Recurrent lymphocytic meningitis, also referred to as Mollaret meningitis, is a rare neurological disease characterized mainly by reactivation of herpes simplex virus 2 (HSV-2) from sensory ganglia. However, the underlying host immune determinants and viral factors rendering some individuals unable to maintain HSV-2 latency are largely unknown. We collected a cohort of 15 patients diagnosed with Mollaret meningitis. By whole-exome sequencing we identified rare host genetic variants predicted to be deleterious in molecules involved in (1) ubiquitin-proteasome pathways, (2) the autophagy machinery, and (3) cell proliferation/apoptosis. Moreover, infection of patient cells with HSV-2 or stimulation by virus-derived double-stranded DNA ligands revealed reduced antiviral interferon responses in most patients. These findings may contribute to a better understanding of disease pathogenesis and protective immunity to HSV in the central nervous system, and may ultimately be of importance for identification of targets for development of improved prophylaxis and treatment of this disease.

Download full-text PDF

Source
http://dx.doi.org/10.1093/infdis/jiaa589DOI Listing

Publication Analysis

Top Keywords

mollaret meningitis
12
whole-exome sequencing
8
sequencing patients
4
patients recurrent
4
hsv-2
4
recurrent hsv-2
4
hsv-2 lymphocytic
4
lymphocytic mollaret
4
meningitis
4
meningitis recurrent
4

Similar Publications

Mollaret meningitis is a rare form of recurrent, self-resolving, aseptic meningitis with a high rate of return. Although it has been associated with several conditions, herpes simplex virus type 2 (HSV-2) is most common. Diagnosis requires recurrent (>3) episodes of aseptic meningitis as defined by pleocytosis in cerebrospinal fluid (CSF) with negative bacterial cultures.

View Article and Find Full Text PDF
Article Synopsis
  • A 41-year-old Japanese woman with MEFV gene mutations presented with symptoms of Kikuchi disease and Mollaret meningitis, including fever, headache, and cervical lymphadenopathy.
  • Diagnostic tests confirmed Kikuchi disease through a lymph node biopsy and identified increased lymphocytes and three pathognomonic Mollaret cells in her cerebrospinal fluid.
  • Treatment with colchicine effectively managed her recurrent episodes of Kikuchi disease and meningitis, suggesting colchicine may be a viable option for similar cases.
View Article and Find Full Text PDF
Article Synopsis
  • Intracranial epidermoid cysts (ECs) are uncommon, non-cancerous growths usually located in specific areas of the brain, and they typically develop from leftover ectodermal cells from embryology.
  • Although these cysts are present from birth, symptoms usually appear in middle age due to pressure effects on surrounding brain tissue.
  • The case presented involves a 69-year-old man with an EC that unexpectedly ruptured and impacted brain tissue, highlighting a rare occurrence and contributing new insights to the understanding of these cysts.
View Article and Find Full Text PDF

Mollaret's meningitis is a rare neurological disorder characterized by recurrent episodes of aseptic lymphocytic meningitis, often associated with herpes simplex virus 2 (HSV-2) infection. We report the case of a 39 y.o.

View Article and Find Full Text PDF

Background And Purpose: Data on clinical features and outcomes of benign recurrent lymphocytic meningitis (BRLM) are limited.

Methods: This was a nationwide population-based cohort study of all adults hospitalized for BRLM associated with herpes simplex virus type 2 (HSV-2) at the departments of infectious diseases in Denmark from 2015 to 2020. Patients with single-episode HSV-2 meningitis were included for comparison.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!