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

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

Sallusto, F., Lenig, D., Förster, R., Lipp, M., & Lanzavecchia, A. (1999) · Nature · doi:10.1038/44385 · Cited by 5,846

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

Meijer, L., Nelson, D. J., Riazanski, V., Gabdoulkhakova, A. G., Héry-Arnaud, G., Berre, R. L., Loaëc, N., Oumata, N., Galons, H., Nowak, E., et al. (2016) · Journal of Innate Immunity · doi:10.1159/000444256 · Cited by 5,008

Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue

Masopust, D., Vezys, V., Marzo, A. L., & Lefrançois, L. (2001) · Science · doi:10.1126/science.1058867 · Cited by 1,952

Lineage relationship and protective immunity of memory CD8 T cell subsets

Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni889 · Cited by 1,864

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

Joshi, N. S., Cui, W., Chandele, A., Lee, H. K., Urso, D. R., Hagman, J., Gapin, L., & Kaech, S. M. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.010 · Cited by 1,861

Immunological memory and protective immunity: understanding their relation

Ahmed, R., & Gray, D. (1996) · Science · doi:10.1126/science.272.5258.54 · Cited by 1,775

Transcriptional control of effector and memory CD8+ T cell differentiation

Kaech, S. M., & Cui, W. (2012) · Nature Reviews Immunology · doi:10.1038/nri3307 · Cited by 1,628

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

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

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

Intlekofer, A. M., Takemoto, N., Wherry, E. J., Longworth, S. A., Northrup, J. T., Palanivel, V., Mullen, A. C., Gasink, C. R., Kaech, S. M., Miller, J. D., et al. (2005) · Nature Immunology · doi:10.1038/ni1268 · Cited by 1,293

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

Gebhardt, T., Wakim, L. M., Eidsmo, L., Reading, P. C., Heath, W. R., & Carbone, F. R. (2009) · Nature Immunology · doi:10.1038/ni.1718 · Cited by 1,157

Persistently primed microglia restrict the reactivation of latent cytomegalovirus at the expense of neuronal synaptic connectivityPreprint

Brizić, I., Mihalić, A., Kveštak, D., Lisnić, B., Krstanović, F., Hosseini, S., Sitnik, K., Golemac, M., Lisnić, V. J., Rashidi, A., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-5144336/v1 · Cited by 2

Type I interferon–driven lung pathology restricts T cell accumulation and motility during tuberculosisPreprint

Caouaille, M., Fromont, L., Shinkawa, T., Faucher, M., Hamid, A. I. A., Béhar, A., Mazères, S., Duvergé, Y., Decarpentrie, E., Lorreyte, Y., et al. (2025) · bioRxiv · doi:10.64898/2025.12.05.692491 · Cited by 1

Research progress of T cells in cholangiocarcinoma

Wang, Z., Dai, Y., Zhou, Y., Wang, Y., Chen, P., Li, Y., Zhang, Y., Wang, X., Hu, Y., Li, H., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1453344 · Cited by 2

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

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

Skin-Resident γδ T Cells Mediate Potent and Selective Antitumor Cytotoxicity through Directed Chemotactic Migration and Mobilization of Cytotoxic Granules

Yang, J., Liu, Z., Hu, X., Zhang, X., Huang, Y., Chen, Y., Chen, C., Shang, R., Tang, Y., Hu, W., et al. (2024) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2024.10.607 · Cited by 2

Herpes stromal keratitis erodes the establishment of tissue-resident memory T cell pool in HSV-1 infected corneas

Setia, M., Suvas, P. K., Rana, M., Chakraborty, A., & Suvas, S. (2024) · Mucosal Immunology · doi:10.1016/j.mucimm.2024.11.003 · Cited by 2

5‐ALA Assisted Surgery of Human Glioblastoma Samples Reveals an Enrichment of T Cells Expressing PD‐1 and CD103 in the Intermediate and Marginal Layers

Vanni, A., Matani, F., Bonaudo, C., Mazzoni, A., Capone, M., Lamacchia, G., Salvati, L., Bartoli, L., Francalanci, S., Petti, M., et al. (2025) · European Journal of Immunology · doi:10.1002/eji.202451681 · Cited by 2

Revealing the significance of tissue-resident memory T cells in lung adenocarcinoma through bioinformatic analysis and experimental validation

Li, Z., Tian, M. L., Yang, Y., Wang, Y., Zhang, L., Huang, F., Xiao, W., Yin, X., Lin, X., & Tian, Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1600863 · Cited by 2

S1P/S1PR4 promotes the differentiation of CD8+ tissue-resident memory T cells aggravating bile duct injury in biliary atresia

Sun, D., Wang, D., Jia, L., Wang, P., Sun, J., Zhao, J., Wu, F., Yang, W., Cai, B., Shi, X., et al. (2025) · Journal of Hepatology · doi:10.1016/j.jhep.2025.08.036 · Cited by 2

Design of Mucosal Vaccines Against Swine Enteric Coronaviruses: From Antigen Delivery to Immune Activation

Pan, Q., Sun, Y., Bai, H., Wang, W., Liu, B., Li, M., Gao, A., Zheng, D., Jiang, W., Hu, H., et al. (2025) · Transboundary and Emerging Diseases · doi:10.1155/tbed/3230453 · Cited by 3

pDCs amplify tissue-resident memory CD8+ T cell responses during viral reinfection

Hernández-García, E., Galán, M., Khouili, S. C., Moya-Ruiz, E., Redondo‐Urzainqui, A., Cueto, F. J., Martínez-Cano, S., Rodrigo-Tapias, M., Tomasello, E., Mañes, S., et al. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20250099 · Cited by 2

Tissue‐Resident Memory T Cells: Pioneering New Avenues in Cancer Immunotherapy

Xiao, Y., Yang, Q., & Sun, Z. (2025) · Cancer Medicine · doi:10.1002/cam4.71429 · Cited by 4

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

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

Neuroinflammation as a result of non‐neurotropic herpesvirus infection

Münz, C. (2026) · Immunology and Cell Biology · doi:10.1111/imcb.70108 · Cited by 2

Multiparametric analysis of vaccine-induced B and T cell responses for optimal evaluation of memory immune responses to Bordetella pertussis in children

Smet, J., Smits, K., Dirix, V., Vermeulen, F., Schutter, I. D., Buisman, A., Corbière, V., Locht, C., & Mascart, F. (2026) · Vaccine · doi:10.1016/j.vaccine.2026.128552 · Cited by 2

Lipid metabolic regulation of pathogenic type 2 immunity in the airway

Yagyu, H., Kiuchi, M., & Hirahara, K. (2026) · International Immunology · doi:10.1093/intimm/dxag015 · Cited by 2

Tissue‐Resident Memory T Cells in the Heart: An Emerging Role in Chronic Inflammation

Manandhar, P., Yan, A., & Moslehi, J. J. (2026) · Immunological Reviews · doi:10.1111/imr.70134 · Cited by 2

The Effects of Sex Hormones and Aging on the Mucosal Immune System in the Human Female Reproductive Tract and Implications for HIV Acquisition

Wira, C. R., Patel, M. V., Faber, G. P., Fu, B., & Rodríguez‐García, M. (2026) · American Journal of Reproductive Immunology · doi:10.1111/aji.70269 · Cited by 2

CD103+ T Cells May Be a Useful Biomarker in Borrmann Type 4 Gastric Cancer

Mori, T., Tanaka, H., Deguchi, S., Miki, Y., Yoshii, M., Tamura, T., Toyokawa, T., Lee, S., Muguruma, K., & Ohira, M. (2022) · Cancer Diagnosis & Prognosis · doi:10.21873/cdp.10121 · Cited by 2

New aspects of the pathogenesis of psoriasis

Zhukov, A. S., Патрушев, А. В., Khairutdinov, V. R., Samtsov, A. V., & Kryukov, E. V. (2022) · Vestnik dermatologii i venerologii · doi:10.25208/vdv1345 · Cited by 2

αβ and γδ T-cell responses to Epstein-Barr Virus: insights in immunocompetence, immune failure and therapeutic augmentation in transplant patients

Eiz‐Vesper, B., Ravens, S., & Maecker‐Kolhoff, B. (2023) · Current Opinion in Immunology · doi:10.1016/j.coi.2023.102305 · Cited by 2

CD100 boosts the inflammatory response in the challenge phase of allergic contact dermatitis in mice

Mraz, V., Funch, A. B., Jee, M. H., Gadsbøll, A.-S. Ø., Weber, J. F., Yeung, K., Lohmann, R. K. D., Hawkes, A. A., Ødum, N., Woetmann, A., et al. (2023) · Contact Dermatitis · doi:10.1111/cod.14414 · Cited by 2

Frequencies of activated T cell populations increase in breast milk of HCMV-seropositive mothers during local HCMV reactivation

Lazar, K., Pawelec, G., Goelz, R., Hamprecht, K., & Wistuba‐Hamprecht, K. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1258844 · Cited by 2

Location versus ID: what matters to lung-resident memory T cells?

Macedo, B. D. G., Masuda, M. Y., & da Silva, H. B. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1355910 · Cited by 2

Evolutionary diversity of CXCL16-CXCR6: Convergent substitutions and recurrent gene loss in sauropsids

Salve, B. G., Sharma, S., & Vijay, N. (2024) · Immunogenetics · doi:10.1007/s00251-024-01357-5 · Cited by 2

RSV Vaccine with Nanoparticle-Based Poly-Sorbitol Transporter (PST) Adjuvant Improves Respiratory Protection Against RSV Through Inducing Both Systemic and Mucosal Humoral Immunity

Jung, S.-M., Kim, S. J., Park, Y. C., Seo, E. S., Kim, C. G., Kim, T., Lee, S., Cho, E., Chang, J., Yun, C., et al. (2024) · Vaccines · doi:10.3390/vaccines12121354 · Cited by 2

Exploring molecular imaging to investigate immune checkpoint inhibitor-related toxicity

Peeters, E., van Genugten, E. A. J., Heskamp, S., de Vries, I. J. M., van Herpen, C., Koenen, H. J. P. M., Kneilling, M., van der Post, R. S., van Dop, W. A., Westdorp, H., et al. (2025) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2024-011009 · Cited by 2

Regulation of Mucosal Immunity in the Genital Tract: Balancing Reproduction and Protective Immunity

Hickey, D. K., Mulvey, P., Bryan, E. R., Trim, L. K., & Beagley, K. W. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-811924-2.00016-x · Cited by 2

Prologue: The “Long Arm” of DAMPs in Shaping Adaptive Immune Responses and Tissue Repairing Processes

Land, W. G. (2018) · Springer eBooks · doi:10.1007/978-3-319-78655-1_30 · Cited by 2

Cell-intrinsic regulation of peripheral memory-phenotype T cell frequencies

Chawla, A. S., Kanodia, P., Mukherjee, A., Jain, V., Kaur, G., Coshic, P., Chatterjee, K., Wadhwa, N., Natchu, U. C. M., Sopory, S., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0200227 · Cited by 2

Heterogeneity of lymphocytes as central operating units of the immune system

Buc, M. (2019) · Vnitřní lékařství · doi:10.36290/vnl.2019.021 · Cited by 2

Mapping Organism-wide Immune Responses

Mackay, L. K., & Prier, J. E. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.11.005 · Cited by 2

Tissue-resident CD8+ memory T cells in multiple sclerosis

Hohlfeld, R., Beltrán, E., Gerdes, L. A., & Dornmair, K. (2020) · Brain · doi:10.1093/brain/awaa352 · Cited by 2

Principles of Vaccinology and Vaccine Immune Response

Montoya, M., & Tchilian, E. Z. (2021) · doi:10.1002/9781119506287.ch2 · Cited by 2

Resident memory T cell precursors in tumor draining lymph nodes require type-1 IFN for optimal differentiationPreprint

Khatwani, N., Searles, T. G., Han, J., Messier, C. M., Mittal, N., Hawkes, A. R., Molodstov, A., Ramirez, D. E., Wilkins, O. M., Huang, Y. H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.02.551658 · Cited by 2

A stitch of CD9 saves nine: CD9+ tissue-resident memory T cells in Sjogren's syndrome and autoimmunity

Li, D., & Zhang, S. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiad096 · Cited by 2

Tissue-resident uterine regulatory T cells support fetal growthPreprint

Flórez, L. V., Fourcade, G., Darrasse-Jèze, G., Barennes, P., Gan-Fernandez, K., Régnier, P., Nehar-Belaid, D., Courau, T., Ruocco, M. G., Zacchigna, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.07.554921 · Cited by 2

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

Kirchmeier, D., Deng, Y., Rieble, L., Läderach, F., Schuhmachers, P., Valencia-Camargo, A. D., Murer, A., Caduff, N., Chatterjee, B., Chijioke, O., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.24.565960 · Cited by 2

Single-Cell Analysis Reveals Tissue-Specific T Cell Adaptation and Clonal Distribution Across the Human Gut-Liver-Blood AxisPreprint

Ran, R., Uslu, M., Siddiqui, M. F., Brubaker, D. K., & Trapečar, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.11.642626 · Cited by 2

CD8 + T cells are primed by cDC1 and exacerbate tau-mediated neurodegenerationPreprint

Hu, H., Lin, P. B., Zeng, C., Sharma, P., Li, Y., Jiang, H., Nulman, J., Ohara, R. A., Wu, T., Li, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.26.708260 · Cited by 2

Immune response to respiratory syncytial virus infection (Orthopneumovirus)

Nikonova, A. A., Isakov, I. Y., & Zverev, V. V. (2020) · Russian Journal of Infection and Immunity · doi:10.15789/2220-7619-irt-1300 · Cited by 1

The mammary gland is intolerant to bacterial intrusion

Rainard, P. (2024) · Exploration of Immunology · doi:10.37349/ei.2024.00128 · Cited by 1

Enzyme replacement therapy (ERT) combined with transient low-dose methotrexate (TLD-MTX) results in age- and disease-dependent immune profile changes in Infantile- vs. late-onset Pompe disease patients

Amirifar, P., Desai, A. K., Jung, S.-H., Young, S. P., Smith, P. B., Lu, C., Abar, B., Kishnani, P. S., & Burt, T. D. (2025) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2024.108637 · Cited by 1

Optimal therapy schedule of chimeric antigen receptor (CAR) T cell immunotherapy

Li, R., & Lei, J. (2025) · Mathematical Biosciences & Engineering · doi:10.3934/mbe.2025061 · Cited by 1

Different densities of Langerhans cells among oral squamous cell carcinoma, lip squamous cell carcinoma and oral potentially malignant disorders: Systematic review and network meta-analysis

Marega, N. A., Silva, L. P. B. D. C. E., de Oliveira, A. B., de Carli, R. L. B., Bufalino, A., Massucato, E. M. S., & Ferrisse, T. M. (2025) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2025.106372 · Cited by 1

The ability of memory CD8 T cell subsets to numerically and functionally recover following whole body irradiation is influenced by their history of cognate antigen exposures

Escue, E., Heidarian, M., Kannan, S. K., Rao, M., Arumugam, S. A., Harty, J. T., & Badovinac, V. P. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf194 · Cited by 1

Pattern of Regulatory T Cells, Resident Memory T Cells, and Exhausted T Cells in Human Pericardial Fluid Samples of Cardiovascular Patients

Érsek, B., Opra, J., Fekete, N., Ifju, M., Molnár, V., Bugyik, E., Pállinger, É., Székely, A. D., Radovits, T., Merkely, B. P., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26209852 · Cited by 1

TGF-β: A silent player regulating CD8 T cell memory

Zambrano-Romero, J. D., Ríos-Ramírez, D. B., García-Rasilla, V. Y., Ruiz-Medina, B. E., & Licona-Limón, P. (2025) · Clinical Immunology · doi:10.1016/j.clim.2025.110612 · Cited by 1

Loss of Dmrta1 alters CD8+ T cell activation and resistance to influenza virus infection

Kondo, H., Otsuka, K., Morimoto, J. O., Arimochi, H., Tsukumo, S., & Yasutomo, K. (2025) · ImmunoHorizons · doi:10.1093/immhor/vlaf054 · Cited by 1

Phenotypic Characterization and Prognostic Impact of CD103+ Tissue-Resident Memory T Cells in Diffuse Large B-cell Lymphoma

Savage, G., Milne, K., Collinge, B. J., Yin, Y., Loos, P., Warren, M. E., Laumont, C. M., Keith, D., Nelson, B. H., Venturutti, L., et al. (2025) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-25-0445 · Cited by 1

The orphan nuclear receptor NR4A3 is dispensable for resident memory CD8+ T-cell generation

Odagiu, L., Boulet, S., Sousa, D. M. D., Daudelin, J., & Labrecque, N. (2026) · ImmunoHorizons · doi:10.1093/immhor/vlaf087 · Cited by 1

From static pathology to dynamic immunity: immunological plasticity and histopathological remodeling in atopic dermatitis and psoriasis

Shen, W., Yao, Y., Ma, Y.-M., Xie, X.-L., Tang, S.-L., Wu, Y., Zhong, H., Li, Y., & Sun, H. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1770896 · Cited by 1

Early-life viral infection generates pathological tissue-resident memory cells that contribute to asthma-like disease

Brown, E., Lan, J., Parks, O. B., Fan, L., Lou, D., McCray, A., Mathews, L. R., Wardropper, A. J., Shull, A., Manni, M. L., et al. (2026) · JCI Insight · doi:10.1172/jci.insight.198712 · Cited by 1

Tissue-Resident Memory T Cells in Diseases: Pathogenic Mechanisms and Emerging Therapeutic Strategies

Xie, D., Tian, Y., Zhang, J., He, M., & Lu, L. W. A. G. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1014806 · Cited by 1

Exercise and tissue-resident memory T cells: from circulating numbers to spatial immune remodeling

Xie, E., He, Y., Cao, T., Li, C., & Wang, Z. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1822561 · Cited by 1

Activated immune cells present a lung interstitial‐to‐airway/alveolar cross‐compartment sharing pattern in severe pneumonia

Zhao, Y., Gong, L., Yu, H., Zhang, S., Yang, G., Wang, C., Wang, W., Cai, X., & Wang, Y. (2026) · Clinical and Translational Medicine · doi:10.1002/ctm2.70696 · Cited by 1

T‐Cell Biology in the Female Reproductive Tract: Relevance to HIV Infection

Shacklett, B. L., Ouattara, R., & Ferre, A. L. (2026) · American Journal of Reproductive Immunology · doi:10.1111/aji.70259 · Cited by 1

CCL3 and IL‐7 Synergistically Enhance CAR‐T Efficacy in Solid Tumors

Chen, H., Luo, X., Gao, H., Ke, Y., Zhan, Y. Q., Xu, X., Xiong, X., Wei, F., Yang, S., Liu, Z., et al. (2026) · Advanced Science · doi:10.1002/advs.75993 · Cited by 1

Rôle des lymphocytes T résidents mémoires dans la physiopathologie des eczémas allergiques de contact

Lefevre, M.-A., Nicolas, J., Vocanson, M., & Nosbaum, A. (2020) · Revue française d'allergologie · doi:10.1016/j.reval.2020.10.003 · Cited by 2

Effects of Astragalus Polysaccharides on CD8+ Tissue-Resident Memory T Cells in Mice with Herpes Simplex

Shi, L., Zhang, C., Liu, L., Xi, Z., & Chen, M. (2022) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2022/7729136 · Cited by 1

Adaptive immunity

Klenerman, P. (2020) · doi:10.1093/med/9780198746690.003.0040 · Cited by 1

Precision Nutrition in Allergy and Immune Function

Nel, A., & Heber, D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-15315-0.00005-5 · Cited by 1

Intranasal Immunization with a Recombinant Adenovirus Encoding Multi-Stage Antigens of Mycobacterium tuberculosis Preferentially Elicited CD8+ T Cell Immunity and Conferred a Superior Protection in the Lungs of Mice than Bacillus Calmette–Guerin

Wang, L., Kang, J., & Jiang, H. X. (2024) · Vaccines · doi:10.3390/vaccines12091022 · Cited by 1

A locally administered single-cycle influenza vaccine expressing a non-fusogenic stabilized hemagglutinin stimulates strong T-cell and neutralizing antibody immunity

Sadler, H. L., Rijal, P., Tan, T. K., & Townsend, A. (2025) · Journal of Virology · doi:10.1128/jvi.00331-24 · Cited by 1

Origin, function and role in the development of skin diseases CLA+T-lymphocytes

Патрушев, А. В., Samtsov, A. V., Nikitin, V. Y., Ivanov, A. M., Gumilevskaya, O. Р., Сухарев, А. В., & Александровна, С. И. (2018) · Vestnik dermatologii i venerologii · doi:10.25208/0042-4609-2018-94-3-20-29 · Cited by 1

Yin and yang of immunological memory in controlling infections: Overriding self defence mechanisms

Roy, R. K., Yadav, R., Jain, A., Tripathi, V., Jain, M., Singh, S. K., & Prakash, H. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.1912037 · Cited by 2

Biomarkers for Immune Modulatory Treatment in Head and Neck Squamous Cell Carcinoma (HNSCC)

Rischin, D. (2021) · Springer eBooks · doi:10.1007/978-3-030-63234-2_6 · Cited by 1

La mystérieuse Œsophagite à Eosinophiles garde encore quelques secrets

Vicari, A. P. (2017) · HEGEL - HEpato-GastroEntérologie Libérale · doi:10.3917/heg.071.0013 · Cited by 1

Vitiligo as a potential degenerative disease: from oxidative stress to cellular senescence

Wang, Y., Chi, J., Wang, T., Zhang, Y., Li, Z., Chen, J., Liu, H., & Li, Q. (2022) · Aging Pathobiology and Therapeutics · doi:10.31491/apt.2022.06.083 · Cited by 1

Assessing the appropriateness of medical care.

Hsu, J. (1998) · PubMed · Cited by 1

CD4 + T cells persist for years in the human small intestine and mediate robust T H 1 immunityPreprint

Bartolomé-Casado, R., Landsverk, O. J. B., Chauhan, S. K., Sætre, F., Hagen, K. T., Yaqub, S., Øyen, O. M., Horneland, R., Aandahl, E. M., Aabakken, L., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/863407 · Cited by 1

Role of herpes simplex virus 1 protein ICP47 in antigen presentation and pathogenesis

Velusamy, T. (2020) · ANU Open Research (Australian National University) · doi:10.25911/5e6f47d5d81d3 · Cited by 1

Immunologic Memory

Abolhassani, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818731-9.00002-1 · Cited by 2

Abnormal lymphatic S1P signaling aggravates lymphatic dysfunction and tissue inflammationPreprint

Kim, D., Tian, W., Wu, T.-H., Xiang, M., Vinh, R., Chang, J., Gu, S., Lee, S., Zhu, Y., Guan, T., et al. (2023) · medRxiv · doi:10.1101/2023.06.08.23291175 · Cited by 1

Immunological profiles in Lynch syndrome colorectal cancers are not specific to mismatch repair gene defectsPreprint

Helderman, N. C., Ijsselsteijn, M. E., Cabuta, M., van der Ploeg, M., van Wezel, T., Ahadova, A., Kloor, M., Morreau, H. M., Nielsen, M., & de Miranda, N. F. C. C. (2024) · medRxiv · doi:10.1101/2024.08.27.24311855 · Cited by 1

Systemic trafficking of mRNA lipid nanoparticle vaccine following intramuscular injection generates potent tissue-specific T cell responsePreprint

Wei, C. Y., Zhu, Y., Lu, X., Goodier, K. D., Yu, D., Liu, X., Choy, J., Calderón, A. T., Ma, J., Su, Y., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.21.649878 · Cited by 1

Tissue-specific clonal selection and differentiation of CD4⁺ T cells during infectionPreprint

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