Anti-Interferon-gamma (IFNg) autoantibody
Test Code
IFNGE
Description
The association of anti-cytokine antibodies with immune dysregulation, immune deficiency or autoimmunity is increasingly being recognized. Anti-IFNγ autoantibodies have been noted to be associated with chronic, treatment refractory, extrapulmonary infections with non-tuberculous mycobacterial (NTM) species, anti-IL17 autoantibodies with chronic mucocutaneous candidiasis (CMC) and anti-IFN-alpha autoantibodies with systemic lupus erythematosus (SLE).
Low titer anti-cytokine autoantibodies may be detected in normal individuals and may serve a regulatory purpose. However, anti-cytokine autoantibodies associated with pathological findings tend to be of high titer and demonstrate significant neutralizing activity in vitro. Recognition of these autoantibodies is of benefit since it may direct the use of adjunctive immunotherapy to modulate the autoantibody titer while continuing with conventional therapies.
Detection of these autoantibodies is performed by ELISA to assess titer. Positive results will reflex to flow cytometry to assess the ability of the autoantibody to neutralize cytokine mediated signaling.
Collect
Collect in a plain red top or SST
Patient Prep
Preferred volume: 1mL serum
Pediatric Collection
Minimum volume: 0.5 mL serum
Unacceptable Conditions
Clotted or hemolyzed samples, plasma
Storage Transport Temp
Send serum Priority Overnight via FedEx and in a well insulated container with an ice pack or frozen on dry ice.
Stability
2-8°C for 48 hours, >1 month at -20°C or below
Performed
Monday - Friday
Methodology
ELISA followed by confirmation by flow cytometry
Turnaround Time
14 days
Department
Immunology Lab - Phenotyping Assays
Synonyms
STAT1 phosphorylation, Functional Autoantibodies to cytokines, Interferon Gamma Autoantibodies, Autoantibody to interferon-gamma, IFNg Autoantibody
Study Offerings
CAP/CLIA
Related Tests
GMCSE
Reference Interval
Negative
CPT Code
83516 – ELISA
86353, 88184, 88185 – flow cytometry reflex
New York Approved
No: Run with Waiver
FDA
LDT