Multiple molecular mimics in Epstein Barr Nuclear Antigen-1, and the pathogenesis of multiple sclerosis.
Overview
- Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Beckman Center for Molecular Medicine, Stanford, CA 94305
- A*STAR Infections Diseases Labs, Agency for Science, Technology and Research, Singapore 138648, Singapore
- Division of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94304
- Department of Neurology, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA 94304
- The Geriatric Research, Education, and Clinical Center, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA 94304
- Institute for Immunity, Transplantation, and Infection, Stanford University, Stanford, CA 94305
Abstract
The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
Code
The paper links to its data, not to its authors' code: see the Data section.
The paper's code and data availability statement is in the Data section.
Tracing map
A tracing map links a paper to the code its authors published: this paper has none, so it has no map.
Data
Datasets cited
- rcsb.org/
structure/ , at PDB; found in the text, “Key role of posttranslational modifications in…”7uqc
Code and data availability statement
The paper has a code and data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- no repository, dataset or request procedure was recognized in it
Read it in the paper: doi.org/10.1073/pnas.2519445123.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 30 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 3 keywords, 9 MeSH terms, 1 funder, 64 references.
Cite
This paper
Lum, F. M., Sattarnezhad, N., Ho, P. P., Orr, N., Robinson, W. H., Lanz, T. V., & Steinman, L. (2026). Multiple molecular mimics in Epstein Barr Nuclear Antigen-1, and the pathogenesis of multiple sclerosis. Proceedings of the National Academy of Sciences of the United States of America, 123(11), e2519445123. https://
BibTeX
@article{lum2026multiple
author = {Lum, Fok Moon and Sattarnezhad, Neda and Ho, Peggy P and Orr, Noga and Robinson, William H and Lanz, Tobias V and Steinman, Lawrence},
title = {{Multiple molecular mimics in Epstein Barr Nuclear Antigen-1, and the pathogenesis of multiple sclerosis}},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
year = {2026},
month = mar,
volume = {123},
number = {11},
pages = {e2519445123},
publisher = {National Academy of Sciences},
issn = {0027-8424},
doi = {10.1073/
url = {https://
pmid = {41790925},
pmcid = {PMC12994170}
}
RIS
TY - JOUR
AU - Lum, Fok Moon
AU - Sattarnezhad, Neda
AU - Ho, Peggy P
AU - Orr, Noga
AU - Robinson, William H
AU - Lanz, Tobias V
AU - Steinman, Lawrence
TI - Multiple molecular mimics in Epstein Barr Nuclear Antigen-1, and the pathogenesis of multiple sclerosis
T2 - Proceedings of the National Academy of Sciences of the United States of America
J2 - Proc Natl Acad Sci U S A
PY - 2026
DA - 2026/
VL - 123
IS - 11
SP - e2519445123
SN - 0027-8424
PB - National Academy of Sciences
DO - 10.1073/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1073/
"type": "article-journal",
"title": "Multiple molecular mimics in Epstein Barr Nuclear Antigen-1, and the pathogenesis of multiple sclerosis",
"container-title": "Proceedings of the National Academy of Sciences of the United States of America",
"author": [
{
"family": "Lum",
"given": "Fok Moon"
},
{
"family": "Sattarnezhad",
"given": "Neda"
},
{
"family": "Ho",
"given": "Peggy P"
},
{
"family": "Orr",
"given": "Noga"
},
{
"family": "Robinson",
"given": "William H"
},
{
"family": "Lanz",
"given": "Tobias V"
},
{
"family": "Steinman",
"given": "Lawrence"
}
],
"container-title-short":
"volume": "123",
"issue": "11",
"page": "e2519445123",
"DOI": "10.1073/
"PMID": "41790925",
"PMCID": "PMC12994170",
"ISSN": "0027-8424",
"publisher": "National Academy of Sciences",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
3,
6
]
]
}
}
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1016/j.ebiom.2026.106324 [code]
- Refined single-cell profiling captures a CCR5&
lt;sup& gt;high& lt;/ sup& gt; CD4& lt;sup& gt;+& lt;/ sup& gt; cytotoxic T-cell precursor in multiple sclerosis. Journal: EBioMedicineIn common: multiple sclerosis, cellular / molecular, 1 reference - [2] doi:10.1186/s12951-026-04551-7
- The role of AI-assisted drug repurposing in neurological disorders: a systematic review of validation strategies, challenges and opportunities.Journal: Journal of nanobiotechnologyIn common: multiple sclerosis, 1 reference
- [3] doi:10.1016/j.isci.2026.115744
- Multiple sclerosis-associated HLA demarcates EBV-specific CD8&
lt;sup& gt;+& lt;/ sup& gt; T cells with an exhausted and brain residency phenotype. Journal: iScienceIn common: multiple sclerosis, 1 reference - [4] doi:10.1038/s41467-026-72997-2
- Endothelial cell-secreted SPARC suppresses astrocytic CD59 expression and promotes astrocytopathy in a mouse model of neuromyelitis optica spectrum disorders.Journal: Nature communicationsIn common: cellular / molecular, 1 reference
- [5] doi:10.1038/s41467-026-71759-4 [code]
- CellNiche represents cellular microenvironments in atlas-scale spatial omics data with contrastive learning.Journal: Nature communicationsIn common: cellular / molecular, 1 reference
- [6] doi:10.1371/journal.pone.0346693
- The normal human lymph node cell classification and landscape defined by high-dimensional spatial proteomics.Journal: PloS oneIn common: cellular / molecular, 1 reference
- [7] doi:10.1038/s41467-026-76762-3 [code]
- PD-1 regulates CD4&
lt;sup& gt;+& lt;/ sup& gt; T cell-mediated CD8& lt;sup& gt;+& lt;/ sup& gt; T cell responses in the brain to balance viral control and neuroinflammation. Journal: Nature communicationsIn common: cellular / molecular, 1 reference - [8] doi:10.1038/s41593-026-02267-3 [code]
- Spatial proteomic analysis in human Alzheimer's disease brains enables identification of microenvironment-depende
nt microglial cell states. Journal: Nature neuroscienceIn common: cellular / molecular, 1 reference - [9] doi:10.1038/s41598-026-51295-3
- Immune landscape of the affected brain in Rasmussen encephalitis.Journal: Scientific reportsIn common: cellular / molecular, 1 reference
- [10] doi:10.1002/jdn.70161 [code]
- Spatio-Temporal Dynamics of Macroglial Cell Organization and Proximity to Blood Vessels During Postnatal Development.Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental NeuroscienceIn common: 1 reference
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
