Tissue-resident memory T cells: local specialists in immune defence

Two subsets of memory T lymphocytes with distinct homing potentials and effector functions

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Modulating Innate and Adaptive Immunity by (R)-Roscovitine: Potential Therapeutic Opportunity in Cystic Fibrosis

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Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue

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Lineage relationship and protective immunity of memory CD8 T cell subsets

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Inflammation Directs Memory Precursor and Short-Lived Effector CD8+ T Cell Fates via the Graded Expression of T-bet Transcription Factor

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Immunological memory and protective immunity: understanding their relation

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Transcriptional control of effector and memory CD8+ T cell differentiation

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

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Effector and memory CD8+ T cell fate coupled by T-bet and eomesodermin

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Memory T cells in nonlymphoid tissue that provide enhanced local immunity during infection with herpes simplex virus

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Medawar and the immunological paradox of pregnancy: in context

Male, V. H. (2020) · Oxford Open Immunology · doi:10.1093/oxfimm/iqaa006 · Cited by 30

Conversations that count: Cellular interactions that drive T cell fate

Duckworth, B. C., & Groom, J. R. (2021) · Immunological Reviews · doi:10.1111/imr.12945 · Cited by 32

Tissue-resident memory T cells in the kidney

Asada, N., Ginsberg, P., Gagliani, N., Mittrücker, H., & Panzer, U. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00927-7 · Cited by 33

Novel approaches for long-term lung transplant survival

Miller, C. L., O, J. M., Allan, J. S., & Madsen, J. C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.931251 · Cited by 30

Biomaterial Approaches for Understanding and Overcoming Immunological Barriers to Effective Oral Vaccinations

Frizzell, H., & Woodrow, K. A. (2020) · Advanced Functional Materials · doi:10.1002/adfm.201907170 · Cited by 30

Long-Lived Skin-Resident Memory T Cells Contribute to Concomitant Immunity in Cutaneous LeishmaniasisPreprint

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From PsO to PsA: the role of TRM and Tregs in psoriatic disease, a systematic review of the literature

Lobão, B., Lourenço, D., Giga, A., & Mendes‐Bastos, P. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1346757 · Cited by 30

Controlled release of ionic carrier hydrogels for sequential immunomodulation to facilitate stage-specific treatment of infectious wound

Lyu, Z., Wu, Y., Hu, F., Zheng, X., Ma, D., Xu, Z., Ding, Y., Liu, X., & Huo, S. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123376 · Cited by 29

Brain-Resident T Cells Following Viral Infection

Prasad, S., & Lokensgard, J. (2019) · Viral immunology · doi:10.1089/vim.2018.0084 · Cited by 29

Single mucosal vaccination targeting nucleoprotein provides broad protection against two lineages of influenza B virus

Kim, M. H., Kang, J.-O., Kim, J., Jung, H. E., Lee, H. K., & Chang, J. (2019) · Antiviral Research · doi:10.1016/j.antiviral.2019.01.002 · Cited by 29

Metabolic regulation of T lymphocyte motility and migration

Vuononvirta, J., Marelli‐Berg, F. M., & Poobalasingam, T. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100888 · Cited by 32

Multiple Levels of Immunological Memory and Their Association with Vaccination

Bugya, Z., Prechl, J., Szénási, T., Nemes, É., Bácsi, A., & Koncz, G. (2021) · Vaccines · doi:10.3390/vaccines9020174 · Cited by 30

Immune Checkpoint Blockade and Skin Toxicity Pathogenesis

Ma, B., & Anandasabapathy, N. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2021.06.040 · Cited by 30

Skin and heart allograft rejection solely by long-lived alloreactive T RM cells in skin of severe combined immunodeficient mice

Tian, Q., Zhang, Z., Tan, L., Yang, F., Xu, Y., Guo, Y., Wei, D., Wu, C., Cao, P., Ji, J., et al. (2022) · Science Advances · doi:10.1126/sciadv.abk0270 · Cited by 29

Tissue-resident memory T cells in chronic liver diseases: Phenotype, development and function

Li, Y., You, Z., Tang, R., & Ma, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.967055 · Cited by 30

Lung-resident CD69+ST2+ TH2 cells mediate long-term type 2 memory to inhaled antigen in mice

Kobayashi, T., Iijima, K., Matsumoto, K., Lama, J. K., & Kita, H. (2023) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2023.01.016 · Cited by 30

Diminished CD103 (aEb7) Expression on Resident T cells from the Female Genital Tract of HIV-positive women

Moylan, D. C., Goepfert, P., Kempf, M.-C., Saag, M. S., Richter, H. E., Mestecky, J. F., & Sabbaj, S. (2017) · Pathogens and Immunity · doi:10.20411/pai.v1i2.166 · Cited by 29

Zymosan by-passes the requirement for pulmonary antigen encounter in lung tissue-resident memory CD8+ T cell development

Caminschi, I., Lahoud, M. H., Pizzolla, A., & Wakim, L. M. (2019) · Mucosal Immunology · doi:10.1038/s41385-018-0124-2 · Cited by 31

Targeting resident memory T cell immunity culminates in pulmonary and systemic protection against Brucella infection

Wang, H., Hoffman, C. A., Yang, X., Clapp, B., & Pascual, D. W. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008176 · Cited by 30

Liver-resident memory T cells: life in lockdown

Pallett, L. J., & Maini, M. K. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00932-w · Cited by 28

Epstein-Barr virus infection induces tissue-resident memory T cells in mucosal lymphoid tissues

Kirchmeier, D., Deng, Y., Rieble, L., Böni, M., Läderach, F., Schuhmachers, P., Valencia-Camargo, A. D., Murer, A., Caduff, N., Chatterjee, B., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.173489 · Cited by 29

Transcription factor BACH2 shapes tissue-resident memory T cell programs to promote HIV-1 persistence

Wei, Y., Ma, H. K., Wong, M. E., Back, H., Papasavvas, E., Mounzer, K., Aberra, F. N., Morgenstern, R., Tebas, P., Konnikova, L., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.07.022 · Cited by 34

Oral typhoid vaccine Ty21a elicits antigen-specific resident memory CD4+ T cells in the human terminal ileum lamina propria and epithelial compartments

Booth, J. S., Goldberg, E., Barnes, R. S., Greenwald, B. D., & Sztein, M. B. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02263-6 · Cited by 28

Rapid detection of SARS‐CoV‐2‐specific memory T‐cell immunity in recovered COVID‐19 cases

Lineburg, K. E., Srihari, S., Altaf, M., Swaminathan, S., Panikkar, A., Raju, J., Crooks, P., Ambalathingal, G. R., Martins, J. P., Matthews, K. K., et al. (2020) · Clinical & Translational Immunology · doi:10.1002/cti2.1219 · Cited by 27

The Tumor Microenvironment and Immunotherapy of Oropharyngeal Squamous Cell Carcinoma

Welters, M. J. P., Santegoets, S. J. A. M., & van der Burg, S. H. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.545385 · Cited by 27

Tissue-resident memory T cells in the multiple sclerosis brain and their relationship to Epstein-Barr virus infected B cells

Serafini, B., Rosicarelli, B., Veroni, C., & Aloisi, F. (2023) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2023.578036 · Cited by 28

Clinically Relevant Reactivation of Polyomavirus BK (BKPyV) in HLA-A02-Positive Renal Transplant Recipients Is Associated with Impaired Effector-Memory Differentiation of BKPyV-Specific CD8+ T Cells

van Aalderen, M. C., Remmerswaal, E. B. M., Heutinck, K. M., ten Brinke, A., Feltkamp, M. C. W., van der Weerd, N. C., der Pant, K. A. M. I. V. D., Bemelman, F. J., van Lier, R. A. W., & ten Berge, I. J. M. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005903 · Cited by 28

CXCR6 + ST2 + memory T helper 2 cells induced the expression of major basic protein in eosinophils to reduce the fecundity of helminth

Obata‐Ninomiya, K., Ishiwata, K., Hisanobu, N., Endo, Y., Ichikawa, T., Onodera, A., Hirahara, K., Okamoto, Y., Kanuka, H., & Nakayama, T. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714731115 · Cited by 29

Epidermal Fatty Acid-Binding Protein: A Novel Marker in the Diagnosis of Dry Eye Disease in Sjögren Syndrome

Shinzawa, M., Doğru, M., Den, S., Ichijima, T., Higa, K., Kojima, T., Seta, N., Nomura, T., Tsubota, K., & Shimazaki, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19113463 · Cited by 28

The Fate Choice Between Effector and Memory T Cell Lineages: Asymmetry, Signal Integration, and Feedback to Create Bistability

Backer, R. A., Hombrink, P., Helbig, C., & Amsen, D. (2018) · Advances in immunology · doi:10.1016/bs.ai.2017.12.003 · Cited by 27

T Cell–Intrinsic CX3CR1 Marks the Most Differentiated Effector CD4+ T Cells, but Is Largely Dispensable for CD4+ T Cell Responses during Chronic Viral Infection

Batista, N. V., Chang, Y.-H., Chu, K.-L., Wang, K. C., Girard, M., & Watts, T. H. (2020) · ImmunoHorizons · doi:10.4049/immunohorizons.2000059 · Cited by 27

CD8+ and CD4+ T Cells Infiltrate into the Brain during Plasmodium berghei ANKA Infection and Form Long-Term Resident Memory

Ghazanfari, N., Gregory, J. L., Devi, S., Fernandez-Ruiz, D., Beattie, L., Mueller, S. N., & Heath, W. (2021) · Journal of Immunology · doi:10.4049/jimmunol.2000773 · Cited by 27

Characteristics of CD8+ and CD4+ Tissue-Resident Memory Lymphocytes in the Gastrointestinal Tract

Li, P., Zhang, Y., Xu, Y., Cao, H., & Li, L. (2022) · Advanced Gut & Microbiome Research · doi:10.1155/2022/9157455 · Cited by 28

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

Long-term maintenance of the influenza-specific cross-reactive memory CD4+ T-cell responses following repeated annual influenza vaccination

Trieu, M.-C., Zhou, F., Lartey, S. L., Jul‐Larsen, Å., Mjaaland, S., Sridhar, S., & Cox, R. J. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw619 · Cited by 27

The TNF Superfamily Molecule LIGHT Promotes the Generation of Circulating and Lung-Resident Memory CD8 T Cells following an Acute Respiratory Virus Infection

Desai, P., Tahiliani, V., Hutchinson, T. E., Dastmalchi, F., Stanfield, J., Abboud, G., Thomas, P. G., Ware, C. F., Song, J. J., Croft, M., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701499 · Cited by 27

Cytomegalovirus infection and progressive differentiation of effector-memory T cells

Pardieck, I. N., Beyrend, G., Redeker, A., & Arens, R. (2018) · F1000Research · doi:10.12688/f1000research.15753.1 · Cited by 26

Vaccine vectors: the bright side of cytomegalovirus

Méndez, A. C., Rodríguez-Rojas, C., & Val, M. D. (2019) · Medical Microbiology and Immunology · doi:10.1007/s00430-019-00597-7 · Cited by 27

Resident Memory T Cells and Their Effect on Cancer

Craig, D. J., Creeden, J. F., Einloth, K. R., Gillman, C. E., Stanbery, L., Hamouda, D., Edelman, G. M., Dworkin, L. D., & Nemunaitis, J. J. (2020) · Vaccines · doi:10.3390/vaccines8040562 · Cited by 27

Nanovaccines for Advancing Long-Lasting Immunity against Infectious Diseases

Gao, X., Wang, X., Li, S., Rahman, M. S. U., Xu, S., & Liu, Y. (2023) · ACS Nano · doi:10.1021/acsnano.3c07741 · Cited by 27

Immune Response Resetting in Ongoing Sepsis

Nowill, A. E., Fornazin, M. C., Spago, M. C., Neto, V. D., Pinheiro, V. R. P., Alexandre, S. S. S., Moraes, E. O., Souza, G. H. M. F., Eberlin, M. N., Marques, L. A., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900104 · Cited by 25

B and T Cell Immunity in Tissues and Across the Ages

Booth, J. S., & Toapanta, F. R. (2021) · Vaccines · doi:10.3390/vaccines9010024 · Cited by 30

Tumor immunotherapy: Mechanisms and clinical applications

Nong, C., Guan, P., Li, L., Zhang, H., & Hu, H. (2022) · MedComm – Oncology · doi:10.1002/mog2.8 · Cited by 27

Tissue-resident and innate-like T cells in patients with advanced chronic liver disease

Ibidapo-Obe, O., & Bruns, T. (2023) · JHEP Reports · doi:10.1016/j.jhepr.2023.100812 · Cited by 25

Single-cycle influenza virus vaccine generates lung CD8 + Trm that cross-react against viral variants and subvert virus escape mutants

Zheng, M. Z. M., Tan, T. K., Villalón‐Letelier, F., Lau, H., Deng, Y., Fritzlar, S., Valkenburg, S. A., Gu, H., Poon, L. L. M., Reading, P. C., et al. (2023) · Science Advances · doi:10.1126/sciadv.adg3469 · Cited by 24

Exercise rejuvenates microglia and reverses T cell accumulation in the aged female mouse brain

Chauquet, S., Willis, E. F., Grice, L. F., Harley, S. B. R., Powell, J. E., Wray, N. R., Nguyen, Q. H., Ruitenberg, M. J., Shah, S. H., & Vukovic, J. (2024) · Aging Cell · doi:10.1111/acel.14172 · Cited by 29

Citrobacter rodentium Induces Tissue-Resident Memory CD4 + T Cells

Bishu, S., Hou, G., Zaatari, M. E., Bishu, S. R., Popke, D. S., Zhang, M., Grasberger, H., Zou, W., Stidham, R. W., Higgins, P., et al. (2019) · Infection and Immunity · doi:10.1128/iai.00295-19 · Cited by 24

Gastric Subserous Vaccination With Helicobacter pylori Vaccine: An Attempt to Establish Tissue-Resident CD4+ Memory T Cells and Induce Prolonged Protection

Liu, W., Zeng, Z., Luo, S., Hu, C., Xu, N., Huang, A., Zheng, L., Sundberg, E. J., Xi, T., & Xing, Y. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01115 · Cited by 25

Intestinal CD8+ T cell responses are abundantly induced early in human development but show impaired cytotoxic effector capacities

Schreurs, R., Sagebiel, A. F., Steinert, F. L., Highton, A. J., Klarenbeek, P. L., Drewniak, A., Bakx, R., The, S., Ribeiro, C. M. S., Perez, D. R., et al. (2021) · Mucosal Immunology · doi:10.1038/s41385-021-00382-x · Cited by 25

Local and Systemic T Cell Immunity in Fighting Pig Viral and Bacterial Infections

Gerner, W., Mair, K. H., & Schmidt, S. (2021) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-013120-044226 · Cited by 25

Systemic priming and intranasal booster with a BcfA-adjuvanted acellular pertussis vaccine generates CD4+ IL-17+ nasal tissue resident T cells and reduces B. pertussis nasal colonization

Yount, K. S., Hall, J. M., Caution, K., Shamseldin, M. M., Guo, M., Marion, K., Fullen, A. R., Huang, Y., Maynard, J. A., Quataert, S. A., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1181876 · Cited by 25

A single-cell transcriptional landscape of immune cells shows disease-specific changes of T cell and macrophage populations in human achalasia

Liu, Z., Dai, H., Yao, L., Chen, W., Wang, Y., Ma, L., Li, X., Lin, S., He, M., Gao, P., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39750-5 · Cited by 26

A Subset of CCL25-Induced Gut-Homing T Cells Affects Intestinal Immunity to Infection and Cancer

Fu, H., Jangani, M., Parmar, A., Wang, G., Coe, D., Spear, S., Sandrock, I., Capasso, M., Coles, M. C., Cornish, G. H., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00271 · Cited by 25

CD4 T cells are required for maintenance of CD8 TRM cells and virus control in the brain of MCMV-infected newborn mice

Brizić, I., Hiršl, L., Šustić, M., Golemac, M., Britt, W. J., Krmpotić, A., & Jonjić, S. (2019) · Medical Microbiology and Immunology · doi:10.1007/s00430-019-00601-0 · Cited by 24

Pivotal role of tissue-resident memory lymphocytes in the control of mucosal infections: can mucosal vaccination induce protective tissue-resident memory T and B cells?

Longet, S., & Paul, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1216402 · Cited by 24

Tissue-resident memory T cells in protective immunity to influenza virus

Lee, S., Yeung, K., & Watts, T. H. (2024) · Current Opinion in Virology · doi:10.1016/j.coviro.2024.101397 · Cited by 24

Dynamic landscapes and protective immunity coordinated by influenza-specific lung-resident memory CD8+ T cells revealed by intravital imaging

van de Wall, S., Anthony, S. M., Hancox, L. S., Pewe, L. L., Langlois, R. A., Zehn, D., Badovinac, V. P., & Harty, J. T. (2024) · Immunity · doi:10.1016/j.immuni.2024.06.016 · Cited by 24

Decreased Frequency of Intestinal CD39+ γδ+ T Cells With Tissue-Resident Memory Phenotype in Inflammatory Bowel Disease

Libera, J., Wittner, M., Kantowski, M., Woost, R., Eberhard, J. M., de Heer, J., Reher, D., Huber, S., Haag, F., & Wiesch, J. S. Z. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.567472 · Cited by 24

Runx proteins and transcriptional mechanisms that govern memory CD8 T cell development

Pipkin, M. E. (2021) · Immunological Reviews · doi:10.1111/imr.12954 · Cited by 24

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

T cell interaction with activated endothelial cells primes for tissue-residency

Wienke, J., Veldkamp, S. R., Struijf, E. M., Yengej, F. A. Y., van der Wal, M., van Royen‐Kerkhof, A., & van Wijk, F. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.827786 · Cited by 25

CD8+ T-cell immunity orchestrated by iNKT cells

Qin, Y., Bao, X., & Zheng, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1109347 · Cited by 24

Depleting CD103+ resident memory T cells in vivo reveals immunostimulatory functions in oral mucosa

Stolley, J. M., Scott, M. C., Joag, V., Dale, A. J., Johnston, T. S., Saavedra, F. M., Gavil, N. V., Lotfi‐Emran, S., Soerens, A. G., Weyu, E., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20221853 · Cited by 24

Local γδ T cells: translating promise to practice in cancer immunotherapy

Zlatareva, I., & Wu, Y. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02303-0 · Cited by 25

Itaconate inhibits CD103+ TRM cells and alleviates hepatobiliary injury in mouse models of primary sclerosing cholangitis

Li, Y., Li, B., Xiao, X., Qian, Q., Wang, R., Lyu, Z., Chen, R., Cui, N., Ou, Y., Pu, X., et al. (2023) · Hepatology · doi:10.1097/hep.0000000000000549 · Cited by 24

Differentiating Immune Cell Targets in Gut-Associated Lymphoid Tissue for HIV Cure

Khan, S., Telwatte, S., Trapečar, M., Yukl, S. A., & Sanjabi, S. (2017) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2017.0153 · Cited by 27

CD103+CD8+ T lymphocytes in non-small cell lung cancer are phenotypically and functionally primed to respond to PD-1 blockade

Wang, P., Huang, B. Y., Gao, Y., Yang, J., Liang, Z., Zhang, N., Fu, X., & Li, L. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.02.002 · Cited by 24

Systemically Administered Sindbis Virus in Combination with Immune Checkpoint Blockade Induces Curative Anti-tumor Immunity

Scherwitzl, I., Hurtado, A. M., Pierce, C. M., Vogt, S., Pampeno, C., & Meruelo, D. (2018) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2018.04.004 · Cited by 25

Dietary Regulation of Memory T Cells

Collins, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124363 · Cited by 25

Engineering Vaccines for Tissue‐Resident Memory T Cells

Knight, F. C., & Wilson, J. T. (2021) · Advanced Therapeutics · doi:10.1002/adtp.202000230 · Cited by 24

Transcriptional programming of CD4 + T RM differentiation in viral infection balances effector- and memory-associated gene expression

Nguyen, Q., Takehara, K. K., Deng, T. Z., O’Shea, S., Heeg, M., Omilusik, K. D., Milner, J. J., Quon, S., Pipkin, M. E., Choi, J., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.abq7486 · Cited by 23

SARS-CoV-2 spike-specific nasal-resident CD49a+CD8+ memory T cells exert immediate effector functions with enhanced IFN-γ production

Rha, M., Kim, G., Lee, S., Kim, J., Jeong, Y., Jung, C. M., Noh, H. E., Noh, J. Y., Kim, Y. M., Cho, H., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52689-5 · Cited by 24

Barrier Integrity and Immunity: Exploring the Cutaneous Front Line in Health and Disease

Fukuda, K., Ito, Y., & Amagai, M. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082323-030832 · Cited by 28

Local Antigen Encounter Is Essential for Establishing Persistent CD8+ T-Cell Memory in the CNS

Schøller, A. S., Fonnes, M. K., Nazerai, L., Christensen, J. P., & Thomsen, A. R. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00351 · Cited by 23

Single-Cell Analysis Reveals Characterization of Infiltrating T Cells in Moderately Differentiated Colorectal Cancer

Yang, X., Quan, Q., Pan, Y., Zhou, Q., Wu, Y., Zhuang, J., Xu, J., Pan, M., & Han, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.620196 · Cited by 24

Nanovaccines Mediated Subcutis‐to‐Intestine Cascade for Improved Protection against Intestinal Infections

Zhong, X., Du, G., Wang, X., Ou, Y., Wang, H., Zhu, Y., Hao, X., Xie, Z., Zhang, Y., Gong, T., et al. (2021) · Small · doi:10.1002/smll.202105530 · Cited by 23

Photoacoustic mediated multifunctional tumor antigen trapping nanoparticles inhibit the recurrence and metastasis of ovarian cancer by enhancing tumor immunogenicity

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