CD69: from activation marker to metabolic gatekeeper

Control of Treg and TH17 cell differentiation by the aryl hydrocarbon receptor

Quintana, F. J., Basso, A. S., Iglesias, A. H., Korn, T., Farez, M. F., Bettelli, E., Caccamo, M., Oukka, M., & Weiner, H. L. (2008) · Nature · doi:10.1038/nature06880 · Cited by 1,865

Control of TH17/Treg Balance by Hypoxia-Inducible Factor 1

Dang, E. V., Barbi, J., Yang, H.-Y., Jinasena, D., Yu, H., Zheng, Y., Bordman, Z., Fu, J., Kim, Y., Yen, H.-R., et al. (2011) · Cell · doi:10.1016/j.cell.2011.07.033 · Cited by 1,595

The developmental pathway for CD103+CD8+ tissue-resident memory T cells of skin

Mackay, L. K., Rahimpour, A., Ma, J. Z., Collins, N., Stock, A. T., Hafon, M.-L., Vega-Ramos, J., Lauzurica, P., Mueller, S. N., Stefanovic, T., et al. (2013) · Nature Immunology · doi:10.1038/ni.2744 · Cited by 1,331

CD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs

Shiow, L. R., Rosen, D. B., Brdičková, N., Xu, Y., An, J., Lanier, L. L., Cyster, J. G., & Matloubian, M. (2006) · Nature · doi:10.1038/nature04606 · Cited by 1,189

The Glucose Transporter Glut1 Is Selectively Essential for CD4 T Cell Activation and Effector Function

Macintyre, A. N., Gerriets, V. A., Nichols, A., Michalek, R. D., Rudolph, M. C., Deoliveira, D., Anderson, S. M., Abel, E. D., Chen, B. J., Hale, L. P., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.05.004 · Cited by 1,169

Control of amino-acid transport by antigen receptors coordinates the metabolic reprogramming essential for T cell differentiation

Sinclair, L. V., Rolf, J., Emslie, E., Shi, Y.-B., Taylor, P. M., & Cantrell, D. A. (2013) · Nature Immunology · doi:10.1038/ni.2556 · Cited by 930

Inflammatory T Cell Responses Rely on Amino Acid Transporter ASCT2 Facilitation of Glutamine Uptake and mTORC1 Kinase Activation

Nakaya, M., Xiao, Y., Zhou, X., Chang, J., Chang, M., Cheng, X., Blonska, M., Lin, X., & Sun, S. (2014) · Immunity · doi:10.1016/j.immuni.2014.04.007 · Cited by 902

Glutamine Uptake and Metabolism Are Coordinately Regulated by ERK/MAPK during T Lymphocyte Activation

Carr, E. L., Kelman, A., Wu, G. S., Gopaul, R., Senkevitch, E., Aghvanyan, A., Turay, A. M., & Frauwirth, K. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903586 · Cited by 830

Transcriptional downregulation of S1pr1 is required for the establishment of resident memory CD8+ T cells

Skon, C. N., Lee, J.-Y., Anderson, K. G., Masopust, D., Hogquist, K. A., & Jameson, S. C. (2013) · Nature Immunology · doi:10.1038/ni.2745 · Cited by 817

The outs and the ins of sphingosine-1-phosphate in immunity

Spiegel, S., & Milstien, S. (2011) · Nature Reviews Immunology · doi:10.1038/nri2974 · Cited by 810

Exposure to aerosolized staphylococcal enterotoxin B potentiated by lipopolysaccharide modifies lung transcriptomes and results in lung injury in the mouse model

Zong, F., Gan, C., Wang, Y., Su, D., Deng, M., Xiao, N., Zhang, Z., Zhou, D., Gao, B., & Yang, H. (2022) · Journal of Applied Toxicology · doi:10.1002/jat.4289 · Cited by 3

T-lymphocyte activation markers in patients with HIV-1-associated neurocognitive disorder

Ferreira, C. M. S., Sunada, N. M. O., & Casseb, J. (2022) · Journal of NeuroVirology · doi:10.1007/s13365-022-01075-2 · Cited by 3

A novel multimeric sCD19 ‐streptavidin fusion protein for functional detection and selective expansion of CD19 ‐targeted CAR‐T cells

Lian, H., Jiang, J., Wang, Y., Yu, X., Zheng, R., Long, J., Zhou, M., Zhou, S., Cheng, W., Zhao, A., et al. (2022) · Cancer Medicine · doi:10.1002/cam4.4657 · Cited by 3

Repeated lipoprotein apheresis and immune response: Effects on different immune cell populations

Walther, R., Wehner, R., Tunger, A., Julius, U., Schatz, U., Tselmin, S., Bornstein, S. R., Schmitz, M., & Graessler, J. (2022) · Therapeutic Apheresis and Dialysis · doi:10.1111/1744-9987.13886 · Cited by 3

Selection of highly responsive T cell receptors by an analysis combining the expression of multiple markers

Ha, M. T. V., Hamana, H., Shitaoka, K., Hayee, A., Kobayashi, E., Yoshikawa, T., Nakatsura, T., Saikawa, R., Sato, E., Osawa, M., et al. (2023) · Cancer Science · doi:10.1111/cas.15776 · Cited by 3

Rhesus macaques show increased resistance to repeated SHIV intrarectal exposure following a heterologous regimen of rVSV vector vaccine expressing HIV antigen

Jelinski, J., Kowatsch, M. M., Lafrance, M.-A., Berger, A., Pedersen, J., Azizi, H., Li, Y., Scholte, F. E. M., Gómez, A., Hollett, N. A., et al. (2023) · Emerging Microbes & Infections · doi:10.1080/22221751.2023.2251595 · Cited by 3

Single-cell analysis of the CD8+ T-cell compartment in multiple myeloma reveals disease specific changes are chiefly restricted to a CD69- subset suggesting potent cytotoxic effectors exist within the tumor bed

Favaloro, J., Bryant, C. E., Abadir, E., Gardiner, S. R., Yang, S., King, T., Nassif, N. T., Sedger, L. M., Boyle, R., Joshua, D., et al. (2023) · Haematologica · doi:10.3324/haematol.2023.283062 · Cited by 3

Quantitative analysis of Tr1 lymphocytes in patients with type 2 diabetes mellitus

Knott-Torcal, C., de la Blanca, N. S., Serrano-Somavilla, A., Martínez‐Hernández, R., Sampedro-Nuñez, M. A., Ruiz-Roso, M. B., Jiménez-Blanco, S., González‐Amaro, R., González-Baranda, L., Garcimartín, A., et al. (2024) · Journal of Endocrinological Investigation · doi:10.1007/s40618-023-02250-w · Cited by 3

Dual regulation effect and mechanism of human myeloid‐derived suppressor cells on anticolorectal cancer cells activity of Vγ9Vδ2 T cells

Zhang, M., Wu, Y., Qin, Y., Shen, J., Cui, Z., Fan, L., Zhang, K., Li, B., Liang, S., & Peng, M. (2024) · Cell Biochemistry and Function · doi:10.1002/cbf.3929 · Cited by 3

Unveiling the immune dynamics of Neisseria persistent oral colonization

Alles, M., Gunasena, M. G. B., Zia, T., D’Mello, A., Bhattarai, S. S., Mulhern, W., Terry, L., Scherger, T., Wijeratne, S., Singh, S., et al. (2024) · Infection and Immunity · doi:10.1128/iai.00048-24 · Cited by 3

Novel Peripherally Selective Cannabinoid Receptor 1 Neutral Antagonist Improves Metabolic Dysfunction-Associated Steatotic Liver Disease in Mice

Laudermilk, L. T., Schlosburg, J. E., Gay, E. A., Decker, A. M., Williams, A., Runton, R., Vasukuttan, V., Kotiya, A., Amato, G. S., & Maitra, R. (2024) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.4c00356 · Cited by 3

Different behavior of NK cells isolated from healthy women and women with recurrent spontaneous abortion after treatment with human amniotic epithelial cells

Rezayat, F., Esmaeil, N., Nikpour, P., Feizi, A., & Rezaei, A. (2025) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiaf020 · Cited by 3

A three-subtype prognostic classification based on base excision repair and oxidative stress genes in lung adenocarcinoma and its relationship with tumor microenvironment

Rao, W., Zhang, Q., Dai, X., Yang, Y., Zhang, L., Kuang, X., Xiao, H., Zhu, J., Xiong, Y., Wang, D., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-98088-8 · Cited by 3

New insights on the monitoring of solid-organ allografts based on immune cell signatures

Mardomi, A., Naderi, S. B., Vahed, S. Z., & Ardalan, M. (2021) · Transplant Immunology · doi:10.1016/j.trim.2021.101509 · Cited by 3

Peripheral blood eosinophils priming and in vitro VEGF stimulation in asthmatics

Gomułka, K., Liebhart, J., Jaskuła, E., & Mędrala, W. (2021) · Advances in Dermatology and Allergology · doi:10.5114/ada.2021.103498 · Cited by 3

Increased CD8+ T cells in patients with Henoch–Schonlein purpura nephritis exhibit suppressive immune activity

Zhao, F., Zhixiang, F., Jiajia, P., Li, Q., Min, Q., Wang, G., & Ziyan, Z. (2022) · Immunology Letters · doi:10.1016/j.imlet.2022.09.003 · Cited by 3

Bacterial vaginosis-driven changes in cervicovaginal immunity that expand the immunological hypothesis for increased HIV susceptibilityPreprint

MacLean, F., Tsegaye, A. T., Graham, J. B., Swarts, J. L., Vick, S. C., Potchen, N. B., Talavera, I. C., Warrier, L., Dubrulle, J., Schroeder, L. K., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.03.601916 · Cited by 3

A longitudinal single-cell atlas to predict outcome and toxicity after BCMA-directed CAR T cell therapy in multiple myelomaPreprint

Rade, M., Fandrei, D., Kreuz, M., Seiffert, S., Wiemers, T. C., Born, P., Fischer, L., Weidner, H., Hofbauer, L. C., Baber, R., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-6165798/v1 · Cited by 3

Immunological characteristics of CD103+CD8+ Tc cells in the liver of C57BL/6 mouse infected with plasmodium NSM

Shi, F., Tang, S., Chen, D., Mo, F., Li, J., Fang, C., Wei, H., Xing, J., Liu, L., Gong, Y., et al. (2023) · Parasitology Research · doi:10.1007/s00436-023-07950-z · Cited by 2

Multi-dimensional characterization of cellular states reveals clinically relevant immunological subtypes and therapeutic vulnerabilities in ovarian cancer

Zhang, C. M., Li, S., Guo, J., Pan, T., Zhang, Y., Gao, Y., Pan, J., Liu, M., Yang, Q., Yu, J., et al. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06521-3 · Cited by 3

T lymphocytes linking autoimmunity and cardiovascular disease in aging

Ortega‐Sollero, E., Ruiz‐Fernández, I., & Martı́n, P. (2025) · The Journal of Cardiovascular Aging · doi:10.20517/jca.2024.40 · Cited by 2

Gene-regulatory programs that specify age-related differences during thymocyte development

Sankaran, D. G., Zhu, H., Maymí, V. I., Forlastro, I. M., Jiang, Y., Laniewski, N. G., Scheible, K. M., Rudd, B. D., & Grimson, A. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115903 · Cited by 2

Idelalisib modulates CD4+ T cell responses to mitigate rejection of allografts in mice

Zhang, W., Zhang, X., Hu, L., Jin, S., Pitts, L., Kofler, M., Wang, Z., Iske, J., Nian, Y., & Shen, Z. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115155 · Cited by 2

Influenza A virus disruption of dendritic cell-natural killer cell crosstalk impacts activation of naïve helper and cytotoxic T cell subsets

Morson, C. A., Uppalapati, C. K., Lopez, B. S., & Kronstad, L. M. (2025) · ImmunoHorizons · doi:10.1093/immhor/vlaf024 · Cited by 2

CD226+ B cells in primary Sjögren’s syndrome: a key player in clinical manifestations and disease pathogenesis

Zhao, P., Song, S., Zhang, S., Peng, C., Cheng, W., Chang, X., Xie, C., Hu, Z., & Liu, C. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1623774 · Cited by 2

CX3CR1–TLR4 Axis as a Shared Neuroimmune Target in COVID-19 and Epilepsy: Integrative Transcriptomics and Gabapentin Repositioning

Pan, N., Cao, P., Chen, B., Chen, L., Liao, X., & Ning, Y. (2025) · Biomedicines · doi:10.3390/biomedicines13092133 · Cited by 3

Mitochondrial Activity Regulates Human T Helper 17 Differentiation and Function

Chen, X., Papadimitriou, T. I., Essen, A., van Brunschot, B., Helsen, M. M. A., Sloetjes, A. W., Vitters, E. L., Koopman, W. J. H., van der Kraan, P. M., van Caam, A., et al. (2025) · Immunology · doi:10.1111/imm.70037 · Cited by 2

Antibody-DNA nanostructure conjugates exhibit inhibited effects on CT26 cells and prevent upregulation of PD-1 in the tumor microenvironment

Li, C., Chen, F., Wu, J., Ren, J., Li, Y., Li, S., & Xia, Z. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.148101 · Cited by 4

SLC7A11-specific CAR-T cell therapy potently targets colorectal and pancreatic cancer

Pan, X., Li, J., Zhu, J. F., Wang, X., Liu, Y., Tian, X., Yang, Y., Wang, P., & Chen, S.-W. (2025) · iScience · doi:10.1016/j.isci.2025.113713 · Cited by 2

Multi-omic analysis of PBMCs in sepsis reveals widespread cytotoxic dysfunction and an increased population of CD69 expressing naïve CD4+ T cells

Flynn, J., Baird, A., Breen, E. P., Carty, M., McNevin, C. S., McDermott, L., Kenny, E. M., Coakley, J. D., Ryan, T., Doherty, D. G., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1667186 · Cited by 2

The impact of low-dose gamma radiation on immune modulation in a mouse model of spontaneous mammary gland tumorigenesis

Khan, A. U. H., Blimkie, M., Marr, B., Wu, J., Pack, T., Kaczmarek, S., Jo, D., Laakso, H., & Lee, S.-H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1635779 · Cited by 2

Deep phenomics of PRR agonist activated human blood

Barman, S., Patel, A., Kelly, A., & Dowling, D. J. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf262 · Cited by 3

Limosilactobacillus reuteri Strains Differentially Stimulate Immunity in Response to Human Milk Oligosaccharides in Newborn Mice

Daniel, R. C., Okeugo, B., Armbrister, S. A., Saleh, Z. M., Wang, J., Luo, M., Taylor, C. M., Lundberg, L. E., Giorgberidze, S., Yin, Z., et al. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10849-z · 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

Hyperglycemia Induced in Sprague–Dawley Rats Modulates the Expression of CD36 and CD69 During Wound Healing

Ho, V., Tran, T., Patel, J., Teshome, B., & Rai, V. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262412032 · Cited by 3

ZIP3 is essential for the encephalitogenic function of pTh17 cells by regulating intracellular zinc levels

Drmic, D., Wang, L. H., Noyer, L., Zhong, L., & Feske, S. (2026) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2026.127819 · Cited by 2

Diverse IL-9-secreting T helper cells direct responses in the allergic lung

Jackson, K. G., & Kaplan, M. H. (2026) · Seminars in Immunology · doi:10.1016/j.smim.2026.102014 · Cited by 2

Discovery of an Adaptive Neuroimmune Response Driving Itch and Fast Tick Removal with Implications for Preventing Pathogen Transmission

Doehl, J. S. P., Serafim, T. D., Doh, S., Grugan, C. S., Iniguez, E., Rogerio, L. A., Frigard, R., Dey, R., Cecílio, P., Gu, X., et al. (2026) · Advanced Science · doi:10.1002/advs.202517742 · Cited by 2

The T Cell Response to Epstein-Barr Virus

Long, H. M., & Taylor, G. S. (2026) · Current topics in microbiology and immunology · doi:10.1007/82_2025_339 · Cited by 3

Immune cell profiling reveals expanded stem cell–like memory T cells in anti-GAD65-associated neurological syndromes

Barman, S., Räuber, S. J., Eisenhut, K., Esser, D., VanDuijn, M. M., Scharf, M., Herrera-Rivero, M., Disse, P., Preuth, L.-M., Gulyaeva, V., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2514753123 · Cited by 4

Ambient temperature regulates CD4+ T cell tonic T cell receptor signaling and responsiveness

Sawada, K., Eom, J., Mahoney-Sutherland, B. A., Stankiewicz, T. E., Oates, J. R., Giles, D. A., Alarcon, P. C., Damen, M. S. M. A., Cannata, A., Hargis, J., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115801 · Cited by 2

Myeloid CD93 binds to CD69 on T cells to drive resistance to T-cell engager therapy

Yu, H., Qian, Y., Huang, Y., Peng, R., Zou, M., Liu, D., Yang, T., Liu, W., Zhang, W., Cao, J., et al. (2026) · Vita · doi:10.15302/vita.2026.08.0064 · Cited by 2

Immunological effects of hybrid minimally invasive versus conventional open pancreatoduodenectomy - A single center cohort study

Himmelsbach, R., Landerer, A., Hipp, J., Hopt, U. T., Fichtner‐Feigl, S., Wittel, U. A., & Ruess, D. A. (2021) · Pancreatology · doi:10.1016/j.pan.2021.03.014 · Cited by 2

Morita-Baylis-Hillman adduct 2-(3-hydroxy-2-oxoindolin-3-yl)acrylonitrile (ISACN) modulates the inflammatory process during LPS-induced acute lung injury

da Silva, J. S. D. F., Carvalho, D. C. M., Silva, L. H. A. C., Lima, É. D. A., de Sales-Neto, J. M., Ferreira, L. A. M. P., Olegário, T. R., Mendes, R. K. S., Lettnin, A. P., Votto, A. P. D. S., et al. (2023) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2023.2177553 · Cited by 2

Function of human skin T cells in wound healing in the in vitro experimental setting

Костоломова, Е. Г., Strelin, S. A., Суховей, Ю. Г., Unger, I., Акунеева, Т. В., Markov, A. A., & Polyanskih, E. D. (2023) · Russian Journal of Immunology · doi:10.46235/1028-7221-12430-foh · Cited by 2

Immunogenicity and reactogenicity of inactivated SARS-CoV-2 vaccines in healthy adults

Wu, Y., Huang, P., Xu, M., Zhao, Q., Xu, Y., Han, S., Li, H., & Wang, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1152899 · Cited by 3

Modulation of CD8+T cells, NK cells and Th1cytokines by metabolic milieu in decline of HBV-viremia in pregnant women treated with tenofovir-disoproxil from second trimester of pregnancy

Pahwa, P., Vyas, A. K., Sevak, J. K., Singh, R., Maras, J. S., Patra, S., Sarin, S. K., & Trehanpati, N. (2024) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2024.104208 · Cited by 2

Polygenic risk associated with Alzheimer’s disease and other traits influences genes involved in T cell signaling and activation

Dressman, D., Tasaki, S., Yu, L., Schneider, J. A., Bennett, D. A. A., Elyaman, W., & Vardarajan, B. N. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1337831 · Cited by 3

A novel metric-based approach of scoring early host immune response from oro-nasopharyngeal swabs predicts COVID-19 outcome

Rajput, Y., Neral, A., Sherwani, N., Jain, V., Sahu, M., Paikra, F., Kushwaha, A., Sahu, A., Lodhi, H., Sundrani, O., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-70161-8 · Cited by 2

Soluble PD-L1 shows no association to relapse and overall survival in early stage non-small cell lung cancer (NSCLC)

Mildner, F., Sykora, M. M., Hackl, H., Amann, A., Zelger, B., Sprung, S., Buch, M. L., Nocera, F., Moser, P., Maier, H., et al. (2024) · Lung Cancer · doi:10.1016/j.lungcan.2024.107955 · Cited by 2

Intravesical chemotherapy enhances anti-tumor immunity in bladder cancer by modulating CD8+ T cell activation and Treg populations

Chen, R., Ding, S., Fu, X., & Liu, G. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.151782 · Cited by 3

Depleting Autoreactive B-Cells Using Targeted Photodynamic Therapy

Venrooij, K. R., Papadimitriou, T. I., Dorst, D. N., & Bonger, K. M. (2025) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.5c00332 · Cited by 2

Vaccination with FasL-/TCL plus MHSP65 induces improved anti-lung cancer immunity in mice

Dong, B., Dai, G., Ding, Y., Wang, B., & Zhang, S. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2017.12.029 · Cited by 2

Prostaglandin-related immune suppression in cattle

Sajiki, Y., Konnai, S., Ikenaka, Y., Okagawa, T., Maekawa, N., Logullo, C., Vaz, I. D. S., Murata, S., & Ohashi, K. (2021) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2021.110238 · Cited by 2

Time-Dependent Serial Changes of Antigen-Presenting Cell Subsets in the Ocular Surface Are Distinct between Corneal Sterile Inflammation and Allosensitization in a Murine Model

Kim, K.-W., Lee, H., Kim, H., & Kim, M. K. (2021) · Cells · doi:10.3390/cells10092210 · Cited by 2

Effect of Poly(I:C) and melanoma B16-F10 on the immunophenotype of murine spleen cells

Ponomarev, А. V., Rudakova, A. A., Za, S., Baryshnikova, M. A., & Kosorukov, V. S. (2021) · Russian Journal of Biotherapy · doi:10.17650/1726-9784-2021-20-4-51-58 · Cited by 2

Tafazzin deficiency attenuates anti-cluster of differentiation 40 and interleukin-4 activation of mouse B lymphocytes

Zegallai, H. M., Abu-El-Rub, E. M., Mejia, E. M., Sparagna, G. C., Cole, L., Marshall, A. J., & Hatch, G. M. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03692-z · Cited by 2

[DNAM-1 regulates the proliferation and function of T regulatory type 1 cells via the IL-2/STAT5 pathway].

Wang, N., Wang, Y., Jiang, P., Lü, M., Hu, Z., & Xu, X. (2022) · PubMed Central · doi:10.12122/j.issn.1673-4254.2022.09.03 · Cited by 2

Investigation on the immune effect of a chitosan-based particle-in-oil-in-water emulsion

Li, L., Li, Y., Peng, Y., Ma, G., & Wu, J. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111468 · Cited by 2

Additional use of α-IgM antibodies potentiates CpG ODN2006-induced B cell activation by targeting mainly naïve and marginal zone-like B cells

Fleige, L., Fillatreau, S., Claus, M., & Capellino, S. (2024) · Cellular Immunology · doi:10.1016/j.cellimm.2024.104846 · Cited by 2

SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses

Chen, W., Fang, X., Gao, Y., Shi, K., Sun, L., Yu, B., Luo, Q., & Xu, Q. (2019) · BMC Pharmacology and Toxicology · doi:10.1186/s40360-019-0377-8 · Cited by 2

Development of a Flow Cytometry–Based Functional Assay to Study Anti-TNF Mechanisms of Action and Capture Donor Heterogeneity

García, C. C., Lefèvre, A., & Busnel, J. (2020) · ImmunoHorizons · doi:10.4049/immunohorizons.2000077 · Cited by 2

Influence of vascular endothelial growth factor on neutrophil activation in asthmatics

Gomułka, K., Liebhart, J., Jaskuła, E., & Mędrala, W. (2022) · Advances in Dermatology and Allergology · doi:10.5114/ada.2022.115888 · Cited by 2

The Peptide/Antibody-Based Surface Decoration of Calcium Phosphate Nanoparticles Carrying siRNA Influences the p65 NF-κB Protein Expression in Inflamed Cells In Vitro

Müller, E. K., Białas, N., Epple, M., & Hilger, I. (2022) · Biomedicines · doi:10.3390/biomedicines10071571 · Cited by 2

A Cell Differentiation Trajectory-Related Signature for Predicting the Prognosis of Lung Adenocarcinoma

Yang, F., Zhao, Y., Huang, X., Zhang, J., & Zhang, T. (2022) · Genetics Research · doi:10.1155/2022/3483498 · Cited by 2

A global map of RNA binding protein occupancy guides functional dissection of post-transcriptional regulation of the T cell transcriptomePreprint

Litterman, A. J., Zhu, W. S., Kageyama, R., Zhao, W., Zaitlen, N., Erle, D. J., & Ansel, K. M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/448654 · Cited by 2

Human placental villi immune cells help maintain homeostasis in uteroPreprint

Toothaker, J. M., Olaloye, O. O., McCourt, B. T., McCourt, C. C., Case, R., Liu, P., Yimlamai, D., Tseng, G. C., & Konnikova, L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.14.452362 · Cited by 2

Mapping the immune landscape in metastatic melanoma reveals localized cell-cell interactions correlating to immunotherapy responsivenessPreprint

Bosisio, F. M., Antoranz, A., Herck, Y. V., Bolognesi, M. M., Lynch, S. M., Rahman, A., Gallagher, W. M., Boecxstaens, V., Marine, J., Cattoretti, G., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1236531/v1 · Cited by 2

Multiple myeloma long-term survivors display sustained immune alterations decades after first line therapyPreprint

Lutz, R., Grünschläger, F., Simon, M., Bauer, M., Yousefian, S., Beumer, N., Jopp‐Saile, L., Awwad, M. H. S., Steinbuß, G., Sedlmeier, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.27.542555 · Cited by 2

Lack of phosphatidylinositol 3-kinase VPS34 in regulatory T cells leads to a fatal lymphoproliferative disorder without affecting their developmentPreprint

Courrèges, C. J. F., Davenport, E. C. M., Bilanges, B., Rebollo-Gómez, E., Hukelmann, J. L., Schoenfelder, P., Edgar, J. R., Sansom, D. M., Scudamore, C. L., Roychudhuri, R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.08.574346 · Cited by 2

A convenient single-cell newly synthesized transcriptome assay reveals FLI1 downregulation during T-cell activationPreprint

Lyu, J., Xu, X., & Chen, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.22.609222 · Cited by 2

Pathogenesis of Graves' Disease Determined Using Single-Cell Sequencing with Thyroid Autoantigens Peptides Stimulation in B CellsPreprint

Kobayashi, G., Okamura, T., Hashimoto, Y., Sakai, K., Sumi, M., Imai, D., Kitagawa, N., Hamaguchi, M., & Fukui, M. (2025) · Research Square · doi:10.21203/rs.3.rs-6167157/v1 · Cited by 2

Sequence and structural determinants of efficacious de novo chimaeric antigen receptors

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Role of CD4 T Cell in Relapsing-Remitting Experimental Autoimmune Encephalomyelitis

Hu, J., Zhou, X., Cao, Y., Tian, H., Li, N., Cheng, X., Yang, X., & Dang, H. (2024) · Journal of Visualized Experiments · doi:10.3791/66553 · Cited by 1

Differential diagnostic value of simultaneous detection of CD69 and HLA-DR on host T and NK cells in QFT-TB assay for identifying active tuberculosis

Yang, Y., Zhang, F., Shi, H., Zhu, Z., Zhou, Y., & Zhou, Y. (2024) · Tuberculosis · doi:10.1016/j.tube.2024.102537 · Cited by 1

Immune suppressive drugs negatively regulate the CD8+T cells function by acetyltransferase p300 induced canonical and non-canonical autophagy

Ni, R., Fan, L., Wang, H., Zhang, Q., Zhang, L., Wang, A., Wang, A., & Liu, B. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e33755 · Cited by 1

Study of Ridostin Pro and Poly(I:C) as adjuvants that enhance the immunogenicity of an antitumor vaccine

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The Influence of Metabolites of Microorganisms of the Genus Bacillus from Permafrost Rocks on T Lymphocyte Differentiation

Petrov, S. A., Sukovei, Y. G., Kalenova, L. F., Костоломова, Е. Г., Михайлович, С. А., Narushko, M., & Бажин, А. С. (2024) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-024-06212-x · Cited by 1

Myosin Light Chain 12b and MASP1 as Novel Biomarker Candidates in Active Juvenile Idiopathic Arthritis─A Combined Proteomics/Bioinformatics Approach

Mohan, V., Krishnan, S., Balan, S., Das, S., Earali, J., Maria, E., Nair, D. R., & John, M. (2025) · Journal of Proteome Research · doi:10.1021/acs.jproteome.4c01054 · Cited by 1

Differential gene expression study in whole blood identifies candidate genes for psychosis in African American individuals

Knowles, E. E. M., Peralta, J. M., Rodrigue, A., Mathias, S. R., Mollon, J. D., Leandro, A. C., Curran, J. E., Blangero, J., & Glahn, D. (2025) · Schizophrenia Research · doi:10.1016/j.schres.2025.04.018 · Cited by 1

Comparison of four different assays to evaluate cellular-mediated immunity against cytomegalovirus in solid organ transplantation

Casas-Parra, A., Veltman, H., Romero-Caballero, A., Gelpi-Remiro, R., Boigués, M., Allalou, I., Linares‐Pardo, I., Vila-Santandreu, A., Martínez-Cáceres, E. M., & Iglesias-Escudero, M. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1567253 · Cited by 1

Single-cell sequencing on PBMCs from patients with HA and HB with inhibitors reveals different immune responses to FVIII and FIX

Li, E., Li, Z., Wang, J., Wu, H., Xue, Y., Lou, C., Chen, Z., Liu, F., Wu, W., Ding, Q.-L., et al. (2025) · Blood Advances · doi:10.1182/bloodadvances.2025015799 · Cited by 1

In vivo labeling reveals that degranulation is increased under supraphysiological TCR stimulation, but not infection, in CD8+ T cells from old mice

Dahlquist, K. J. V., Dehm, E. M., Smith, D. M., Lucas, E. D., Pierson, M. J., Hamilton, S. E., & Camell, C. D. (2025) · GeroScience · doi:10.1007/s11357-025-01723-5 · Cited by 1

Diatom-Based Artificial Antigen-Presenting Cells: A Novel Approach for Adaptive Immune Modulation

Rahman, A. A., Isa, I. L. M., Biggs, M. J. P., & Pandit, A. S. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c07766 · Cited by 1

ALK2/3 recruitment to the immunological synapse is required for T cell activation and death

Shi, J.-G., Ma, Z.-W., Ruan, Z.-L., Xu, Y., Hang, W.-H., Liu, R., Xiong, Y., Shu, H., & Li, S. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20250121 · Cited by 1

Germinal center formation is resilient to CD69 deletion on T follicular helper cells

Guillaume, S. M., Carslaw, H. A., Innocentin, S., Webb, L. M. C., Liston, A., Foster, W. S., & Linterman, M. A. (2025) · Immunology and Cell Biology · doi:10.1111/imcb.70051 · Cited by 1

γδ T cells in pediatric sepsis

Zhou, W., Feng, T., Li, L., He, Z., Mu, Y., Liu, D., & Li, H. (2025) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiaf118 · Cited by 1

Requirements for development of T helper 1 and T follicular helper cells from a common precursor

Bosma, D. M. T., Busselaar, J., Staal, M. D., de Koning, M., Reljić, M., Lei, X., de Wit, T., Xiao, Y., Borst, J. G., & Salerno, F. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117296 · Cited by 1

A natural oil-based nanoadjuvant enhances the immunogenicity of enterotoxigenic Escherichia coli (ETEC) in an experimental vaccine

Cecchini, M. E., Arsaute, S., Montironi, I. D., Roma, D. A., Raviolo, J. M., Moreno, F. R., Maletto, B. A., Camacho, N. M., Mañas, F., Bellingeri, R. V., et al. (2025) · Vaccine X · doi:10.1016/j.jvacx.2025.100724 · Cited by 1

Blood transcriptomic profiling reveals gene expression alterations in patients with SFTS-associated encephalitis

Wu, D., Wang, A., Shi, J., Zhang, Y., Geng, Y., Liu, H., Wu, Y., Kong, W., Zhu, Y., & Chen, Y. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.01161-25 · Cited by 1

A PD-1/PD-L1-Sensitive Co-culture-Based Primary T-Cell Activation Assay

Kocik-Krol, J., Stec, M., Siedlar, M., Vo, T. H., Rani, S., & Skalniak, Ł. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4734-9_6 · Cited by 1

NFATc1 regulates LAG3+CD8+ T cells in the spleen of mice infected with Plasmodium yoelii NSM

Pan, X., Mo, F., Li, P., Xiao, W. L., Liang, G., Xie, X., Yuan, H., Wei, H., Zhao, S., Li, L., et al. (2025) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0013605 · Cited by 1

IL2/IL15 Signaling Induces NK Cell Production of FLT3LG, Augmenting Anti–PD-1 Immunotherapy

Avanessian, S. C., van den Bijgaart, R. J. E., Chew, N. W., Supper, V. M., Tang, T. T., Zhang, Y., Zhao, Y., Abe, K., Gauthier, J., & Barry, K. C. (2025) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-24-1259 · Cited by 1

Cell Surface Markers of HIV Latency: Current Insights and Future Directions

Zaongo, S. D., Tang, S., Lu, Y., & Chen, Y.-K. (2025) · Reviews in Medical Virology · doi:10.1002/rmv.70077 · Cited by 1

Alterations in Circulating T-Cell Subsets with Gut-Homing/Residency Phenotypes Associated with HIV-1 Status and Subclinical Atherosclerosis

Gabriel, E. M., Dias, J., Filali-Mouhim, A., Caballero, R. E., Salinas, T. R. W., Nayrac, M., Chartrand‐Lefebvre, C., Routy, J., Durand, M., Far, M. E., et al. (2025) · Cells · doi:10.3390/cells14211732 · Cited by 1

Integration of Transcriptome Profiling and Single‐Cell Sequencing Analysis to Establish a CD8 + T Cell–Related Prognostic Model for Patients With NSCLC : From Assessment to Therapy

Jiang, Y., Yu, M., Cui, X., Li, X., Li, B., Zhang, J. I.-X., & Xu, F. (2025) · Cancer Medicine · doi:10.1002/cam4.71337 · Cited by 1

Pre‐Existing Th1 Immunity Outperforms Age in Predicting Antibody Responses to SARS‐CoV‐2 Inactivated Vaccines

Ye, C., Zhang, X., Qiu, L., Ji, J., Gu, J., Jia, H., Lu, Y., Chen, J., Meng, Z., Lian, J., et al. (2025) · Advanced Science · doi:10.1002/advs.202514147 · Cited by 1

A Spatial Gene Expression Signature of the Mouse Brain Post-Injury at the Focal Point of Contusion

Kounelis-Wuillaume, S., Frank, A. M., Goguet, E., Alba, C., Sukumar, G., Wilkerson, M. D., Dalgard, C. L., McCabe, J. T., & Doughty, M. L. (2025) · Journal of Neurotrauma · doi:10.1177/08977151251390528 · Cited by 1

Activation status of airway immune cells is a defining feature of severe asthma, regardless of fungal sensitisation

Plumpton, E. L., Colombo, S. A. P., Steward, M., Brown, S. L., Khan, S., Tavernier, G., Francis, H., Platt, H., Hussell, T., Horsnell, W. G. C., et al. (2025) · Mucosal Immunology · doi:10.1016/j.mucimm.2025.11.004 · Cited by 3

CD69 Regulates Gingival Inflammation and Microbiome in Periodontitis

Saavedra, F. M., Fischer, L., Bittner‐Eddy, P. D., Johnstone, K. F., Stolley, J. M., Williams, D. W., Herzberg, M. C., & Costalonga, M. (2025) · Journal of Dental Research · doi:10.1177/00220345251383827 · Cited by 1

The Leukocyte Activation Receptor CD69 Controls T Cell Differentiation through Its Interaction with Galectin-1

de la Fuente, H., Cruz‐Adalia, A., del Hoyo, G. M., Cibrián, D., Bonay, P., Pérez-Hernández, D., Vázquez, J., Navarro, P., Gallego, R. G., Ramírez‐Huesca, M., et al. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00348-14 · Cited by 101

CD69 Promotes Rapid Activation of Skin-Resident Memory T Cells 2309788

Hallisey, V. M., & Schwab, S. R. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkag141.1614

The activation antigen CD69

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CD69 is an immunoregulatory molecule induced following activation

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