CSF and blood signatures support classification of limbic encephalitis subtypes Article Swipe
Andreas Schulte‐Mecklenbeck
,
Andre Dik
,
Christine Strippel
,
Laura Bierhansl
,
Niklas Meyer
,
Lisanne Korn
,
Matthias Pawlowski
,
Saskia Räuber
,
Judith Alferink
,
Sven G. Meuth
,
Nico Melzer
,
Gerd Meyer zu Hörste
,
Harald Prüß
,
Heinz Wiendl
,
Catharina C. Groß
,
Stjepana Kovac
·
YOU?
·
· 2024
· Open Access
·
· DOI: https://doi.org/10.1016/j.bbi.2024.10.018
YOU?
·
· 2024
· Open Access
·
· DOI: https://doi.org/10.1016/j.bbi.2024.10.018
Autoimmune limbic encephalitis (ALE) represents a heterogeneous disease associated with antibodies targeting extracellular (ALEextra) epitopes, intracellular (ALEintra) epitopes, anti-glutamic acid decarboxylase65 ALE (ALEGAD65), and ALE without detectable antibodies (ALEabneg). Combining analysis of cellular parameters, investigated by flow cytometry, and soluble parameters in the blood and cerebrospinal fluid (CSF) from a large cohort of 148 ALE patients (33 ALEextra, 12 ALEintra, 28 ALE-GAD65, 37 ALEabneg) in comparison to paradigmatic examples for neuro-inflammatory (51 relapsing remitting MS patients (RRMS)), and neuro-degenerative (34 Alzheimer's disease patients (AD)) diseases revealed discrete immune signatures in ALE subgroups. Identification of ALE-subtype specific markers facilitated classification of rare ALE-associated tumors, which may prompt further diagnostic efforts in clinical practice. While ALEintra exhibited features of neuro-inflammation, ALEextra displayed features of neuro-inflammation as well as neuro-degeneration. Moreover, ALEGAD65 and ALEabneg lacked hallmarks of inflammation. This may explain the low efficacy of anti-inflammatory treatment regimens in ALEGAD65 and presumably also ALEabneg.
Related Topics
Concepts
Limbic encephalitis
Limbic system
Limbic lobe
Medicine
Psychology
Neuroscience
Encephalitis
Immunology
Virus
Central nervous system
Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1016/j.bbi.2024.10.018
- OA Status
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- References
- 24
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4403348616
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4403348616Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1016/j.bbi.2024.10.018Digital Object Identifier
- Title
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CSF and blood signatures support classification of limbic encephalitis subtypesWork title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2024Year of publication
- Publication date
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2024-10-12Full publication date if available
- Authors
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Andreas Schulte‐Mecklenbeck, Andre Dik, Christine Strippel, Laura Bierhansl, Niklas Meyer, Lisanne Korn, Matthias Pawlowski, Saskia Räuber, Judith Alferink, Sven G. Meuth, Nico Melzer, Gerd Meyer zu Hörste, Harald Prüß, Heinz Wiendl, Catharina C. Groß, Stjepana KovacList of authors in order
- Landing page
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https://doi.org/10.1016/j.bbi.2024.10.018Publisher landing page
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YesWhether a free full text is available
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hybridOpen access status per OpenAlex
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https://doi.org/10.1016/j.bbi.2024.10.018Direct OA link when available
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Limbic encephalitis, Limbic system, Limbic lobe, Medicine, Psychology, Neuroscience, Encephalitis, Immunology, Virus, Central nervous systemTop concepts (fields/topics) attached by OpenAlex
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0Total citation count in OpenAlex
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24Number of works referenced by this work
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10Other works algorithmically related by OpenAlex
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| publication_year | 2024 |
| referenced_works | https://openalex.org/W2544465965, https://openalex.org/W2961171977, https://openalex.org/W3128726177, https://openalex.org/W3160922307, https://openalex.org/W2564964128, https://openalex.org/W3216615419, https://openalex.org/W4310130646, https://openalex.org/W2280783985, https://openalex.org/W3152673411, https://openalex.org/W3133136253, https://openalex.org/W3217473669, https://openalex.org/W2133096503, https://openalex.org/W1785671910, https://openalex.org/W3091932761, https://openalex.org/W1917986498, https://openalex.org/W3181107652, https://openalex.org/W2909247417, https://openalex.org/W4205661108, https://openalex.org/W2805188161, https://openalex.org/W7075608323, https://openalex.org/W2777074421, https://openalex.org/W4385829919, https://openalex.org/W4319263061, https://openalex.org/W4225771916 |
| referenced_works_count | 24 |
| abstract_inverted_index.a | 5, 49 |
| abstract_inverted_index.12 | 58 |
| abstract_inverted_index.28 | 60 |
| abstract_inverted_index.37 | 62 |
| abstract_inverted_index.MS | 74 |
| abstract_inverted_index.as | 123, 125 |
| abstract_inverted_index.by | 35 |
| abstract_inverted_index.in | 41, 64, 89, 109, 145 |
| abstract_inverted_index.of | 31, 52, 93, 99, 116, 121, 133, 141 |
| abstract_inverted_index.to | 66 |
| abstract_inverted_index.(33 | 56 |
| abstract_inverted_index.(34 | 79 |
| abstract_inverted_index.(51 | 71 |
| abstract_inverted_index.148 | 53 |
| abstract_inverted_index.ALE | 21, 24, 54, 90 |
| abstract_inverted_index.and | 23, 38, 44, 77, 129, 147 |
| abstract_inverted_index.for | 69 |
| abstract_inverted_index.low | 139 |
| abstract_inverted_index.may | 104, 136 |
| abstract_inverted_index.the | 42, 138 |
| abstract_inverted_index.This | 135 |
| abstract_inverted_index.acid | 19 |
| abstract_inverted_index.also | 149 |
| abstract_inverted_index.flow | 36 |
| abstract_inverted_index.from | 48 |
| abstract_inverted_index.rare | 100 |
| abstract_inverted_index.well | 124 |
| abstract_inverted_index.with | 9 |
| abstract_inverted_index.(AD)) | 83 |
| abstract_inverted_index.(ALE) | 3 |
| abstract_inverted_index.(CSF) | 47 |
| abstract_inverted_index.While | 112 |
| abstract_inverted_index.blood | 43 |
| abstract_inverted_index.fluid | 46 |
| abstract_inverted_index.large | 50 |
| abstract_inverted_index.which | 103 |
| abstract_inverted_index.cohort | 51 |
| abstract_inverted_index.immune | 87 |
| abstract_inverted_index.lacked | 131 |
| abstract_inverted_index.limbic | 1 |
| abstract_inverted_index.prompt | 105 |
| abstract_inverted_index.disease | 7, 81 |
| abstract_inverted_index.efforts | 108 |
| abstract_inverted_index.explain | 137 |
| abstract_inverted_index.further | 106 |
| abstract_inverted_index.markers | 96 |
| abstract_inverted_index.soluble | 39 |
| abstract_inverted_index.tumors, | 102 |
| abstract_inverted_index.without | 25 |
| abstract_inverted_index.(RRMS)), | 76 |
| abstract_inverted_index.analysis | 30 |
| abstract_inverted_index.cellular | 32 |
| abstract_inverted_index.clinical | 110 |
| abstract_inverted_index.discrete | 86 |
| abstract_inverted_index.diseases | 84 |
| abstract_inverted_index.efficacy | 140 |
| abstract_inverted_index.examples | 68 |
| abstract_inverted_index.features | 115, 120 |
| abstract_inverted_index.patients | 55, 75, 82 |
| abstract_inverted_index.regimens | 144 |
| abstract_inverted_index.revealed | 85 |
| abstract_inverted_index.specific | 95 |
| abstract_inverted_index.Combining | 29 |
| abstract_inverted_index.Moreover, | 127 |
| abstract_inverted_index.displayed | 119 |
| abstract_inverted_index.epitopes, | 14, 17 |
| abstract_inverted_index.exhibited | 114 |
| abstract_inverted_index.hallmarks | 132 |
| abstract_inverted_index.practice. | 111 |
| abstract_inverted_index.relapsing | 72 |
| abstract_inverted_index.remitting | 73 |
| abstract_inverted_index.targeting | 11 |
| abstract_inverted_index.treatment | 143 |
| abstract_inverted_index.ALE-GAD65, | 61 |
| abstract_inverted_index.Autoimmune | 0 |
| abstract_inverted_index.antibodies | 10, 27 |
| abstract_inverted_index.associated | 8 |
| abstract_inverted_index.comparison | 65 |
| abstract_inverted_index.cytometry, | 37 |
| abstract_inverted_index.detectable | 26 |
| abstract_inverted_index.diagnostic | 107 |
| abstract_inverted_index.parameters | 40 |
| abstract_inverted_index.presumably | 148 |
| abstract_inverted_index.represents | 4 |
| abstract_inverted_index.signatures | 88 |
| abstract_inverted_index.subgroups. | 91 |
| abstract_inverted_index.ALE-subtype | 94 |
| abstract_inverted_index.Alzheimer's | 80 |
| abstract_inverted_index.facilitated | 97 |
| abstract_inverted_index.parameters, | 33 |
| abstract_inverted_index.encephalitis | 2 |
| abstract_inverted_index.investigated | 34 |
| abstract_inverted_index.paradigmatic | 67 |
| abstract_inverted_index.anti-glutamic | 18 |
| abstract_inverted_index.cerebrospinal | 45 |
| abstract_inverted_index.extracellular | 12 |
| abstract_inverted_index.heterogeneous | 6 |
| abstract_inverted_index.inflammation. | 134 |
| abstract_inverted_index.intracellular | 15 |
| abstract_inverted_index.ALE-associated | 101 |
| abstract_inverted_index.Identification | 92 |
| abstract_inverted_index.classification | 98 |
| abstract_inverted_index.decarboxylase65 | 20 |
| abstract_inverted_index.anti-inflammatory | 142 |
| abstract_inverted_index.neuro-degenerative | 78 |
| abstract_inverted_index.neuro-inflammation | 122 |
| abstract_inverted_index.neuro-inflammatory | 70 |
| abstract_inverted_index.ALE<sub>GAD65</sub> | 128, 146 |
| abstract_inverted_index.ALE<sub>abneg</sub> | 130 |
| abstract_inverted_index.ALE<sub>extra</sub> | 118 |
| abstract_inverted_index.ALE<sub>intra</sub> | 113 |
| abstract_inverted_index.neuro-degeneration. | 126 |
| abstract_inverted_index.neuro-inflammation, | 117 |
| abstract_inverted_index.ALE<sub>abneg</sub>) | 63 |
| abstract_inverted_index.ALE<sub>abneg</sub>. | 150 |
| abstract_inverted_index.ALE<sub>extra</sub>, | 57 |
| abstract_inverted_index.ALE<sub>intra</sub>, | 59 |
| abstract_inverted_index.(ALE<sub>extra</sub>) | 13 |
| abstract_inverted_index.(ALE<sub>intra</sub>) | 16 |
| abstract_inverted_index.(ALE<sub>GAD65</sub>), | 22 |
| abstract_inverted_index.(ALE<sub>abneg</sub>). | 28 |
| cited_by_percentile_year | |
| countries_distinct_count | 2 |
| institutions_distinct_count | 16 |
| citation_normalized_percentile.value | 0.31063648 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |