INTRODUCTION
Discovery of the spectrum of autoimmune encephalitis (AIE) is among the most attractive
events of neurology in the past decade. AIE includes a heterogeneous group of encephalitic
syndromes, which generally include two major categories: classic paraneoplastic limbic
encephalitis (LE) associated with the so-called well-characterized onconeural autoantibodies
against intracellular neuronal antigens (e.g., Hu, Ma2, etc.) and new-type AIE associated
with autoantibodies to the neuronal surface or synaptic antigens.[1] Paraneoplastic
LE occurs in the context of malignant tumors and results from an immunological response
to tumor antigens, which mimic intracellular antigens expressed in neurons. The autoantibodies
in this situation might not be pathogenic but can serve as diagnostic markers for
paraneoplastic LE. The new-type AIE occurs in association with pathogenic autoantibodies
against synaptic receptors or membrane antigens, and the binding of autoantibodies
to their targets causes neuronal dysfunction, usually irreversibly. Over a dozen new-type
autoantibodies have been identified since the discovery of anti-N-methyl-D-aspartate
receptor (NMDAR) antibody by Dalmau et al. in 2007.[2] Most of these autoantibodies
associated with specific and well-characterized symptoms and the detection of these
autoantibodies confirm the diagnosis. Since the introduction and establishment of
the diagnostic test for anti-NMDAR antibody in China in 2010,[3] hundreds of cases
of AIE have been diagnosed and treated, which has changed our clinical approach to
encephalitis management. The following sections will focus on a few recent advances
as well as related clinical research on AIE in China.
EPIDEMIOLOGY
Autoimmune encephalitis is not a rare cause of encephalitis. However, it is still
difficult to estimate its incidence. Anti-NMDAR encephalitis is the major component
of the disease spectrum. According to the UK-based prospective surveillance study
in children, the incidence of anti-NMDAR encephalitis is 0.85 per million children
annually.[4] No data about incidence in adults is available. Gable et al.[5] reported
that the frequency of anti-NMDAR encephalitis surpassed that of individual viral etiologies
in young individuals enrolled in the California Encephalitis Project. Increasing numbers
of AIE cases have been identified in China since the autoantibody assay was introduced
to some neurological centers after 2010. The frequency of AIE also surpassed that
of viral encephalitis in our project in Peking Union Medical College Hospital (PUMCH).
A total of 4106 cases of encephalitis of unidentified etiology were registered to
PUMCH encephalitis and paraneoplastic neurological syndrome project for autoantibody
assay between May, 2013 and December, 2014. A total of 531 cases (12.9%) were positive
for autoantibodies, including 423 cases (10.3%) with anti-NMDAR antibodies, 68 cases
(1.66%) with anti-leucine-rich glioma-inactivated 1 (LGI1) antibodies, thirty cases
(0.73%) with anti-γ-aminobutyric acid B receptor (GABABR) antibodies, seven cases
(0.17%) with anti-contactin associated protein 2 (CASPR2) antibodies, and three cases
(0.073%) with anti-α-amino-3-hydroxy-5-methyl-4-isoxazole propionate receptor (AMPAR)
antibodies. The relative frequencies of the NMDAR, LGI1, GABABR, CASPR2, and AMPAR
antoantibodies were 79.7%, 12.8%, 5.6%, 1.3%, and 0.6%, respectively, in patients
with AIE [Figure 1]. Our findings indicate that AIE associated with autoantibodies
is one of the major causes of encephalitis. Anti-NMDAR encephalitis is the most common
cause of AIE, followed by anti-LGI1 encephalitis. However, the frequency of anti-LGI1
encephalitis may be underestimated due to potentially unrecognized cases with insidious
onset in elderly patients which mimic neurodegenerative disorders.
Figure 1
The laboratory experience of PUMCH encephalitis and paraneoplastic neurological syndrome
project. A total of 4106 cases with encephalitis of unidentified etiology were test
for antibodies against neuronal cell-surface or synaptic protein: 531 cases (12.9%)
were positive for autoantibodies, including 423 cases (10.3%) with anti-NMDAR antibodies,
68 cases (1.66%) with anti-LGI1 antibodies, thirty cases (0.73%) with anti-GABABR
antibodies, seven cases (0.17%) with anti-CASPR2 antibodies and three cases (0.073%)
with anti-AMPAR antibodies. PUMCH: Peking Union Medical College Hospital; Ab: Antibody;
NMDAR: N-methyl-D-aspartate receptor; LGI1: Leucine-rich glioma-inactivated 1; GABABR:
γ-aminobutyric acid B receptor; CASPR2: Contactin-associated protein 2; AMPAR: α-amino-3-hydroxy-5-methyl-4-isoxazole
propionate receptor.
PATHOGENIC MECHANISM
Understanding the pathogenic mechanisms is critical for research and clinical management
of AIE. Most data focus on anti-NMDAR antibodies, which recognize an extracellular
epitope in the GluN1 subunit of the NMDAR. The autoantibodies crosslink the NMDARs
and promote internalization of the receptors, which reduces the receptor density on
the neuronal surface, resulting in neuronal dysfunction.[6] This process is reversible
after removal of autoantibodies and may explain the good recovery of patients after
immunotherapy.[7] The internalization of receptors was also described as an effect
of autoantibodies in AMPAR encephalitis.[8] Other autoantibodies may work through
different mechanisms. For example, anti-LGI1 antibodies block the binding sites of
LGI1, which results in a decrease of AMPAR via unknown mechanisms.[9] Anti-GABABR
antibodies influence receptor function and block the inhibitory effects of baclofen
on the spontaneous firing of cultured neurons.[10]
Pathological studies on anti-NMDAR encephalitis indicated that the intrathecal antibody
synthesis in the disease is associated with the colonization of B-cells and plasma
cells in the central nerve system (CNS). Analysis of the inflammatory infiltrates
in brain samples from autopsy or biopsy demonstrated numerous plasma cells (CD138+)
in perivascular, interstitial, and Virchow–Robin spaces, and B- and T-cells predominantly
located in perivascular regions. Complement-mediated mechanisms did not play a substantial
pathogenic role in anti-NMDAR encephalitis.[11]
Tumors and infections may trigger the onset of AIE. According to Dr. Dalmau et al.,
46% of female patients with anti-NMDAR encephalitis had tumors, mainly ovarian teratoma
and Asian patients were more likely to have a teratoma (45%) than Caucasians (31%)
or Hispanics (27%).[7] However, in our series of 115 Chinese patients with anti-NMDAR
encephalitis, only 26.5% (18/68) of female patients had ovarian teratoma, while the
series reported by other centers in China showed even lower percentages of related
tumor.[12] The CNS is an immune-privileged organ. Neuronal cell surface antigens do
not activate the immune system under physiological conditions. However, the activation
can be induced elsewhere either by a systemic tumor or an infection. Neural tissues
with NMDAR are always present in teratoma and represent potential autoantigens. Tabata
et al.[13] reported a pathological observation of neuronal tissues obtained from ovarian
teratoma in patients with anti-NMDAR encephalitis. Lymphocyte infiltration was more
frequent in the encephalitis group than in the nonencephalitis group. Dense B-lymphocyte
infiltration near neural tissues was observed in the encephalitis group. Differences
in lymphocyte infiltration in ovarian teratoma between anti-NMDAR encephalitis and
nonencephalitis patients underscore the immunological importance of the ovarian teratoma
as the site of initial antigen presentation in anti-NMDAR encephalitis.
Herpes simplex virus encephalitis (HSVE) is a triggering factor for anti-NMDAR encephalitis.[14]
The so-called post-HSVE choreoathetosis in children is confirmed now as post-HSVE
anti-NMDAR encephalitis due to the fact that patients with relapsing symptoms had
no evidence of viral reactivation but harbor NMDAR antibodies and respond well to
immunotherapy. Other viral infections are suspected to play a role in triggering anti-NMDAR
encephalitis and still need further confirmation.[15]
However, the triggering factor remains unknown for a considerable percentage of patients
with AIE. We recently reported two female cases with tumor-negative anti-NMDAR encephalitis
after resection of melanocytic nevus.[16] Our observation suggests a possible link
between AIE and melanocytic nevus. Melanoblasts migrate from the neural crest to the
epidermis and hair follicles, where they differentiate and become mature melanocytes
that synthesize melanin. Hoogduijn et al.[17] found that cultured melanocytes express
NMDAR. Therefore, NMDAR in melanocytic nevus may be a potential autoantigen in the
pathogenesis of anti-NMDAR encephalitis. It might be reasonable to pay attention to
prominent melanocytic nevus in patients with relapsing anti-NMDAR encephalitis without
detectable tumor.
CLINICAL PRESENTATION
The degree of syndrome specificity should not be overlooked because each of the neuronal
cell-surface autoantibodies is associated with a relatively specific syndrome [Table
1].[1
18] For example, the manifestations of anti-NDMAR encephalitis can be categorized
into eight groups: behavior and cognition, memory, speech, seizures, movement disorder,
loss of consciousness, autonomic dysfunction, and central hypoventilation.[7] Fever
and headache have been suggested as prodromal symptoms without specificity. However,
the cerebrospinal fluid (CSF) pleocytosis and meningeal enhancement in magnetic resonance
imaging (MRI) in some cases indicate meningeal involvement which is consistent with
neuropathological findings of this disorder. Persistent fever in the active phase
of anti-NDMAR encephalitis may result from CNS dysfunction or sympathetic hyperactivity
when infection can be ruled out. The presentation of anti-NDMAR encephalitis differs
from classical LE in its diffuse CNS involvement and represents a unique type of AIE.[1]
On the other hand, AIE associated with autoantibodies against LGI1, GABABR, and AMPAR
often presents with limbic syndrome, for example, epilepsy, short-term memory loss,
and psychiatric symptoms.
Table 1
Autoimmune encephalitis with antibodies against neuronal cell-surface or synaptic
protein
Antigen
Clinical syndrome
Tumor
NMDAR
Diffuse encephalitis Prodromal symptoms, psychiatric, seizures, amnesia, movement
disorders, catatonia, autonomic instability, and coma
10–45% female adult patients; ovarian teratoma
LGI1
Limbic encephalitis, hyponatremia, and occasional FBDS
Rare
GABABR
Limbic encephalitis and prominent seizures
30–50%; SCLC
AMPAR
Limbic encephalitis and psychiatric symptoms
70%; lung, breast, and thymoma
Caspr2
Encephalitis, Morvan syndrome, and neuromyotonia
0–40%; thymoma
mGluR5
Limbic encephalitis (reported in less than ten patients)
Frequent; Hodgkin lymphoma
D2R
Basal ganglia encephalitis and Sydenham chorea
Infrequent
DPPX
Diarrhea, encephalitis with CNS hyperexcitability Confusion, psychiatric symptoms,
tremor, myoclonus, nystagmus, hyperekplexia, PERM-like symptoms, and ataxia
No tumor association
GABAAR
Refractory seizures, status epilepticus, or epilepsia partialis continua, stiff-person,
opsoclonus
Infrequent
GlyR
Stiff-person, PERM, limbic encephalitis, ataxia
Infrequent
IgLON5
Abnormal sleep movements and behaviors, obstructive sleep apnea, stridor, dysarthria,
dysphagia, ataxia, and chorea
No tumor association
Modified according to autoimmune encephalopathies by Leypoldt et al.[1] NMDAR: N-methyl-D-aspartate
receptor; LGI1: Leucine-rich glioma-inactivated 1; GABABR: γ-aminobutyric acid B receptor;
FBDS: Faciobrachial seizures; SCLC: Small cell lung cancer; CASPR2: Contactin-associated
protein 2; AMPAR: α-amino-3-hydroxy-5-methyl-4-isoxazole propionate receptor; mGluR5:
Metabotropic glutamate receptor 5; D2R: Dopamine-2 receptor; DPPX: Dipeptidyl-peptidase-like
protein 6; GABAAR: γ-aminobutyric acid B receptor; GlyR: Glycine receptor; IgLON5:
IgLON family member 5; CNS: Central nerve system; PERM: Progressive encephalomyelitis
with rigidity and myoclonus.
The so-called autoimmune epilepsy is another frontier of AIE. Faciobrachial dystonic
seizures and temporal lobe epilepsy with amygdala enlargement may be the characteristic
type of seizure in anti-LGI1 encephalitis.[19
20
21] Recently, Li et al.[22] described a negative myoclonus in a Chinese child with
anti-NMDAR encephalitis. Our study [23] demonstrated that most Chinese patients with
anti-GABABR antibody-associated LE presented with prominent refractory epilepsy, which
usually improved neurologically with immunotherapy.
DIAGNOSTIC APPROACH
Different techniques are available for the diagnosis of neuronal cell-surface antibodies.
Most laboratories in China use the cell-based assay (CBA, Euroimmun, Germany) commercially
available for the diagnosis of neuronal cell-surface autoantibodies, which is a highly
sensitive and specific assay. Tissue-based assays (TBAs, Euroimmun, Germany) are used
in confirmative tests in addition to CBA if only serum is available. TBA can also
be used as a screening method to reveal yet-to-be-identified autoantigens when so-called
unknown fluorescence object (UFO) is observed. However, resources for identification
of new autoantigens underlying the UFO are still limited in China. Timely diagnosis
of AIE is usually hindered by the lack of laboratory resources in some areas of China.
The rule of “CSF ONLY” has been emphasized in the diagnosis of anti-NMDAR encephalitis
because the autoantibodies always exist in CSF and the determination of serum autoantibodies
alone carries the risk of diagnostic errors. The sensitivity of NMDAR antibody testing
is higher in CSF than in serum. However, it may not be true for anti-LGI1 antibodies
or anti-GABABR antibodies which might be more prevalent in serum than in CSF. Titers
of anti-NMDAR encephalitis in CSF and serum were higher in patients with poor outcome
or teratoma than in patients with a good outcome or no tumor. The titer change in
CSF was more closely related with relapses than was that in serum. Our laboratory
at PUMCH always requires serum-CSF pairs for autoantibody assay to minimize errors
of interpretation and misleading diagnoses.[24]
A recent report of anti-NMDAR antibodies after plasma exchange and removal of ovarian
teratoma in a patient with encephalopathy suggested that the antibodies may be undetectable
in an early phase in some cases.[25] We also experienced two female patients with
encephalitis and ovarian teratoma without detectable autoantibodies either on CBA
or TBA (no UFO identified) but showed good recovery after immunotherapy and teratoma
resection. Under these circumstances, the anti-NMDAR antibodies which were produced
by the localized plasma cells and cause neuronal dysfunction may not reach a detectable
level in lumbar CSF due to a concentration gradient.
Other CSF findings of anti-NMDAR encephalitis include increased CSF pressure and mild
elevation of white cell counts and protein.[26] Mild lymphocytic inflammation with
activated lymphocytes and plasma cells was identified in CSF cytology studies of anti-NMDAR
encephalitis [Figure 2]. The presence of oligoclonal bands and plasma cells in CSF
indicates intrathecal immunoglobulin synthesis. The clinical significance of the co-existence
of multiple anti-neuronal antibodies in single patients is an interesting question.
This immunophenotype affects clinical manifestation resulting in variation or overlap
of neurological syndromes. For example, the co-existence of anti-AQP4 antibodies in
anti-NMDAR encephalitis may contribute to additional demyelination features and tendency
to relapse. The presence of additional onconeural antibodies (e.g., anti-Hu antibodies)
warrants investigation for occult tumor and indicates a poor prognosis.[27]
Figure 2
CSF cytology of a patient with anti-NMDAR encephalitis. Lymphocytic inflammation is
typical CSF findings of anti-NMDAR encephalitis, and plasma cells are often identified
in CSF. CSF: Cerebrospinal fluid; NMDAR: N-methyl-D-aspartate receptor (May-Grunwald-Giemsa
stain, original magnification ×200).
A recent study demonstrated CXCL13, a B-cell-attracting chemokine produced by plasma
cells and monocytes/macrophages, as a potential biomarker for anti-NMDAR encephalitis.
Seventy percent of patients with new onset of anti-NMDAR encephalitis showed elevated
CXCL13 levels in the CSF. Prolonged or secondary elevation of CXCL13 was associated
with limited response to treatment and relapses.[28]
Neuroimaging findings of mesial temporal involvement are significant for the diagnosis
of LE related to GABABR or LGI1 antibodies. Though routine MRI may not aid diagnosis
in most cases of anti-NMDAR encephalitis [Figure 3]. Positron emission tomography
(PET) provides evidence of cerebral functional change underlying the clinical manifestation.
PET results of patients diagnosed with anti-NMDAR encephalitis showed inconsistent
results. However, relative hypometabolism of the bilateral occipital lobes and hypermetabolism
of the bilateral frontal, temporal, and parietal lobes are characteristic findings
in the acute phase of the disease.
Figure 3
Brain MRI of autoimmune encephalitis. (a) High signals on bilateral mesial temporal
lobe in a patient with limbic encephalitis associated with anti-GABABR antibodies.
(b) High signals on the bilateral mesial temporal lobe and right amygdala enlargement
in a patient with limbic encephalitis associated with anti-LGI1 antibodies. (c) Abnormalities
in the right mesial temporal lobe in a patient with anti-NMDAR encephalitis during
her initial episode. (d) New lesions more prominent at left mesial temporal lobe and
brain stem during her relapse. MRI: Magnetic resonance imaging; GABABR: γ-aminobutyric
acid B receptor; LGI1: Leucine-rich glioma-inactivated 1; NMDAR: N-methyl-D-aspartate
receptor.
TREATMENT
Underlying tumors are the major trigger for AIE, and therefore, patients should be
screened for systemic tumors during diagnosis. The ovarian teratoma, once detected,
should be removed promptly in patients with anti-NMDAR encephalitis. Critical neurological
and systemic complications should not be looked as contraindications for surgery.
First-line immunotherapy for anti-NMDAR encephalitis includes steroids, intravenous
immunoglobulin, or plasma exchange; second-line immunotherapy includes rituximab or
cyclophosphamide. The protocol suggested by Dalmau et al. emphasizes the indications
of the second-line therapy and long-term immunotherapy.[7] The systemical review by
Nosadini et al.[29] demonstrated that patients given immunotherapy do better and relapse
less than patients given no treatment and second-line therapy, for example, rituximab
improves outcomes and reduces relapses. However, administration of rituximab is limited
in China due to an off-label indication of the medicine. The retrial of first-line
therapy is still an option in resource-limited settings [Figure 4]. On the other hand,
according to the study by Zekeridou et al.[30] despite a higher rate of second-line
immunotherapy in their case series, the outcome in their series was very similar to
the outcome reported in the previous series. Randomized clinical trial is needed to
determine the optimal treatment of anti-NMDAR encephalitis.
Figure 4
Proposed pathway for the treatment of anti-NMDAR encephalitis. The algorithm demonstrates
indications of first-line, second-line, and chronic immunotherapy. The retrial of
first-line therapy is an option in patients with little or no response to the initial
immunotherapy. Chronic immunosuppression: mycophenolate mofetil or azathioprine for
1 year. NMDAR: N-methyl-D-aspartate receptor; IVIg: Intravenous immunoglobulin; PE:
Plasma exchange.
Intrathecal administration of methotrexate (MTX) was reported to be effective in a
few pediatric cases with anti-NMDAR encephalitis.[31] We recently used intrathecal
therapy in three patients refractory to first-line and second-line immunotherapy.
The patients demonstrated remarkable clinical improvement and decrease of anti-NMDAR
antibody titers after 4–5 cycles of intrathecal administration of MTX and dexamethasone.
Intrathecal immunotherapy might be a promising option for refractory cases since it
may directly affect intrathecal antibody synthesis in anti-NMDAR encephalitis.
Cases with relapsing AIE represent a new challenge to neurologists. Relapse of anti-NMDAR
encephalitis is defined as the new onset or worsening of symptoms after at least 2
months of improvement or stabilization. Dalmau et al. reported that 12% of patients
showed clinical relapses during a 24-month follow-up.[7] Our observations in a Chinese
series suggest a higher relapse among patients (23.5%) in our series, with multiple
relapses in half of relapsing cases.[32] Inadequacy of second-line and long-term immunotherapy,
absence of teratoma, and potential demyelinating mechanism might contribute to the
relapse of anti-NMDAR encephalitis.[7]
Specific symptomatic treatment for anti-NMDAR encephalitis might play a role based
on the mechanism of NMDAR dysfunction in this disorder. D-cycloserine, known as anti-tuberculotic
medicine, has been widely used in neuropsychiatric studies, since it acts as a partial
NMDA-agonist at low doses, at the glycine-binding site of NR1 subunit.[33] We recently
observed clinical improvement in one refractory case with anti-NMDAR encephalitis
after administration of D-cycloserine (125–250 mg/d).
In conclusion, the discovery of AIE broadens the horizons of neuroimmunology and alters
the strategies for diagnosis and treatment of encephalitic syndrome. The characteristics
of Chinese patients with AIE need to be fully defined based on multicenter clinical
studies in the future. Further studies focusing on the antibody – receptor interaction
and intrathecal antibody synthesis will contribute to our understanding of the immune
mechanisms and developing more specific and effective treatment.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.