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Sorted By Test Name - Mayo Medical Laboratories

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TOXOG<br />

8267<br />

amniotic fluid specimens (PTOX/81795 Toxoplasma gondii, Molecular Detection, PCR). For<br />

confirmation of a diagnosis, the FDA issued a Public Health Advisory (7/25/1997) suggesting that sera<br />

found to be positive/equivocal for Toxoplasma gondii IgM antibody be sent to a Toxoplasma reference<br />

laboratory. CDC or Jack Remington, M.D., Palo Alto <strong>Medical</strong> Foundation, 860 Bryant Street, Palo Alto,<br />

CA 94301, were recommended. (Reviewed 12/2011)<br />

Reference Values:<br />

Toxoplasma ANTIBODY, IgG<br />

or =8 IU/mL (positive)<br />

Toxoplasma ANTIBODY, IgM<br />

<strong>Test</strong> value threshold or =0.55- or =0.65 is positive<br />

Clinical References: 1. Luft BJ, Remington JS: Toxoplasmic encephalitis in AIDS. Clin Infect Dis<br />

1992 August;15(2):211-222 2. Wong SY, Remington JS: Toxoplasmosis in pregnancy. Clin Infect Dis<br />

1994 June;18(6):853-862<br />

Toxoplasma Antibody, IgG, Serum<br />

Clinical Information: Toxoplasma gondii is an obligate intracellular parasite that is capable of<br />

infecting a variety of intermediate hosts including humans. Infected definitive hosts (cats) shed oocysts in<br />

feces that rapidly mature in soil and become infectious. Toxoplasmosis is acquired by humans via<br />

ingestion of food or water contaminated with cat feces or undercooked meats containing oocysts.<br />

Infection of the normal adult is commonly asymptomatic. In cases with clinical manifestations, the most<br />

common symptom is lymphadenopathy that may be accompanied by an array of other symptoms making<br />

differential diagnosis difficult. Severe-to-fatal infections do occur in adults immunocompromised by<br />

cancer chemotherapy or other immunosuppressive treatment and in patients with AIDS. These infections<br />

are thought to be caused by reactivation of latent infections and often involve the central nervous system.<br />

Transplacental transmission of the parasites resulting in congenital toxoplasmosis can occur during the<br />

acute phase of acquired maternal infection. The risk of fetal infection is a function of the time at which<br />

acute maternal infection occurs during gestation. The incidence of congenital toxoplasmosis increases as<br />

pregnancy progresses; conversely, the severity of congenital toxoplasmosis is greatest when maternal<br />

infection is acquired early during pregnancy. A majority of infants infected in utero are asymptomatic at<br />

birth, particularly if maternal infection occurs during the third trimester, with sequelae appearing later in<br />

life. Congenital toxoplasmosis results in severe generalized or neurologic disease in about 20% to 30% of<br />

the infants infected in utero; approximately 10% exhibit ocular involvement only and the remainder are<br />

asymptomatic at birth. Subclinical infection may result in premature delivery and subsequent neurologic,<br />

intellectual, and audiologic defects.<br />

Useful For: Indication of past or recent infection with Toxoplasma gondii<br />

Interpretation: Diagnosis of acute central nervous system, intrauterine, or congenital toxoplasmosis is<br />

difficult by routine serological methods. A single positive IgG result is only indicative of exposure to<br />

toxoplasma at some point in time (past or recent) and is present in up to 70% of the adult United States<br />

population. The absence of IgG is helpful in that it usually indicates the absence of infection. However, a<br />

negative result could mean either no previous exposure or could also be seen in cases of remote exposure<br />

with subsequent loss of detectable antibody. Seroconversion from negative to positive IgG is indicative of<br />

recent Toxoplasma gondii infection. Seroconversion indicates infection subsequent to the first negative<br />

specimen. Specimens interpreted as equivocal may contain very low levels of IgG. A second specimen<br />

should be drawn and tested.<br />

Reference Values:<br />

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