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Reference range: <1:64, >1:64
The E. Chaffeensis Ab IgG test is a specialized diagnostic tool pivotal in the field of infectious diseases, particularly in the context of tick-borne illnesses. Ehrlichia chaffeensis is the bacterium responsible for Ehrlichiosis, a condition transmitted through tick bites, primarily in regions where ticks are endemic. The IgG antibody test for E. chaffeensis plays a crucial role in the diagnosis and management of this infection.
Reference range: <1:20, =>1:20
Ehrlichia chaffeensis Ab (IgM) testing plays a critical role in the early diagnosis of human monocytic ehrlichiosis (HME), a tick-borne illness caused by the bacterium Ehrlichia chaffeensis. This test specifically looks for IgM antibodies, which are among the first antibodies produced by the immune system in response to an infection. The presence of IgM antibodies against E. chaffeensis typically indicates a recent or ongoing infection, as these antibodies usually develop within the first week or two after exposure to the bacterium and can be detected before the IgG antibodies.
Reference range: <1:20, >1:20
The E. Chaffeensis Ab IgM test is a crucial diagnostic tool in the realm of infectious diseases, specifically for the timely detection of Ehrlichiosis, a tick-borne illness caused by the Ehrlichia chaffeensis bacterium. This test detects IgM antibodies, which are among the first antibodies produced by the immune system in response to an infection.
Optimal range: 0 - 999 Units
LEARN MOREOptimal range: 0.8 - 2.6 Ratio
The Etiocholanolone/Androsterone (E/A) Ratio assesses androgen metabolism by comparing the enzymatic activity of 5b-reductase/5a-reductase. Etiocholanolone is produced via the 5b-reductase pathway and androsterone is produced via the 5a-reductase pathway.
Optimal range: 0.34 - 1.76 Ratio
The Etiocholanolone/Androsterone (E/A) Ratio assesses androgen metabolism by comparing the enzymatic activity of 5β-reductase/5α-reductase.
Optimal range: 0.55 - 2.45 Ratio
The Etiocholanolone/Androsterone (E/A) Ratio assesses androgen metabolism by comparing the enzymatic activity of 5β-reductase/5α-reductase.
Optimal range: 0.3 - 2 Ratio
The ratio of potentially toxic urinary estrogens (i.e. 2- and 4-catechols of estradiol and estrone) to inert estriol has been used for many years as an index of breast cancer risk.
Optimal range: 0 - 18 U/mL
The EBV (Epstein Barr) Nuclear Antigen Antibodies, IgG test looks for a type of antibody which the body typically develops in response to Epstein-Barr Virus.
EBNA antibodies usually appear 2-4 months after infection and persist for the life of the person.
This test is usually performed to establish a past infection with EBV.
Optimal range: 0 - 10 Relative Abundance
The marker "EBNA1 (IgG)" is a crucial indicator for assessing neurological health and potential autoimmune conditions affecting the nervous system. EBNA1 stands for Epstein-Barr Nuclear Antigen 1, and the IgG designation refers to Immunoglobulin G, a type of antibody. This particular marker is significant because it helps detect past infections with the Epstein-Barr virus (EBV), which is known to be associated with a variety of neurological disorders. EBV is a common virus, and while it often causes mild symptoms or goes unnoticed in many people, its connection to neurological conditions can be significant in a subset of individuals. The presence of IgG antibodies against EBNA1 indicates that a person has been infected with EBV at some point in their life, and their immune system has produced antibodies to fight off the virus. In the context of the NeuralZoomer Plus panel, testing for EBNA1 (IgG) antibodies helps healthcare providers understand whether a past EBV infection might be contributing to neurological symptoms or conditions. This information is valuable for developing a comprehensive picture of a patient's neurological health and tailoring treatment approaches to address any identified autoimmune or viral-related issues.
Optimal range: 0 - 18 U/mL
EBV-VCA, IgG is an antibody (protein) that is produced by the body in an immune response to an Epstein-Barr virus antigen.
Optimal range: 0 - 36 U/mL
EBV-VCA, IgM is an antibody (protein) that is produced by the body in an immune response to an Epstein-Barr virus antigen.
EBV stands for Epstein-Barr virus.
Epstein-Barr virus is a virus that typically causes a mild to moderate illness. Blood tests for Epstein-Barr virus detect antibodies to EBV in the blood and help establish a diagnosis of EBV infection.
VCA stands for Viral capsid antigen.
– Anti-VCA IgM appears early in EBV infection and usually disappears within four to six weeks.
– Anti-VCA IgG appears in the acute phase of EBV infection, peaks at two to four weeks after onset, declines slightly then persists for the rest of a person’s life.
Optimal range: 0 - 18 U/mL
EBV CAPSID Ag.ab/IgG is an antibody (protein) that is produced by the body in an immune response to an Epstein-Barr virus antigen.
Optimal range: 0 - 36 U/mL
EBV CAPSID Ag.Ab/IgM is an antibody (protein) that is produced by the body in an immune response to an Epstein-Barr virus antigen.
Optimal range: 0 - 100 U/mL
If the result of the Epstein-Barr Virus Early Antigen IgG (EBV EA IgG) test falls within the reference range, it generally indicates one of the following scenarios:
No Active or Recent EBV Infection: A result within the reference range typically suggests that there is no active or recent infection by the Epstein-Barr Virus. EBV EA IgG antibodies are usually present during the acute phase of an EBV infection. Their absence or low levels within the normal range implies that the individual is likely not in the acute phase of EBV infection.
Past Infection: Individuals who have had an EBV infection in the past and have since recovered will often have EBV EA IgG levels within the reference range. After the acute phase of the infection, these antibody levels usually decline and may fall back into the reference range.
Latency: EBV can remain latent in the body after the initial infection. A reference range result for EBV EA IgG indicates that the virus is not actively replicating or causing active symptoms, consistent with a latent or dormant state of the virus.
Possible Immunity: If a person has been exposed to EBV in the past, they may have developed immunity to the virus. In such cases, other types of EBV antibodies (like VCA IgG or EBNA IgG) might be present, while EA IgG remains within the reference range, indicating a past infection and possible immunity.
Early or Very Late Stage of Infection: In very early stages of an EBV infection or in cases where a significant amount of time has passed since the infection, EA IgG levels might still be within the reference range. This is because it takes time for these antibodies to develop post-infection, and they tend to decline in later stages.
It's important to interpret these results in the context of other EBV-specific antibody tests (like VCA IgM, VCA IgG, and EBNA IgG) and the clinical presentation of the patient. The EBV antibody profile, including the EA IgG result, provides a more comprehensive understanding of the individual's infection status. A healthcare provider can best interpret what this result means in the context of an individual's symptoms, history, and overall health.
Optimal range: 0 - 9 U/mL
Aid in the diagnosis of acute EBV (infectious mononucleosis) and EBV reactivation in conjunction with other serologic tests. The appearance of IgG antibodies to Early antigen-diffuse [EA(D)] is generally associated with the primary (acute) stage of EBV infection. For most individuals these antibodies are transient and are often undetectable after 6 months.
Optimal range: 0 - 9 U/mL
The EBV Early Antigen Ab, IgG is a valuable biomarker in the diagnosis and management of Epstein-Barr virus infections. By understanding the presence and levels of these antibodies, healthcare providers can better determine the phase of EBV infection and provide appropriate treatment strategies. If you suspect an EBV infection or are experiencing prolonged symptoms, consult your healthcare provider about testing for EBV Early Antigen Ab, IgG.