 2017 to 2026
$4.4M
Regulation of TLR signaling, Inflammation and Antigen Presentation by VPS33BR01AI155426 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI KRAMER, HELMUT J, PASARE, CHANDRASHEKHAR · 2021 to 2025
$3.4M
Mechanisms of CD8+ T cell-induced Innate Immune ActivationF30AI188599 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI Charles Vallez · 2025 to 2026
$86k
NIAID NIH HHS F30 AI188599NIAID NIH HHS R01 AI123176NIAID NIH HHS R01 AI155426
6 · The paper itself

Abstract

Effective bidirectional communication between the innate and adaptive immune systems is crucial for tissue homeostasis and protective immunity against infections. The innate immune system is responsible for the early sensing of and initial response to threats, including microbial ligands, toxins, and tissue damage. Pathogen-related information, detected primarily by the innate immune system via dendritic cells, is relayed to adaptive immune cells, leading to the priming and differentiation of naive T cells into effector and memory lineages. Memory T cells that persist long after pathogen clearance are integral for durable protective immunity. In addition to rapidly responding to reinfections, memory T cells also directly instruct the interacting myeloid cells to induce innate inflammation, which resembles microbial inflammation. As such, memory T cells act as newly emerging activators of the innate immune system and function independently of direct microbial recognition. While T cell-mediated activation of the innate immune system likely evolved as a protective mechanism to combat reinfections by virulent pathogens, the detrimental outcomes of this mechanism manifest in the forms of autoimmunity and other T cell-driven pathologies. Here, we review the complexities and layers of regulation at the interface between the innate and adaptive immune systems to highlight the implications of adaptive instruction of innate immunity in health and disease.

Indexed as

Adaptive ImmunityCell CommunicationImmunity, InnateAnimalsDendritic CellsHumansImmunologic MemoryMemory T CellsT-LymphocytesautoimmunityCAR-T cellscytokine stormsmicrobial defensesterile inflammationT cell memoryTNF superfamily

Identifiers

PMID40279312
PMCPMC12120936

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.