Evidence map›Paper›PMID 42094502›Full record

ArticlebioRxiv : the preprint server for biology2026

Pro-Cognitive Effects of IgM Isotype Anti-NMDAR1 Autoantibodies in Mice.

Jenna M DeWit, Tina Tebyanian, Alexandra Unapanta, Melonie N Vaughn, Susan B Powell, Victoria B Risbrough, Xianjin Zhou

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jenna M DeWitSchool of Biological Sciences, University of California San Diego, La Jolla, California, CA 92093, United States of America.
Tina TebyanianSchool of Biological Sciences, University of California San Diego, La Jolla, California, CA 92093, United States of America.
Alexandra UnapantaDepartment of Psychiatry, University of California San Diego, La Jolla, California, CA 92093, United States of America.
Melonie N VaughnDepartment of Psychiatry, University of California San Diego, La Jolla, California, CA 92093, United States of America.
Susan B PowellDepartment of Psychiatry, University of California San Diego, La Jolla, California, CA 92093, United States of America.
Victoria B RisbroughDepartment of Psychiatry, University of California San Diego, La Jolla, California, CA 92093, United States of America.
Xianjin ZhouDepartment of Psychiatry, University of California San Diego, La Jolla, California, CA 92093, United States of America.

Funding

Effects of Different Isotypes of Anti-NMDAR1 Autoantibodies on Cognitive Function and NeuroprotectionR01NS135620 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Victoria B Risbrough, XIANJIN ZHOU · 2024 to 2026
$1.6M
NINDS NIH HHS R01 NS135620
6 · The paper itself

Abstract

Natural anti-NMDAR1 autoantibodies are present at varying levels in the general human population, but their effects on cognitive function remain unclear. Recent human studies reported significant associations between higher blood levels of natural anti-NMDAR1 autoantibodies and potential neuroprotective outcomes in Alzheimer's disease, traumatic brain injury-associated depression and PTSD symptoms, and schizophrenia. However, whether these natural autoantibodies play a causal role in emotional and cognitive function has not been investigated. Since natural autoantibodies in human blood are predominantly of the IgM isotype, we immunized Aicda mutant mice to produce only IgM isotype anti-NMDAR1 autoantibodies without IgG and IgA isotypes. Mice were tested for sensorimotor gating and conditioned fear and extinction, cross species measures of information processing and emotional memory, respectively. Mice with higher levels of IgM anti-NMDAR1 autoantibodies exhibited significantly increased sensorimotor gating and improved fear extinction recall compared with mice with baseline levels of these autoantibodies. These findings indicate that IgM anti-NMDAR1 autoantibodies are pro-cognitive, unlike previous reports of poor cognition associated with IgG anti-NMDAR1 autoantibodies. Together, these studies suggest that IgM may hold therapeutic potential for a range of neurodegenerative, neurological, and psychiatric disorders.

Indexed as

Aicda Mutant MiceCognitive FunctionExcitotoxicityFear ConditioningIgM Anti-NMDAR1 autoantibodyPrepulse Inhibition

Identifiers

PMID42094502
PMCPMC13142351

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.