Helper T cell differentiation

Control of Regulatory T Cell Development by the Transcription Factor Foxp3

Hori, S., Nomura, T., & Sakaguchi, S. (2003) · Science · doi:10.1126/science.1079490 · Cited by 8,187

Foxp3 programs the development and function of CD4+CD25+ regulatory T cells

Fontenot, J. D., Gavin, M. A., & Rudensky, A. Y. (2003) · Nature Immunology · doi:10.1038/ni904 · Cited by 7,745

Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins.

Mosmann, T. R., Cherwinski, H. M., Bond, M. W., Giedlin, M. A., & Coffman, R. L. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.136.7.2348 · Cited by 7,553

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

Bettelli, E., Carrier, Y., Gao, W., Korn, T., Strom, T. B., Oukka, M., Weiner, H. L., & Kuchroo, V. K. (2006) · Nature · doi:10.1038/nature04753 · Cited by 6,992

Signaling by intrathymic cytokines, not T cell antigen receptors, specifies CD8 lineage choice and promotes the differentiation of cytotoxic-lineage T cells

Park, J., Adoro, S., Guinter, T. I., Erman, B., Alag, A., Catálfamo, M., Kimura, M. Y., Cui, Y., Lucas, P. J., Gress, R. E., et al. (2010) · Nature Immunology · doi:10.1038/ni.1840 · Cited by 5,835

Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor α-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases

Sakaguchi, S., Sakaguchi, N., Asano, M., Itoh, M., & Toda, M. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.155.3.1151 · Cited by 5,608

The Orphan Nuclear Receptor RORγt Directs the Differentiation Program of Proinflammatory IL-17+ T Helper Cells

Ivanov, I. I., McKenzie, B. S., Zhou, L., Tadokoro, C. E., Lepelley, A., Lafaille, J. J., Cua, D. J., & Littman, D. R. (2006) · Cell · doi:10.1016/j.cell.2006.07.035 · Cited by 5,145

Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages

Harrington, L. E., Hatton, R. D., Mangan, P. R., Turner, H., Murphy, T. L., Murphy, K. M., & Weaver, C. T. (2005) · Nature Immunology · doi:10.1038/ni1254 · Cited by 4,742

Conversion of Peripheral CD4+CD25− Naive T Cells to CD4+CD25+ Regulatory T Cells by TGF-β Induction of Transcription Factor Foxp3

Chen, W., Jin, W., Hardegen, N. J., Lei, K.-J., Li, L., Marinos, N. J., McGrady, G., & Wahl, S. M. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20030152 · Cited by 4,678

A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17

Park, H., Li, Z., Yang, X. O., Chang, S. H., Nurieva, R., Wang, Y.-H., Wang, Y., Hood, L., Zhu, Z., Tian, Q., et al. (2005) · Nature Immunology · doi:10.1038/ni1261 · Cited by 4,265

The rising roles of exosomes in the tumor microenvironment reprogramming and cancer immunotherapy

Wu, Y., Han, W., Dong, H., Liu, X., & Su, X. (2024) · MedComm · doi:10.1002/mco2.541 · Cited by 36

Cytokines that target immune killer cells against tumors

Qiao, J., & Fu, Y. (2020) · Cellular and Molecular Immunology · doi:10.1038/s41423-020-0481-0 · Cited by 36

TRP Ion Channels in Immune Cells and Their Implications for Inflammation

Yan, Q., Gao, C., Li, M., Lan, R., Wei, S., Fan, R., & Cheng, W. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052719 · Cited by 35

Interactions Between HDL and CD4+ T Cells: A Novel Understanding of HDL Anti-Inflammatory Properties

Atehortúa, L., Davidson, W. S., & Chougnet, C. A. (2024) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.124.320851 · Cited by 35

The Potential Roles of T Cells in Periapical Lesions

Wang, L., Yang, F., Qiu, Y., Ye, L., Song, D., & Huang, D. (2021) · Journal of Endodontics · doi:10.1016/j.joen.2021.09.016 · Cited by 35

Gut immune homeostasis: the immunomodulatory role of Bacillus clausii , from basic to clinical evidence

Wong‐Chew, R. M., de Castro, J.-A. A., Morelli, L., Perez, M. I., & Özen, M. (2022) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2022.2085559 · Cited by 35

Regulation of T helper cell differentiation by the interplay between histone modification and chromatin interaction

Liu, S., Cao, Y., Cui, K., Ren, G., Zhao, T., Wang, X., Wei, D., Chen, Z., Gurram, R. K., Liu, C., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.03.018 · Cited by 34

Immune system-mediated cellular and molecular mechanisms in idiopathic membranous nephropathy pathogenesis and possible therapeutic targets

Motavalli, R., Etemadi, J., Kahroba, H., Mehdizadeh, A., & Yousefi, M. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.116923 · Cited by 34

Biomimetic Metallacage Nanoparticles with Aggregation-Induced Emission for NIR-II Fluorescence Imaging-Guided Synergistic Immuno-Phototherapy of Tumors

Zhang, J., Ma, W., Yang, B., Shi, T., Liao, S., Li, Y., & Yin, S. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c17413 · Cited by 33

T cells in cancer: mechanistic insights and therapeutic advances

Pu, J., Liu, T., Zhou, Y., Chen, M., Fu, X., Wan, Y., Wang, J., Chen, B., Sharma, A., Lukacs‐Kornek, V., et al. (2025) · Biomarker Research · doi:10.1186/s40364-025-00807-w · Cited by 33

The Multiple Roles of the Cytosolic Adapter Proteins ADAP, SKAP1 and SKAP2 for TCR/CD3 -Mediated Signaling Events

Dadwal, N., Mix, C., Reinhold, A., Witte, A., Freund, C., Schraven, B. L., & Kliche, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.703534 · Cited by 36

Impact of inflammation and Treg cell regulation on neuropathic pain in spinal cord injury: mechanisms and therapeutic prospects

Zhang, C., Li, Y., Yu, Y., Li, Z., Xu, X., Talifu, Z., Liu, W., Yang, D., Gao, F., Wei, S., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1334828 · Cited by 32

Increased proportion of follicular helper T cells is associated with B cell activation and disease severity in IgA nephropathy

Du, W., Gao, C., You, X., Li, L., Zhao, Z.-B., Fang, M., Ye, Z., Si, M., Lian, Z., & Yu, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.901465 · Cited by 32

Hepatitis B and Hepatitis D Viruses: A Comprehensive Update with an Immunological Focus

Sausen, D. G., Shechter, O., Bietsch, W., Shi, Z., Miller, S. M., Gallo, E. S., Dahari, H., & Borenstein, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415973 · Cited by 32

Gingival mesenchymal stem cells: Biological properties and therapeutic applications

Peng, Y., Jaar, J. C., & Tran, S. D. (2024) · Journal of Oral Biology and Craniofacial Research · doi:10.1016/j.jobcr.2024.07.003 · Cited by 30

Testicular immunity

Li, S., Kumar, S., Gu, X., & DeFalco, T. (2024) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2024.101323 · Cited by 30

From “Traditional” to “Trained” Immunity: Exploring the Novel Frontiers of Immunopathogenesis in the Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Romeo, M., Silvestrin, A., Senese, G., Nardo, F. D., Napolitano, C., Vaia, P., Coppola, A., Federico, P., Dallio, M., & Federico, A. (2025) · Biomedicines · doi:10.3390/biomedicines13082004 · Cited by 29

Specific Targeting of Notch Ligand-Receptor Interactions to Modulate Immune Responses: A Review of Clinical and Preclinical Findings

Goruganthu, M., Shanker, A., Dikov, M. M., & Carbone, D. P. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01958 · Cited by 29

The role of metabolism in Th17 cell differentiation and autoimmune diseases

Wang, G., Su, Z., Li, H. J., Xiao, L., Li, C., & Lian, G. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.108450 · Cited by 29

The Role of Dendritic Cell Subsets in Recurrent Spontaneous Abortion and the Regulatory Effect of Baicalin on It

Lai, N., Fu, X., Hei, G., Song, W., Wei, R., Zhu, X., Guo, Q., Zhang, Z., Chu, C., Xu, K., et al. (2022) · Journal of Immunology Research · doi:10.1155/2022/9693064 · Cited by 29

Crucial role of T cells in NAFLD-related disease: A review and prospect

Mao, T., Yang, R. X., Luo, Y., & He, K. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1051076 · Cited by 30

Immunopathogenesis of multiple sclerosis: molecular and cellular mechanisms and new immunotherapeutic approaches

Aliyu, M., Zohora, F. T., Ceylan, A., Hossain, F., Yazdani, R., & Azizi, G. (2024) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2024.2330642 · Cited by 31

The Role of T Helper 22 Cells in Dermatological Disorders

Pan, Y., Du, D., Wang, L., Wang, X., He, G., & Jiang, X. L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.911546 · Cited by 28

Vaccine-based immunotherapy and related preclinical models for glioma

Yao, L., Hatami, M., Ma, W., & Skutella, T. (2024) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2024.06.009 · Cited by 28

Remodeling of T-cell mitochondrial metabolism to treat autoimmune diseases

Lin, L., Ren, R., Xiong, Q., Zheng, C., Yang, B., & Wang, H. (2024) · Autoimmunity Reviews · doi:10.1016/j.autrev.2024.103583 · Cited by 28

MAIT cell plasticity enables functional adaptation that drives antibacterial immune protection

Wang, H., Souter, M. N. T., Moreira, M. L., Li, S., Zhou, Y., Nelson, A. G., Yu, J., Meehan, L. J., Meehan, B. S., Eckle, S. B. G., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adp9841 · Cited by 27

Sex Differences Distinctly Impact High-Fat Diet-Induced Immune Dysfunction in Wistar Rats

Tibães, J. R. B., Azarcoya‐Barrera, J., Wollin, B., Veida-Silva, H., Makarowski, A., Vine, D. F., Tsai, S. J., Jacobs, R. L., & Richard, C. (2022) · Journal of Nutrition · doi:10.1093/jn/nxac024 · Cited by 27

The Metabolic Basis of ILC Plasticity

Pelletier, A., & Stockmann, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.858051 · Cited by 27

Abnormal Lymphatic Sphingosine-1-Phosphate Signaling Aggravates Lymphatic Dysfunction and Tissue Inflammation

Kim, D., Tian, W., Wu, T.-H., Xiang, M., Vinh, R., Chang, J., Gu, S., Lee, S., Zhu, Y., Guan, T., et al. (2023) · Circulation · doi:10.1161/circulationaha.123.064181 · Cited by 27

Dysregulated MicroRNAs in the Pathogenesis of Systemic Lupus Erythematosus: A Comprehensive Review

Choi, D., Kim, J., Yang, J. W., Kim, J. H., Park, S., & Shin, J. I. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.74315 · Cited by 26

Atherosclerosis antigens as targets for immunotherapy

Raposo-Gutiérrez, I., Rodríguez-Ronchel, A., & Ramiro, A. R. (2023) · Nature Cardiovascular Research · doi:10.1038/s44161-023-00376-x · Cited by 26

Contribution of Th17 cells to tissue injury in hypertension

Basile, D. P., Abais‐Battad, J. M., & Mattson, D. L. (2020) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0000000000000680 · Cited by 26

Cancer-associated mesenchymal stem/stromal cells: role in progression and potential targets for therapeutic approaches

Hazrati, A., Malekpour, K., Mirsanei, Z., Khosrojerdi, A., Rahmani-Kukia, N., Heidari, N., Abbasi, A., & Soudi, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1280601 · Cited by 27

A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer

Yao, P., Su, L., Liu, Z., & Xu, C. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1343316 · Cited by 26

Inflammasomes in T cells

Linder, A., & Hornung, V. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167275 · Cited by 26

TIGIT Deficiency Protects Mice From DSS-Induced Colitis by Regulating IL-17A–Producing CD4+ Tissue-Resident Memory T Cells

Chen, B., Ye, B., Li, M., Wang, S., Li, J., Lai, Y., Yang, N., Ke, Z., & Zhang, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.931761 · Cited by 25

E26 transformation-specific transcription variant 5 in development and cancer: modification, regulation and function

Wei, Y., Han, S., Wen, J., Liao, J., Liang, J., Yu, J., Chen, X., Xiang, S., Huang, Z., & Zhang, B. (2023) · Journal of Biomedical Science · doi:10.1186/s12929-023-00909-3 · Cited by 25

IL-21+ CD4+ T helper cells co-expressing IFN-γ and TNF-α accumulate in the joints of antinuclear antibody positive patients with juvenile idiopathic arthritis

Fischer, J., Dirks, J., Haase, G., Holl‐Wieden, A., Hofmann, C., Girschick, H. J., & Morbach, H. (2020) · Clinical Immunology · doi:10.1016/j.clim.2020.108484 · Cited by 25

Non-canonical Hippo signaling regulates immune responses

Chen, L. (2019) · Advances in immunology · doi:10.1016/bs.ai.2019.07.001 · Cited by 24

Effector Memory T Cells and CD45RO+ Regulatory T Cells in Metastatic vs. Non-Metastatic Lymph Nodes in Lung Cancer Patients

Kwiecień, I., Rutkowska, E., Sokołowski, R., Bednarek, J., Raniszewska, A., Jahnz‐Różyk, K., Rzepecki, P., & Domagala-Kulawik, J. J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.864497 · Cited by 24

The mTOR signalling in corneal diseases: A recent update

Li, X., Chen, K., Wang, Z., Li, J., Wang, X., Xie, C., Tong, J., & Shen, Y. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115620 · Cited by 24

Analysis of the heterogeneity and complexity of murine extraorbital lacrimal gland via single-cell RNA sequencing

Huang, D., Jiao, X., Huang, S., Liu, J., Si, H., Qi, D., Pei, X., Lu, D., Wang, Y., & Li, Z. (2024) · The Ocular Surface · doi:10.1016/j.jtos.2024.06.005 · Cited by 23

Iron Supplementation Interferes With Immune Therapy of Murine Mammary Carcinoma by Inhibiting Anti-Tumor T Cell Function

Tymoszuk, P., Nairz, M., Brigo, N., Petzer, V., Heeke, S., Kircher, B., Hermann‐Kleiter, N., Klepsch, V., Theurl, I., Weiß, G., et al. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.584477 · Cited by 23

The Role of Kupffer Cells and Liver Macrophages in the Pathogenesis of Metabolic Dysfunction-Associated Steatotic Liver Disease

Tsomidis, I., Tsakou, A., Voumvouraki, A., & Kouroumalis, E. (2026) · Biomedicines · doi:10.3390/biomedicines14010151 · Cited by 22

Live Imaging of Innate and Adaptive Immune Responses in the Liver

Li, L., & Zeng, Z. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.564768 · Cited by 22

Umbilical mesenchymal stem cells mitigate T-cell compartments shift and Th17/Treg imbalance in acute ischemic stroke via mitochondrial transfer

Chen, S., Han, C., Shi, Z., Guan, X., Cheng, L., Wang, L., Zou, W., & Liu, J. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04224-6 · Cited by 22

The many-sided contributions of NF-κB to T-cell biology in health and disease

Voisin, A., & Grinberg‐Bleyer, Y. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.10.006 · Cited by 22

T-helper 22 cells develop as a distinct lineage from Th17 cells during bacterial infection and phenotypic stability is regulated by T-bet

Barnes, J. L., Plank, M. W., Asquith, K. L., Maltby, S., Sabino, L. R., Kaiko, G. E., Lochrin, A. J., Horvat, J. C., Mayall, J., Kim, R., et al. (2021) · Mucosal Immunology · doi:10.1038/s41385-021-00414-6 · Cited by 22

Exosomal microRNAs shuttling between tumor cells and macrophages: cellular interactions and novel therapeutic strategies

Xu, W., Wang, D., Zhao, Z., Zhang, H.-D., Yang, S., Zhang, Q., Li, L., & Zhang, J. (2022) · Cancer Cell International · doi:10.1186/s12935-022-02594-y · Cited by 21

Transcript Engineered Extracellular Vesicles Alleviate Alloreactive Dynamics in Renal Transplantation

Lin, J., Lv, J., Yu, S., Chen, Y., Wang, H., & Chen, J. (2022) · Advanced Science · doi:10.1002/advs.202202633 · Cited by 21

The molecular mechanism of actions and clinical utilities of tumor infiltrating lymphocytes in gastrointestinal cancers: a comprehensive review and future prospects toward personalized medicine

Piroozkhah, M., Gholinezhad, Y., Piroozkhah, M., Shams, E., & Mojarad, E. N. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1298891 · Cited by 21

Alcohol Consumption and Autoimmune Diseases

Terracina, S. A., Caronti, B., Lucarelli, M., Francati, S., Piccioni, M. G., Tarani, L., Ceccanti, M., Caserta, M., Verdone, L., Venditti, S., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020845 · Cited by 22

Plasma EVs Display Antigen-Presenting Characteristics in Patients With Allergic Rhinitis and Promote Differentiation of Th2 Cells

Fang, S., Zhou, Z., Peng, Y., Liu, X., He, B., Chen, D., Chen, D., & Fu, Q. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.710372 · Cited by 21

Immunity and Extracellular Matrix Characteristics of Breast Cancer Subtypes Based on Identification by T Helper Cells Profiling

Zhou, Y., Tian, Q., Gao, H., Zhu, L., Zhang, Y., Zhang, C., Yang, J., & Wang, B. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.859581 · Cited by 21

The altered immunological status of children conceived by assisted reproductive technology

Xu, X., Wu, H., Bian, Y., Cui, L., Man, Y., Wang, Z., Zhang, X., Zhang, C., & Geng, L. (2021) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-021-00858-2 · Cited by 20

CRL4B complex-mediated H2AK119 monoubiquitination restrains Th1 and Th2 cell differentiation

Qin, L., Song, Y., Zhang, F., Wang, R., Li, Z., Jin, S., Chen, C., Li, C., Wang, Μ., Jiang, B., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01155-8 · Cited by 20

Tackling of Immunorefractory Tumors by Targeting Alternative Immune Checkpoints

Dulal, D., Boring, A. R., Terrero, D., Johnson, T. L., Tiwari, A. K., & Raman, D. (2023) · Cancers · doi:10.3390/cancers15102774 · Cited by 20

Cross-talk between biometal ions and immune cells for bone repair

Liu, S., Lin, Z., Qiao, W., Chen, B., & Shen, J. (2024) · Engineered Regeneration · doi:10.1016/j.engreg.2024.01.003 · Cited by 20

Harnessing m1A modification: a new frontier in cancer immunotherapy

Wang, X., Ma, X., Chen, S., Fan, M., Jin, C., Chen, Y., Wang, S., Wang, Z., Meng, F., Zhang, C., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1517604 · Cited by 19

Ovarian cancer metastasis to the human omentum disrupts organ homeostasis and induces fundamental tissue reprogramming

Lischetti, U., Liang, C.-Y., Carrara, M., Coelho, R., Hanns, A., Lombardo, F. C., Dondi, A., Goetze, S., Hensler, M., Kurzeder, C., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-67557-z · Cited by 19

Novel insights: crosstalk with non-puerperal mastitis and immunity

Zhou, Y., Gong, J., Deng, X., Shen, L., & Liu, L. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1431681 · Cited by 19

Maintenance of X chromosome inactivation after T cell activation requires NF-κB signaling

Forsyth, K. S., Toothacre, N. E., Jiwrajka, N., Driscoll, A. M., Shallberg, L. A., Cunningham‐Rundles, C., Barmettler, S., Farmer, J. R., Verbsky, J. W., Routes, J. M., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.ado0398 · Cited by 19

Potent T cell‐mediated anti‐inflammatory role of the selective CB2 agonist lenabasum in multiple sclerosis

Tiberi, M., Evron, T., Saracini, S., Boffa, L., Mercuri, N. B., Chintalacharuvu, S. R., Atamas, S. P., & Chiurchiù, V. (2021) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12768 · Cited by 19

The balance of interleukin‐12 and interleukin‐23 determines the bias of MAIT1 versus MAIT17 responses during bacterial infection

Wang, H., Nelson, A. G., Wang, B., Zhao, Z., Lim, X. Y., Shi, M., Meehan, L. J., Jia, X., Kedzierska, K., Meehan, B. S., et al. (2022) · Immunology and Cell Biology · doi:10.1111/imcb.12556 · Cited by 19

Effects of Calcium Hydroxide Intracanal Medications on T Helper (Th1, Th2, Th9, Th17, and Tfh) and Regulatory T (Treg) Cell Cytokines in Apical Periodontitis: A CONSORT RCT

Teixeira, F. F. C., Cardoso, F. G. R., Ferreira, N. S., Corazza, B. J. M., Valera, M. C., Nascimento, G. G., & Martinho, F. C. (2022) · Journal of Endodontics · doi:10.1016/j.joen.2022.04.010 · Cited by 18

Consensus cluster analysis of apoptosis-related genes in patients with osteoarthritis and their correlation with immune cell infiltration

Yu, E., Zhang, M., Xu, G., Liu, X., & Yan, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1202758 · Cited by 18

Tumor vaccines: Toward multidimensional anti-tumor therapies

Tan, Y., Chen, H., Gou, X., Fan, Q., & Chen, J. (2023) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2023.2271334 · Cited by 18

Microenvironmental regulation and remodeling of breast cancer angiogenesis: from basic mechanisms to clinical therapeutic implications

Zhou, Z., Zhong, H., Wang, H., Wang, S., Kridis, W. B., Wang, R., Shen, K., Wang, Z., & Huang, R. (2025) · Discover Oncology · doi:10.1007/s12672-025-03797-1 · Cited by 17

The emerging importance of skull-brain interactions in traumatic brain injury

Goodman, G. W., Devlin, P., West, B. E., & Ritzel, R. M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1353513 · Cited by 19

Cuproptosis‐related gene DLAT is a biomarker of the prognosis and immune microenvironment of gastric cancer and affects the invasion and migration of cells

Peng, Y., Shi, R., Yang, S., & Zhu, J. (2024) · Cancer Medicine · doi:10.1002/cam4.70012 · Cited by 17

Posttransplant complications: molecular mechanisms and therapeutic interventions

Liu, X., Shen, J., Yan, H., Hu, J., Liao, G., Ding, L., Zhou, S., Zhang, J., Liao, J., Guo, Z., et al. (2024) · MedComm · doi:10.1002/mco2.669 · Cited by 17

Nanoparticles in Subunit Vaccines: Immunological Foundations, Categories, and Applications

Liang, J., Yao, L., Liu, Z., Chen, Y., Lin, Y., & Tian, T. (2024) · Small · doi:10.1002/smll.202407649 · Cited by 18

Sex differences in neuro(auto)immunity and chronic sciatic nerve pain

Linher‐Melville, K., Shah, A. A., & Singh, G. (2020) · Biology of Sex Differences · doi:10.1186/s13293-020-00339-y · Cited by 17

Are BET Inhibitors yet Promising Latency-Reversing Agents for HIV-1 Reactivation in AIDS Therapy?

Salahong, T., Schwartz, C., & Sungthong, R. (2021) · Viruses · doi:10.3390/v13061026 · Cited by 17

Inhibition of DYRK1B suppresses inflammation in allergic contact dermatitis model and Th1/Th17 immune response

Wongchang, T., Pluangnooch, P., Hongeng, S., Wongkajornsilp, A., Thumkeo, D., & Soontrapa, K. (2023) · Scientific Reports · doi:10.1038/s41598-023-34211-x · Cited by 16

Multi-omic analysis reveals dynamic changes of three-dimensional chromatin architecture during T cell differentiation

Zhang, G., Li, Y., & Wei, G. (2023) · Communications Biology · doi:10.1038/s42003-023-05141-1 · Cited by 16

Intranasally inoculated bacterium-like particles displaying porcine epidemic diarrhea virus S1 protein induced intestinal mucosal immune response in mice

Su, K., Wang, Y., Yuan, C., Zhang, Y., Li, Y., Li, T., & Song, Q. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1269409 · Cited by 16

Protective effect of low‐intensity pulsed ultrasound on immune checkpoint inhibitor-related myocarditis via fine-tuning CD4+ T-cell differentiation

Fu, S., Guo, Z., Xu, X., Li, Y., Choi, S. Y. C., Zhao, P., Shen, W., Gao, F., Wang, C., Chen, S., et al. (2024) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-023-03590-5 · Cited by 17

Generation of an Inhibitory NK Cell Subset by TGF-β1/IL-15 Polarization

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