The DOI matches its Crossref record; 123 of the 124 references it cites were found in a registry or an index.
CD8+ T-cells infiltrate Alzheimer’s disease brains and regulate neuronal- and synapse-related gene expression in APP-PS1 transgenic mice
Open accessAbstract
Neuroinflammation is a major contributor to disease progression in Alzheimer’s disease (AD) and is characterized by the activity of brain resident glial cells, in particular microglia cells. However, there is increasing evidence that peripheral immune cells infiltrate the brain at certain stages of AD progression and shape disease pathology. We recently identified CD8+ T-cells in the brain parenchyma of APP-PS1 transgenic mice being tightly associated with microglia as well as with neuronal structures. The functional role of CD8+ T-cells in the AD brain is however completely unexplored. Here, we demonstrate increased numbers of intra-parenchymal CD8+ T-cells in human AD post-mortem hippocampus, which was replicated in APP-PS1 mice. Also, aged WT mice show a remarkable infiltration of CD8+ T-cells, which was more pronounced and had an earlier onset in APP-PS1 mice. To address their functional relevance in AD, we successfully ablated the pool of CD8+ T-cells in the blood, spleen and brain from 12 months-old APP-PS1 and WT mice for a total of 4 weeks using an anti-CD8 antibody treatment. While the treatment at this time of disease stage did neither affect the cognitive outcome nor plaque pathology, RNAseq analysis of the hippocampal transcriptome from APP-PS1 mice lacking CD8+ T-cells revealed highly altered neuronal- and synapse-related gene expression including an up-regulation for neuronal immediate early genes (IEGs) such as the Activity Regulated Cytoskeleton Associated Protein (Arc) and the Neuronal PAS Domain Protein 4 (Npas4). Gene ontology enrichment analysis illustrated that the biological processes “regulation of neuronal synaptic plasticity” and the cellular components “postsynapses” were over-represented upon CD8+ T-cell ablation. Additionally, Kegg pathway analysis showed up-regulated pathways for “calcium signaling”, “long-term potentiation”, “glutamatergic synapse” and “axon guidance”. Therefore, we conclude that CD8+ T-cells infiltrate the aged and AD brain and that brain CD8+ T-cells might directly contribute to neuronal dysfunction in modulating synaptic plasticity. Further analysis will be essential to uncover the exact mechanism of how CD8+ T-cells modulate the neuronal landscape and thereby contribute to AD pathology.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Dysfunctional meninges also represent an important contributor to neuroinflammation in neurodegenerative diseases by acting as a checkpoint for T-cell infiltration.”
From Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases (2024) · cites this paper as [684]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400
clusterProfiler: an R Package for Comparing Biological Themes Among Gene Clusters
Yu, G., Wang, L.-G., Han, Y., & He, Q.-Y. (2012) · OMICS: A Journal of Integrative Biology · doi:10.1089/omi.2011.0118 · Cited by 36,259
HTSeq—a Python framework to work with high-throughput sequencing data
Anders, S., Pyl, P. T., & Huber, W. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btu638 · Cited by 21,464
Neuropathological stageing of Alzheimer-related changes.
Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
Edgar, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.207 · Cited by 13,288
REVIGO summarizes and visualizes long lists of gene ontology terms
Supek, F., Bošnjak, M., Škunca, N., & Šmuc, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021800 · Cited by 6,264
Neuroinflammation in Alzheimer's disease
Heneka, M. T., Carson, M. J., Khoury, J. E., Landreth, G. E., Brosseron, F., Feinstein, D. L., Jacobs, A. H., Wyss-Coray, T., Vitorica, J., Ransohoff, R. M., et al. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)70016-5 · Cited by 6,226
Self-citationThe amyloid hypothesis of Alzheimer's disease at 25 years
Selkoe, D. J., & Hardy, J. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201606210 · Cited by 6,164
Flagged first, then by citations
1 of the 124 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases
Loh, J. S., Mak, W. Q., Tan, L. K. S., Ng, C. X., Chan, H. H., Yeow, S. H., Foo, J. B., Ong, Y. S., How, C. W., & Khaw, K. Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01743-1 · Cited by 1,193
Zhang, J., Zhang, Y., Wang, J., Xia, Y., Zhang, J., & Chen, L. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01911-3 · Cited by 1,138
Emerging roles of innate and adaptive immunity in Alzheimer’s disease
Chen, X., & Holtzman, D. M. (2022) · Immunity · doi:10.1016/j.immuni.2022.10.016 · Cited by 297
The neuroimmune axis of Alzheimer’s disease
Jorfi, M., Maaser‐Hecker, A., & Tanzi, R. E. (2023) · Genome Medicine · doi:10.1186/s13073-023-01155-w · Cited by 313
Jorfi, M., Park, J., Hall, C. K., Lin, C.-C. J., Chen, M., von Maydell, D., Kruskop, J. M., Kang, B., Choi, Y., Prokopenko, D., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01415-3 · Cited by 214
CXCR6 orchestrates brain CD8+ T cell residency and limits mouse Alzheimer’s disease pathology
Su, W., Saravia, J., Risch, I., Rankin, S. L., Guy, C. S., Chapman, N. M., Shi, H., Sun, Y., Anil, K. C., Li, W., et al. (2023) · Nature Immunology · doi:10.1038/s41590-023-01604-z · Cited by 222
Schonhoff, A. M., Figge, D. A., Williams, G. P., Jurkuvenaite, A., Gallups, N. J., Childers, G. M., Webster, J. M., Standaert, D. G., Goldman, J. E., & Harms, A. S. (2023) · Nature Communications · doi:10.1038/s41467-023-39060-w · Cited by 161
Blood-to-brain communication in aging and rejuvenation
Bieri, G., Schroer, A. B., & Villeda, S. A. (2023) · Nature Neuroscience · doi:10.1038/s41593-022-01238-8 · Cited by 156
Yang, S., Wang, L., Zeng, Y., Wang, Y., Pei, T., Xie, Z., Xiong, Q., Wei, H., Li, W., Li, J., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154762 · Cited by 153
Kann, O., Almouhanna, F., & Chausse, B. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.10.007 · Cited by 155
Brain-spleen axis in health and diseases: A review and future perspective
Wei, Y., Wang, T., Liao, L., Fan, X., Chang, L., & Hashimoto, K. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.02.008 · Cited by 134
Microglia in Alzheimer’s Disease in the Context of Tau Pathology
Perea, J. R., Bolós, M., & Ávila, J. (2020) · Biomolecules · doi:10.3390/biom10101439 · Cited by 134
Neuroinflammation in Alzheimer’s disease: insights from peripheral immune cells
Zhang, Q., Yang, G., Luo, Y., Jiang, L., Chi, H., & Tian, G. (2024) · Immunity & Ageing · doi:10.1186/s12979-024-00445-0 · Cited by 138
The role of the immune system in Alzheimer’s disease
Wu, K., Zhang, Y.-R., Huang, Y., Dong, Q., Tan, L., & Yu, J. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101409 · Cited by 119
Dysregulation of Systemic Immunity in Aging and Dementia
Lutshumba, J., Nikolajczyk, B. S., & Bachstetter, A. D. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.652111 · Cited by 104
Expression of Immune Related Genes and Possible Regulatory Mechanisms in Alzheimer’s Disease
Lu, Y., Li, K., Hu, Y., & Wang, X. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.768966 · Cited by 93
Zhao, Y., Zheng, Q., Hong, Y., Gao, Y., Hu, J., Lang, M., Zhang, H., Zhou, Y., Luo, H., Zhang, X., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01352-1 · Cited by 87
Peripheral and central neuroimmune mechanisms in Alzheimer’s disease pathogenesis
Zhang, S., Gao, Y., Zhao, Y., Huang, T. Y., Zheng, Q., & Wang, X. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00812-5 · Cited by 78
Common Peripheral Immunity Mechanisms in Multiple Sclerosis and Alzheimer's Disease
Rossi, B., Santos-Lima, B., Terrabuio, E., Zenaro, E., & Constantin, G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.639369 · Cited by 84
Neuroimmune contributions to Alzheimer’s disease: a focus on human data
Haage, V., & De Jager, P. L. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01637-0 · Cited by 74
Altendorfer, B., Unger, M. S., Poupardin, R., Hoog, A., Asslaber, D., Gratz, I. K., Mrowetz, H., Benedetti, A., de Sousa, D. M. B., Greil, R., et al. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100737 · Cited by 77
Self-citationRegulators of cholinergic signaling in disorders of the central nervous system
Winek, K., Soreq, H., & Meisel, A. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15332 · Cited by 75
The impact of neuroinflammation on neuronal integrity
Tastan, B., & Heneka, M. T. (2024) · Immunological Reviews · doi:10.1111/imr.13419 · Cited by 81
Self-citationRole of Peripheral Immune Cells-Mediated Inflammation on the Process of Neurodegenerative Diseases
Yang, Q., Wang, G., & Zhang, F. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.582825 · Cited by 73
Roles of Cytokines in Alzheimer’s Disease
Chen, Z., Balachandran, Y. L., Chong, W. P., & Chan, K. W. Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115803 · Cited by 75
How the immune system shapes neurodegenerative diseases
Mason, H. D., & McGavern, D. B. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.08.001 · Cited by 67
Role of Neuron and Glia in Alzheimer’s Disease and Associated Vascular Dysfunction
Bandyopadhyay, S. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.653334 · Cited by 64
Immunotherapies for Alzheimer’s Disease—A Review
Valiukas, Z., Ephraim, R., Tangalakis, K., Davidson, M., Apostolopoulos, V., & Feehan, J. (2022) · Vaccines · doi:10.3390/vaccines10091527 · Cited by 70
Immune mechanisms and shared immune targets in neurodegenerative diseases
Weiner, H. L. (2024) · Nature Reviews Neurology · doi:10.1038/s41582-024-01046-7 · Cited by 72
Garofalo, S., Cocozza, G., Bernardini, G., Savage, J. C., Raspa, M., Aronica, E., Tremblay, M., Ransohoff, R. M., Santoni, A., & Limatola, C. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.06.004 · Cited by 59
Batterman, K. V., Cabrera, P. E., Moore, T. L., & Rosene, D. L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.607691 · Cited by 53
Modeling the neuroimmune system in Alzheimer’s and Parkinson’s diseases
Balestri, W., Sharma, R., da Silva, V. A., Bobotis, B. C., Curle, A. J., Kothakota, V., Kalantarnia, F., Hangad, M. V., Hoorfar, M., Jones, J., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03024-8 · Cited by 55
Oberlin, L. E., Erickson, K. I., Mackey, R. H., Klunk, W. E., Aizenstein, H. J., Lopresti, B. J., Kuller, L. H., López, O. L., & Snitz, B. E. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.03.015 · Cited by 56
Adaptive immune changes associate with clinical progression of Alzheimer’s disease
van Olst, L., Kamermans, A., Halters, S., van der Pol, S. M. A., Rodríguez, E., Verberk, I. M. W., Verberk, S. G. S., Wessels, D. W. R., Rodriguez-Mogeda, C., Verhoeff, J., et al. (2024) · Molecular Neurodegeneration · doi:10.1186/s13024-024-00726-8 · Cited by 61
Alzheimer’s disease pathogenesis: standing at the crossroad of lipid metabolism and immune response
Wang, Z., Zhang, L., & Qin, C. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00857-6 · Cited by 60
Michael, J., Zirknitzer, J., Unger, M. S., Poupardin, R., Rieß, T., Paiement, N., Zerbe, H., Hutter‐Paier, B., Reitsamer, H. A., & Aigner, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052782 · Cited by 50
Self-citationMicroglial MHC-I induction with aging and Alzheimer’s is conserved in mouse models and humans
Kellogg, C. M., Pham, K. D., Machalinski, A. H., Porter, H. L., Blankenship, H. E., Tooley, K. B., Stout, M. B., Rice, H. C., Sharpe, A. L., Beckstead, M. J., et al. (2023) · GeroScience · doi:10.1007/s11357-023-00859-6 · Cited by 51
The role of the CD8+ T cell compartment in ageing and neurodegenerative disorders
Terrabuio, E., Zenaro, E., & Constantin, G. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1233870 · Cited by 51
CD8+ T cells in brain injury and neurodegeneration
Zhang, Z., Duan, Z., & Cui, Y. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1281763 · Cited by 51
Ghosh, P., Singh, R. B., Ganeshpurkar, A., Pokle, A. V., Singh, R. B., Singh, S. K., & Kumar, A. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105212 · Cited by 44
Crossing borders in Alzheimer’s disease: A T cell’s perspective
van Olst, L., Coenen, L., Nieuwland, J. M., Rodriguez-Mogeda, C., de Wit, N. M., Kamermans, A., Middeldorp, J., & de Vries, H. E. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114398 · Cited by 45
Afsar, A., Castro, M. D. C. C., Soladogun, A. S., & Li, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087258 · Cited by 45
The Role of Sphingolipids and Specialized Pro-Resolving Mediators in Alzheimer’s Disease
de Wit, N. M., Mol, K., Rodríguez‐Lorenzo, S., de Vries, H. E., & Kooij, G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.620348 · Cited by 40
Immune Regulatory Functions of Macrophages and Microglia in Central Nervous System Diseases
Poppell, M., Hammel, G., & Ren, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065925 · Cited by 39
The anti-inflammatory effects of itaconate and its derivatives in neurological disorders
Kong, X., Xu, L., Mou, Z., Lyu, W., Shan, K., Wang, L., Liu, F., Rong, F., Li, J., & Wei, P. (2024) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2024.07.001 · Cited by 38
Rao, A. T., Chen, N., Kim, M. J., Blumenfeld, J. R., Yip, O., Liang, Z., Shostak, D. M., Hao, Y., Nelson, M. R., Koutsodendris, N., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.10.005 · Cited by 48
Systemic inflammation as a central player in the initiation and development of Alzheimer’s disease
Bayraktaroğlu, I., Ortí-Casañ, N., Dam, D. V., Deyn, P. P. D., & Eisel, U. L. M. (2025) · Immunity & Ageing · doi:10.1186/s12979-025-00529-5 · Cited by 49
Ma, C., Wu, Y., Song, L., Yin, L., Yin, J.-J., Wang, Q., Yu, J., & Xiao, B. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.355747 · Cited by 37
Liu, Y., Tan, Y., Zhang, Z., Li, H., Yi, M., Zhang, Z., Hui, S., & Peng, W. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101831 · Cited by 34
T cell aging and Alzheimer’s disease
Guo, L., Li, X., Gould, T. M., Wang, Z., & Cao, W. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1154699 · Cited by 35
CD8+ T cells recognizing a neuron-restricted antigen injure axons in a model of multiple sclerosis
Clarkson, B. D. S., Grund, E. M., Standiford, M. M., Mirchia, K., Westphal, M. S., Muschler, L. S., & Howe, C. L. (2023) · Journal of Clinical Investigation · doi:10.1172/jci162788 · Cited by 32
Discerning the Role of Blood Brain Barrier Dysfunction in Alzheimer’s Disease
Tao, Q., Lin, R.-R., Chen, Y.-H., & Wu, Z. (2022) · Aging and Disease · doi:10.14336/ad.2022.0130-1 · Cited by 34
Li, X., Wang, H., Zhang, Q., Sun, X., Zhang, M., & Wang, G. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02910-x · Cited by 32
Antigen-specific age-related memory CD8 T cells induce and track Alzheimer’s-like neurodegeneration
Panwar, A., Rentsendorj, A., Jhun, M., Cohen, R. M., Cordner, R., Gull, N., Pechnick, R. N., Duvall, G., Mardiros, A., Golchian, D., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2401420121 · Cited by 36
Alzheimer’s disease: The role of T lymphocytes in neuroinflammation and neurodegeneration
Asamu, M. O., Oladipo, O. O., Abayomi, O. A., & Adebayo, A. A. (2023) · Brain Research · doi:10.1016/j.brainres.2023.148589 · Cited by 32
Terrabuio, E., Pietronigro, E. C., Bani, A., Bianca, V. D., Laudanna, C., Rossi, B., Finotti, G., Santos-Lima, B., Zenaro, E., Turano, E., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62405-6 · Cited by 33
Endothelial-Ercc1 DNA repair deficiency provokes blood-brain barrier dysfunction
Hansen, C. E., Vacondio, D., van der Molen, L., Jüttner, A. A., Fung, W. K., Karsten, M., van het Hof, B., Fontijn, R. D., Kooij, G., Witte, M. E., et al. (2025) · Cell Death & Disease · doi:10.1038/s41419-024-07306-0 · Cited by 27
He, H., Yang, Y., Wang, L., Guo, Z., Ye, L., Ou-Yang, W., & Yang, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1182307 · Cited by 27
Ye, Y., Gao, M., Shi, W., Gao, Y., Li, Y., Yang, W., Zheng, X., & Lu, X. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1325530 · Cited by 29
Basic principles of neuroimmunology
Yoshida, T. M., Wang, A., & Hafler, D. A. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00951-7 · Cited by 27
Glia as antigen-presenting cells in the central nervous system
Sutter, P. A., & Crocker, S. J. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102646 · Cited by 24
Pathogenesis of miR-155 on nonmodifiable and modifiable risk factors in Alzheimer’s disease
Liu, J.-J., Long, Y.-F., Xu, P., Guo, H.-D., & Cui, G.-H. (2023) · Alzheimer s Research & Therapy · doi:10.1186/s13195-023-01264-z · Cited by 26
Chen, H., Liao, Y., Zhang, X., Shen, H., Shang, D., He, Z., Zhou, W., & Song, Z. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02790-1 · Cited by 24
CD28null T cells in aging and diseases: From biology to assessment and intervention
Guan, Y., Cao, M., Wu, X., Yan, J., Hao, Y., & Zhang, C. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111807 · Cited by 27
Sun, Y., Zhang, H.-L., Liu, R.-Y., Wang, Y.-Q., Zhang, X.-R., Huang, R.-M., Zhu, B.-R., & Wu, H.-X. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155802 · Cited by 24
The role of m6A modification in the risk prediction and Notch1 pathway of Alzheimer’s disease
Qiao, Y., Mei, Y., Xia, M., Luo, D., & Gao, L. (2024) · iScience · doi:10.1016/j.isci.2024.110235 · Cited by 24
Jacobs, T., Jacobson, S. R., Fortea, J., Berger, J. S., Vedvyas, A., Marsh, K., He, T., Gutiérrez‐Jiménez, E., Fillmore, N. R., Gonzalez, M., et al. (2024) · Immunity & Ageing · doi:10.1186/s12979-024-00435-2 · Cited by 27
CD8+ T cells exacerbate AD-like symptoms in mouse model of amyloidosis
Wang, X., Campbell, B., Bodogai, M., McDevitt, R. A., Patrikeev, A., Gusev, F. E., Ragonnaud, E., Kumaraswami, K., Shirenova, S. D., Vardy, K., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.08.045 · Cited by 30
Netzahualcoyotzi, C., Santillán‐Cigales, J. J., Adalid-Peralta, L. V., & Velasco, I. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16106 · Cited by 24
Lorenz, L. M., Hirmer, S., Schmalen, A., Hauck, S. M., & Deeg, C. A. (2021) · Cells · doi:10.3390/cells10030711 · Cited by 22
Innate and adaptive immunity in neurodegenerative disease
Huang, Y., Zhang, G., Li, S., Feng, J., & Zhang, Z. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05533-4 · Cited by 22
Ghareghani, M., & Rivest, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310905 · Cited by 20
Identification ferroptosis-related hub genes and diagnostic model in Alzheimer’s disease
Zhao, H., Wang, J., Li, Z., Wang, S., Yu, G., & Wang, L. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1280639 · Cited by 20
Immune Response at the Crossroads of Atherosclerosis and Alzheimer's Disease
Stahr, N. A., & Galkina, E. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.870144 · Cited by 18
Identification of Biomarkers Related to M2 Macrophage Infiltration in Alzheimer’s Disease
Lin, C., Xu, C., Zhou, Y., Chen, A., & Jin, B. (2022) · Cells · doi:10.3390/cells11152365 · Cited by 20
MacPherson, K. P., Eidson, L. N., Houser, M. C., Weiss, B. E., Gollihue, J. L., Herrick, M. K., Rodrigues, M. E. D. S., Sniffen, L. J., Weekman, E. M., Hamilton, A. M., et al. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.895017 · Cited by 19
de Sousa, D. M. B., Poupardin, R., Villeda, S., Schroer, A. B., Fröhlich, T., Frey, V., Staffen, W., Mrowetz, H., Altendorfer, B., Unger, M. S., et al. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1196083 · Cited by 20
Self-citationA glance through the effects of CD4 + T cells, CD8 + T cells, and cytokines on Alzheimer's disease
Afsar, A., Chen, M., Xuan, Z., & Li, Z. (2023) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2023.10.058 · Cited by 20
Zhang, Y., Shen, S., Li, X., Wang, S., Xiao, Z., Cheng, J., & Li, R. (2023) · Neuroscience Letters · doi:10.1016/j.neulet.2023.137609 · Cited by 19
Immunological aspects of central neurodegeneration
Niso‐Santano, M., Fuentes, J. M., & Galluzzi, L. (2024) · Cell Discovery · doi:10.1038/s41421-024-00666-z · Cited by 17
TLR2 immunotherapy suppresses neuroinflammation, tau spread, and memory loss in rTg4510 mice
Kim, Y., Ryu, S.-H., Hyun, J., Cho, Y.-J., & Jung, Y. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.08.002 · Cited by 17
Effects of Qi-Fu-Yin on aging of APP/PS1 transgenic mice by regulating the intestinal microbiome
Xiao, Q., Ye, T., Wang, X., Qi, D., & Cheng, X. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1048513 · Cited by 17
The Role of Immunity in Alzheimer's Disease
McManus, R. M. (2022) · Advanced Biology · doi:10.1002/adbi.202101166 · Cited by 16
CD8+ T cells contribute to diet-induced memory deficits in aged male rats
Butler, M. J., Sengupta, S., Muscat, S. M., Amici, S. A., Biltz, R. G., Deems, N. P., Dravid, P., Mackey-Alfonso, S. E., Ijaz, H., Bettes, M. N., et al. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.02.003 · Cited by 18
de Sousa, D. M. B., Benedetti, A., Altendorfer, B., Mrowetz, H., Unger, M. S., Schallmoser, K., Aigner, L., & Kniewallner, K. M. (2023) · Aging · doi:10.18632/aging.204502 · Cited by 15
Self-citationStress regulates Alzheimer’s disease progression via selective enrichment of CD8+ T cells
Feng, Y., Fan, J., Cheng, Y., Dai, Q., & Ma, S. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113313 · Cited by 19
Wang, Y., Jiang, R., Li, M., Wang, Z., Yang, Y., & Sun, L. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-230784 · Cited by 18
Fernando, N., Gopalakrishnan, J., Behensky, A. A., Reich, L. N., Liu, C., Bass, V., Bono, M., Montgomery, W., Pace, R. D., Mattapallil, M. J., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.18.533293 · Cited by 15
Immunity in Alzheimer’s disease: From mechanisms to therapies
Chen, X., Holtzman, D. M., & Colonna, M. (2026) · Immunity · doi:10.1016/j.immuni.2026.02.004 · Cited by 18
Role of sex hormones in neuroinflammation in Alzheimer's disease
Maekawa, K., & Yamanaka, K. (2023) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12744 · Cited by 14
Garces, A., Martinez, B., Garza, R. D. L., Roy, D., Vallee, K.-A. J., Fields, J. A., Moore, D. J., Rodrigo, H., & Roy, U. (2023) · Scientific Reports · doi:10.1038/s41598-022-27276-7 · Cited by 15
Lee, E. J., Bae, S., Suh, M., Choi, Y., Choi, Y., Hwang, D. W., & Lee, D. S. (2024) · BMC Genomics · doi:10.1186/s12864-024-10434-8 · Cited by 15
Neutrophil-to-Lymphocyte Ratio in the Alzheimer’s Disease Continuum
Aprile, D., Marchi, F. D., Menegon, F., Comi, C., & Tondo, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115157 · Cited by 14
Chen, Y., & Colonna, M. (2022) · Current Opinion in Immunology · doi:10.1016/j.coi.2022.102233 · Cited by 14
Duan, K., Ma, Y., Jin, T., Miao, Y., & Zhang, Q. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.947781 · Cited by 14
An insight into the TAM system in Alzheimer’s disease
Zhou, S., Li, Y., Zhang, Z., & Yuan, Y. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109791 · Cited by 14
de Fàbregues, O., Sellés, M. C., Ramos-Vicente, D., Roch, G., Vila, M., & Bové, J. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106308 · Cited by 12
Rui, W., Wu, Y., Yang, Y., Xie, W., Qin, D., Ming, J., Ye, Z., Liu, L., Zong, M., Tang, X., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03255-9 · Cited by 15
Integrated analysis and identification of hub genes as novel biomarkers for Alzheimer’s disease
Zhao, K., Zhang, H., Wu, Y., Liu, J., Li, X., & Lin, J. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.901972 · Cited by 13
Adaptive immunity in the neuroinflammation of Alzheimer’s disease
Liu, H., Chen, Y., Zhang, J., & Chen, X. (2025) · Chinese Medical Journal · doi:10.1097/cm9.0000000000003695 · Cited by 13
Metadata
- Authors
- Unger, M. S., Li, E., Scharnagl, L., Poupardin, R., Altendorfer, B., Mrowetz, H., Hutter-Paier, B., Weiger, T. M., Heneka, M. T., Attems, J., & Aigner, L.
- Affiliations
- Paracelsus Medical University (AT)
- University of Salzburg (AT)
- University Hospital Bonn (DE)
- Newcastle University (GB)
- Corresponding author
- Aigner, L.
- ORCID
- Venue
- Brain, Behavior, and Immunity
- Publisher
- Elsevier BV
- Published
- 2020-10
- Volume
- 89
- Pages
- 67-86
- ISSN
- 0889-1591 (ISSN-L)
- OpenAlex
- W3032539442
- Cited by
- 248
- References
- 124
- Citations by year
- 2026: 34 · 2025: 43 · 2024: 63 · 2023: 62 · 2022: 28 · 2021: 15 · 2020: 3
- FWCI
- 10.43
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Brain Behavior and Immunity (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Open Repository and Bibliography (University of Luxembourg) (submittedVersion, other-oa)
- DZNE Pub (submittedVersion, cc-by)
- Funders
- Austrian Science Fund (P 31362-B34, F4413-B23)
- Seventh Framework Programme (HEALTH-F2-2011-278850)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- CD8+ T cells, Alzheimer's disease, APP/PS1 mice, neuroinflammation, hippocampus, synaptic plasticity, neuronal gene expression, Arc, Npas4, immediate early genes, calcium signaling, long-term potentiation, glutamatergic synapses, axon guidance
- MeSH terms
- Alzheimer Disease, Animals, Brain, Disease Models, Animal, Mice, Transgenic, Synapses, Gene Expression, Amyloid beta-Peptides, Amyloid beta-Protein Precursor, CD8-Positive T-Lymphocytes, Mice, Presenilin-1
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review