# Anti-NMDAR encephalitis following malaria: expanding the spectrum of post−malarial neurological syndromes

**Authors:** Shuwen Deng, Wenlong Wang, Wei Lu, Shige Wang

PMC · DOI: 10.3389/fimmu.2026.1762504 · 2026-03-12

## TL;DR

This paper reports the first confirmed case of anti-NMDAR encephalitis following malaria, expanding the known neurological complications of the disease.

## Contribution

The study presents the first antibody-confirmed case of anti-NMDAR encephalitis triggered by Plasmodium falciparum malaria.

## Key findings

- Anti-NMDAR encephalitis occurred in a patient 11 days after recovering from P. falciparum malaria.
- The patient showed rapid improvement after immunotherapy, with no evidence of other infections or tumors.
- The case highlights the need for early antibody testing for AIE in post-malarial neuropsychiatric symptoms.

## Abstract

Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is the most common form of autoimmune encephalitis (AIE), often triggered by viral infections or tumors. This report describes a rare case following a parasitic infection.

We report a rare case of anti-NMDAR encephalitis developing in a 40-year-old man following recovery from Plasmodium falciparum malaria. Despite confirmed parasite clearance, he presented eleven days later with seizures, altered consciousness, and acute psychosis. Anti-NMDAR antibodies were detected in the cerebrospinal fluid (CSF) via both immunofluorescence and cell-based assay, with no evidence of concurrent infection or malignancy. The patient showed rapid clinical improvement after first-line immunotherapy.

This report represents the first antibody-confirmed case of anti-NMDAR encephalitis following Plasmodium falciparum infection, highlighting malaria as a novel post-infectious trigger and expanding the recognized spectrum of post-malarial neurological syndromes (PMNS). It underscores that clinicians in endemic regions should maintain a high index of suspicion for AIE in patients with new neuropsychiatric symptoms after malaria and pursue early antibody testing and immunotherapy.

## Linked entities

- **Diseases:** autoimmune encephalitis (MONDO:0020640), malaria (MONDO:0005136)
- **Species:** Plasmodium falciparum (taxon 5833)

## Full-text entities

- **Diseases:** Plasmodium falciparum infection (OMIM:248310), viral infections (MESH:D014777), malignancy (MESH:D009369), seizures (MESH:D012640), acute psychosis (MESH:D011605), altered consciousness (MESH:D003244), infection (MESH:D007239), PMNS (MESH:D000094025), AIE (MESH:D020274), malaria (MESH:D008288), Plasmodium falciparum malaria (MESH:D016778), neuropsychiatric symptoms (MESH:D001523), Anti-N-methyl-D-aspartate receptor ( (MESH:D060426), parasitic infection (MESH:D010272)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13019358/full.md

---
Source: https://tomesphere.com/paper/PMC13019358