Evidence map›Paper›PMID 41601146›Full record

ReviewAnnals of medicine2026

Neuroimmune circuits in respiratory pathophysiology: decoding molecular crosstalk for precision therapeutic targeting.

Qian Chen, Nan Jia, Junling Liu, Caiyou Xu, Zherui Shen, Shihua Shi, Fei Wang, Zhenxing Wang

Abstract readReview
In one paragraph

Review in Annals of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. The Role of the Nervous System in Lung Disease.Current neurology and neuroscience reports · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. 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

8 authors.

Qian ChenHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.ORCID 0009-0005-1528-1006
Nan JiaHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Junling LiuHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Caiyou XuFirst School of Clinical Medicine, Nanjing University of Traditional Chinese Medicine, Nanjing, China.
Zherui ShenHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Shihua ShiHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.ORCID 0000-0001-6475-2349
Fei WangHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Zhenxing WangHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.ORCID 0000-0001-6832-9652

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe lung is a uniquely innervated barrier organ with dynamic neuroimmune interactions that critically regulate respiratory homeostasis. Despite the well-characterized gut-brain axis, pulmonary neuroimmune crosstalk remains an underexplored frontier. Emerging evidence implicates dysregulated neuron-immune dialogues as key drivers of respiratory pathologies, yet systematic dissection of their bidirectional mechanisms - from neurogenic immunomodulation to immune-mediated neural plasticity - is lacking. MAIN BODY: This review establishes a hierarchical framework for pulmonary neuroimmune crosstalk. We first delineate the lung's specialized neuroimmune architecture, then synthesize cutting-edge evidence on neuron-immune dialogues across five major respiratory diseases: pulmonary infections, asthma, chronic obstructive pulmonary disease, pulmonary fibrosis and lung cancer. Notably, we identify feedback-regulated circuits encompassing intricate networks mediated by neurotransmitters (e.g. acetylcholine, norepinephrine), neuropeptides (e.g. substance P, CGRP), immune cells (e.g. ILC2s, macrophages, T cells), and cytokines (e.g. TNF-α, IL-1β).

conclusionsDecoding key molecular targets within the neuroimmune axis provides novel strategies for predicting disease biomarkers (e.g. CGRP in early allergic inflammation) and refining therapeutic interventions (e.g. purposing anti-NGF biologics for neuropathic airway inflammation). This review specifically identifies promising targets - such as CGRP signalling in asthma and infections, and cholinergic pathways in COPD and lung cancer - for next-generation biologics and neuromodulatory therapies. This synthesis bridges neuroimmunology and clinical pulmonology, positioning neuroimmune crosstalk as a promising frontier in precision respiratory medicine and paving the way for an innovative therapeutic paradigm.

Indexed as

LungNeuroimmunomodulationAnimalsAsthmaCytokinesHumansLung NeoplasmsNeurotransmitter AgentsPrecision MedicineCytokinesNeurotransmitter Agentsbidirectional crosstalkNeuroimmune axisprecision medicinerespiratory diseasestranslational therapeutics

Identifiers

PMID41601146
PMCPMC12854227

What Socratic 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 Socratic graph.