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Gamma delta T-cell-based immune checkpoint therapy: attractive candidate for antitumor treatment

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SARS-CoV-2-specific T cells in the changing landscape of the COVID-19 pandemic

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BCG immunization induces CX3CR1hi effector memory T cells to provide cross-protection via IFN-γ-mediated trained immunity

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Longitudinal liver sampling in patients with chronic hepatitis B starting antiviral therapy reveals hepatotoxic CD8+ T cells

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The diversity of CD8+ T cell dysfunction in cancer and viral infection

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IL-15 in T-Cell Responses and Immunopathogenesis

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Single cell dynamics of tumor specificity vs bystander activity in CD8+ T cells define the diverse immune landscapes in colorectal cancer

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Tissue‐resident memory T cells and lung immunopathology

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Role of T cells in severe COVID-19 disease, protection, and long term immunity

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Multi-modal generative modeling for joint analysis of single-cell T cell receptor and gene expression data

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High-titer AAV disrupts cerebrovascular integrity and induces lymphocyte infiltration in adult mouse brain

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The gene regulatory basis of bystander activation in CD8 + T cells

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Updated Insights into the T Cell-Mediated Immune Response against SARS-CoV-2: A Step towards Efficient and Reliable Vaccines

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Severe respiratory viral infections: T-cell functions diverging from immunity to inflammation

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Lymph node sharing between pancreas, gut, and liver leads to immune crosstalk and regulation of pancreatic autoimmunity

Brown, H. M., Komnick, M. R., Brigleb, P. H., Dermody, T. S., & Esterházy, D. (2023) · Immunity · doi:10.1016/j.immuni.2023.07.008 · Cited by 44

Immunopathology and Immunotherapy of Inflammatory Skin Diseases

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Multiomic single-cell sequencing defines tissue-specific responses in Stevens-Johnson syndrome and toxic epidermal necrolysis

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Mechanisms governing bystander activation of T cells

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PSGL-1 attenuates early TCR signaling to suppress CD8+ T cell progenitor differentiation and elicit terminal CD8+ T cell exhaustion

Hope, J. L., Otero, D. C., Bae, E., Stairiker, C. J., Palete, A. B., Faso, H. A., Lin, M. P., Henriquez, M. L., Roy, S. B., Seo, H., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112436 · Cited by 39

KIR+CD8+ and NKG2A+CD8+ T cells are distinct innate-like populations in humans

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Identification of a distinct NK-like hepatic T-cell population activated by NKG2C in a TCR-independent manner

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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

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

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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 30

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

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

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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 28

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

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

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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 26

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

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Regulation and function of poised mRNAs in lymphocytes

Turner, M. (2023) · BioEssays · doi:10.1002/bies.202200236 · Cited by 19

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 21

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

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

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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 20

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

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

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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 13

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

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 13

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

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

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

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 12

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

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

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

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

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

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

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 11

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

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

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 8

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 4

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

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

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., Coquet, J. M., Geisler, C., et al. (2025) · British Journal of Dermatology · doi:10.1093/bjd/ljaf427 · Cited by 4

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

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

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 3

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

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

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., Cho, H., Fu, W., Li, Q., Zhang, R., Nasri, U., Zheng, M., Wu, A., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69975-z · Cited by 3

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

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

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

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

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

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

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

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

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

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

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 2

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

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

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

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

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

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

Maurice, N. J., Taber, A. K., & Prlic, M. (2021) · The Journal of Immunology · doi:10.4049/jimmunol.2000937 · Cited by 57

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

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 32

Memory CD8 T cells that are bystander-activated during an infection control early pathogen replication in an innate-like manner (P4371)

Prlic, M., & Chu, T. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.190.supp.183.21

Bystander activation proceeds independently of TCR machinery and co-inhibitory pathways but is regulated by the cell-extrinsic cytokine milieu 2483

Maurice, N. J., Dalzell, T. S., Jarjour, N. N., DePauw, T. A., Wall, S. M., Tankersly, T. N., Hamilton, S. E., & Jameson, S. C. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf283.395