Test ID PNEFS Neuroimmunology Antibody Follow-up, Serum
Useful For
Monitoring patients who have previously tested positive for 1 or more antibodies in a Neuroimmunology Laboratory evaluation
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
ANN1S | Anti-Neuronal Nuclear Ab, Type 1 | No | No |
ANN2S | Anti-Neuronal Nuclear Ab, Type 2 | No | No |
ANN3S | Anti-Neuronal Nuclear Ab, Type 3 | No | No |
AGN1S | Anti-Glial Nuclear Ab, Type 1 | No | No |
PCABP | Purkinje Cell Cytoplasmic Ab Type 1 | No | No |
PCAB2 | Purkinje Cell Cytoplasmic Ab Type 2 | No | No |
PCATR | Purkinje Cell Cytoplasmic Ab Type Tr | No | No |
AMPHS | Amphiphysin Ab, S | No | No |
CRMS | CRMP-5-IgG, S | No | No |
CCPQ | P/Q-Type Calcium Channel Ab | No | No |
CCN | N-Type Calcium Channel Ab | No | No |
GANG | AChR Ganglionic Neuronal Ab, S | No | No |
VGKC | Neuronal (V-G) K+ Channel Ab, S | No | No |
ARMO | ACh Receptor (Muscle) Modulating Ab | No | No |
NMOCS | NMO/AQP4-IgG CBA, S | No | No |
NMDCS | NMDA-R Ab CBA, S | No | No |
AMPCS | AMPA-R Ab CBA, S | No | No |
GABCS | GABA-B-R Ab CBA, S | No | No |
NMDIS | NMDA-R Ab IF Titer Assay, S | No | No |
AMPIS | AMPA-R Ab IF Titer Assay, S | No | No |
GABIS | GABA-B-R Ab IF Titer Assay, S | No | No |
Method Name
This follow-up evaluation is used to monitor patients who tested positive for 1 or more antibodies in the Neuroimmunology Laboratory in the past 15 months.
Reporting Name
Neuroimmunology Ab Follow-up, SSpecimen Type
SerumContainer/Tube:
Preferred: Red top
Acceptable: Serum gel
Specimen Volume: 4 mL
Forms: If not ordering electronically, complete, print, and send a Neurology Test Request Form-General (T732) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/neurology-request-form.pdf)
Specimen Minimum Volume
0.8 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Serum | Refrigerated (preferred) | 14 days |
Ambient | 72 hours | |
Frozen |
Clinical Information
Paraneoplastic autoimmune neurological disorders reflect a patient's humoral and cellular immune responses to cancer. The cancer may be new or recurrent, is usually limited in metastatic volume, and is often occult by standard imaging procedures. Autoantibodies specific for onconeural proteins found in the plasma membrane, cytoplasm, and nucleus of neurons or muscle are generated in this immune response and serve as serological markers of paraneoplastic autoimmunity. The most commonly recognized cancers in this context are small-cell lung carcinoma (SCLC), thymoma, ovarian (or related mullerian) carcinoma, breast carcinoma, and Hodgkin's lymphoma. Pertinent childhood neoplasms recognized thus far include neuroblastoma, thymoma, Hodgkin's lymphoma, and chondroblastoma. An individual patient's autoantibody profile can predict a specific neoplasm with 90% certainty, but not the neurological syndrome.
Four classes of autoantibodies are recognized:
-Neuronal nuclear (antineuronal nuclear antibody-type 1 [ANNA-1], ANNA-2, ANNA-3)
-Neuronal and muscle cytoplasmic (Purkinje cell cytoplasmic antibody, type 1 [PCA-1], PCA-2, PCA-Tr, CRMP-5, amphiphysin, and striational)
-Glial nuclear (anti-glial nuclear antibody)
-Plasma membrane cation channel Antibodies (neuronal P/Q-type and N-type calcium channel and muscle acetylcholine receptor autoantibodies). These autoantibodies are potential effectors of neurological dysfunction.
Seropositive patients usually present with subacute neurological symptoms and signs. The patient may present with encephalopathy, cerebellar ataxia, myelopathy, radiculopathy, plexopathy, sensory, sensorimotor, or autonomic neuropathy, with or without coexisting evidence of a neuromuscular transmission disorder: Lambert-Eaton syndrome (LES), myasthenia gravis, or neuromuscular hyperexcitability. Initial signs may be subtle, but a subacute multifocal and progressive syndrome usually evolves. Sensorimotor neuropathy and cerebellar ataxia are common presentations, but the clinical picture in some patients is dominated by striking gastrointestinal dysmotility, limbic encephalopathy, basal ganglionitis, or cranial neuropathy (especially loss of vision, hearing, smell, or taste). Cancer risk factors include past or family history of cancer, history of smoking or social/environmental exposure to carcinogens. Early diagnosis and treatment of the neoplasm favor less neurological morbidity and offer the best hope for survival.
Reference Values
NEURONAL NUCLEAR ANTIBODIES
Antineuronal Nuclear Antibody-Type 1 (ANNA-1)
<1:240
Antineuronal Nuclear Antibody-Type 2 (ANNA-2)
<1:240
Antineuronal Nuclear Antibody-Type 3 (ANNA-3)
<1:240
NEURONAL AND MUSCLE CYTOPLASMIC ANTIBODIES
Purkinje Cell Cytoplasmic Antibody, Type 1 (PCA-1)
<1:240
Purkinje Cell Cytoplasmic Antibody, Type 2 (PCA-2)
<1:240
Purkinje Cell Cytoplasmic Antibody, Type Tr (PCA-Tr)
<1:240
Amphiphysin Antibody
<1:240
CRMP-5-IgG
<1:240
Striational (Striated Muscle) Antibodies
<1:60
Paraneoplastic Autoantibody Western Blot Confirmation
Negative
CRMP-5-IgG Western Blot
Negative
CATION CHANNEL ANTIBODIES
N-Type Calcium Channel Antibody
≤0.03 nmol/L
P/Q-Type Calcium Channel Antibody
≤0.02 nmol/L
ACh Receptor (Muscle) Binding Antibody
≤0.02 nmol/L
AChR Ganglionic Neuronal Antibody
≤0.02 nmol/L
ACh Receptor (Muscle) Modulating Antibodies
0-20% (reported as __% loss of AChR)
GAD65 ANTIBODY ASSAY
≤0.02 nmol/L
Neuron-restricted patterns of IgG staining that do not fulfill criteria for amphiphysin, ANNA-1, ANNA-2, ANNA-3, PCA-1, PCA-2, PCA-Tr, or CRMP-5-IgG may be reported as "unclassified antineuronal IgG." Complex patterns that include non-neuronal elements may be reported as "uninterpretable."
Note: Titers lower than 1:240 are detectable by recombinant CRMP-5 Western blot analysis. CRMP-5 Western blot analysis will be done on request on stored serum (held 4 weeks). This supplemental testing is recommended in cases of chorea, vision loss, and cranial neuropathy and myelopathy. Call the Neuroimmunology Laboratory at 800-533-1710 or 507-266-5700 to request CRMP-5 Western blot.
Cautions
This test should only be utilized when the presence of paraneoplastic autoantibodies has been previously documented.
This test should not be requested in patients who have recently received radioisotopes, therapeutically or diagnostically, because of potential assay interference. The specific waiting period before specimen collection will depend on the isotope administered, the dose given and the clearance rate in the individual patient. Specimens will be screened for radioactivity prior to analysis. Radioactive specimens received in the laboratory will be held one week and assayed if sufficiently decayed, or canceled if radioactivity remains.
Day(s) Performed
ANNA-1, ANNA-2, ANNA-3, PCA-1, PCA-2, PCA-Tr, Amphiphysin, CRMP-5-IgG: Monday through Friday; 11:30 a.m.
Striational (striated muscle) antibodies: Monday through Friday
P/Q-type calcium channel antibody, N-type calcium channel antibody; Monday through Thursday, Sunday; 2 p.m.
ACh receptor (muscle) binding antibody: Monday through Friday, Sunday; 2 p.m.
AChR ganglionic neuronal antibody: Monday through Thursday, Sunday; 2 p.m.
Paraneoplastic autoantibody Western blot confirmation, CRMP-5-IgG Western blot: Monday through Friday; 8 a.m.
ACh receptor (muscle) modulating antibodies: Monday through Thursday; 11 a.m.
GAD65: Monday through Friday; 6 a.m.
Report Available
VariesPerforming Laboratory

CPT Code Information
83519-59-ACh receptor (muscle) binding antibody (if appropriate)
83519-59-ACh receptor (muscle) modulating antibodies (if appropriate)
83519-59-AChR ganglionic neuronal antibody (if appropriate)
83519-59-N-type calcium channel antibody (if appropriate)
83519-59-P/Q-type calcium channel antibody (if appropriate)
83520-Striational (striated muscle) antibodies (if appropriate)
84182-CRMP-5-IgG Western blot (if appropriate)
84182-Paraneoplastic autoantibody Western blot confirmation (if appropriate)
86255-Amphiphysin (if appropriate)
86255-ANNA-1 (if appropriate)
86255-ANNA-2 (if appropriate)
86255-ANNA-3 (if appropriate)
86255-CRMP-5-IgG (if appropriate)
86255-PCA-1 (if appropriate)
86255-PCA-2 (if appropriate)
86255-PCA-Tr (if appropriate)
86341-GAD65 antibody assay (if appropriate)