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Microglia in the Neuroinflammatory Pathogenesis of Alzheimer’s Disease and Related Therapeutic Targets
Open accessAbstract
Alzheimer’s disease (AD) is the most prevalent neurodegenerative disease worldwide, characterized by progressive neuron degeneration or loss due to excessive accumulation of β-amyloid (Aβ) peptides, formation of neurofibrillary tangles (NFTs), and hyperphosphorylated tau. The treatment of AD has been only partially successful as the majority of the pharmacotherapies on the market may alleviate some of the symptoms. In the occurrence of AD, increasing attention has been paid to neurodegeneration, while the resident glial cells, like microglia are also observed. Microglia, a kind of crucial glial cells associated with the innate immune response, functions as double-edge sword role in CNS. They exert a beneficial or detrimental influence on the adjacent neurons through secretion of both pro-inflammatory cytokines as well as neurotrophic factors. In addition, their endocytosis of debris and toxic protein like Aβ and tau ensures homeostasis of the neuronal microenvironment. In this review, we will systematically summarize recent research regarding the roles of microglia in AD pathology and latest microglia-associated therapeutic targets mainly including pro-inflammatory genes, anti-inflammatory genes and phagocytosis at length, some of which are contradictory and controversial and warrant to further be investigated.
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“Microglia may help contain amyloid plaques, phagocytose pathological material, support synapses, and limit inflammatory spread; yet they may also release pro-inflammatory mediators, promote complement-associated synapse loss, propagate neurotoxic signaling, and contribute to chronic tissue damage.”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [19]
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“The central unresolved issue is that the same broad category of “microglial activation” can describe processes with opposite biological consequences.”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [19]
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“Reviews and experimental studies now increasingly describe Alzheimer’s neuroinflammation as a dynamic balance between protective and harmful microglial programs, with disease stage and local tissue environment determining whether immune activation is beneficial, insufficient, maladaptive, or toxic [13,19].”
From Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis? (2026) · cites this paper as [19]
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Cites
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., & Pericak-Vance, M. A. (1993) · Science · doi:10.1126/science.8346443 · Cited by 9,429
Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023
Glutamate neurotoxicity and diseases of the nervous system
Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,184
Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971
Macrophage activation and polarization: nomenclature and experimental guidelines
Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.008 · Cited by 6,337
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
Martinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066
Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo
Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493
Synaptic Pruning by Microglia Is Necessary for Normal Brain Development
Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244
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Liu, Y., Peng, H., Liu, Q., Hao, J., Tang, C., & Yan, H. (2024) · NeuroMolecular Medicine · doi:10.1007/s12017-024-08821-1 · Cited by 3
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Naffaa, M. M. (2025) · Lifespan development and mental health. · doi:10.70322/ldmh.2025.10005 · Cited by 3
Yang, X., Li, K., Zhang, Y., Sun, R., & Yu, J. (2025) · Psychiatry and Clinical Psychopharmacology · doi:10.5152/pcp.2025.241016 · Cited by 3
Wang, H., Yang, Q., Ge, C., Liu, J., Mistry, H., Jia, Y., & He, G. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251361042 · Cited by 4
Self-citationWang, X.-C., Wu, G., Cai, H., Chu, C.-L., Liu, Y., Li, H.-C., Zheng, J. G., Chen, H., Lin, H., Li, S., et al. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04515-7 · Cited by 3
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Tidke, B., Itekar, S., Khobragade, R., Vinchurney, M. D., Trivedi, R., Taksande, B. G., & Umekar, M. J. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115785 · Cited by 3
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Sharma, S., Gupta, M., & Sharma, S. (2025) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2025.2554239 · Cited by 4
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Melhem, N. Y., Qutifan, S., Alsalem, M., & Saleh, T. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102896 · Cited by 4
Li, Y., Fan, H., Han, X., Ni, M., Hou, X., Xia, H., Shi, Y., Zhang, L., & Sun, J. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05287-5 · Cited by 3
Wozniczka, C. M., & Weaver, D. F. (2026) · NeuroSci · doi:10.3390/neurosci7010013 · Cited by 3
Xu, Z., Xu, W., He, J., Qian, J., Wang, H., Li, C., & Zhou, X. (2026) · CNS Neuroscience & Therapeutics · doi:10.1002/cns.70771 · Cited by 3
Yang, N., Jiang, J., Shi, J., Liu, X., Yu, C., Guo, S., Zhang, C., Gao, F., Yang, Z., Feng, H., et al. (2026) · Inflammation · doi:10.1007/s10753-025-02435-w · Cited by 4
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Xu, F., Liu, Z., Wang, Z., Zhang, Y., Zhao, Y., & Fang, W. (2025) · Cell Biochemistry and Function · doi:10.1002/cbf.70089 · Cited by 3
Sun, X., Liu, H., Li, W., Li, L., Tian, Q., Cao, Q., Meng, Y., Shen, Y., Che, F., Chiu, J. C., et al. (2025) · Journal of Inflammation · doi:10.1186/s12950-025-00449-7 · Cited by 3
Zhai, Z., Kong, F., Zhu, Z., Dai, J., Cai, J., Xie, D., Shen, Y., Xu, Y., & Sun, T. (2023) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2023.11.011 · Cited by 4
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Julius, A., Malakondaiah, S., Subbarayalu, R., Renuka, R. R., & Pothireddy, R. B. (2025) · SN Comprehensive Clinical Medicine · doi:10.1007/s42399-025-01936-x · Cited by 3
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Spetz, M. R., Kim, H., Ligocki, A. P., Shekharan, S. R., Brien, H. J., Chavarría, D., Conger, D. J., Shattuck-Brandt, R. L., Shostak, A., Embalabala, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.12.642808 · Cited by 3
Perez‐Alcantara, M., Washer, S. J., Chen, Y., Steer, J., González‐Padilla, D., McWilliam, J., Willé, D. R., Panousis, N., Kolberg, P., Navarro‐Guerrero, E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.18.670767 · Cited by 3
de Andrade, Á. D. B., Ide, F. C., Mangia, A. S., Martins, A. C., Nascimento, A. Q., & do Nascimento, I. B. (2024) · Revista Brasileira de Geriatria e Gerontologia · doi:10.1590/1981-22562024027.240007.en · Cited by 2
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Raza, H., Ali, A., Kumar, A., Adnan, F., Shah, S. A. W., Ghazanfar, S., Roshan, F. N. U., Shamim, Z., Opare, A. D., & Tanveer, F. S. (2025) · Annals of Medicine and Surgery · doi:10.1097/ms9.0000000000002887 · Cited by 2
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Saramak, K. (2025) · Allergies · doi:10.3390/allergies5020018 · Cited by 2
Wu, Y., Zhan, Y., Zhu, W., & Pei, J. (2025) · Medicine · doi:10.1097/md.0000000000042651 · Cited by 2
Zhang, Y., Wu, Y., Zhang, X., Guo, S., He, J., Hu, N., Huang, Y., Kong, Y., Li, Q., Sui, A., et al. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70124 · Cited by 2
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Lin, Y., Wang, J., Liu, B., Hu, T., & Gu, J. (2025) · Gene · doi:10.1016/j.gene.2025.149722 · Cited by 2
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Kumar, R. M. R., Logesh, R., & Chidambaram, S. B. (2025) · Pharmaceutical Medicine · doi:10.1007/s40290-025-00584-9 · Cited by 4
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Teng, M., Ma, R., Liu, S., Zhang, G., Zou, J., & Fu, Q. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.169535 · Cited by 3
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Chauhan, A., Devi, R., Singh, S., Bhutani, K., Prasad, S., Singh, A., Bhaskar, N., Kumar, S., Saini, A. K., & Thakur, R. (2025) · Discover Neuroscience · doi:10.1186/s13064-025-00217-6 · Cited by 5
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Lai, Y., & Zhao, H. (2025) · Scientific Reports · doi:10.1038/s41598-025-23434-9 · Cited by 2
Bhatia, N., Khan, M. M. U., Masih, D., & Srinivas, U. (2025) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-025-00318-w · Cited by 2
Cheng, Y., Santucci, K., Gao, Y., Takenaka, K., Lindner, G., Xu, S.-M., & Janitz, M. (2026) · Journal of Molecular Neuroscience · doi:10.1007/s12031-025-02469-7 · Cited by 3
Ahn, N.-H., Hong, S.-C., Hong, C. R., Lee, E. H., Lee, J. H., Choi, S.-B., Jung, J., Kim, Y., Kim, J.-S., Park, K., et al. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05680-8 · Cited by 2
Khzem, A. H. A., & Gomaa, M. S. (2026) · Drug Design Development and Therapy · doi:10.2147/dddt.s597087 · Cited by 3
Kumar, D., Kondaveeti, S. B., Agrawal, M., Kumar, A., Awasthi, A., Mahmood, S., Singh, T. G., & Kumar, M. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05857-1 · Cited by 2
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Lopez, D. M., Keavey, L., & Bowles, K. R. (2026) · Bioscience Reports · doi:10.1042/bsr20250131 · Cited by 2
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Zhu, C., Xu, J., Lin, J., Liu, J., & Yu, E. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.110994 · Cited by 2
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Guan, J., Wu, P., Liu, M., Jiang, C., Meng, X., Wu, X., Lu, M., Fan, Y., & Gan, L. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.12.022 · Cited by 3
Emokpae, M. A., Osifo, J. O., Emokpae, L. A., ERHUNMWUNSE, R. U., & Ayomide, I. B. (2024) · Journal of Behavioral and Brain Science · doi:10.4236/jbbs.2024.1412020 · Cited by 2
Shu, H., Ding, G., Xu, X., Huang, X., & He, R. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1481526 · Cited by 2
Rodrigues, A. B. M., Passetti, F., & Guimarães, A. C. R. (2025) · Neuroinformatics · doi:10.1007/s12021-024-09713-2 · Cited by 2
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Wang, A., Zhang, F., Zhang, W., Gong, J., & Sun, X. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115218 · Cited by 2
Mirehei, M., Motamedi, F., Maghsoudi, N., Mansouri, Z., Naderi, S., Khodagholi, F., & Abbaszadeh, F. (2025) · Experimental Gerontology · doi:10.1016/j.exger.2025.112746 · Cited by 2
Babaker, M. A., Ghany, K. A. E., Elshafey, N., Algohary, A. M., Elgohary, E., Hamouda, R. A., Abol-Fetouh, G. M., Elbawab, R. H., & Ahmed-Farid, O. A.-H. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.107194 · Cited by 2
Asthana, A., Agarwal, R., & Tripathi, S. (2023) · Advances in Alzheimer s Disease · doi:10.4236/aad.2023.122002 · Cited by 2
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Yang, F., Gao, W., Wang, J. Z., Li, X., & Li, H. (2024) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x24500873 · Cited by 1
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Li, N., Liu, N., Ye, Y., Shi, H., Shi, J., Luo, G., Guo, J., Liu, Y., & Chen, H. (2025) · IEEE Journal of Selected Topics in Quantum Electronics · doi:10.1109/jstqe.2025.3564366 · Cited by 1
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Omutindo Nyakayo, A. (2025) · NEWPORT INTERNATIONAL JOURNAL OF RESEARCH IN MEDICAL SCIENCES · doi:10.59298/nijrms/2025/6.2.4752 · Cited by 1
Lin, Z., Qiao, W., Wang, J., Tang, Z., Shi, L., Qian, Q., Hu, W., Zhang, R., & Chen, X. (2025) · Phytochemistry · doi:10.1016/j.phytochem.2025.114566 · Cited by 1
Li, D., Mu, X., Ma, Y., Lu, W., & Wang, R. (2025) · Food Science and Human Wellness · doi:10.26599/fshw.2025.9250621 · Cited by 1
Sandrine, M. N. Y., Owona, P. E., Ella, F. A., Bilanda, D. C., Julie, A. O. J., Cynthia, B. Y. P., Michel, B. G., Dzeufiet, P. D. D., Binsaleh, A. Y., Alwethaynani, M. S., et al. (2025) · Journal of Computational Biophysics and Chemistry · doi:10.1142/s2737416525501248 · Cited by 1
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Bottaccioli, F., & Bottaccioli, A. G. (2025) · Brain Behavior and Immunity Integrative · doi:10.1016/j.bbii.2025.100138 · Cited by 1
Akash, A., Ahamed, M., Porel, P., & Aran, K. R. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149949 · Cited by 2
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TLRs and NLRs modulate oral microbiome involvement in Alzheimer’s disease
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Jain, A., Srivastava, S., Kumar, S., Sahu, R., Tariq, M., & Ashraf, G. M. (2026) · Springer eBooks · doi:10.1007/978-981-95-4751-7_5 · Cited by 1
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Sangineto, M., & Serviddio, G. (2026) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-25-01035 · Cited by 1
Zhao, G., Cui, B., Lu, Y., Ma, K., Gao, X., She, X., Zhu, Y., Ji, X., Yang, H. M., & Yang, H. (2026) · Biomolecules · doi:10.3390/biom16020200 · Cited by 1
Self-citationYadav, S., Pandey, S. K., & Awasthi, S. (2026) · Advanced Therapeutics · doi:10.1002/adtp.202500576 · Cited by 1
Yang, Z., Zhang, M., Zhi, W., Lizhen, Hu, X., Zou, Y., & Wang, L. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27031492 · Cited by 3
A systemic and dialectical paradigm for Psychoneuroendocrineimmunology and integrated care science
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Cao, J., Song, J., Yin, Z., & Tang, Z. (2026) · British Journal of Pharmacology · doi:10.1111/bph.70289 · Cited by 1
Guidotti, L., Lucchesi, M., Daghini, E., Amato, R., Neri, G., Corsi, F., Marracci, S., Gargini, C., Borello, U., Cammalleri, M., et al. (2026) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.67.2.31 · Cited by 1
Zhu, S., Li, Y., Lin, C., Liu, X., Luo, Y., Qian, H., & Tang, Z. (2026) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-026-05225-9 · Cited by 1
Ye, Q., & Ma, S. (2026) · Molecules · doi:10.3390/molecules31081272 · Cited by 2
DHCR24 in cholesterol metabolism and diseases of the nervous system
Zhu, H. G., Li, S., Yang, Y. Z., 张似青, Wang, Y., & Xiong, T. (2026) · Lipids in Health and Disease · doi:10.1186/s12944-026-02954-x · Cited by 2
Druszczyńska, M., Sadowska, B., Kulesza, J., Kulesza, E., & Fol, M. (2026) · Vaccines · doi:10.3390/vaccines14050412 · Cited by 2
Setiawan, A. W., Choi, J. T., Park, S., Choi, M., Tjandrawinata, R. R., Hadinata, E., Park, M. N., Ikrar, T., Nurkolis, F., & Kim, B. (2026) · Pharmaceuticals · doi:10.3390/ph19050792 · Cited by 1
Tian, M., Feng, R., Gong, C., Ben, X., Ma, Z., Yi, X., & Guo, Q. (2026) · Biomolecules · doi:10.3390/biom16060798 · Cited by 1
Singh, G., Singh, G., Shreya, Kumari, A., & Aran, K. R. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1819432 · Cited by 1
Kumar, N., Mir, P. A., Bhutia, G. T., Chaudhary, P., Kaur, G., Alam, Q., Pawar, S. D., & Gupta, S. K. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05983-w · Cited by 1
Hill, N., AlMuallim, H. Y. O., Maddock, E., Hobbs, C., Clarke, E. E., Goncalves, M. B. C. V., & Corcoran, J. P. T. (2026) · FEBS Open Bio · doi:10.1002/2211-5463.70284 · Cited by 1
Sa, Y., Yuan, H., Ma, J., Yang, Z., Wang, M., Wang, W., Yang, L., Ma, F., Zhang, W., Wilson, G., et al. (2026) · Advanced Science · doi:10.1002/advs.76863 · Cited by 1
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唐, 琼. (2024) · Open Journal of Natural Science · doi:10.12677/ojns.2024.122032 · Cited by 1
Mudimela, S., Giridharan, V. V., & Saravanan, J. (2024) · Chemistry & Biodiversity · doi:10.1002/cbdv.202301260 · Cited by 1
Pal, S., & Melnik, R. (2024) · Lecture notes in computer science · doi:10.1007/978-3-031-64636-2_4 · Cited by 1
Phikud navakot extract acts as an ER stress inhibitor to ameliorate ER stress and neuroinflammation
Temviriyanukul, P., Chansawhang, A., Inthachat, W., Supasawat, P., Phochantachinda, S., Pitchakarn, P., & Chantong, B. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e39700 · Cited by 1
McGregor, B. A., Raihan, M. O., Brishti, A., Hur, J., & Porter, J. E. (2025) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1544971 · Cited by 1
Bong, S., Choi, H., Song, H., Kim, D. K., Mook‐Jung, I., & Lee, D. Y. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70030 · Cited by 1
Chen, S., Chen, R., Luo, M., Luo, Y., Ma, X., Zhao, H., & Xu, Z. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123537 · Cited by 1
Biney, A. K., Schultz, C. R., Stone, M. F., Nguyen, D. A., Wang, A., Furtado, M. D. A., & Lumley, L. A. (2025) · Experimental Biology and Medicine · doi:10.3389/ebm.2025.10598 · Cited by 1
Fatima, E., & Fatima, A. (2025) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2025.07.002 · Cited by 1
Sun, X., Li, W., Li, L., Tian, Q., Cao, Q., Fu, Q., Meng, Y., Shen, Y., Yu, J., & Che, F. (2023) · Research Square · doi:10.21203/rs.3.rs-3481982/v1 · Cited by 1
Miao, J., Wang, J., Li, Y., Zhang, H., Zhang, Y., Li, Q., Xiao, B., Zhou, W., & Guo, J. (2026) · Advanced Science · doi:10.1002/advs.77929
“This contributes to CAA, BBB breakdown, and microglial overactivation [ 15, 21–23 ].”
Lymphoid-like Suppressive Microglia in Alzheimer’s Disease: A New Neuroimmune Regulatory Axis?
Chmiel, J., Gawełczyk, W., Soczyńska, J., & Leszek, J. (2026) · Cells · doi:10.3390/cells15131151
CUIDADOS PALIATIVOS NA DOENÇA DE ALZHEIMER: RELATO DE EXPERIÊNCIA
Moura, C. A. D., & Lopes, G. D. S. (2023) · Revista Contemporânea · doi:10.56083/rcv3n12-151
Role of Exosomes in Management of Depression
Nigade, A., Pathak, G., Anitha, K., Mishra, N., Bali, V., & Bhatt, S. (2024) · Springer eBooks · doi:10.1007/978-981-99-8373-5_8
Vijayan, V., Siddique, I. A., Gupta, S., Madan, E., Raj, N., & gupta, S. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4863165
de Andrade, Á. D. B., Ide, F. C., Mangia, A. S., Martins, A. C., Nascimento, A. Q., & do Nascimento, I. B. (2024) · Revista Brasileira de Geriatria e Gerontologia · doi:10.1590/1981-22562024027.240007.pt
Bastos, S. (2024) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2024.tde-25072024-110328
Alzheimer's disease: therapeutic potential of phytocannabinoids
da Silva, T. C. C., da Silva, A. R., Campagnone, C. H. D. S., Alves, A. J., & da Silva, V. A. (2024) · Concilium · doi:10.53660/clm-3910-24q30
Levenson, J. M., Kam, H., & Chen, D. F. (2024) · eLife · doi:10.7554/elife.103535
Murshid, N. M., Sahardi, N. F. N. M., & Makpol, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms26010241
Metadata
- Authors
- Cai, Y., Liu, J., Wang, B., Sun, M., & Yang, H.
- Affiliations
- First Affiliated Hospital of Soochow University (CN)
- Corresponding author
- Sun, Miao
- Yang, Hao
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2022-04-26
- Volume
- 13
- Pages
- 856376-856376
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC9086828
- OpenAlex
- W4281554374
- Cited by
- 351
- References
- 169
- Citations by year
- 2026: 70 · 2025: 148 · 2024: 88 · 2023: 41 · 2022: 4
- FWCI
- 7.24
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (81,570,960, 81,974,244, 82071551, 2019YFA0802600)
- Government of Jiangsu Province
- 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 › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- microglia, Alzheimer's disease, neuroinflammation, neurodegeneration, amyloid-beta, tau hyperphosphorylation, neurofibrillary tangles, inflammatory cytokines, anti-inflammatory genes, phagocytosis, microglial homeostasis, therapeutic target
- MeSH terms
- Alzheimer Disease, Humans, Neurons, Amyloid beta-Peptides, Microglia, Neurodegenerative Diseases
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