Anatomy and Neuroscience - Research Publications

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    Prognosis in autoimmune encephalitis: Database
    Broadley, J ; Seneviratne, U ; Beech, P ; Buzzard, K ; Butzkueven, H ; O'Brien, T ; Monif, M (ELSEVIER SCIENCE BV, 2018-12)
    Autoimmune encephalitis is a rare and debilitating disease. An important question in clinical neurology is what factors may be correlated with outcomes in autoimmune encephalitis. There is observational data describing statistical analyses on such variables, but there are no review articles that collaborate and interpret this information. This data in brief article represents the data collection for such a review (Broadley et al., 2018). Herein we summarize clinical information from 44 research articles, in particular pertaining to outcomes and prognostic variables.
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    Characterization of the human myelin oligodendrocyte glycoprotein antibody response in demyelination
    Tea, F ; Lopez, JA ; Ramanathan, S ; Merheb, V ; Lee, FXZ ; Zou, A ; Pilli, D ; Patrick, E ; van der Walt, A ; Monif, M ; Tantsis, EM ; Yiu, EM ; Vucic, S ; Henderson, APD ; Fok, A ; Fraser, CL ; Lechner-Scott, J ; Reddel, SW ; Broadley, S ; Barnett, MH ; Brown, DA ; Lunemann, JD ; Dale, RC ; Brilot, F ; Sinclair, A ; Kermode, AG ; Kornberg, A ; Bye, A ; McGettigan, B ; Trewin, B ; Brew, B ; Taylor, B ; Bundell, C ; Miteff, C ; Troedson, C ; Pridmore, C ; Spooner, C ; Yiannikas, C ; O'Gorman, C ; Clark, D ; Suan, D ; Jones, D ; Kilfoyle, D ; Gill, D ; Wakefield, D ; Hofmann, D ; Mathey, E ; O'Grady, G ; Jones, HF ; Beadnall, H ; Butzkueven, H ; Joshi, H ; Andrews, I ; Sutton, I ; MacIntyre, J ; Sandbach, JM ; Freeman, J ; King, J ; O'Neill, JH ; Parratt, J ; Barton, J ; Garber, J ; Ahmad, K ; Riney, K ; Buzzard, K ; Kothur, K ; Cantrill, LC ; Menezes, MP ; Paine, MA ; Marriot, M ; Ghadiri, M ; Boggild, M ; Lawlor, M ; Badve, M ; Ryan, M ; Aaqib, M ; Shuey, N ; Jordan, N ; Urriola, N ; Lawn, N ; White, O ; McCombe, P ; Patel, R ; Leventer, R ; Webster, R ; Smith, R ; Gupta, S ; Mohammad, SS ; Pillai, S ; Hawke, S ; Simon, S ; Calvert, S ; Blum, S ; Malone, S ; Hodgkinson, S ; Nguyen, TK ; Hardy, TA ; Kalincik, T ; Ware, T ; Fung, VSC ; Huynh, W (BMC, 2019-09-03)
    Over recent years, human autoantibodies targeting myelin oligodendrocyte glycoprotein (MOG Ab) have been associated with monophasic and relapsing central nervous system demyelination involving the optic nerves, spinal cord, and brain. While the clinical relevance of MOG Ab detection is becoming increasingly clear as therapeutic and prognostic differences from multiple sclerosis are acknowledged, an in-depth characterization of human MOG Ab is required to answer key challenges in patient diagnosis, treatment, and prognosis. Herein, we investigated the epitope, binding sensitivity, and affinity of MOG Ab in a cohort of 139 and 148 MOG antibody-seropositive children and adults (n = 287 patients at baseline, 130 longitudinal samples, and 22 cerebrospinal fluid samples). MOG extracellular domain was also immobilized to determine the affinity of MOG Ab. MOG Ab response was of immunoglobulin G1 isotype, and was of peripheral rather than intrathecal origin. High affinity MOG Ab were detected in 15% paediatric and 18% adult sera. More than 75% of paediatric and adult MOG Ab targeted a dominant extracellular antigenic region around Proline42. MOG Ab titers fluctuated over the progression of disease, but affinity and reactivity to Proline42 remained stable. Adults with a relapsing course intrinsically presented with a reduced immunoreactivity to Proline42 and had a more diverse MOG Ab response, a feature that may be harnessed for predicting relapse. Higher titers of MOG Ab were observed in more severe phenotypes and during active disease, supporting the pathogenic role of MOG Ab. Loss of MOG Ab seropositivity was observed upon conformational changes to MOG, and this greatly impacted the sensitivity of the detection of relapsing disorders, largely considered as more severe. Careful consideration of the binding characteristics of autoantigens should be taken into account when detecting disease-relevant autoantibodies.
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    Innate Immunity in the Central Nervous System: A Missing Piece of the Autoimmune Encephalitis Puzzle?
    Wesselingh, R ; Butzkueven, H ; Buzzard, K ; Tarlinton, D ; O'Brien, TJ ; Monif, M (FRONTIERS MEDIA SA, 2019-09-10)
    The autoimmune encephalitides are a group of autoimmune conditions targeting the central nervous system and causing severe clinical symptoms including drug-resistant seizures, cognitive dysfunction and psychiatric disturbance. Although these disorders appear to be antibody mediated, the role of innate immune responses needs further clarification. Infiltrating monocytes and microglial proliferation at the site of pathology could contribute to the pathogenesis of the disease with resultant blood brain barrier dysfunction, and subsequent activation of adaptive immune response. Both innate and adaptive immune cells can produce pro-inflammatory molecules which can perpetuate ongoing neuroinflammation and drive ongoing seizure activity. Ultimately neurodegenerative changes can ensue with resultant long-term neurological sequelae that can impact on ongoing patient morbidity and quality of life, providing a potential target for future translational research.