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Reactive microglia in patients with senile dementia of the Alzheimer type are positive for the histocompatibility glycoprotein HLA-DR
Abstract
HLA-DR is a class II cell surface glycoprotein of the human histocompatibility complex usually expressed on the surface of cells that are simultaneously presenting foreign antigen to T-lymphocytes. Using immunohistochemical procedures with two specific monoclonal antibodies to HLA-DR, HLA-DR-positive reactive microglia were found in gray matter throughout the cortex of postmortem brains of patients with senile dementia of the Alzheimer type (SDAT) and were particularly concentrated in the areas of senile plaque formation. Double immunostaining with antibodies to glial fibrillary acidic protein (GFAP) showed that the HLA-DR-positive cells were different from the reactive astrocytes although the occasional positively staining giant astrocyte was also seen. Small numbers of resting microglia were HLA-DR-positive in white matter of both normal and SDAT brains. The SDAT cases also had reduced cortical choline acetyltransferase (ChAT) levels. In the 11 brains studied, the number of hippocampal HLA-DR-positive cells was positively correlated with the numbers of plaques and negatively correlated with average cortical ChAT.
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“AD is accompanied by activation of microglia and astrocytes1,2 that affects the clearance and production of Aβ42,3,4 development and propagation of tau pathology,5 exacerbates neurodegeneration, and influences disease progression and severity.6,7”
From CSF biomarkers of neuroinflammation and cerebrovascular dysfunction in early Alzheimer disease (2018) · cites this paper as [1]
In the citing paper
“Reactive gliosis and neural inflammation are hallmarks of AD4,122–125.”
From Microglial signatures and their role in health and disease (2018) · cites this paper as [122]
In the citing paper
“Microglia in AD have long been known to acquire what is typically considered a “reactive” morphology, with short, thick, and poorly ramified processes [67–69].”
From Microglial dysfunction in brain aging and Alzheimer's disease (2014) · cites this paper as [69]
Citations
Cites
Handbook of Histopathological and Histochemical Techniques
(1974) · Elsevier eBooks · doi:10.1016/c2013-0-04011-x · Cited by 508
THE DETAILED DISTRIBUTION OF MHC CLASS II ANTIGENS IN NORMAL HUMAN ORGANS
Daar, A. S., Fuggle, S., Fabre, J. W., Ting, A., & Morris, P. J. (1984) · Transplantation · doi:10.1097/00007890-198409000-00019 · Cited by 432
Lampson, L. A., & Hickey, W. F. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.136.11.4054 · Cited by 230
Interferon-γ induces the expression of H-2 and Ia antigens on brain cells
Wong, G. H., Bartlett, P. F., Clark‐Lewis, I., McKimm‐Breschkin, J. L., & Schrader, J. W. (1984) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(84)80026-0 · Cited by 181
Distribution of choline acetyltransferase-containing neurons of the hypothalamus
Tago, H., McGeer, P. L., Bruce, G., & Hersh, L. B. (1987) · Brain Research · doi:10.1016/0006-8993(87)90268-x · Cited by 142
Self-citationMizukawa, K., McGeer, P. L., Tago, H., Peng, J. H., McGeer, E. G., & Kimura, H. (1986) · Brain Research · doi:10.1016/0006-8993(86)90253-2 · Cited by 120
Self-citationDemonstration of HLA-DR antigens in normal human brain.
de Tribolet, N., Hamou, M., Mach, J. P., Carrel, S., & Schreyer, M. (1984) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.47.4.417 · Cited by 57
Immunofluorescence studies of the monocytes in the injured rat brain
Tsuchihashi, Y., Kitamura, T., & Fujita, S. (1981) · Acta Neuropathologica · doi:10.1007/bf00688024 · Cited by 48
McGeer, E. G., Singh, E. A., & McGeer, P. L. (1987) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-198701000-00005 · Cited by 15
Self-citation
Research works printed but not linked: 3
- McGeer, 1987, Biochemistry and pathology of the basal ganglia, Can. J. Neurol. Sci., 19
- del Rio Hortega, 1932, Microglia, Vol. 2, 483
- Tago, H., McGeer, P.L., Bruce, G. and Hersh, L.B., Distribution of cholineacetyltransferase-containing neurons of the hypothalamus, Brain Res., in press.
Cited by
Sorted by citations
Items 601–700 of 834
Pollack, I. F., Lee, L. H., Zhou, H. F., & Lund, R. D. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490310106 · Cited by 17
Manipulation of microglial activity as a therapy for Alzheimer s disease
Ling, E. (2012) · Frontiers in Bioscience-Scholar · doi:10.2741/s342 · Cited by 15
The Role of Immunity in Alzheimer's Disease
McManus, R. M. (2022) · Advanced Biology · doi:10.1002/adbi.202101166 · Cited by 16
Acidic FGF Expression in the Surroundings of Senile Plaques.
Kimura, H., Tooyama, I., & McGeer, P. L. (1994) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.174.279 · Cited by 16
Self-citationImmunoblot detection of antibodies to myelin basic protein in Alzheimer's disease patients
Singh, V. K., Yang, Y., & Singh, E. A. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90766-z · Cited by 16
Amyloid β-Induced Inflammarafts in Alzheimer’s Disease
Ding, S., Choi, S., & Miller, Y. I. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104592 · Cited by 19
Emerging trends in IRAK-4 kinase research
Yadav, H. K., & Shirumalla, R. K. (2023) · Molecular Biology Reports · doi:10.1007/s11033-023-08438-w · Cited by 15
Tsering, W., Hery, G. P., Phillips, J. L., Lolo, K., Bathe, T., Villareal, J. A. B., Ruan, I. Y., & Prokop, S. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01688-6 · Cited by 15
Oxygen Sensing and Signaling in Alzheimer’s Disease: A Breathtaking Story!
Correia, S. C., & Moreira, P. I. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01148-6 · Cited by 14
Hensley, K., Danekas, A., Farrell, W., Garcia, T. M. D. N., Mehboob, W., & White, M. C. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.11.039 · Cited by 15
Löffler, T., Flunkert, S., Havas, D., Schweinzer, C., Uger, M. D., Windisch, M., Steyrer, E., & Hutter‐Paier, B. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-84 · Cited by 15
Walker, D. G., Lue, L., Beach, T., & Tooyama, I. (2019) · Cells · doi:10.3390/cells8070766 · Cited by 15
Oligomeric amyloid-β(1–42) induces THP-1 human monocyte adhesion and maturation
Crouse, N. R., Ajit, D., Udan, M. L. D., & Nichols, M. R. (2008) · Brain Research · doi:10.1016/j.brainres.2008.11.093 · Cited by 17
Sato, M., Ikeda, K., Haga, S., Allsop, D., & Ishii, T. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90702-u · Cited by 15
Immunologic and tissue culture approaches to the neurobiology of aging
Rpgers, J., & Rovigatti, U. (1988) · Neurobiology of Aging · doi:10.1016/s0197-4580(88)80143-x · Cited by 16
Yu, L., Che, R., Zhang, W., Xu, J., Lian, W., He, J., Tu, S., Bai, X., & He, X. (2023) · Phytotherapy Research · doi:10.1002/ptr.7765 · Cited by 14
MRI reveals differential effects of amphetamine exposure on neuroglia in vivo
Liu, C. H., Yang, J., Ren, J. Q., Liu, C., You, Z., & Liu, P. K. (2012) · The FASEB Journal · doi:10.1096/fj.12-220061 · Cited by 14
A Protective Role of Translocator Protein in Alzheimer’s Disease Brain
Jung, M. E. (2020) · Current Alzheimer Research · doi:10.2174/1567205017666200217105950 · Cited by 17
Chronic inflammation in Alzheimer’s disease offers therapeutic opportunities
McGeer, E. G., & McGeer, P. L. (2001) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.1.1.53 · Cited by 14
Self-citationExpression Profile Analysis of Brain Aging
Ginsberg, S. D. (2007) · CRC Press eBooks · doi:10.1201/9781420005523-7 · Cited by 15
HLA-DR4 influences glial activity in Alzheimer's disease hippocampus
Aisen, P. S. S., Luddy, A., Durner, M., Reinhard, J. F., & Pasinetti, G. M. (1998) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(98)00268-8 · Cited by 14
Interleukin-1α polymorphism has influence on late-onset sporadic Parkinson’s disease in Taiwan
Wu, Y., Chen, C. M., Hwang, J. C., Chen, S. T., Feng, I., Hsu, H. C., Liu, C. N., Liu, Y. T., Lai, Y. Y., Huang, H. J., et al. (2007) · Journal of Neural Transmission · doi:10.1007/s00702-007-0726-4 · Cited by 14
Induction of resting microglia in culture medium devoid of glycine and serine
Tanaka, J., Toku, K., Matsuda, S., Sudo, S., Fujita, H. M., Sakanaka, M., & Maeda, N. (1998) · Glia · doi:10.1002/(sici)1098-1136(199810)24:2 · Cited by 88
Jöhren, O., Viswanathan, M., & Saavedra, J. M. (1995) · Brain Research · doi:10.1016/0006-8993(95)01035-3 · Cited by 14
Inflammatory Mechanisms of Alzheimer’s Disease
Rogers, J., & Griffin, W. S. T. (1998) · Humana Press eBooks · doi:10.1007/978-1-59259-473-3_6 · Cited by 14
Gliosis in relation to Alzheimer's hallmark lesions in aging and Alzheimer's disease
Overmyer, M. (2002) · Cited by 14
Traub, J., Frey, A., & Störk, S. (2023) · Life · doi:10.3390/life13020329 · Cited by 14
Rubino, V., Rosa, G. L., Pipicelli, L., Carriero, F., Damiano, S., Santillo, M., Terrazzano, G., Ruggiero, G., & Mondola, P. (2023) · Antioxidants · doi:10.3390/antiox12091747 · Cited by 14
Murata, T., Tago, K., Miyata, K., Moriwaki, Y., Misawa, H., Kobata, K., Nakazawa, Y., Tamura, H., & Funakoshi‐Tago, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010316 · Cited by 17
Zia, B., Elmeky, M., Azimullah, S., Jha, N. K., Meeran, M. F. N., & Ojha, S. K. (2025) · Current Neuropharmacology · doi:10.2174/011570159x365720250225080257 · Cited by 13
McRae‐Degueurce, A., Martins, R. N., Fonte, J., Kraftsik, R., Hirt, L., & Judith Miklossy, A. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.10.015 · Cited by 13
Wang, F., Awan, M. U. F., Wang, Y., Wang, L., Qing, H., Ma, H., & Deng, Y. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150610738 · Cited by 13
Fehrenbach, M. K., Tjwa, M., Bechmann, I., & Krueger, M. (2018) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2018.03.004 · Cited by 14
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Self-citationThu, V. T. A., Hoang, T. X., & Kim, J. Y. (2023) · BioMed Research International · doi:10.1155/2023/3483411 · Cited by 12
Ashraf, A., Guillen, J. A. A., Aljuhani, M., Hubens, C. J., & So, P. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00181 · Cited by 12
Changes in neocortical and hippocampal microglial cells during hibernation
León‐Espinosa, G., Regalado-Reyes, M., DeFelipe, J., & Muñoz, A. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1596-7 · Cited by 14
Bagheri, S., Saboury, A. A., Haertlé, T., Rongioletti, M. C. A., & Saso, L. (2022) · Inorganics · doi:10.3390/inorganics10010006 · Cited by 14
Nonsteroidal Anti-Inflammatory Drugs and Alzheimer??s Disease
Lucca, U. (1999) · CNS Drugs · doi:10.2165/00023210-199911030-00005 · Cited by 11
Cras, P. P., Gheuens, J., Lübke, U., Boons, J., Vandermeeren, M., HEUVERSWYN, H. V., & Martin, J. (1990) · Journal of Histochemistry & Cytochemistry · doi:10.1177/38.8.2195115 · Cited by 12
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Thrupp, N., Frigerio, C. S., Wolfs, L., Skene, N., Poovathingal, S., Fourne, Y., Matthews, P. M., Theys, T., Mancuso, R., Strooper, B. D., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.13.035386 · Cited by 11
Sue, W.-C., Griffin, T. W., & Stanley, L. C. (1993) · Springer eBooks · doi:10.1007/978-1-4757-9486-1_32 · Cited by 12
Yamakawa, M., & Rexach, J. E. (2024) · Biomedicines · doi:10.3390/biomedicines12020308 · Cited by 14
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Sandoval, K. E., & WITT, K. A. (2024) · Pharmacological Reviews · doi:10.1124/pharmrev.124.001117 · Cited by 14
Swanson, M. E. V., Mrkela, M., Turner, C. P., Curtis, M. A., Faull, R. L. M., Walker, A. K., & Scotter, E. L. (2025) · Acta Neuropathologica Communications · doi:10.1186/s40478-025-01941-0 · Cited by 14
Toledano‐Díaz, A., Álvarez, M., & Tolédano, A. (2022) · Journal of Central Nervous System Disease · doi:10.1177/11795735221128703 · Cited by 11
The role of macrophages in models of neurological and psychiatric disorder
Perry, V. H. (1992) · Psychological Medicine · doi:10.1017/s0033291700038009 · Cited by 11
Moura, E. L. R., dos Santos, H., Celes, A. P. M., Bassani, T. B., Souza, L. C., & Vital, M. A. B. F. (2020) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-200175 · Cited by 11
The Alzheimer Pandemic: Is Paracetamol to Blame?
Jones, G. R. N. (2014) · Inflammation & Allergy - Drug Targets · doi:10.2174/1871528112666131219163405 · Cited by 11
Effects of Alzheimer's peptide and α1-antichymotrypsin on astrocyte gene expression
Baker, C., Nielsen, H. M., Minthon, L., Wright, H. T., Chappell, S., Okyere, J., May, S. T., Morgan, K., Kalsheker, N. A., & Janciauskiene, S. M. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.10.017 · Cited by 11
Chronically active: activation of microglial proteolysis in ageing and neurodegeneration
Stolzing, A., Sethe, S. C., & Grune, T. (2005) · Redox Report · doi:10.1179/135100005x70198 · Cited by 11
Immunization of Rats With Cholinergic Neurons Induces Behavioral Deficits
Chapman, J., Feldon, J., Alroy, G., & Michaelson, D. M. (1989) · Neural Plasticity · doi:10.1155/np.1989.63 · Cited by 11
Akiyama, H., Yamada, T., McGeer, P. L., Kawamata, T., Tooyama, I., & Ishii, T. (1993) · Acta Neuropathologica · doi:10.1007/bf00334451 · Cited by 11
Self-citationRat Microglia Exhibit Increased Density on Alzheimer's Plaquesin Vitro
Joshi, S. N., & Crutcher, K. A. (1998) · Experimental Neurology · doi:10.1006/exnr.1997.6678 · Cited by 11
Leng, F., Initiative, O. B. O. A. D. N., Zhan, Z., Sun, Y., Liu, F., Edison, P., Sun, Y., & Wang, Z. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220102 · Cited by 11
Balzano, T., Esteban-García, N., & Blesa, J. (2022) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2023.2160440 · Cited by 11
Lana, D., Branca, J. J. V., Delfino, G., Giovannini, M. G., Casamenti, F., Nardiello, P., Bucciantini, M., Stefani, M., Zach, P., Zecchi‐Orlandini, S., et al. (2023) · Cells · doi:10.3390/cells12182258 · Cited by 10
Current Conceptual View of Alzheimer’s Disease
Herrup, K. (2012) · Advances in biological psychiatry · doi:10.1159/000335378 · Cited by 10
Jiamvoraphong, N., Jantaratnotai, N., Sanvarinda, P., Tuchinda, P., Piyachaturawat, P., Thampithak, A., & Sanvarinda, P. (2017) · Journal of Pharmacy and Pharmacology · doi:10.1111/jphp.12723 · Cited by 10
Imamura, K., Sawada, M., Ozaki, N., Naito, H., Iwata, N., Ishihara, R., Takeuchi, T., & Shibayama, H. (2001) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-200101000-00006 · Cited by 11
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Karki, S., & Nichols, M. R. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.10.081 · Cited by 10
Chabot, S., & Yong, V. W. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-108-4_14 · Cited by 10
Part III. Neuropathology of Alzheimer's disease
Arnold, S. E. (2000) · Disease-a-Month · doi:10.1016/s0011-5029(00)90030-0 · Cited by 10
Cell cycle and chromosome segregation defects in alzheimer's disease
Potter, H., Geller, L. N., Thomas, A. E., Conforto, D., & Chichkova, R. I. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)83340-0 · Cited by 10
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Tu, J., Yang, L., Zhou, X., Qi, K., Wang, J., Kouadir, M., Xu, L., Yin, X., & Zhao, D. (2013) · Journal of Molecular Neuroscience · doi:10.1007/s12031-013-0140-3 · Cited by 9
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McGeer, P. L., & McGeer, E. G. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-179913 · Cited by 8
Self-citation[46] Inflammatory responses to amyloid fibrils
Yates, S. L., Kocsis‐Angle, J., Embury, P., & Brunden, K. R. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)09048-5 · Cited by 9
Bradford, H. F., Foley, P., Docherty, M., Fillit, H. M., Luine, V. N., McEwen, B. S., Bucht, G., Winbald, B., & Hardy, J. (1989) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100029875 · Cited by 9
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(2001) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8225-5 · Cited by 9
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Womack, T., Vollert, C. T., Ohia-Nwoko, O., Schmitt, M. E., Montazari, S., Beckett, T. L., Mayerich, D. M., Murphy, M. P., & Eriksen, J. L. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.769347 · Cited by 8
Chen, M., Liang, J., Liu, Y., Liu, Y., Zhou, C., Hong, P., Zhang, Y., & Qian, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24020905 · Cited by 9
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Prčina, M., Novak, M., Cigankova, V., & Kontseková, E. (2018) · Bratislavské lekárske listy/Bratislava medical journal · doi:10.4149/bll_2018_040 · Cited by 8
Nagao, M., Yamano, S., Imagawa, N., Igami, K., Miyazaki, T., Ito, H., Watanabe, T., Kubota, K., Katsurabayashi, S., & Iwasaki, K. (2019) · Traditional & Kampo Medicine · doi:10.1002/tkm2.1220 · Cited by 8
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Bernstein, H. (2006) · Springer eBooks · doi:10.1007/0-387-23101-3_1 · Cited by 8
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Jeon, S. W., & Kim, Y. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-981-19-7376-5_1 · Cited by 7
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Kostić, M. S., Živković, N., Cvetanović, A., Bašić, J., & Stojanović, I. R. (2024) · Reviews in the Neurosciences · doi:10.1515/revneuro-2024-0090 · Cited by 8
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Cohen, R. M. (2009) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/foc.7.1.foc28 · Cited by 8
Rad, F. R., Akbari, M. G., Zamani, M., Bayat, S., & Zamani, M. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02295-z · Cited by 7
Pollock, T. B., Mack, J. M., Day, R. J., Isho, N. F., Brown, R. J., Oxford, A. E., Morrison, B. E., Hayden, E. J., & Rohn, T. T. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/5123565 · Cited by 7
Do, M. H., Kim, M. K., Choi, S. Y., Lee, P., Kim, Y., & Hur, J. (2021) · Applied Biological Chemistry · doi:10.1186/s13765-021-00604-7 · Cited by 7
Development of antiinflammatory therapy for Alzheimer's disease
Aisen, P. S. S. (2002) · Drug Development Research · doi:10.1002/ddr.10094 · Cited by 7
Weiner, M., Edland, S. D., & Luszczynska, H. (2014) · Cited by 7
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Cotman, C. W., Kahle, J. S., & Korotzer, A. R. (1995) · Comprehensive physiology · doi:10.1002/cphy.cp110113 · Cited by 7
Microglial cerebrospinal fluid antibodies
McRae‐Degueurce, A., Ling, E., Wigander, A., & Dahlström, A. B. (1996) · Molecular and Chemical Neuropathology · doi:10.1007/bf02815209 · Cited by 7
Implications of immunomodulant therapy in Alzheimer’s disease
Singh, V. K., & Fudenberg, H. H. (1988) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-9154-7_2 · Cited by 7
Singh, A. S., Naqvi, A. R., & Chanu, M. T. (2026) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2026.01.050 · Cited by 7
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Tiwari, P., & Tolwinski, N. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054300 · Cited by 7
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Potter, H. (2005) · Springer eBooks · doi:10.1007/0-387-29390-6_5 · Cited by 6
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Ramkissoon, A., Shapiro, A. M., Loniewska, M. M., & Wells, P. G. (2013) · Wiley eBooks · doi:10.1002/9781118355886.ch10 · Cited by 6
Cerebrospinal fluid antibodies : an indicator for immune responses in alzheimer's disease
McRae‐Degueurce, A., & Dahlström, A. B. (1992) · Research in Immunology · doi:10.1016/0923-2494(92)80053-n · Cited by 6
Identical Tau Filaments in Subacute Sclerosing Panencephalitis and Chronic Traumatic EncephalopathyPreprint
Qi, C., Hasegawa, M., Takao, M., Sakai, M., Sasaki, M., Mizutani, M., Akagi, A., Iwasaki, Y., Miyahara, H., Yoshida, M., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.02.526771 · Cited by 6
Jacob, C., Tollenaere, M., Kachar, H., Potier, M., Deyn, P. P. D., & Dam, D. V. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e41445 · Cited by 6
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Navarro, N. V., Mundim, G. D. N., & Čudić, M. (2025) · Molecules · doi:10.3390/molecules30091895 · Cited by 5
Su, W.-S., Wu, M.-T., Cheng, I. H.-J., & Yang, F. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115420 · Cited by 5
Mutti, V., Carini, G., Marizzoni, M., Filippini, A., Bono, F., Fiorentini, C., Saleri, S., Cillis, F. D., Cattaneo, A., Gennarelli, M., et al. (2025) · Biomolecules · doi:10.3390/biom15091322 · Cited by 5
Donev, R., & Howell, O. W. (2012) · Advances in protein chemistry and structural biology · doi:10.1016/b978-0-12-394287-6.00004-5 · Cited by 5
Inflammatory Processes Exacerbate Degenerative Neurological Disorders
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Faltraco, F., Lista, S., Garaci, F., & Hampel, H. (2012) · Cineca Institutional Research Information System (Tor Vergata University) · Cited by 5
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Metadata
- Authors
- McGeer, P. L., Itagaki, S., Tago, H., & McGeer, E. G.
- Affiliations
- University of British Columbia (CA)
- Corresponding author
- McGeer, Patrick L.
- ORCID
- McGeer, Patrick L.
- Venue
- Neuroscience Letters
- Publisher
- Elsevier BV
- Published
- 1987-08
- Volume
- 79
- Issue
- 1-2
- Pages
- 195-200
- ISSN
- 0304-3940 (ISSN-L)
- OpenAlex
- W2074274825
- Cited by
- 836
- References
- 9
- Citations by year
- 2026: 7 · 2025: 19 · 2024: 24 · 2023: 36 · 2022: 32 · 2021: 30 · 2020: 40 · 2019: 31 · 2018: 26 · 2017: 28 · 2016: 21 · 2015: 27 · 2014: 34 · 2013: 27 · 2012: 27
- FWCI
- 14.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience Letters (publishedVersion)
- PubMed (publishedVersion)
- 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
- reactive microglia, HLA-DR, senile dementia of the Alzheimer type, Alzheimer's disease, amyloid plaques, glial fibrillary acidic protein, astrocytes, choline acetyltransferase, hippocampus, neuroinflammation
- MeSH terms
- Aged, Aged, 80 and over, Alzheimer Disease, Cerebral Cortex, Hippocampus, HLA-D Antigens, HLA-DR Antigens, Humans, Neuroglia
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