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Hair Follicle Melanocytes Initiate Autoimmunity in Alopecia Areata: a Trigger Point

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A review of recent advancement in covalent organic framework (COFs) synthesis and characterization with a focus on their applications in antibacterial activity

Al-dolaimy, F., Saraswat, S. K., Hussein, B. A., Hussein, U. A., Saeed, S. M., Kareem, A. T., Abdulwahid, A. S., Mizal, T. L., Muzammil, K., Alawadi, A. H., et al. (2024) · Micron · doi:10.1016/j.micron.2024.103595 · Cited by 32 · see citing works

Bystander activation in memory and antigen-inexperienced memory-like CD8 T cells

Paprčková, D., Šályová, E., Michalik, J., & Štěpánek, O. (2023) · Current Opinion in Immunology · doi:10.1016/j.coi.2023.102299 · Cited by 31 · see citing works

Shaping immunity for life: Layered development of CD8 + T cells

Tabilas, C., Smith, N. L., & Rudd, B. D. (2023) · Immunological Reviews · doi:10.1111/imr.13185 · Cited by 29 · see citing works

Bystander activation of Bordetella pertussis ‐induced nasal tissue‐resident memory CD4 T cells confers heterologous immunity to Klebsiella pneumoniae

Curham, L. M., Mannion, J. M., Daly, C. M., Wilk, M. M., Borkner, L., Lalor, S. J., McLoughlin, R. M., & Mills, K. H. G. (2023) · European Journal of Immunology · doi:10.1002/eji.202250247 · Cited by 28 · see citing works

Altered T-cell reactivity in the early stages of Alzheimer's disease

Rickenbach, C., Mallone, A., Häusle, L., Frei, L., Seiter, S., Sparano, C., Kirabali, T., Blennow, K., Zetterberg, H., Ferretti, M. T., et al. (2025) · Brain · doi:10.1093/brain/awaf167 · Cited by 27 · see citing works

T cells in the skin: Lymphoma and inflammatory skin disease

Roediger, B., & Schlapbach, C. (2022) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2022.02.015 · Cited by 27 · see citing works

Liver-resident CD8+ T cells in viral hepatitis: not always good guys

Luxenburger, H., & Neumann‐Haefelin, C. (2023) · Journal of Clinical Investigation · doi:10.1172/jci165033 · Cited by 25 · see citing works

Memory T cells possess an innate-like function in local protection from mucosal infection

Arkatkar, T., Davé, V., Cruz Talavera, I., Graham, J. B., Swarts, J. L., Hughes, S. M., Bell, T. A., Hock, P., Farrington, J., Shaw, G. D., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci162800 · Cited by 25 · see citing works

T cell receptor sequences are the dominant factor contributing to the phenotype of CD8+ T cells with specificities against immunogenic viral antigens

Chen, D. G., Xie, J., Su, Y., & Heath, J. R. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113279 · Cited by 25 · see citing works

Association of T Cell Senescence with Radiation Pneumonitis in Patients with Non-small Cell Lung Cancer

Kim, K. H., Pyo, H., Lee, H., Oh, D., Noh, J. M., Ahn, Y. C., Kim, C. G., Yoon, H. I., Lee, J., Park, S., et al. (2022) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2022.07.018 · Cited by 23 · see citing works

Regulation and function of poised mRNAs in lymphocytes

Turner, M. (2023) · BioEssays · doi:10.1002/bies.202200236 · Cited by 20 · see citing works

MAITs and their mates: “Innate-like” behaviors in conventional and unconventional T cells

Hackstein, C.-P., & Klenerman, P. (2023) · Clinical & Experimental Immunology · doi:10.1093/cei/uxad058 · Cited by 20 · see citing works

Smart proteins as a new paradigm for meeting dietary protein sufficiency of India: a critical review on the safety and sustainability of different protein sources

Kumar, R., Guleria, A., Padwad, Y. S., Srivatsan, V., & Yadav, S. K. (2024) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2024.2367564 · Cited by 20 · see citing works

IL-15 induced bystander activation of CD8+ T cells may mediate endothelium injury through NKG2D in Hantaan virus infection

Zhang, X., Zhang, Y., Liu, H., Tang, K., Zhang, C., Wang, M., Xue, M., Jia, X., Hu, H., Li, N., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1084841 · Cited by 18 · see citing works

Autoantibodies in COVID-19: implications for disease severity and clinical outcomes

Galipeau, Y., Cooper, C., & Langlois, M. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1509289 · Cited by 18 · see citing works

Biofilm-derived oxylipin 10-HOME–mediated immune response in women with breast implants

Khan, I., Minto, R. E., Kelley-Patteson, C., Singh, K., Timsina, L., Suh, L., Rinne, E., Natta, B. W. V., Neumann, C. R., Mohan, G., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci165644 · Cited by 18 · see citing works

Senescence-associated lineage-aberrant plasticity evokes T-cell-mediated tumor control

Belenki, D., Richter‐Pechańska, P., Shao, Z., Bhattacharya, A., Lau, A., de Freitas, J. A. N. L. F., Kandler, G., Hick, T., Cai, X., Scharnagl, E., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57429-x · Cited by 15 · see citing works

TLR2-induced CD8+ T-cell deactivation shapes dendritic cell differentiation in the bone marrow during sepsis

Antoni, A.-C., Pylaeva, E., Budeus, B., Jabłońska, J., Klein‐Hitpaß, L., Dudda, M., & Flohé, S. B. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.945409 · Cited by 14 · see citing works

Poly(I:C) and R848 ligands show better adjuvanticity to induce B and T cell responses against the antigen(s)

Tandel, N., Patel, D., Thakkar, M., Shah, J. V., Tyagi, R. K., & Dalai, S. K. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e26887 · Cited by 14 · see citing works

IFN-λ uniquely promotes CD8 T cell immunity against SARS-CoV-2 relative to type I IFN

Solstad, A., Denz, P. J., Kenney, A. D., Mahfooz, N. S., Speaks, S., Gong, Q., Robinson, R., Long, M. E., Forero, A., Yount, J. S., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.171830 · Cited by 12 · see citing works

CCL5-Secreting Virtual Memory CD8+ T Cells Inversely Associate With Viral Reservoir Size in HIV‐1−Infected Individuals on Antiretroviral Therapy

Hu, W., Li, Y.-J., Zhen, C., Wang, Y.-Y., Huang, H.-H., Zou, J., Zheng, Y.-Q., Huang, G.-C., Meng, S.-R., Jin, J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.897569 · Cited by 14 · see citing works

CXCR6+CD69+ CD8+ T cells in ascites are associated with disease severity in patients with cirrhosis

Niehaus, C., Klein, S., Strunz, B., Freyer, E., Maasoumy, B., Wedemeyer, H. H., Björkström, N. K., Kraft, A. R. M., & Cornberg, M. (2024) · JHEP Reports · doi:10.1016/j.jhepr.2024.101074 · Cited by 13 · see citing works

Infection, vaccination and narcolepsy type 1: Evidence and potential molecular mechanisms

Ayoub, I., Freeman, S. A., Saoudi, A., & Liblau, R. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2024.578383 · Cited by 13 · see citing works

IFITM3 Is Upregulated Characteristically in IL-15–Mediated Bystander-Activated CD8+ T Cells during Influenza Infection

Jeong, S., Jeon, M., Lee, H., Kim, S., Park, S., & Shin, E. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100629 · Cited by 13 · see citing works

CD5 Suppresses IL-15–Induced Proliferation of Human Memory CD8+ T Cells by Inhibiting mTOR Pathways

Choi, Y. J., Lee, H., Kim, J. H., Kim, S., Koh, J., Sa, M., Park, S., & Shin, E. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100854 · Cited by 12 · see citing works

Infectious agents and pathogenesis of Behçet's disease: An extensive review

Cheng, L., Zhan, H., Liu, Y., Chen, H., Zhang, F., Zheng, W., & Li, Y. (2023) · Clinical Immunology · doi:10.1016/j.clim.2023.109631 · Cited by 12 · see citing works

Alopecia areata following ChAdOx1 nCoV-19 vaccination (Oxford/AstraZeneca)

Su, H., Juan, C.-K., & Chen, Y. (2022) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2022.03.006 · Cited by 12 · see citing works

Temperature impacts the bovine ex vivo immune response towards Mycoplasmopsis bovis

Démoulins, T., Yimthin, T., Lindtke, D., Eggerschwiler, L., Siegenthaler, R., Labroussaa, F., & Jores, J. (2024) · Veterinary Research · doi:10.1186/s13567-024-01272-3 · Cited by 11 · see citing works

The recombinant zoster vaccine induces trained immunity in monocytes through persistent downregulation of TGFβ

Johnson, M. J., Crotteau, M., Ghosh, D., Vu, T., Trinity, L., Marcheş, R., Ucar, D., Levin, M. J., & Weinberg, A. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013759 · Cited by 10 · see citing works

Immunization-induced antigen archiving enhances local memory CD8+ T cell responses following an unrelated viral infection

Doan, T. A., Forward, T. S., Schafer, J. B., Lucas, E. D., Fleming, I., Uecker-Martin, A., Ayala, E., Guthmiller, J. J., Hesselberth, J. R., Morrison, T. E., et al. (2024) · npj Vaccines · doi:10.1038/s41541-024-00856-6 · Cited by 9 · see citing works

Variable Normalization of Naïve CD4+ Lymphopenia and Markers of Monocyte and T Cell Activation over the Course of Direct-Acting Anti-Viral Treatment of Chronic Hepatitis C Virus Infection

Auma, A. W. N., Shive, C. L., Kostadinova, L., & Anthony, D. D. (2021) · Viruses · doi:10.3390/v14010050 · Cited by 9 · see citing works

Endotoxemia Associated with Liver Disease Correlates with Systemic Inflammation and T Cell Exhaustion in Hepatitis C Virus Infection

Shive, C. L., Kowal, C. M., Desotelle, A., Nguyen, Y., Carbone, S., Kostadinova, L., Davitkov, P., O’Mara, M., Reihs, A., Siddiqui, H., et al. (2023) · Cells · doi:10.3390/cells12162034 · Cited by 8 · see citing works

Single-dose of hybrid eukaryotic-prokaryotic nanovesicles to drive a rapid and controllable immune response against Klebsiella pneumoniae induced nosocomial pneumonia

Jiang, L., Ding, L., Long, Q., Liu, X., Li, J., Li, J., Zheng, Y., & Liu, G. (2023) · Nano Today · doi:10.1016/j.nantod.2023.102135 · Cited by 8 · see citing works

Dual Activation‐Induced Marker Combinations Efficiently Identify and Discern Antigen‐Specific and Bystander‐Activated Human CD4 + T Cells

Ceraolo, M. G., Leccese, M., Cassotta, A., Triolo, S., Bombaci, M., Coluccio, E. B., Prati, D., Ungaro, R., Abrignani, S., Bandera, A., et al. (2024) · European Journal of Immunology · doi:10.1002/eji.202451404 · Cited by 7 · see citing works

Interleukins 15 and 18 synergistically prime the antitumor function of natural killer cells through noncanonical activation of mTORC1

Fallone, L., Pouxvielh, K., Arbez, L., Rousseaux, N., Picq, L., Drouillard, A., Mathieu, A., Nombel, A., Benezech, S., Bourdonnay, E., et al. (2025) · Science Signaling · doi:10.1126/scisignal.adq8778 · Cited by 8 · see citing works

Apoptotic Vesicles Derived from Mesenchymal Stem Cells Ameliorate Hypersensitivity Responses via Inducing CD8 + T Cells Apoptosis with Calcium Overload and Mitochondrial Dysfunction

Liu, A., Peng, P., Wei, C., Meng, F., Huang, X., Liu, P., Fan, S., Cai, X., Wu, M., Xuan, Z., et al. (2025) · Advanced Science · doi:10.1002/advs.202407446 · Cited by 7 · see citing works

Bacterial Foreignization Nanosystem Elicits Multi‐Phenotypic T Cells for Antitumor Immunity

Zhuang, W., Xue, W., Liang, C., Liu, P., Lei, Y., He, J., Cheng, R., Nie, W., Wang, J., Tang, J., et al. (2025) · Advanced Science · doi:10.1002/advs.202504155 · Cited by 6 · see citing works

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 · see citing works

Herpes simplex virus lymphadenitis is associated with tumor reduction in a patient with chronic lymphocytic leukemia

Chang, A., Sholukh, A. M., Wieland, A., Jaye, D. L., Carrington, M. N., Huang, M.-L. W., Xie, H. J., Jerome, K. R., Roychoudhury, P., Greninger, A. L., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci161109 · Cited by 6 · see citing works

Act Early and at the Right Location: SARS-CoV-2 T Cell Kinetics and Tissue Localization

Bertoletti, A., Bert, N. L., & Tan, A. T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810679 · Cited by 6 · see citing works

After virus exposure, early bystander naïve CD8 T cell activation relies on NAD+ salvage metabolism

Holay, N., Kennedy, B. E., Murphy, J. P., Konda, P., Giacomantonio, M., Brauer-Chapin, T., Paulo, J. A., Kumar, V., Kim, Y., Elaghil, M., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1047661 · Cited by 6 · see citing works

Revisiting the role of human memory CD8+ T cells in immune surveillance

Wang, Y.-Y., Hu, W., Wang, F., & Zhang, C. (2022) · Cellular and Molecular Immunology · doi:10.1038/s41423-022-00900-2 · Cited by 6 · see citing works

Antigen specific activation of cytotoxic CD8+ T cells by Staphylococcus aureus infected dendritic cells

Friot, A., Djebali, S., Valsesia, S., Parroche, P., Dubois, M., Baude, J., Vandenesch, F., Marvel, J., & Leverrier, Y. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1245299 · Cited by 5 · see citing works

Human genetic errors of immunity illuminate an adaptive arsenal model of rapid defenses

Lucas, C. L. (2024) · Trends in Immunology · doi:10.1016/j.it.2023.12.006 · Cited by 5 · see citing works

Regulatory T cells restrict immunity and pathology in distal tissue sites following a localized infection

Graham, J. B., Swarts, J. L., Koehne, A. L., Watson, C., & Lund, J. M. (2024) · Mucosal Immunology · doi:10.1016/j.mucimm.2024.06.007 · Cited by 5 · see citing works

De-coupling immune parameters and toxicity associated with IL-12 agonism

Lanzar, Z. R., Aldridge, D. L., Jayaraman, B., Haskins, B. E., Howard, C. A., Arana, K., Bunkofske, M. E., Mulka, K. R., Pardy, R. D., Byerly, J. H., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115840 · Cited by 5 · see citing works

Monomeric C-reactive protein evokes TCR Signaling-dependent bystander activation of CD4+ T cells

Zhou, L., Chen, S.-J., Chang, Y., Liu, S.-H., Zhou, Y., Huang, X.-P., Hua, Y.-X., An, H., Zhang, S.-H., Сергеевич, М. И., et al. (2023) · Molecular Immunology · doi:10.1016/j.molimm.2023.03.025 · Cited by 5 · see citing works

Bystander activation of tissue‐resident memory CD4 T cells: Getting by with a little help from unfamiliar T‐cell friends

Cornelis, R., & Shulman, Z. (2023) · European Journal of Immunology · doi:10.1002/eji.202350413 · Cited by 5 · see citing works

Bystander CAR − CD8 + T cells in a CAR-T cell product can expand and enhance the antitumor effects of a bispecific antibody

Kato, J., Konishi, T., Honda, T., Maruta, M., Nabe, S., Masuda, Y., Matsumoto, M., Kawasaki, N., Miyazaki, Y., Doi, Y., et al. (2025) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-011690 · Cited by 4 · see citing works

IL-2 mediates human bystander CD8+ T-cell responses to innate immune signals

Schenk, T. J. C., Vos, M. W., van Sleen, Y., Hoeboer, J., van Baarle, D., & Guichelaar, T. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf196 · Cited by 4 · see citing works

Type 1 diabetes risk and severity after SARS-CoV-2 infection or vaccinationPreprint

Stene, L. C., Ruiz, P. L., Ljung, R., Bøås, H., Gulseth, H. L., Pihlström, N., Sundström, A., Zethelius, B., Størdal, K., Gani, O., et al. (2024) · medRxiv · doi:10.1101/2024.07.03.24309894 · Cited by 4 · see citing works

Functions and features of circulating memory T cells

Jameson, S. C., & Hamilton, S. E. (2026) · Immunity · doi:10.1016/j.immuni.2026.03.014 · Cited by 3 · see citing works

Successful salvage of a severe COVID-19 patient previously with lung cancer and radiation pneumonitis by mesenchymal stem cells: a case report and literature review

Huang, X., Tan, X., Xie, X., Jiang, T., Xiao, Y., & Liu, Z. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1321236 · Cited by 3 · see citing works

Accurate enumeration of pathogen-specific and virtual memory CD8 T cells after infection

Berton, R. R., Heidarian, M., Kannan, S. K., Shah, M., Butler, N. S., Harty, J. T., & Badovinac, V. P. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf007 · Cited by 3 · see citing works

Heterogeneous generation and expansion of epidermal-resident memory T cells in individuals allergic to nickel

Yeung, K., Weber, J. F., Stegenborg-Grathwohl, S. M., Bischofberger, N., Vaher, H., Jacobsen, J. C., Sørensen, F. N. F., Khodosevich, K. V., Coquet, J. M., Geisler, C., et al. (2025) · British Journal of Dermatology · doi:10.1093/bjd/ljaf427 · Cited by 3 · see citing works

Pathogenic CD8 T cells defined by longitudinal liver sampling in chronic hepatitis B patients starting antiviral therapyPreprint

Nkongolo, S., Mahamed, D., Kuipery, A., Vásquez, J. D. S., Kim, S., Mehrotra, A., Patel, A. B., Hu, C., McGilvray, I. D., Feld, J. J., et al. (2021) · medRxiv · doi:10.1101/2021.12.16.21267870 · Cited by 3 · see citing works

Human Th17- and IgG3-associated autoimmunity induced by a translocating gut pathobiontPreprint

Gronke, K., Nguyen, M. T., de Souza, N. S., Schumacher, J., Yang, Y., Sonnert, N. D., Leopold, S. R., Martin, A. L., Hallet, R., Richter, K., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.29.546430 · Cited by 3 · see citing works

MHC-II presentation by oral Langerhans cells impacts intraepithelial Tc17 abundance and Candida albicans oral infection via CD4 T cells

Bittner‐Eddy, P. D., Fischer, L. A., Parachuru, P., & Costalonga, M. (2024) · Frontiers in Oral Health · doi:10.3389/froh.2024.1408255 · Cited by 2 · see citing works

Retinoic acid receptor-related orphan receptor α regulates bystander activation of memory CD8+ T cells

Cai, Z., Kozai, M., Mita, H., Takeuchi, H., Mizuno, S., Matsuo, K., & Takada, K. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1647746 · Cited by 2 · see citing works

Discovery of intrahepatic CD103+ cDC1/CD8+ TRM protective immune axis against acetaminophen-induced acute liver injury

Lee, J., Kang, M.-H., Kwon, K.-H., Cha, M.-S., Hong, J., Bae, Y.-S., Park, S., Yang, S., Kim, H. Y., Yoon, K. C., et al. (2025) · Experimental and Molecular Medicine · doi:10.1038/s12276-025-01565-3 · Cited by 2 · see citing works

Stem-like memory-T maintenance and differentiation into tissue-resident T cells sustain chronic graft-versus-host disease in mice

Kong, X., Wang, B., Wu, X.-W., Cho, H.-J., Fu, W., Li, Q.-J., Zhang, R., Nasri, U., Zheng, M., Wu, A. Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69975-z · Cited by 2 · see citing works

Innate and Adaptive Cell-Mediated Immune Responses to a COVID-19 mRNA Vaccine in Young Children

Weinberg, A., Johnson, M. J., Garth, K. M., Hsieh, E. W. Y., Kedl, R. M., Weiskopf, D., Cassaday, M., Rester, C., Cabrera-Martinez, B., Baxter, R. M., et al. (2023) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofad608 · Cited by 2 · see citing works

Longitudinal multiomic profiling and corticosteroid modulation of the immediate innate immune response to an adenovirus-vector vaccine

Choi, S. J., Lee, W., Kim, S. C., Jo, H.-Y., Park, H., Kim, H. B., Park, W., Park, S. H., Ko, J., & Lee, J. S. (2024) · Vaccine · doi:10.1016/j.vaccine.2024.07.019 · Cited by 2 · see citing works

Epidemiological Characteristics of Neuro‐Specific Antibodies Following Viral Infections

Su, Y., Wang, J., Ren, Y. D., Xu, L., Si, Y., Tang, M., Li, Y., & Wang, M. (2024) · Journal of Medical Virology · doi:10.1002/jmv.70050 · Cited by 2 · see citing works

Decoding Immunobiology Through Genetic Errors of Immunity

Bender, M. J., & Lucas, C. L. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082323-124920 · Cited by 2 · see citing works

Characterization of tumoricidal activities mediated by a novel immune cell regimen composing interferon-producing killer dendritic cells and tumor-specific cytotoxic T lymphocytes

Fang, C.-H., Cheng, W., Cheng, Y., Lan, K.-L., & Lee, J. (2024) · BMC Cancer · doi:10.1186/s12885-024-12101-3 · Cited by 2 · see citing works

Skin-resident T cells play an important role in controlling skin colonization of Candidozyma (Candida) auris

Xie, J., Yan, L., Kadosh, D., & Xiong, N. (2026) · iScience · doi:10.1016/j.isci.2026.115862 · Cited by 1 · see citing works

Potential mechanisms linking bacterial factors to the development and progression of multiple sclerosis

Jafari-Nakhjavanlou, A., Irajian, P., & Bialvaei, A. Z. (2025) · Infectious Medicine · doi:10.1016/j.imj.2025.100219 · Cited by 1 · see citing works

Recombinant attenuated Salmonella vaccine promotes CD8+ T cell-dependent antitumor immunity via IFN-γ-induced IRF-1-mediated upregulation of IL-7

Jeong, J.-H., Kim, D.-J., Kim, C.-W., Han, Y. H., Jang, A., Park, J.-H., Tae, N., Ahn, J.-H., Cho, J., Choi, S. S., et al. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01510-x · Cited by 1 · see citing works

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 · see citing works

Network and machine learning analyses approach towards understanding the effects of bystander infection on both myeloid-related normal and clonal hematopoietic systems

Cueno, M. E., & Imai, K. (2026) · In Silico Research in Biomedicine · doi:10.1016/j.insi.2026.100270 · Cited by 1 · see citing works

Living rent free in your head: resident memory T cells

Degefu, H. N., Kleist, S. A., & Rosato, P. C. (2026) · ImmunoHorizons · doi:10.1093/immhor/vlaf074 · Cited by 1 · see citing works

Herbs for Autoimmune Diseases

Mukne, A., Dangat, S. V., Shirodkar, P. Y., & Sawate, K. (2023) · Springer eBooks · doi:10.1007/978-981-99-7703-1_18 · Cited by 1 · see citing works

Mutual regulation of CD4+ T cells and intravascular fibrin in infections

Mueller, T. T., Pilartz, M., Thakur, M., LangHeinrich, T., Luo, J., Block, R., Hoeflinger, J. K. L., Meister, S., Karaj, F., Pérez, L. G., et al. (2024) · Haematologica · doi:10.3324/haematol.2023.284619 · Cited by 1 · see citing works

Activation of bystander CD8 + T cells in a pediatric patient with acute hepatitis E

Morita, A., Imagawa, K., Iwasaki, T., Yaita, K., Sakai, A., & Takada, H. (2024) · Immunological Medicine · doi:10.1080/25785826.2024.2378542 · Cited by 1 · see citing works

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 · see citing works

T cell – macrophage interactions in tuberculosis as barriers to vaccine-induced immunity: What we’ve got here is failure to communicatePreprint

Mortensen, R. J., Arlehamn, C. S. L., Coler, R. N., Gerner, M. Y., Goletti, D., Lewinsohn, D. A., Modlin, R. L., Musvosvi, M., Rengarajan, J., Urdahl, K. B., et al. (2025) · doi:10.12688/verixiv.1865.1 · Cited by 1 · see citing works

The Ugly Duckling Turned to Swan: A Change in Perception of Bystander-Activated Memory CD8 T Cells

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Bystander activation in CD8 memory T cells is an innate program that is standalone from, yet influences TCR and TCR-driven responses 2259216

Maurice, N. J., Dalzell, T. S., Jarjour, N. N., & Jameson, S. C. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkag141.674

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Paprčková, D., Šályová, E., Michalik, J., & Štěpánek, O. (2023) · Current Opinion in Immunology · doi:10.1016/j.coi.2023.102299 · Cited by 31 · see citing works

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