Sign in →

Test Code AAGTS Alpha-3 Beta-4 Ganglionic Neuronal Acetylcholine Receptor Binding Antibody, Flow Cytometry Titer, Serum (Non-Orderable)


Specimen Required


Only orderable as a reflex. For more information see:

-DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

-GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum


Useful For

Only orderable as a reflex. For more information see:

DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum

 

Evaluating patients with suspected autoimmune autonomic ganglionopathy and autoimmune gastrointestinal dysmotility using serum specimens

 

Reporting alpha-3 beta-4 ganglionic neuronal acetylcholine receptor binding antibody end titer results of as part of a profile

Reporting Name

AChR Alpha3 Gang Flow Titer, S

Specimen Type

Serum

Specimen Minimum Volume

Serum: 1 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 28 days
  Frozen  28 days
  Ambient  72 hours

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject
Gross icterus Reject

Reference Values

Only orderable as a reflex. For more information see:

-DYS2 / Dysautonomia, Autoimmune/Paraneoplastic Evaluation, Serum

-GID2 / Gastrointestinal Dysmotility, Autoimmune/Paraneoplastic Evaluation, Serum

 

<1:10

Method Description

This assay is a live cell-based binding assay using flow cytometry to detect ganglionic acetylcholine receptor (AChR) binding antibodies in patient serum. Human embryonic kidney cells (HEK293) transiently expressing human alpha-3 beta-4 ganglionic AChR subunits, along with accessory proteins required for receptor expression, are used as the antigen source. Receptor expression is enhanced prior to analysis under controlled culture conditions. Cells are incubated with diluted patient serum to allow binding of AChR-specific antibodies to surface-expressed receptors. Bound human IgG is detected using a fluorophore-conjugated anti-human IgG secondary antibody, with a viability dye included to exclude non-viable cells. Fluorescence intensity is measured by flow cytometry, and antibody binding is assessed by comparing signal from AChR-expressing cells to control cells lacking receptor expression. A humanized AChR-specific monoclonal antibody is used as an assay calibrator. The IgG binding index (IBI) of patient samples is compared to the assay calibrator to calculate a cut-off Index (COI). Patient samples with a COI greater than or equal to 1.0 are reported as positive. Positive samples are further titrated to determine the end-point dilution, defined as the highest serum dilution that remains above the calibrator.(Unpublished Mayo method)

Day(s) Performed

Varies

Report Available

3 to 7 days

Specimen Retention Time

2 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

86256

LOINC Code Information

Test ID Test Order Name Order LOINC Value
AAGTS AChR Alpha3 Gang Flow Titer, S In Process

 

Result ID Test Result Name Result LOINC Value
623083 AChR Alpha3 Gang Flow Titer, S In Process