Neuronal regulation of type 2 innate lymphoid cells via neuromedin U

limma powers differential expression analyses for RNA-sequencing and microarray studies

Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv007 · Cited by 40,458

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

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A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

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affy—analysis of Affymetrix GeneChip data at the probe level

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Orchestrating high-throughput genomic analysis with Bioconductor

Huber, W. K., Carey, V. J., Gentleman, R. C., Anders, S., Carlson, M. R. J., Carvalho, B. S., Bravo, H. C., Davis, S. R., Gatto, L., Girke, T., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3252 · Cited by 3,614

RAG-2-deficient mice lack mature lymphocytes owing to inability to initiate V(D)J rearrangement

Shinkai, Y. (1992) · Cell · doi:10.1016/0092-8674(92)90029-c · Cited by 2,651

Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function.

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Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity

Neill, D. R., Wong, S. H., Bellosi, A., Flynn, R. J., Daly, M. G., Langford, T. K. A., Bucks, C. M., Kane, C. M., Fallon, P. G., Pannell, R., et al. (2010) · Nature · doi:10.1038/nature08900 · Cited by 2,079

Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus

Monticelli, L. A., Sonnenberg, G. F., Abt, M. C., Alenghat, T., Ziegler, C. G. K., Doering, T. A., Angelosanto, J., Laidlaw, B. J., Yang, C. Y., Sathaliyawala, T., et al. (2011) · Nature Immunology · doi:10.1038/ni.2131 · Cited by 1,327

Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus

Monticelli (2011) · PubMed · doi:10.1031/ni.2131 · Cited by 1,286

Neuromedin U Signaling Map: Toward Neuropeptide Focused Therapeutic Targets in Cancer and Human Diseases

Dcunha, L., Edakkad, B., Fathima, I., Dagamajalu, S., Raju, R., Balaya, R. D. A., & Kanekar, S. (2026) · OMICS A Journal of Integrative Biology · doi:10.1177/15578100261422815 · Cited by 1

Genetic deletion of neuromedin U and neuromedin S confers transient reno-protection in adenine-induced chronic kidney disease

Yoshida, H., Teranishi, H., Shikano, K., Kato, H., Apolinario, M. E. C., Hanada, T., Hikida, T., & Hanada, R. (2026) · Peptides · doi:10.1016/j.peptides.2026.171474 · Cited by 1

Harnessing innate lymphoid cells (ILCs) for cancer immunotherapy: A new frontier in precision immuno-oncology

Ghezel, M. A., Aram, C., Alishvandi, A., Barancheshmeh, M., Firuzpour, F., Khodabandehloo, M. H., Mohammadian, S., Rahimi, M., & Keikha, M. (2026) · Translational research · doi:10.1016/j.trsl.2026.03.001 · Cited by 1

Single-cell analysis of recruited ILC2 cell fate during transition from circulation to establishment of tissue residency

Kashyap, A., Can, U. I., Miller, M. M., Farwell, B., Stenske, S. E., Verma, M., & Reinhardt, R. L. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkaf352 · Cited by 1

Overview of allergic disease: Pathogenesis of allergic inflammation – WAO White Book on Allergy 2026 – 2.1

Caraballo, L. R., & Llinás-Caballero, K. (2026) · World Allergy Organization Journal · doi:10.1016/j.waojou.2026.101384 · Cited by 1

The Neuroimmune Connectome: Understanding how the Peripheral Nervous System shapes Immunity

Tsuda, S., & Globig, A.-M. (2026) · ImmunoHorizons · doi:10.1093/immhor/vlaf080 · Cited by 1

Innate Lymphoid Cells in Tissue Homeostasis and Diseases

Zhan, Z., Sun, H., Li, C., Hong, Q., Zhu, S., Yu, Y., Zhang, H., & Guo, K. (2026) · MedComm · doi:10.1002/mco2.70743 · Cited by 1

Group 2 innate lymphoid cells: Where are we 15 years out?

Doherty, T. A. (2026) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2026.04.013 · Cited by 1

γδ T Cell-Mediated Neuroimmune Interactions in Skin Inflammation and Allergy

Peng, S., & Honda, T. (2026) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-026-09168-0 · Cited by 1

Molecular functions and applications of peptide agonists acting on mouse neuromedin U receptor 1

Takayama, K., Mori, K., Nomura, E., Hanano, M., Kuruma, M., Morito, K., Taguchi, A., Taniguchi, A., Miyazato, M., & Hayashi, Y. (2026) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2026.118702 · Cited by 1

Type 2 neuroimmune interaction-mediated functional homeostasis and tissue repair

Chang, X., Zhang, J., Li, J. N., Liu, L., & Wang, F. (2026) · Oral Science and Homeostatic Medicine · doi:10.26599/oshm.2026.9610057 · Cited by 1

Longitudinal profiling reveals immune dynamics and distinct plasma cell signatures during B-cell depletion in IgG4-related disease

Kim, H. J., Kim, M.-G., Kim, S., Kim, M. H., Kim, S. U., Kwon, H. S., Choi, S. Y., Kang, H. R., Heo, S. Y., Cho, S. I., et al. (2026) · Annals of the Rheumatic Diseases · doi:10.1016/j.ard.2026.05.024 · Cited by 1

The enteric nervous system: A neuroimmune conductor regulating intestinal homeostasis and inflammation

Wang, Y., & Xu, H. (2026) · Molecular Immunology · doi:10.1016/j.molimm.2026.07.004 · Cited by 1

Group 2 innate lymphoid cells activate myelin-reactive T cells to augment neuroinflammation

Huang, H., Liu, G., Han, Y., Miao, Y., Zhu, Z., Wang, Y., Wang, J., Shi, M., Li, J., Yang, H., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.07.011 · Cited by 1

Hypothesis of immune homeostasis regulator: The nervous system regulates glucose immunometabolism to control immunity

Luan, W., & Qi, F. (2022) · Medical Hypotheses · doi:10.1016/j.mehy.2022.110841 · Cited by 1

ILC2s touch a nerve

Bordon, Y. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.119 · Cited by 1

Group 2 ILC Functional Assays in Allergic Airway Inflammation

Entwistle, L. J., Puttur, F. K., Gregory, L. G., & Lloyd, C. M. (2020) · Methods in molecular biology · doi:10.1007/978-1-0716-0338-3_10 · Cited by 1

L’actualité scientifique de ce début 2018 vue par les étudiants de l’AMPS

Désveaux, I., Gaudet, C., Raulet, R., Scherlinger, M., Varennes, O., & Schaeverbeke, T. (2018) · médecine/sciences · doi:10.1051/medsci/20183401012 · Cited by 1

Guest editorial: Innate lymphocytes: Development, homeostasis, and disease

Sciumè, G. (2018) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2018.08.002 · Cited by 1

Lack of mucosal cholinergic innervation is associated with increased risk of enterocolitis in Hirschsprung’s diseasePreprint

Keck, S., Galati-Fournier, V., Kym, U., Moesch, M., Usemann, J., Subotic, U., Tharakan, S. J., Krebs, T. F., Stathopoulos, E., Schmittenbecher, P., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.15.151621 · Cited by 1

SAT0024 JAK-INHIBITION WITH BARICTINIB INHIBITS ACTIVATION OF NLRP1/CASPASE1/GDMSD PYROPTOSIS PATHWAY IN RHEUMATOID ARTHRITIS SYNOVIAL FIBROBLASTS

Xie, W., & Zhang, Z. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-eular.5062 · Cited by 1

Unveiling the Neuron-mediated Group 2 Innate Lymphoid Cell Activation in Human Asthma

Kabata, H., & Ueki, S. (2024) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202404-0844ed · Cited by 1

Nociceptor Neurons Control Pollution-Mediated Neutrophilic AsthmaPreprint

Wang, J.-C., Kulle, A., Crosson, T., Nikpoor, A. R., Gupta, S., Roger, A., Rafei, M., Thanabalasuriar, A., & Talbot, S. (2025) · eLife · doi:10.7554/elife.101988.2 · Cited by 1

Reprogramming the gut immune system: featured advances in intestinal immunity in 2025

Murakami, M., & Takeda, K. (2026) · Immunology and Cell Biology · doi:10.1111/imcb.70117 · Cited by 1

Can U Turn ILC2s Up?

Muller, P. A., & Mucida, D. (2017) · Cell · doi:10.1016/j.cell.2017.10.013

Papers of note in Nature 549 (7671)

VanHook, A. M. (2017) · Science Signaling · doi:10.1126/scisignal.aap9538

Wheeze No More: Growing Out of Your Dopaminergic Nerves

Barr, J., Su, Y., & Sun, X. (2019) · Immunity · doi:10.1016/j.immuni.2019.11.006

Microbiota–modulated enteric neuron translational profiling uncovers a CART+ glucoregulatory subsetPreprint

Muller, P. A., Schneeberger, M., Matheis, F., Kerner, Z. J., & Mucida, D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.09.983841

SAT0022 CXCL7 PROMOTES OSTEOCLASTOGENESIS IN RHEUMATOID ARTHRITIS

Wang, X., Sun, L., & Zhao, J. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-eular.1474

1) Gut Controls Brain

Nakazato, M. (2020) · Nihon Naika Gakkai Zasshi · doi:10.2169/naika.109.445

Neuronal GPCR regulates the specificity of innate immunity against pathogen infectionPreprint

Wibisono, P., Wibisono, S., Watteyne, J., Chen, C.-H., Sellegounder, D., Beets, I., Liu, Y., & Sun, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.06.442992

T Cells and Group 2 Innate Lymphoid Cells 2

Kato, A., & Schleimer, R. P. (2022) · Springer eBooks · doi:10.1007/978-981-16-0784-4_6

Innate Lymphoid Cells in Atopic Dermatitis and Psoriasis

Sugita, K. (2021) · The Nishinihon Journal of Dermatology · doi:10.2336/nishinihonhifu.83.503

Resident T cells orchestrate adipose tissue remodeling in a site peripheral to infectionPreprint

Kabat, A. M., Hackl, A., Sanin, D. E., Zeis, P., Grzes, K. M., Baixauli, F., Kyle, R. L., Caputa, G., Edwards-Hicks, J., Villa, M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.24.481701

Faculty Opinions recommendation of Neuropeptide CGRP Limits Group 2 Innate Lymphoid Cell Responses and Constrains Type 2 Inflammation.

Belz, G. T. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736283453.793567128

Faculty Opinions recommendation of Nociceptor sensory neurons suppress neutrophil and γδ T cell responses in bacterial lung infections and lethal pneumonia.

Mucida, D. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732801082.793545021

L’actualité scientifique de ce début 2018 vue par les étudiants de l’AMPS

Désveaux, I., Gaudet, C., Raulet, R., Scherlinger, M., Varennes, O., & Schaeverbeke, T. (2018) · médecine/sciences · doi:10.1051/medsci/20183401121

Faculty Opinions recommendation of LIGHT-HVEM Signaling in Innate Lymphoid Cell Subsets Protects Against Enteric Bacterial Infection.

Kolls, J. K., & Matsunaga, Y. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733793319.793549716

Peptide Tool-Driven Functional Elucidation of Biomolecules Related to Endocrine System and Metabolism

Takayama, K. (2022) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.c22-00048

Fabrication d’un épithélium bronchique innervé à partir d’une prise de sang

Foisset, F., Lehalle, C., Nasri, A., Bourdais, C., Morichon, L., Petit, A., Vachier, I., Assou, S., BOURDIN, A. A., Frossard, N., et al. (2023) · Revue des Maladies Respiratoires · doi:10.1016/j.rmr.2023.01.021

Sensory Systems in the Peripheral and Central Nervous Systems Shape Host Response During Infections

Wyart, C., Jim, K. K., & Prendergast, A. E. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.07.008 · Cited by 1

WITHDRAWN: Neuron-dependent tuft cell expansion initiates sinonasal allergic Type 2 inflammationPreprint

Ortiz-Carpena, J. F., Inclan-Rico, J. M., Pastore, C., Hung, L., Wilkerson, W. B., Weiner, M., Lin, C., Gentile, M. E., Cohen, N. A., Abdus-Saboor, I., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.04.547596

PARKİNSON HASTALIĞI İLE TIRAP GEN POLİMORFİZMİ ARASINDAKİ İLİŞKİNİN ARAŞTIRILMASI

KAYAN, M. K., & Calapoğlu, N. Ş. (2024) · SDÜ Tıp Fakültesi Dergisi · doi:10.17343/sdutfd.1360587

RAG suppresses group 2 innate lymphoid cellsPreprint

Heul, A. V., Mack, M. R., Zamidar, L., Tamari, M., Yang, T.-L., Trier, A. M., Kim, D.-H., Janzen-Meza, H., Dyken, S. J. V., Hsieh, C., et al. (2024) · eLife · doi:10.7554/elife.98287.1

Nociceptor Neurons Control Pollution-Mediated Neutrophilic AsthmaPreprint

Wang, J.-C., Crosson, T., Nikpoor, A. R., Gupta, S., Rafei, M., & Talbot, S. (2024) · eLife · doi:10.7554/elife.101988.1

Le neuropeptide VIP potentialise l’immunité de type 2 et de type 3 lors de la prise alimentaire

Pascal, M., Kazakov, A., Chevalier, G., Belkaid, Y., Lepousez, G., Lledo, P., Wilhelm, C., & Eberl, G. (2024) · La Revue de Médecine Interne · doi:10.1016/j.revmed.2024.10.429

Recent advances in research on common targets of neurological and sex hormonal influences on asthma

Zhou, W., Chen, H., Chen, X., Gao, J., & Ji, W. (2025) · Clinical and Translational Allergy · doi:10.1002/clt2.70022

A Sustainable Solution in Supply Chain in the Contemporary Business World: An Integrated Model

SEN, P. C., Mukherjee, S., Agrawal, P., Mondal, S., & Ghosh, A. (2025) · Emerald Group Publishing Limited eBooks · doi:10.1108/978-1-83549-246-820251005

Early Progenitors of Innate Lymphoid Cells (ILC)

Das, A., Ding, Y., & Bhandoola, A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-128-24465-4.00045-4

RAG suppresses group 2 innate lymphoid cellsPreprint

Heul, A. V., Mack, M. R., Zamidar, L., Tamari, M., Yang, T.-L., Trier, A. M., Kim, D.-H., Janzen-Meza, H., Dyken, S. J. V., Hsieh, C., et al. (2025) · eLife · doi:10.7554/elife.98287.2

Prevalent cross-cell type QTL trans -regulatory genetic effects impacting innate lymphoid cells in the small intestinePreprint

Xu, M., Gosik, K., Zang, Y., Ashenberg, O., Li, C., Li, H., Liu, K., Churchill, G. A., Gatti, D. M., Choi, K., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.16.649031

Innate Lymphoid Cells Type 3

Cao, W. H. J., Belz, G. T., & Jacquelot, N. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-824465-4.00136-8

The Immunobiology of Asthma

Cho, J. L. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-824465-4.00252-0

Haplotypes, Genotypes, and DNA Methylation Levels of Neuromedin U Gene Are Associated with Cardio-Metabolic Parameters: Results from the Moli-sani Study

Noro, F., Marotta, A., Costanzo, S., Izzi, B., Gialluisi, A., Curtis, A. D., Pepe, A., Grossi, S., Castelnuovo, A. F. D., Cerletti, C., et al. (2025) · Biomedicines · doi:10.3390/biomedicines13081906

Enteric ChAT-expressing neurons as new target for Lactobacillus plantarum ameliorates inflammatory bowel diseasesPreprint

Xia, B., Sun, Y., Wang, J., Liu, Y., Wang, L., Jiang, S., Bai, G., Zhang, R., Zhang, Y., Kou, R.-W., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.09.673902

Progenitor T cells drive chronic pulmonary type 2 inflammation

Kratchmarov, R., Jia, X., Nagai, J., Pacheco, G. A., Perniss, A., Bell, M. A., Gül, E., Thompson, T. W., Hayashi, H., Saghaei, S., et al. (2026) · Nature Immunology · doi:10.1038/s41590-026-02619-y

Escherichia coli -induced gut IL-33 release inhibits lung type 2 allergic responsesPreprint

Salgado, C. L., Ayupe, M. C., Rodrigues, J. F., Gonçalves, L. M., Menezes-Silva, L., Pizzolante, B. C., Oliveira, B. D. C., da Silva, G. W., Moreira, F., de Oliveira, É. E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.07.687219

Additional file 4 of Moniezia benedeni infection enhances neuromedin U (NMU) expression in sheep (Ovis aries) small intestine

Yao, W., Liu, L.-P., Wen, Y.-Q., 王宝山, Dong, J., WanHong, H., 范希萍, Wang, W.-H., & Zhang, W. (2022) · Figshare · doi:10.6084/m9.figshare.19619475

Additional file 3 of Moniezia benedeni infection enhances neuromedin U (NMU) expression in sheep (Ovis aries) small intestine

Yao, W., Liu, L.-P., Wen, Y.-Q., 王宝山, Dong, J., WanHong, H., 范希萍, Wang, W.-H., & Zhang, W. (2022) · Figshare · doi:10.6084/m9.figshare.19619472

Additional file 6 of Moniezia benedeni infection enhances neuromedin U (NMU) expression in sheep (Ovis aries) small intestine

Yao, W.-L., Liu, L.-P., Wen, Y.-Q., 王宝山, Dong, J., WanHong, H., 范希萍, Wang, W.-H., & Zhang, W. (2022) · Figshare · doi:10.6084/m9.figshare.19619481

Additional file 5 of Moniezia benedeni infection enhances neuromedin U (NMU) expression in sheep (Ovis aries) small intestine

Yao, W., Liu, L.-P., Wen, Y.-Q., 王宝山, Dong, J., WanHong, H., 范希萍, Wang, W.-H., & Zhang, W. (2022) · Figshare · doi:10.6084/m9.figshare.19619478

Additional file 1 of Moniezia benedeni infection enhances neuromedin U (NMU) expression in sheep (Ovis aries) small intestine

Yao, W., Liu, L.-P., Wen, Y.-Q., 王宝山, Dong, J., WanHong, H., 范希萍, Wang, W.-H., & Zhang, W. (2022) · Figshare · doi:10.6084/m9.figshare.19619466

Additional file 2 of Moniezia benedeni infection enhances neuromedin U (NMU) expression in sheep (Ovis aries) small intestine

Yao, W., Liu, L.-P., Wen, Y.-Q., 王宝山, Dong, J., WanHong, H., 范希萍, Wang, W.-H., & Zhang, W. (2022) · Figshare · doi:10.6084/m9.figshare.19619469

Acute stress alleviates type 2 lung inflammation by restricting ILC2s through corticosterone-glucocorticoid receptor signaling

Zhu, L., Huang, Y., Peng, B., Zhong, S., Zhang, X., Xiao, F., Asim, D., Pakezhati, J., Ma, J., Sun, S., et al. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01407-w

Regulation of innate lymphoid cells development by transcription factors : a multi-transcription factors reporter mouse model approach

Cherrier, D. E. (2020) · theses.fr (ABES) · doi:10.70675/bbb87cfaz35e5z49bbzb2b8zb242dde3bfb3

(-)-Epigallocatechin-3-gallate alleviates diarrhea in piglets by suppressing the NMU-NMUR1-ILC2 axis and modulating microbiota-associated energy metabolism

Ma, Z., Gao, L., Hou, W., Wu, J., Wen, X., Zhang, Y., Dong, N., Dou, X., & Shan, A. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.158119

Innate Lymphoid Cells under Neuronal Control in the Small Intestine : vasoactive Intestinal Peptide potentiates ILC2 and ILC3 functions

Pascal, M. (2019) · theses.fr (ABES) · doi:10.70675/32d591dez8b4ez4ce3zaa43z45e944fffcaf

Rôle de l’IL-33 et des cellules lymphoïdes innées de type 2 dans l’inflammation allergique pulmonaire

Schmitt, P. (2019) · theses.fr (ABES) · doi:10.70675/910c14fdzc720z4a3fza364z6abf25ce9c20

Contribution des cellules innées lymphoïdes de groupe 1 dans le développement de la stéatohépathie non alcoolique du foie

Vieira, É. (2020) · theses.fr (ABES) · doi:10.70675/a3d3dfefzd83dz4502zb987z5b0a8fe8cff5

Caractérisation transcriptomique des cellules lymphoïdes innées

Crinier, A. (2020) · theses.fr (ABES) · doi:10.70675/850e38aazc227z4187z9c41z07c47cac00d9

Cellular and molecular dissection of bacterial peptidoglycan-mediated Drosophila melanogaster behavioral immunity

Masuzzo, A. (2020) · theses.fr (ABES) · doi:10.70675/6ab77a8cz5137z4357za03az56573aa0d5f8

Régulation métabolique de la plasticité des ILC2 au cours de l'infection par Mycobacterium tuberculosis

Corral, D. (2020) · theses.fr (ABES) · doi:10.70675/5891ec8az223cz458dzb5cezd92ba38e80aa

Identification et caractérisation de métabolites lipidiques bactériens impliqués dans l'homéostasie intestinale

Petitfils, C. (2021) · theses.fr (ABES) · doi:10.70675/bc778947z305ez4f0cz8866z05cc7ee3d466

Rôle du système immunitaire intestinal au sein de l’axe microbiote-intestin-cerveau dans les symptômes psycho-comportementaux

Gabriel-Segard, T. (2023) · theses.fr (ABES) · doi:10.70675/2f469c9fz7a22z4f47z9e37zcf0e1f890660

ILC2s and their immune checkpoints in the antitumor response

Ciancaglini, C., Santopolo, S., Vacca, P., Moretta, L., & Quatrini, L. (2026) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-014183

Osteoarthritis: An Immuno‐Inflammatory Disease‐Mechanisms of Immune Cell Dysregulation and Potential Therapeutic Strategies

Lei, Q., Lou, X., Su, X., Liu, S., Tong, Y., Chen, J., Chen, X., Mao, W., Yu, H., & Lin, L. (2026) · Med Research · doi:10.1002/mdr2.70072

Exploration of the regulatory mechanism of the vasoactive intestinal peptide-eosinophil axis in sheep resistance to Moniezia benedeni infection

Zhang, W., Yao, W., Wang, B., Meng, Y., Jiang, L., Li, Z., & Huang, Z. (2026) · Veterinary Parasitology · doi:10.1016/j.vetpar.2026.110822

Effect of calcitonin gene-related peptide on group 2 innate lymphoid cell in allergic rhinitis

Yi, X., Zeng, Y., Qin, J., Liu, Y., Luo, X., Zeng, Q., & Liu, W. (2026) · European journal of medical research · doi:10.1186/s40001-026-04735-9

Therapeutic Potential of Group 2 Innate Lymphoid Cells in Neuroinflammatory Diseases

Ye, Q., Yu, Q., & Ping, A. (2026) · Scandinavian Journal of Immunology · doi:10.1111/sji.70131

Bridging neural and immune networks in barrier defense

Gu, Z., Guo, X., Xu, W., Wang, F., & Chu, C. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117653

Intracellular metabolic regulation of the fate and function of innate lymphoid cells

Wang, J., Chen, B., & Ren, W. (2026) · Trends Open · doi:10.1016/j.treopn.2026.06.011

Trichinella spiralis infection remodels intestinal neurotransmitter metabolism during LPS-induced systemic inflammation

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A pulmonary innate lymphoid cell-driven serotonergic neuroimmune axis orchestrates airway hyperreactivity and cough hypersensitivity

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