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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.
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Sorted by citations
Items 101–200 of 834
Role of neuroinflammation in neurodegeneration: new insights
McManus, R. M., & Heneka, M. T. (2017) · Alzheimer s Research & Therapy · doi:10.1186/s13195-017-0241-2 · Cited by 258
Szczepanik, A. M. (2001) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(00)00404-5 · Cited by 250
Senile plaques stimulate microglia to release a neurotoxin found in Alzheimer brain
Giulian, D., Haverkamp, L. J., Li, J., Karshin, W. L., Yu, J., Tom, D., Li, X., & Kirkpatrick, J. B. (1995) · Neurochemistry International · doi:10.1016/0197-0186(95)00067-i · Cited by 242
NLRP3 Inflammasome Inhibitor Ameliorates Amyloid Pathology in a Mouse Model of Alzheimer’s Disease
Yin, J., Zhao, F., Chojnacki, J. E., Fulp, J., Klein, W. L., Zhang, S., & Zhu, X. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0467-9 · Cited by 244
Sánchez-Guajardo, V., Barnum, C. J., Tansey, M. G., & Romero‐Ramos, M. (2013) · ASN NEURO · doi:10.1042/an20120066 · Cited by 246
The changing phenotype of microglia from homeostasis to disease
Luo, X., & Chen, S. (2012) · Translational Neurodegeneration · doi:10.1186/2047-9158-1-9 · Cited by 246
Microglial Expression of MHC Class II Increases in Normal Aging of Nonhuman Primates
Sheffield, L. G., & Berman, N. E. J. (1998) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00168-1 · Cited by 234
MHC class II‐positive microglia in human brain: Association with alzheimer lesions
Perlmutter, L. S., Scott, S. A., Barrón, E., & Chui, H. C. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490330407 · Cited by 228
Peripheral infection evokes exaggerated sickness behaviour in pre-clinical murine prion disease
Combrinck, M. I., Perry, V. H., & Cunningham, C. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00030-1 · Cited by 231
Down’s syndrome, neuroinflammation, and Alzheimer neuropathogenesis
Wilcock, D. M., & Griffin, W. S. T. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-84 · Cited by 230
Hjorth, E., Zhu, M., Toro, V. C., Vedin, I., Palmblad, J. E. W., Cederholm, T., Freund‐Levi, Y., Irving, G. F., Wahlund, L., Basun, H., et al. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-130131 · Cited by 237
Barrientos, R. M., Frank, M. G., Hein, A. M., Higgins, E. A., Watkins, L. R., Rudy, J. W., & Maier, S. F. (2009) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2008.07.002 · Cited by 226
Inflammation, anti-inflammatory agents and Alzheimer disease: The last 12 years
McGeer, P. L., Rogers, J., & McGeer, E. G. (2006) · Journal of Alzheimer s Disease · doi:10.3233/jad-2006-9s330 · Cited by 222
Self-citationChoi, S., Aïd, S., Kim, H., Jackson, S. H., & Bosetti, F. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07572.x · Cited by 228
Inflammation markers in relation to cognition in a healthy aging population
Teunissen, C. E., van Boxtel, M. P. J., Bosma, H., Bosmans, E., Delanghe, J., Bruijn, C. D., Wauters, A., Maes, M. H. J., Jolles, J., Steinbusch, H. W. M., et al. (2003) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00398-3 · Cited by 220
Cerebral pattern of pro- and anti-inflammatory cytokines in dementias
Tarkowski, E., Liljeroth, A.-M., Minthon, L., Tarkowski, A., Wallin, A., & Blennow, K. (2003) · Brain Research Bulletin · doi:10.1016/s0361-9230(03)00088-1 · Cited by 219
Microglia Gone Rogue: Impacts on Psychiatric Disorders across the Lifespan
Tay, T. L., Béchade, C., D’Andrea, I., St‐Pierre, M., Henry, M. S., Roumier, A., & Tremblay, M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00421 · Cited by 217
Inflammation, Antiinflammatory Agents, and Alzheimer’s Disease: The Last 22 Years
McGeer, P. L., Rogers, J., & McGeer, E. G. (2016) · Journal of Alzheimer's Disease · doi:10.3233/jad-160488 · Cited by 215
Self-citationTerai, K., Matsuo, A., & McGeer, P. L. (1996) · Brain Research · doi:10.1016/0006-8993(96)00310-1 · Cited by 215
Self-citation(1990) · PubMed Central · Cited by 214
Svoboda, D. S., Barrasa, M. I., Shu, J., Rietjens, R. G. J., Zhang, S., Mitalipova, M., Berube, P., Fu, D., Shultz, L. D., Bell, G. W., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1913541116 · Cited by 206
Increased microglial activation and protein nitration in white matter of the aging monkey☆
Sloane, J. A., Hollander, W., Moss, M. B., Rosene, D. L., & Abraham, C. R. (1999) · Neurobiology of Aging · doi:10.1016/s0197-4580(99)00066-4 · Cited by 208
The role of complement and activated microglia in the pathogenesis of Alzheimer's disease
Eikelenboom, P., & Veerhuis, R. (1996) · Neurobiology of Aging · doi:10.1016/0197-4580(96)00108-x · Cited by 206
Pro-Resolving Lipid Mediators Improve Neuronal Survival and Increase Aβ42 Phagocytosis
Zhu, M., Wang, X., Hjorth, E., Colas, R. A., Schroeder, L., Granholm, A.-C., Serhan, C. N., & Schultzberg, M. (2016) · Molecular Neurobiology · doi:10.1007/s12035-015-9544-0 · Cited by 204
NADPH oxidase as a therapeutic target in Alzheimer's disease
Block, M. L. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-s2-s8 · Cited by 203
Tweedie, D., Ferguson, R. A., Fishman, K., Frankola, K. A., van Praag, H., Holloway, H. W., Luo, W., Li, Y., Caracciolo, L., Russo, I., et al. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-106 · Cited by 208
Yates, S. L., Burgess, L. H., Kocsis‐Angle, J., Antal, J. M., Dority, M. D., Embury, P. B., Piotrkowski, A. M., & Brunden, K. R. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0741017.x · Cited by 202
Yang, X., Sheng, W., Sun, G. Y., & Lee, J. C. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.12.004 · Cited by 215
Emerging roles of pathogens in Alzheimer disease
Miklossy, J. (2011) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399411002006 · Cited by 206
Sawada, M., Suzumura, A., Yamamoto, H., & Marunouchi, T. (1990) · Brain Research · doi:10.1016/0006-8993(90)90317-5 · Cited by 201
Human APOE4 increases microglia reactivity at Aβ plaques in a mouse model of Aβ deposition
Rodriguez, G. A., Tai, L. M., LaDu, M. J., & Rebeck, G. W. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-111 · Cited by 193
Styren, S. D., Civin, W. H., & Rogers, J. (1990) · Experimental Neurology · doi:10.1016/0014-4886(90)90054-v · Cited by 191
Mori, T., Koyama, N., Guillot‐Sestier, M., Tan, J., & Town, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055774 · Cited by 191
Sequestration of RNA in Alzheimer's disease neurofibrillary tangles and senile plaques
Ginsberg, S. D., Crino, P. B., Lee, V. M. ‐., Eberwine, J. H., & Trojanowski, J. Q. (1997) · Annals of Neurology · doi:10.1002/ana.410410211 · Cited by 188
β-amyloid, microglia, and the inflammasome in Alzheimer’s disease
Gold, M., & El Khoury, J. (2015) · Seminars in Immunopathology · doi:10.1007/s00281-015-0518-0 · Cited by 187
Microglial Scavenger Receptors and Their Roles in the Pathogenesis of Alzheimer's Disease
Wilkinson, K., & Khoury, J. B. E. (2012) · International Journal of Alzheimer s Disease · doi:10.1155/2012/489456 · Cited by 197
Role of microglia in senile plaque formation
Mackenzie, I. R. A., Hao, C., & Munoz, D. G. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(95)00092-s · Cited by 183
Amyloid β protein (Aβ) removal by neuroglial cells in culture
Shaffer, L. M., Dority, M. D., Gupta‐Bansal, R., Frederickson, R. C. A., Younkin, S. G., & Brunden, K. R. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(95)00055-j · Cited by 180
Tooyama, I., Kimura, H., Akiyama, H., & McGeer, P. L. (1990) · Brain Research · doi:10.1016/0006-8993(90)91496-4 · Cited by 180
Self-citationMori, T., Rezai-Zadeh, K. P., Koyama, N., Arendash, G. W., Yamaguchi, H., Kakuda, N., Horikoshi‐Sakuraba, Y., Tan, J., & Town, T. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.294025 · Cited by 189
Udan, M. L. D., Ajit, D., Crouse, N. R., & Nichols, M. R. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05001.x · Cited by 179
Arginine Deprivation and Immune Suppression in a Mouse Model of Alzheimer's Disease
Kan, M. J., Lee, J. E., Wilson, J. G., Everhart, A. L., Brown, C. M., Hoofnagle, A. N., Jansen, M., Vitek, M. P., Gunn, M. D., & Colton, C. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4668-14.2015 · Cited by 178
Interleukin-2 improves amyloid pathology, synaptic failure and memory in Alzheimer’s disease mice
Alves, S., Churlaud, G., Audrain, M., Michaelsen‐Preusse, K., Fol, R. R., Souchet, B., Braudeau, J., Körte, M., Klatzmann, D., & Cartier, N. (2016) · Brain · doi:10.1093/brain/aww330 · Cited by 178
Rozemüller, A. J. M., Eikelenboom, P., Pals, S. T., & Stam, F. C. (1989) · Neuroscience Letters · doi:10.1016/0304-3940(89)90547-8 · Cited by 173
Myerowitz, R., Lawson, D., Mizukami, H., Mi, Y.-D., Tifft, C., & Proia, R. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.11.1343 · Cited by 161
Mechanisms of microglia accumulation in Alzheimer’s disease: therapeutic implications
Khoury, J. E., & Luster, A. D. (2008) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2008.08.004 · Cited by 171
A Phenotypic Change But Not Proliferation Underlies Glial Responses in Alzheimer Disease
Serrano-Pozo, A., Gómez-Isla, T., Growdon, J. H., Frosch, M. P., & Hyman, B. T. (2013) · The American Journal of Pathology · doi:10.1016/j.ajpath.2013.02.031 · Cited by 169
Microglial response to 6-hydroxydopamine-induced substantia nigra lesions
Akiyama, H., & McGeer, P. L. (1989) · Brain Research · doi:10.1016/0006-8993(89)90857-3 · Cited by 169
Self-citationYoshimura, K., Sakurai, Y., Nishimura, D., Tsuruo, Y., Nomura, M., Kawato, S., Seiwa, C., Iguchi, T., Itoh, K., & Asou, H. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19981001)54:1 · Cited by 15
Complement gene expression in human brain: comparison between normal and Alzheimer disease cases
Walker, D. G., & McGeer, P. L. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90017-6 · Cited by 167
Self-citationBiochemical markers related to Alzheimer’s dementia in serum and cerebrospinal fluid
Teunissen, C. E., de Vente, J., Steinbusch, H. W. M., & Bruijn, C. D. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00328-1 · Cited by 169
Early and Late CNS Inflammation in Alzheimer’s Disease: Two Extremes of a Continuum?
Cuello, A. C. (2017) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2017.07.005 · Cited by 170
Wiley, C. A., Lopresti, B. J., Venneti, S., Price, J. C., Klunk, W. E., DeKosky, S. T., & Mathis, C. A. (2009) · Archives of Neurology · doi:10.1001/archneurol.2008.511 · Cited by 160
Microglia Demonstrate Age-Dependent Interaction with Amyloid-β Fibrils
Floden, A. M., & Combs, C. K. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101014 · Cited by 166
Akiyama, H., Itagaki, S., & McGeer, P. L. (1988) · Journal of Neuroscience Research · doi:10.1002/jnr.490200202 · Cited by 160
Self-citationChoi, S., Langenbach, R. I., & Bosetti, F. (2007) · The FASEB Journal · doi:10.1096/fj.07-9411com · Cited by 159
Zhao, F., Cai, T., Liu, M., Zheng, G., Luo, W., & Chen, J. (2008) · Toxicological Sciences · doi:10.1093/toxsci/kfn213 · Cited by 157
Retinal pathological features and proteome signatures of Alzheimer’s disease
Koronyo, Y., Rentsendorj, A., Mirzaei, N., Regis, G. C., Sheyn, J., Shi, H., Barrón, E., Cook‐Wiens, G., Rodriguez, A., Medeiros, R., et al. (2023) · Acta Neuropathologica · doi:10.1007/s00401-023-02548-2 · Cited by 162
Gene expression profiling of amyloid beta peptide-stimulated human post-mortem brain microglia
Walker, D. G. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00306-2 · Cited by 155
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Chamak, B., Morandi, V., & Mallat, M. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490380213 · Cited by 164
Dystrophic microglia in late‐onset Alzheimer's disease
Streit, W. J., Khoshbouei, H., & Bechmann, I. (2020) · Glia · doi:10.1002/glia.23782 · Cited by 152
Amyloid-β-induced chemokine production in primary human macrophages and astrocytes
Smits, H. A., Rijsmus, A., van Loon, J. H., Wat, J. W. Y., Verhoef, J., Boven, L. A., & Nottet, H. S. L. M. (2002) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(02)00112-1 · Cited by 150
Microglial degeneration in the aging brain - bad news for neurons?
Streit, W. (2008) · Frontiers in Bioscience · doi:10.2741/2937 · Cited by 150
Rojanathammanee, L., Puig, K. L., & Combs, C. K. (2013) · Journal of Nutrition · doi:10.3945/jn.112.169516 · Cited by 150
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Geller, L. N., & Potter, H. (1999) · Neurobiology of Disease · doi:10.1006/nbdi.1999.0236 · Cited by 147
Mhatre, M., Floyd, R. A., & Hensley, K. (2004) · Journal of Alzheimer s Disease · doi:10.3233/jad-2004-6206 · Cited by 148
Glial cells in Alzheimer’s disease: From neuropathological changes to therapeutic implications
Uddin, M. S., & Lim, L. W. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101622 · Cited by 154
Neuroinflammatory responses in Alzheimer’s disease
Dansokho, C., & Heneka, M. T. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1831-7 · Cited by 146
Cell surface morphology identifies microglia as a distinct class of mononuclear phagocyte
Giulian, D., Li, J., Bartel, S., Broker, J., Li, X., & Kirkpatrick, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07712.1995 · Cited by 142
Microglia and the Immune Pathology of Alzheimer Disease
Giulian, D. (1999) · The American Journal of Human Genetics · doi:10.1086/302477 · Cited by 141
The effects of a novel NSAID on chronic neuroinflammation are age dependent☆
Hauss‐Wegrzyniak, B., Vraniak, P., & Wenk, G. L. (1999) · Neurobiology of Aging · doi:10.1016/s0197-4580(99)00028-7 · Cited by 141
COLTON, C., BROWN, C., COOK, D., NEEDHAM, L., XU, Q., CZAPIGA, M., SAUNDERS, A., SCHMECHEL, D., RASHEED, K., & VITEK, M. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00016-7 · Cited by 108
Evolution of neuroinflammation across the lifespan of individuals with Down syndrome
Flores-Aguilar, L., Iulita, M. F., Kovecses, O., Torres, M. D., Levi, S. M., Zhang, Y., Askenazi, M., Wisniewski, T., Busciglio, J., & Cuello, A. C. (2020) · Brain · doi:10.1093/brain/awaa326 · Cited by 138
Jefferies, W. A., Food, M. R., Gabathuler, R., Rothenberger, S., Yamada, T., Yasuhara, O., & McGeer, P. L. (1996) · Brain Research · doi:10.1016/0006-8993(95)01407-1 · Cited by 137
Self-citationThe role of microglia in human disease: therapeutic tool or target?
Cartier, N., Lewis, C. B., Zhang, R., & Rossi, F. M. V. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1330-y · Cited by 142
Neuropathology after active Aβ42 immunotherapy: implications for Alzheimer’s disease pathogenesis
Boche, D., Denham, N., Holmes, C., & Nicoll, J. A. R. (2010) · Acta Neuropathologica · doi:10.1007/s00401-010-0719-5 · Cited by 135
Mallach, A., Zielonka, M., van Lieshout, V., An, Y., Khoo, J. H., Vanheusden, M., Chen, W.-T., Moechars, D., Arancibia-Carcamo, I. L., Fiers, M., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114216 · Cited by 135
Nerve growth factor metabolic dysfunction in Alzheimer's disease and Down syndrome
Iulita, M. F., & Cuello, A. C. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.04.010 · Cited by 141
Moon, M., Choi, J. G., Nam, D. W., Hong, H., Choi, Y.-J., Oh, M. S., & Mook‐Jung, I. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-101263 · Cited by 136
Respiratory infection promotes T cell infiltration and amyloid-β deposition in APP/PS1 mice
McManus, R. M., Higgins, S. C., Mills, K. H. G., & Lynch, M. A. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.07.025 · Cited by 134
Gehrmann, J., Banati, R. B., & Kreutzberg, G. W. (1993) · Journal of Neuroimmunology · doi:10.1016/0165-5728(93)90191-z · Cited by 133
Kocherhans, S., Madhusudan, A., Doehner, J., Breu, K. S., Nitsch, R. M., Fritschy, J.-M., & Knuesel, I. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0418-10.2010 · Cited by 132
Targeting monocyte chemoattractant protein-1 signalling in disease
Dawson, J., Miltz, W., Mir, A. K., & Wießner, C. (2003) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.7.1.35 · Cited by 132
Choi, S., Aïd, S., Caracciolo, L., Minami, S., Niikura, T., Matsuoka, Y., Turner, R. S., Mattson, M. P., & Bosetti, F. (2012) · Journal of Neurochemistry · doi:10.1111/jnc.12059 · Cited by 136
Banati, R. B., Gehrmann, J., Czech, C., Mönning, U., Jones, L. L., König, G., Beyreuther, K. T., & Kreutzberg, G. W. (1993) · Glia · doi:10.1002/glia.440090305 · Cited by 132
Targeting microglia-mediated neurotoxicity: the potential of NOX2 inhibitors
Surace, M. J., & Block, M. L. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1015-4 · Cited by 134
Inflammasomes: Molecular Regulation and Implications for Metabolic and Cognitive Diseases
Choi, A. J. S., & Ryter, S. W. (2014) · Molecules and Cells · doi:10.14348/molcells.2014.0104 · Cited by 132
Modulation of human microglial cell superoxide production by cytokines
Chao, C. C., Hu, S., & Peterson, P. K. (1995) · Journal of Leukocyte Biology · doi:10.1002/jlb.58.1.65 · Cited by 131
Immune system associated antigens expressed by cells of the human central nervous system
Luber‐Narod, J., & Rogers, J. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90263-7 · Cited by 131
Leveugle, B., Spik, G., Perl, D. P., Bouras, C., Fillit, H. M., & Hof, P. R. (1994) · Brain Research · doi:10.1016/0006-8993(94)90202-x · Cited by 131
Donepezil inhibits the amyloid-beta oligomer-induced microglial activation in vitro and in vivo
Kim, H. G., Moon, M., Choi, J. G., Park, G., Kim, A., Hur, J., Lee, K., & Oh, M. S. (2013) · NeuroToxicology · doi:10.1016/j.neuro.2013.10.004 · Cited by 127
Walker, D. G., Tang, T. M., Mendsaikhan, A., Tooyama, I., Serrano, G. E., Sue, L. I., Beach, T. G., & Lue, L.-F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020678 · Cited by 128
Review: Impact of Helicobacter pylori on Alzheimer's disease: What do we know so far?
Doulberis, M., Kotronis, G., Thomann, R., Pοlyzos, S. A., Boziki, M. K., Gialamprinou, D., Deretzi, G., Katsinelos, P., & Kountouras, J. (2017) · Helicobacter · doi:10.1111/hel.12454 · Cited by 134
Cognitive and neuroinflammatory consequences of mild repeated stress are exacerbated in aged mice
Buchanan, J. B., Sparkman, N. L., Chen, J., & Johnson, R. W. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.02.013 · Cited by 128
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Béland, L.-C., Markovinovic, A., Jakovac, H., De Marchi, F., Bilic, E., Mazzini, L., Kriz, J., & Munitic, I. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa124 · Cited by 125
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Hu, X., Zhang, D., Pang, H., Caudle, W. M., Li, Y., Gao, H., Liu, Y., Li, Q., Wilson, B. C., Monte, D. A. D., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.10.7194 · Cited by 128
Handattu, S. P., Garber, D. W., Monroe, C. E., van Groen, T., Kadish, I., Nayyar, G., Cao, D., Palgunachari, M. N., Li, L., & Anantharamaiah, G. M. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.03.007 · Cited by 125
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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