Evidence map›Paper›PMID 35479088›Full record

ArticleFrontiers in immunology2022

Identification of Anti-Collapsin Response Mediator Protein 2 Antibodies in Patients With Encephalitis or Encephalomyelitis.

Kaibiao Xu, Dongmei Wang, Yan He, Shengnan Wang, Guanghui Liu, Yue Pan, Haishan Jiang, Yu Peng, Fenliang Xiao, Yihua Huang and 4 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Kaibiao XuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Dongmei WangDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yan HeDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shengnan WangDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guanghui LiuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yue PanDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Haishan JiangDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yu PengDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Fenliang XiaoDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yihua HuangDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Qiqi WangDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yongming WuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Suyue PanDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yafang HuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Southern Medical University · CNNanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Purpose: An increasing number of autoimmune encephalitis (AE)-associated autoantibodies have been successfully characterized. However, many cases of AE remain unexplained on account of unknown antibodies. The aim of the present study was to identify a novel antibody against collapsin response mediator protein 2 (CRMP2) in suspected AE patients. Methods: A patient's serum and cerebrospinal fluid samples tested negative for known AE antibodies; however, strong immunolabel signals were observed in the neuronal cytoplasm of the cortex, hippocampus, and Purkinje cells on rat brain sections. Immunoprecipitation from the rat brain protein lysate, followed by mass spectrometry analysis, was used to identify the targeting antigen. Western blotting and cell-based assay with antigen-overexpressing HEK293T cells were used for antibody specificity, epitope, IgG subtype determination, and retrospective study. Results: An antibody against CRMP2, a synaptic protein involved in axon guidance, was identified. The immunostains of the patient's samples on rat brain sections were eliminated by pre-absorption with HEK293T cells overexpressing CRMP2. The samples specifically immunoreacted with CRMP2, but not with CRMP1, CRMP3, CRMP4, and CRMP5. The C-terminus of CRMP2 with 536 amino acids contained the epitope for antibody binding. The subtype analysis showed that the anti-CRMP2 antibody was IgG4. Furthermore, a screening of 46 patients with neurological disoders and neuro-cytoplasm immunostainings on rat brain sections resulted in the identification of anti-CRMP2 antibodies in a case of encephalomyelitis. The two patients responded well to immunotherapies. Conclusions: This study discovered that a novel anti-CRMP2 antibody was associated with suspected AE and thus should be included in the testing list for AE.

Indexed as

EncephalitisEncephalomyelitisAnimalsEpitopesHashimoto DiseaseHEK293 CellsHumansRatsRetrospective StudiesEpitopesautoantibodiesbrain inflammationCRMP2 proteininflammatory encephalomyelitisneurologic autoimmune diseases

Identifiers

PMID35479088
PMCPMC9036435
OpenAlexW4223605540

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.