IL-15 functions as a danger signal to regulate tissue-resident T cells and tissue destruction

Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells

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Tumor-associated B7-H1 promotes T-cell apoptosis: A potential mechanism of immune evasion

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The Role of Tumoral FOXP3 on Cell Proliferation, Migration, and Invasion in Gastric Cancer

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European Society for Pediatric Gastroenterology, Hepatology, and Nutrition Guidelines for the Diagnosis of Coeliac Disease

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X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

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Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid

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The Combined Use of Cytokine Serum Values with Laboratory Parameters Improves Mortality Prediction of COVID-19 Patients: The Interleukin-15-to-Albumin Ratio

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CD8+ TEMRAs in severe asthma associate with asthma symptom duration and escape proliferation arrest

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The immune response modulated by inoculation of commensal bacteria at birth impacts the gut microbiota and prevents Salmonella colonization

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Advances in IL-2 Family Cytokine-Based Cancer Therapies: Overcoming Challenges Through Molecular Engineering and Delivery Strategies

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High-Dimensional Analyses Reveal IL15 Enhances Activation of Sipuleucel-T Lymphocyte Subsets and Reverses Immunoresistance

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Signals that control MAIT cell function in healthy and inflamed human tissues

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Restoring tolerance with antigen delivery

Jabrì, B., & Abadie, V. (2024) · Science · doi:10.1126/science.adg7505 · Cited by 7

DAMP-ing IBD: Extinguish the Fire and Prevent Smoldering

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Loss of tolerance to dietary proteins: From mouse models to human model diseases

Levescot, A., & Cerf–Bensussan, N. (2024) · Immunological Reviews · doi:10.1111/imr.13395 · Cited by 8

Gamma-Chain Receptor Cytokines & PD-1 Manipulation to Restore HCV-Specific CD8+ T Cell Response during Chronic Hepatitis C

Peña‐Asensio, J., Sánchez, H. C., Torralba, M., Miquel, J., Sanz‐de‐Villalobos, E., & Larrubia, J. R. (2021) · Cells · doi:10.3390/cells10030538 · Cited by 8

4‐1BB and cytokines trigger human NK, γδ T, and CD8+ T cell proliferation and activation, but are not required for their effector functions

Vidard, L. (2022) · Immunity Inflammation and Disease · doi:10.1002/iid3.749 · Cited by 6

Recombinant Human Interleukin-15 and Anti-PD-L1 Combination Therapy Expands a CXCR3+PD1−/low CD8 T-Cell Subset in Simian Immunodeficiency Virus-Infected Rhesus Macaques

Chen, P., Chen, H., Moussa, M., Cheng, J., Li, T., Qin, J., Lifson, J. D., Sneller, M. C., Krymskaya, L., Godin, S., et al. (2019) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiz485 · Cited by 7

TCR signaling via NFATc1 constrains IL-15-induced bystander activation of human memory CD8+ T cells

Lee, H., Kim, S., Kim, S.-H., Jeong, S., Kim, K. H., Kim, C. G., Koh, J., Kim, H., Han, J. W., Yu, H., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.10.002 · Cited by 7

Profibrogenic role of IL-15 through IL-15 receptor alpha-mediated trans-presentation in the carbon tetrachloride-induced liver fibrosis model

Cloutier, M., Variya, B. C., Akbari, S. A., Rexhepi, F., Ilangumaran, S., & Ramanathan, S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1404891 · Cited by 6

Immune dysregulation is an important factor in the underlying complications in Influenza infection. ApoH, IL-8 and IL-15 as markers of prognosis

Garcinuño, S., Lalueza, A., Gil‐Etayo, F. J., Díaz‐Simón, R., Lizasoaín, I., Moraga, A., Díaz-Benito, B., Naranjo, L., Cabrera-Marante, Ó., Pleguezuelo, D. E., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1443096 · Cited by 7

Elevated IL-15 levels in systemic lupus erythematosus: potential pathogenesis insight and therapeutic target

Jiang, J., Yang, M., Yang, B., Wu, H., & Lu, Q. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112973 · Cited by 6

Tissue-resident immune cells in cervical cancer: emerging roles and therapeutic implications

Li, X., Deng, J., Liu, X., Zhou, Y., Bi, T., Chen, J., & Wang, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1541950 · Cited by 7

Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis

Gu, A., Sun, C., Shan, Y., Husile, H., & Bai, H. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.993492 · Cited by 6

Granulocyte–macrophage colony‐stimulating factor–stimulated human macrophages demonstrate enhanced functions contributing to T‐cell activation

Farzam‐kia, N., Lemaître, F., Moratalla, A. C., Solorio, Y. C., Cal, S. D., Jamann, H., Klément, W., Antel, J. P., Duquette, P., Girard, M., et al. (2022) · Immunology and Cell Biology · doi:10.1111/imcb.12600 · Cited by 6

Regulatory T cell‐derived interleukin‐15 promotes the diversity of immunological memory

Madi, A., Wu, J., Ma, S., Weisshaar, N., Mieg, A., Hering, M., Ming, Y., Zettl, F., Möhr, K., ten Bosch, N., et al. (2022) · European Journal of Immunology · doi:10.1002/eji.202149400 · Cited by 6

Tissue-Resident Cytolytic Innate Lymphocytes in Cancer

Nixon, B. G., & Li, M. O. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701124 · Cited by 8

Diversity of T cells in the skin: Novel insights

Novak, N., Tordesillas, L., & Cabanillas, B. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.1985116 · Cited by 6

Dynamics of IL‐15/IL‐15R‐α expression in response to HSV‐1 infection reveal a novel mode of viral immune evasion counteracted by iNKT cells

Sobkowiak, M. J., Paquin‐Proulx, D., Bosnjak, L., Moll, M., Chen, M., & Sandberg, J. K. (2021) · European Journal of Immunology · doi:10.1002/eji.202149287 · Cited by 6

Human small intestine contains 2 functionally distinct regulatory T-cell subsets

Chauhan, S. K., Bartolomé-Casado, R., Landsverk, O. J. B., Johannessen, H., Phung, D., Nilsen, H. R., Sætre, F., Jahnsen, J., Horneland, R., Yaqub, S., et al. (2023) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2023.02.030 · Cited by 9

Natural killer cells in kidney immune surveillance, injury and fibrosis

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The Path Towards Effective Long-Lasting Tissue-Targeted Prime/Pull/Keep Herpes Simplex Therapeutic Vaccines

Quadiri, A., Lekbach, Y., Elfatimi, E., Prakash, S., Vahed, H., Karan, S., Rehman, A., Ng, S. X. L., Maurya, C., Chow, R., et al. (2025) · Vaccines · doi:10.3390/vaccines13090908 · Cited by 5

Microscopic Colitis and Celiac Disease: Sharing More than a Diagnostic Overlap

González-Castro, A. M., Fernández‐Bañares, F., Zabana, Y., Farago-Pérez, G., Jonathan, D. O.-B., Expósito, E., & Guagnozzi, D. (2024) · Nutrients · doi:10.3390/nu16142233 · Cited by 6

Liver-resident CD8+ T cells: learning lessons from the local experts.

Swadling, L., Pallett, L., & Maini, M. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.02.001 · Cited by 5

Beneficial Role of Microbial Transglutaminase in the Pathogenetic Mechanisms of Coeliac Disease

Treppiccione, L., Picarelli, A., & Rossi, M. (2022) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000003451 · Cited by 5

Inflammatory Diseases of the Gastrointestinal Tract and Pharmacological Treatments

Mathias, C. B., McAleer, J. P., & Szollosi, D. E. (2019) · Springer eBooks · doi:10.1007/978-3-030-19922-7_6 · Cited by 5

Strategies for the Development of NK Cell-Based Therapies for Cancer Treatment

Budagova, T., Efremova, A. S., Maiak, M. A., & Goldshtein, D. V. (2025) · Cells · doi:10.3390/cells14231858 · Cited by 4

Is the microbiome important in celiac disease?

Galipeau, H. J., & Verdu, E. F. (2025) · Journal of the Canadian Association of Gastroenterology · doi:10.1093/jcag/gwae047 · Cited by 4

IL-15-Activated CD38+HLA-DR+CD8+ T cells induce liver injury in cirrhosis via JAK/STAT5 and PI3K/mTOR pathways

Liu, K., Dong, H., Zhang, K., Yan, W., Wu, H., Fan, J., & Ye, W. (2025) · Scientific Reports · doi:10.1038/s41598-025-02693-6 · Cited by 4

Treatment of gluten-related disorders

Yoosuf, S., & Makharia, G. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821846-4.00006-1 · Cited by 4

Activation and in vivo evolution of the MAIT cell transcriptome in mice and humans reveals diverse functionalityPreprint

Hinks, T., Marchi, E., Jabeen, M., Olshansky, M., Kurioka, A., Pediongco, T. J., Meehan, B. S., Kostenko, L., Turner, S. J., Corbett, A. J., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/490649 · Cited by 4

IL-15 and IL-7: keys to dysregulated inflammation in acute coronary syndromes

Nosalski, R., & Guzik, T. J. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab189 · Cited by 4

Serum interleukin 15 level may serve as a new marker for alopecia areata

Omar, N. M., Ghanem, B. M., Abdelsalam, M., & Elmogy, M. H. (2021) · Egyptian Journal of Dermatology and Venerology · doi:10.4103/ejdv.ejdv_57_20 · Cited by 3

Effect of acetylcholinesterase inhibition on immune cells in the murine intestinal mucosa

Al-Mansori, A., Al-Sbiei, A., Bashir, G. H., Qureshi, M. M., Tariq, S., Altahrawi, A., al-Ramadi, B. K., & Fernández-Cabezudo, M. J. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e33849 · Cited by 2

Amyloid beta-induced signalling in leptomeningeal cells and its impact on astrocyte response

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Immunology in Celiac Disease

Marietta, E. V., Choung, R. S., Rubio‐Tapia, A., & Murray, J. A. (2025) · Gastrointestinal Endoscopy Clinics of North America · doi:10.1016/j.giec.2024.12.009 · Cited by 3

Pregnancy probabilistically augments potential precursors to chronic, immune-mediated or autoimmune lacrimal gland infiltrates

Mircheff, A. K., Wang, Y., Li, M., Pan, B. X., & Ding, C. (2017) · The Ocular Surface · doi:10.1016/j.jtos.2017.09.005 · Cited by 3

Cytokine and metabolite networks shape T cell residency and functionality at the term human maternal-fetal interface

Maurice, N. J., Erickson, J. R., DeJong, C. S., Mair, F., Taber, A. K., Frutoso, M., Islas, L., Vigil, A.-L. B. G., Lawler, R. L., McElrath, M. J., et al. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf093 · Cited by 5

Microbial Peptidases: Key Players in Reducing Gluten Immunogenicity Through Peptide Degradation

Sanchiz, Á., San-Martín, M. I., Navasa, N., Martı́nez-Blanco, H., Ferrero, M. Á. M., Rodrı́guez-Aparicio, L. B., & Chamizo‐Ampudia, A. (2025) · Applied Sciences · doi:10.3390/app15148111 · Cited by 3

IL-15 Promotes the Survival of Anti-Inflammatory (M2), Immunoinhibitory (IL-10+) Dermal Macrophages in Human Eyelid Skin Under IFNγ-Dominated Inflammatory Conditions

Demetrius, D., Perez, S. M., Suzuki, T., Gherardini, J., Lee, W., Chéret, J., & Paus, R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26167811 · Cited by 2

Tissue‐Resident Memory T Cells: Pioneering New Avenues in Cancer Immunotherapy

Xiao, Y., Yang, Q., & Sun, Z. (2025) · Cancer Medicine · doi:10.1002/cam4.71429 · Cited by 4

Schistosoma mansoni Infection Is Associated With Increased Monocytes and Fewer Natural Killer T Cells in the Female Genital Tract

Kingery, J. R., Chalem, A., Mukerebe, C., Shigella, P., Miyaye, D., Magawa, R., Ward, M., Kalluvya, S. E., McCormick, J., Maganga, J. K., et al. (2022) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofac657 · Cited by 2

Biological variability of human intraepithelial lymphocytes throughout the human gastrointestinal tract in health and coeliac disease

Fiz‐López, A., Prado, Á. D., Arribas‐Rodríguez, E., García‐Alonso, F. J., Izquierdo, S., Martín‐Muñoz, Á., Garrote, J. A., Arranz, E. M., Barrio, J., Fernández-Salazar, L. I., et al. (2024) · European Journal of Clinical Investigation · doi:10.1111/eci.14304 · Cited by 2

Functional genomic analysis of the 68-1 RhCMV-Mycobacteria tuberculosis vaccine reveals an IL-15 response signature that is conserved with vector attenuation

Sung, C.-J., Whitmore, L. S., Smith, E. A., Chang, J., Tisoncik-Go, J., Barber-Axthelm, A. M., Selseth, A. N., Feltham, S., Ojha, S., Hansen, S. G., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460344 · Cited by 2

The Role of T‐Helper 17 Cells and Regulatory T Cells in Acute Diffuse and Total Alopecia: The Increased Function of Regulatory T Cells May Explain the Favorable Prognosis

Lim, J., Kang, D., Moon, H., Kwon, S., & Lew, B. (2025) · The Journal of Dermatology · doi:10.1111/1346-8138.17745 · Cited by 2

Microbiota promote enhanced CD39 expression in γδ intraepithelial lymphocytes through the activation of TCR and IL-15 signaling

Alonso, S., Kaur, H., Luo, J., Nguyen, M.-U., Laguerta, A. M., Fong, A., Skariah, N., Argüello, R. J., Verzi, M. P., Swamy, M., et al. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.07.005 · Cited by 2

Specific Genetic Polymorphisms Contributing in Differential Binding of Gliadin Peptides to HLA-DQ and TCR to Elicit Immunogenicity in Celiac Disease

Banerjee, P., Chaudhary, R., Singh, A. K., Parulekar, P., Kumar, S., & Senapati, S. (2023) · Biochemical Genetics · doi:10.1007/s10528-023-10377-x · Cited by 2

Standing in the GAP : To Formulate a Novel Radioimmunotherapy Regime to Improve the Long-Term Outcome in Breast Cancer

Ho, L. P., Teo, Y. W. B., Hoon, T. P., Iqbal, J., Linn, Y. C., Tee, G. Y., Tan, K. W., Chong, T. H., Wee, O. K., & Wei, Y. K. (2018) · Immunotherapy · doi:10.2217/imt-2017-0080 · Cited by 2

STAT3 gain-of-function mutations connect leukemia with autoimmune disease by pathological dysregulation of NKG2D hi CD8 killer T cellsPreprint

Masle‐Farquhar, E., Jackson, K., Peters, T. J., Al‐Eryani, G., Singh, M., Payne, K. J., Rao, G., Apps, G., Kingham, J., Jara, C. J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.11.480027 · Cited by 2

Converging cytokine and metabolite networks shape asymmetric T cell fate at the term human maternal-fetal interfacePreprint

Maurice, N. J., Erickson, J. R., DeJong, C. S., Mair, F., Taber, A. K., Frutoso, M., Islas, L., Vigil, A.-L. B. G., Lawler, R. L., McElrath, M. J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.10.598377 · Cited by 2

ASSESSMENT OF SERUM LEVELS OF ANTIGLIADIN ANTIBODIES (IgG and IgA) IN PATIENTS WITH ALOPECIA AREATA AND THEIR RELATION TO SEVERITY OF THE DISEASE

Mohamed, A. M., Darwish, H. M. A., Al-Sebaay, H. K., & El-Aziz, S. Y. (2023) · Al-Azhar Medical Journal · doi:10.21608/amj.2023.315119 · Cited by 1

Interleukins Signature Profile in the Etiopathogenesis of Oral Submucous Fibrosis: A Comprehensive Study

Yadahalli, R., Sarode, G. S., Sarode, S. C., & Vyas, N. (2024) · Medical Journal of Dr D Y Patil Vidyapeeth · doi:10.4103/mjdrdypu.mjdrdypu_553_23 · Cited by 1

Gut Microbiota Dysbiosis in Celiac Disease, Exploring the Probiotic Solution

Ali, H. M., Mohammed, Z. A., & Abbas, O. K. (2025) · Iraqi Journal of Community Medicine · doi:10.4103/irjcm.irjcm_45_24 · Cited by 1

Colonic neoplasia and celiac disease: A systematic review

Khayyat, Y. M. (2025) · World Journal of Gastroenterology · doi:10.3748/wjg.v31.i36.110210 · Cited by 1

IL-15 Promotes Inflammatory Th17 Cells in the Intestine

Hou, G., Lee, A. A., Golob, J. L., Grasberger, H., Berinstein, E. M., Swanson, B. J., Bishu, S., Zataari, M. E., Khaykin, V. M., Berinstein, J. A., et al. (2025) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izaf222 · Cited by 1

Longitudinal analysis identifies bystander-activated innate cytotoxic CD8+ T cells as predictors and therapeutic biomarkers for acute graft-versus-host disease

Chen, Y., Zhou, R., Zhong, L., Deng, H., Yu, J., Wang, H., Jiang, X., Mo, W., Wang, S., & Liu, Y. (2026) · hLife · doi:10.1016/j.hlife.2025.10.006 · Cited by 1

Predictive significance of interleukin-15 in urinary tract infections caused by beta-lactamase-producing Klebsiella pneumoniae

Finjan, N. M., & Mahmood, A. S. (2021) · Materials Today Proceedings · doi:10.1016/j.matpr.2021.07.415 · Cited by 1

Effects of Common Myokines on Diabetes Mellitus

Yu, Z., Liu, Q., Zhu, Y., Guo, T., Jin, M., Hao, J., Qi, C., Miao, X., Xi, D., Fan, J., et al. (2022) · Journal of Diabetes Mellitus · doi:10.4236/jdm.2022.123013 · Cited by 1

Short-chain fatty acids and their impact on human health – a review

Czachajda, M., Góral, A., Duszyńska, K., Dolepski, K., Żuk, K., & Firlej, E. (2024) · Medycyna Ogólna i Nauki o Zdrowiu · doi:10.26444/monz/190750 · Cited by 2

The Relationship of Circulatory miRNA-21 Expression with IL-15 Level in Celiac Disease Patients in Karbala Province

Al-Janabi, R. A. S., & Ali, A. J. M. (2025) · Medical Journal of Babylon · doi:10.4103/mjbl.mjbl_411_24 · Cited by 1

A quantitative systems pharmacology model to inform clinical translation of dynamic PKPD relationships of engineered IL-15

Joslyn, L. R., Jafarnejad, M., Yadav, R., Holder, P. G., Sanjabi, S., Shivva, V., Liu, K., Leung, I., Hassanzadeh‐Kiabi, N., Schubbert, S., et al. (2025) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2025.107303 · Cited by 1

Low responsiveness to a hepatitis B virus vaccine in a Chinese population lacks association with ITGAL, CD58, TNFSF15, CCL15, TGFB3, and BCL6 gene variants

Xu, X., Li, Y., Liang, Y., Yin, M., Zhang, Y., Huang, L., Yu, Z., & Ni, J. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.06.010 · Cited by 1

Perspectives for the application of interleukin 15 in anti-cancer therapy

Węgierek‐Ciura, K., & Pajtasz‐Piasecka, E. (2019) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0013.7194 · Cited by 1

Non-dietary therapies for celiac disease

Yoosuf, S., Therrien, A., & Leffler, D. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821571-5.00011-8 · Cited by 1

La mystérieuse Œsophagite à Eosinophiles garde encore quelques secrets

Vicari, A. P. (2017) · HEGEL - HEpato-GastroEntérologie Libérale · doi:10.3917/heg.071.0013 · Cited by 1

Converting to adapt

Colonna, M., & Cervantes‐Barragán, L. (2016) · Science · doi:10.1126/science.aag1719 · Cited by 1

Sustained IL-15 response signature predicts RhCMV/SIV vaccine efficacyPreprint

Barrenäs, F., Hansen, S. G., Law, G. L., Driscoll, C. B., Green, R. R., Smith, E. A., Chang, J., Golez, I., Urion, T., Peng, X., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.11.426199 · Cited by 1

Human enteric viruses shape disease phenotype through divergent innate immunomodulationPreprint

Adiliaghdam, F., Amatullah, H., Digumarthi, S., Saunders, T. L., Rahman, R., Wong, L., Sadreyev, R. I., Droit, L., Paquette, J., Goyette, P., et al. (2021) · bioRxiv · doi:10.1101/2021.10.14.464404 · Cited by 1

IL-15 promotes inflammatory T h 17 cells in the intestinePreprint

Golob, J. G., Hou, G., Lee, A. A., Grasberger, H., Berinstein, E. M., Zataari, M. E., Khaykin, V. M., Fry, C., Berinstein, J., Nemzek, J. A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.11.532227 · Cited by 1

TCR signaling via NFATc1 constrains IL-15-induced NK-like activation of human memory CD8 + T cellsPreprint

Lee, H., Kim, S., Kim, S.-H., Jeong, S., Kim, K. H., Kim, C. G., Koh, J., Kim, H., Han, J. W., Yu, H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.13.632884 · Cited by 1

Constraints and tunability of antigen-agnostic memory durabilityPreprint

Tripathi, S., Liu, C., Lau, W. W., Sparks, R., & Tsang, J. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.18.663399 · Cited by 1

Hidden immune memory niches in inflammatory skin diseasesPreprint

Steele, L., Foster, A. R., Roberts, K., Admane, C., Birk, S., Mazin, P., Akbarnejad, A., Tudor, C., Rumney, B. M., Chan, H. M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.20.713219 · Cited by 2

Celiac Disease and Its Association with Organ-Specific Auto-Immune Diseases

Buchke, S., Bora, A., Mehta, B., Relekar, M., Varsha, P., Kumar, J., & Bhanu, P. (2021) · International Journal of Innovative Research in Medical Science · doi:10.23958/ijirms/vol06-i10/1214

Estudio de los mecanismos de muerte celular en la mucosa de intestino delgado

Ruera, C. N. (2022) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/133567

Faculty Opinions recommendation of The activation of bystander CD8+ T cells and their roles in viral infection.

Lionakis, M. S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737082332.793572046

Faculty Opinions recommendation of T cells in celiac disease.

Cerf–Bensussan, N. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727506738.793561387

Faculty Opinions recommendation of Chronic Inflammation Permanently Reshapes Tissue-Resident Immunity in Celiac Disease.

Cerf–Bensussan, N. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735060192.793561397

Faculty Opinions recommendation of CD4 T-cell cytokines synergize to induce proliferation of malignant and nonmalignant innate intraepithelial lymphocytes.

Cerf–Bensussan, N. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727165354.793561402

Faculty Opinions recommendation of Coeliac disease and mast cells.

Kawakami, T. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736760232.793571856

Innate riddle of CD4+ T cells and the control of enteric infections

Malik, A., & Jabrì, B. (2022) · Immunity · doi:10.1016/j.immuni.2022.06.017

Let's be adaptable

Lutter, L. (2022) · Utrecht University Repository (Utrecht University) · doi:10.33540/1160

Shaping mucosal and systemic immunity by non-digestible oligosaccharides and postbiotics

Ayechu-Muruzabal, V. (2022) · doi:10.33540/1552

Data from Rapid Depletion of Intratumoral Regulatory T Cells Induces Synchronized CD8 T- and NK-cell Activation and IFNγ-Dependent Tumor Vessel Regression

Kurebayashi, Y., Olkowski, C. P., Lane, K. C., Vasalatiy, O. V., Xu, B., Okada, R., Furusawa, A., Choyke, P. L., Kobayashi, H., & Sato, N. (2023) · doi:10.1158/0008-5472.c.6513648.v1

Data from IL15 and Anti–PD-1 Augment the Efficacy of Agonistic Intratumoral Anti-CD40 in a Mouse Model with Multiple TRAMP-C2 Tumors

Chen, W., Bamford, R. N., Edmondson, E. F., & Waldmann, T. A. (2023) · doi:10.1158/1078-0432.c.6531092

Data from IL15 and Anti–PD-1 Augment the Efficacy of Agonistic Intratumoral Anti-CD40 in a Mouse Model with Multiple TRAMP-C2 Tumors

Chen, W., Bamford, R. N., Edmondson, E. F., & Waldmann, T. A. (2023) · doi:10.1158/1078-0432.c.6531092.v1

IL-15 enhances anti-tumor immunity of sipuleucel-T by activating lymphocyte subsets and reversing immunoresistancePreprint

Saeed, M. A., Peng, B., Kim, K., Borkowski, A., Tine, B. A. V., Sheikh, N. A., Vu, T., Thorek, D. L. J., Fehniger, T. A., & Pachynski, R. K. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.23.550213

Transcriptome Heterogeneity in COVID-19-induced Acute Respiratory Distress SyndromePreprint

Nishii, M., Honzawa, H., Oki, H., Matsumura, R., Sakai, K., Saji, R., Ban, T., Tamura, T., & Takeuchi, I. (2024) · Research Square · doi:10.21203/rs.3.rs-3908055/v1

A flexible model for correlated count data, with application to multicondition differential expression analyses of single-cell RNA sequencing data

Liu, Y. K., Carbonetto, P. S., Takahama, M., Gruenbaum, A., Xie, D., Chevrier, N., & Stephens, M. (2024) · The Annals of Applied Statistics · doi:10.1214/24-aoas1894 · Cited by 1

Characterizing the mechanisms underpinning interleukin-15Rα-mediated protection against sepsis and candidiasis

Yang, J., Xu, B., Cao, J., Liu, Y., Tang, L., Zhao, P., Li, S., Li, X., Liu, J., Yu, R., et al. (2025) · Cytokine · doi:10.1016/j.cyto.2025.157026

Additional file 2 of Lung cancer cell-intrinsic IL-15 promotes cell migration and sensitizes murine lung tumors to anti-PD-L1 therapy

Hu, S., Meng, K., Wang, T., Qu, R., Wang, B., Xi, Y., Yu, T., Yuan, Z., Cai, Z., Tian, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25649466

Additional file 1 of Excessive IL-15 promotes cytotoxic CD4 + CD28− T cell-mediated renal injury in lupus nephritis

Zhang, T., Liu, X., Zhao, Y., Xu, X., Liu, Y., & Wu, X. (2022) · Figshare · doi:10.6084/m9.figshare.21456176

Additional file 9 of Lung cancer cell-intrinsic IL-15 promotes cell migration and sensitizes murine lung tumors to anti-PD-L1 therapy

Hu, S., Meng, K., Wang, T., Qu, R., Wang, B., Xi, Y., Yu, T., Yuan, Z., Cai, Z., Tian, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26708804

Additional file 6 of Lung cancer cell-intrinsic IL-15 promotes cell migration and sensitizes murine lung tumors to anti-PD-L1 therapy

Hu, S., Meng, K., Wang, T., Qu, R., Wang, B., Xi, Y., Yu, T., Yuan, Z., Cai, Z., Tian, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26708795

Additional file 8 of Lung cancer cell-intrinsic IL-15 promotes cell migration and sensitizes murine lung tumors to anti-PD-L1 therapy

Hu, S., Meng, K., Wang, T., Qu, R., Wang, B., Xi, Y., Yu, T., Yuan, Z., Cai, Z., Tian, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26708801

Additional file of Upregulation of IL-15 in the placenta alters trophoblasts behavior contributing to gestational diabetes mellitus

Li, J., Li, Y., Zhou, X., Wei, L., Zhang, J., Zhu, S., Zhang, H., Gao, X., Sharifu, L. M., Wang, S., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14432411

Emerging roles for IL-15 in the activation and function of T-cells during immune stimulation

Schluns, K. S., & Anthony, S. M. (2015) · Research and Reports in Biology · doi:10.2147/rrb.s57685 · Cited by 28

IL-15 controls T cell functions through its influence on CD30 and OX40 antigens in Celiac Disease

Períolo, N., Guillén, L., Arruvito, M. L., Alegre, N. S., Niveloni, S. I., Hwang, J. H., Bai, J., & Cherñavsky, A. C. (2014) · Cytokine · doi:10.1016/j.cyto.2014.01.004 · Cited by 3

Signalling mechanisms driving homeostatic and inflammatory effects of interleukin-15 on tissue lymphocytes

Skariah, N., James, O. J., & Swamy, M. (2024) · Discovery Immunology · doi:10.1093/discim/kyae002 · Cited by 31

S1823 Neutralizing IL-15 Inhibits Pro-inflammatory Cytokine Production and Promote Protective Immune Responses

Iaquinto, G., Aufiero, V. R., Giardullo, N., Capuano, F., & Mazzarella, G. (2023) · The American Journal of Gastroenterology · doi:10.14309/01.ajg.0000956932.84681.2d

IL-15 in T-Cell Responses and Immunopathogenesis

Lee, H., Park, S., & Shin, E. (2024) · Immune Network · doi:10.4110/in.2024.24.e11 · Cited by 76