Other Titles

Rising Star Poster/Presentation - Rapid Presentation Round

Abstract

Autoimmune Encephalitis (AE) is a disease in which the cells of the immune system attack the brain, causing inflammation also known as encephalitis. Brain Inflammation diminishes its proper functioning and can severely impact basic processing skills. The presentation of AE is difficult to identify, because it varies depending on the antibodies involved and the location of inflammation. Autoimmune encephalitis can gradually worsen over time, and can even be fatal. The disease is rare, but as diagnosis methods improve, more and more cases are being discovered. Autoimmune Encephalitis has been found to be more common in women than men. There are 13 known forms of autoimmune encephalitis, and there is no cure for any form. Anti N-methyl-D-aspartate (NMDA) receptor encephalitis, the most common form of AE, has a recovery rate of ~ 80% after two years of treatment. The sudden onset of symptoms and often rapid decline in health leaves families completely unprepared for how much their lives will change. People with AE after recovery are twice as likely to develop an anxiety disorder, and nearly three times as likely to develop depression.

Psychiatric symptoms of autoimmune encephalitis are commonly preceded by infections or flu-like illnesses and begin weeks to months after infection. Typically, diagnosis of autoimmune encephalitis requires:

  • Short term memory loss and altered mental state within three months of each other
  • At least one of the following
    • Numbness, weakness, or paralysis in a specific limb/area of the body
    • Unexplained seizures
    • Elevated WBC count
    • MRI showing brain inflammation

Further testing may be done to identify the targeted antigen type of encephalitis. For example tumor screening may be necessary for anti-NMDA receptor encephalitis, as it commonly associated with teratoma, a tumor found in the ovaries (this may contribute to the reason why a large majority of people diagnosed with anti-NMDA receptor encephalitis are women).

Intravenous Immunoglobulin (IVIG) is a common treat for autoimmune encephalitis. IVIG removes harmful antibodies from a patient’s blood, and replaces them with antibodies from the plasma of healthy donors to reduce inflammation. Studies have shown IVIG to be effective in improving the functional outcomes of autoimmune encephalitis. Immunosuppressant medications, such as Rituximab, work by suppressing the immune system function to improve inflammation, though there is a higher risk of infection. Steroids can also be prescribed to reduce inflammation.

Oftentimes patients with AE may experience mental and behavioral abnormalities, so nurses may have to collaborate with psychiatrists to create a care plan. It is crucial to pay particular attention to nonverbal cues, because patients with communication impairments may not be able to express pain or discomfort. Nurses should also be informed on the past medical history of the patient so that they can recognize risks. Basic vital signs should be monitored regularly, especially after receiving treatment. Teaching and reinforcing healthy coping strategies is crucial to the overall well being of patients with autoimmune encephalitis. mental health should be assessed by the nurse daily to gauge an understanding of how a patient is coping.

Notes

References:

Autoimmune Encephalitis Alliance (n.d). What is AE? https://aealliance.org/patient-support/what-is-ae/

Cleveland Clinic (n.d). Diagnosis and Management of Autoimmune Encephalitis. https://my.clevelandclinic.org/departments/neurological/depts/multiple-sclerosis/ms-approaches/diagnosis-and-management-of-autoimmune-encephalitis

Dubey, D., Pittock, S. J., Kelly, C. R., McKeon, A., Lopez-Chiriboga, A. S., Lennon, V. A., Gadoth, A., Smith, C. Y., Bryant, S. C., Klein, C. J., Aksamit, A. J., Toledano, M., Boeve, B. F., Tillema, J. M., & Flanagan, E. P. (2018). Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis. Annals of neurology, 83(1), 166–177. https://doi.org/10.1002/ana.25131

Gole S, Anand A. Autoimmune Encephalitis. [Updated 2023 Jan 2]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK578203/

Oregon Health & Science University Brain Institute (n.d). Autoimmune Encephalitis. https://www.ohsu.edu/brain-institute/autoimmune-encephalitis#:~:text=What%20is%20autoimmune%20encephalitis%3F,that%20mistakenly%20attack%20brain%20cells

Samanta D, Lui F. Anti-NMDAR Encephalitis. [Updated 2023 Jul 17]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK551672/

University of Pennsylvania Perelman School of Medicine (n.d). Anti-NMDAR Encephalitis. https://www.med.upenn.edu/autoimmuneneurology/nmdar-encephalitis.html

Yang, L., Jiang, Q., Guan, H., & Bo, H. (2019). Nursing care in anti-N-methyl-D-aspartate receptor encephalitis: A case series. Medicine, 98(46), e17856. https://doi.org/10.1097/MD.0000000000017856

Description

When the brain is under attack, every mechanism in our bodies is susceptible to impairment, especially when the perpetrator is your own immune system. This is the case with Autoimmune Encephalitis, a disease in which antigens of the brain are targeted, causing inflammation and symptoms resembling schizophrenia.

Author Details

Ophelia Hyde, NIH SIP University of Miami

Sigma Membership

Non-member

Type

Poster

Format Type

Text-based Document

Study Design/Type

Other

Research Approach

Other

Keywords:

Demyelinating Diseases, Inflammation, Demyelinating Diseases -- Psychosocial Factors, Autoimmune Encephalitis, Brain Inflamation

Conference Name

Creating Healthy Work Environments

Conference Host

Sigma Theta Tau International

Conference Location

Washington, DC, USA

Conference Year

2024

Rights Holder

All rights reserved by the author(s) and/or publisher(s) listed in this item record unless relinquished in whole or part by a rights notation or a Creative Commons License present in this item record. All permission requests should be directed accordingly and not to the Sigma Repository. All submitting authors or publishers have affirmed that when using material in their work where they do not own copyright, they have obtained permission of the copyright holder prior to submission and the rights holder has been acknowledged as necessary.

Review Type

Abstract Review Only: Reviewed by Event Host

Acquisition

Proxy-submission

Date of Issue

2026-02-17

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Autoimmune Encephalitis: The Psychological Impact of Brain Inflammation

Washington, DC, USA

Autoimmune Encephalitis (AE) is a disease in which the cells of the immune system attack the brain, causing inflammation also known as encephalitis. Brain Inflammation diminishes its proper functioning and can severely impact basic processing skills. The presentation of AE is difficult to identify, because it varies depending on the antibodies involved and the location of inflammation. Autoimmune encephalitis can gradually worsen over time, and can even be fatal. The disease is rare, but as diagnosis methods improve, more and more cases are being discovered. Autoimmune Encephalitis has been found to be more common in women than men. There are 13 known forms of autoimmune encephalitis, and there is no cure for any form. Anti N-methyl-D-aspartate (NMDA) receptor encephalitis, the most common form of AE, has a recovery rate of ~ 80% after two years of treatment. The sudden onset of symptoms and often rapid decline in health leaves families completely unprepared for how much their lives will change. People with AE after recovery are twice as likely to develop an anxiety disorder, and nearly three times as likely to develop depression.

Psychiatric symptoms of autoimmune encephalitis are commonly preceded by infections or flu-like illnesses and begin weeks to months after infection. Typically, diagnosis of autoimmune encephalitis requires:

  • Short term memory loss and altered mental state within three months of each other
  • At least one of the following
    • Numbness, weakness, or paralysis in a specific limb/area of the body
    • Unexplained seizures
    • Elevated WBC count
    • MRI showing brain inflammation

Further testing may be done to identify the targeted antigen type of encephalitis. For example tumor screening may be necessary for anti-NMDA receptor encephalitis, as it commonly associated with teratoma, a tumor found in the ovaries (this may contribute to the reason why a large majority of people diagnosed with anti-NMDA receptor encephalitis are women).

Intravenous Immunoglobulin (IVIG) is a common treat for autoimmune encephalitis. IVIG removes harmful antibodies from a patient’s blood, and replaces them with antibodies from the plasma of healthy donors to reduce inflammation. Studies have shown IVIG to be effective in improving the functional outcomes of autoimmune encephalitis. Immunosuppressant medications, such as Rituximab, work by suppressing the immune system function to improve inflammation, though there is a higher risk of infection. Steroids can also be prescribed to reduce inflammation.

Oftentimes patients with AE may experience mental and behavioral abnormalities, so nurses may have to collaborate with psychiatrists to create a care plan. It is crucial to pay particular attention to nonverbal cues, because patients with communication impairments may not be able to express pain or discomfort. Nurses should also be informed on the past medical history of the patient so that they can recognize risks. Basic vital signs should be monitored regularly, especially after receiving treatment. Teaching and reinforcing healthy coping strategies is crucial to the overall well being of patients with autoimmune encephalitis. mental health should be assessed by the nurse daily to gauge an understanding of how a patient is coping.