Mantoux test

Mantoux test
The Mantoux skin test consists of an intradermal injection of one-tenth of a milliliter (ml) of PPD tuberculin. The circular shape is known as a wheal response.
Synonyms	Mantoux screening test
Purpose	screen for tuberculosis

The Mantoux test or Mendel–Mantoux test (also known as the Mantoux screening test, tuberculin sensitivity test, Pirquet test, or PPD test for purified protein derivative) is a tool for screening for tuberculosis (TB) and for tuberculosis diagnosis. It is one of the major tuberculin skin tests used around the world, largely replacing multiple-puncture tests such as the tine test. The Heaf test, a form of tine test, was used until 2005 in the UK, when it was replaced by the Mantoux test. The Mantoux test is endorsed by the American Thoracic Society and Centers for Disease Control and Prevention. It was also used in the USSR and is now prevalent in most of the post-Soviet states, although Soviet mantoux produced many false positives due to children's allergic reaction.

History

The size of induration is measured 48–72 hours later. Erythema (redness) should not be measured.

Mantoux test injection site in a subject without chronic conditions or in a high-risk group clinically diagnosed as negative at 50 hours

Tuberculin is a glycerol extract of the tubercle bacillus. Purified protein derivative (PPD) tuberculin is a precipitate of species-nonspecific molecules obtained from filtrates of sterilized, concentrated cultures. The tuberculin reaction was first described by Robert Koch in 1890. The test was first developed and described by the German physician Felix Mendel in 1908. It is named after Charles Mantoux, a French physician who built on the work of Koch and Clemens von Pirquet to create his test in 1907. However, the test was unreliable due to impurities in tuberculin which tended to cause false results.

Esmond R. Long and Florence B. Seibert identified the active agent in tuberculin as a protein. Seibert then spent a number of years developing methods for separating and purifying the protein from Mycobacterium tuberculosis, obtaining purified protein derivative (PPD) and enabling the creation of a reliable test for tuberculosis. Her first publication on the purification of tuberculin appeared in 1934. By the 1940s, Seibert's PPD was the international standard for tuberculin tests. In 1939, Russian M.A. Linnikova created a modified version of PPD. In 1954, the Soviet Union started mass production of PPD-L, named after Linnikova.

Procedure

In the Mantoux test, a standard dose of 5 tuberculin units (TU - 0.1 ml), according to the CDC, or 2 TU of Statens Serum Institute (SSI) tuberculin RT23 in 0.1 ml solution, according to the National Health Service, is injected intradermally (between the layers of dermis) on the flexor surface of the left forearm, mid-way between elbow and wrist. The injection should be made with a tuberculin syringe, with the needle bevel facing upward. When placed correctly, injection should produce a pale wheal of the skin, 6 to 10 mm in diameter. The result of the test is read after 48–96 hours, ideally after 72 hours/3rd day. This procedure is termed the 'Mantoux technique'. A person who has been exposed to the bacteria would be expected to mount an immune response in the area of skin containing the bacterial proteins. This response is a classic example of 'delayed-type hypersensitivity reaction' (DTH), a type IV of hypersensitivities. T cells and myeloid cells are attracted to the site of reaction in 1–3 days and generate local inflammation. The reaction is read by measuring the diameter of induration (palpable raised, hardened area) across the forearm (perpendicular to the long axis) in millimeters. If there is no induration, the result should be recorded as "0 mm". Erythema (redness) should not be measured. In the Pirquet version of the test tuberculin is applied to the skin via scarification.

Classification of tuberculin reaction

The results of this test must be interpreted carefully. The person's medical risk factors determine at which increment (5 mm, 10 mm, or 15 mm) of induration the result is considered positive. A positive result indicates TB exposure.

• 5 mm or more is positive in
  • An HIV-positive person
  • Persons with recent contacts with a TB patient
  • Persons with nodular or fibrotic changes on chest X-ray consistent with old healed TB
  • Patients with organ transplants, and other immunosuppressed patients
• 10 mm or more is positive in
  • Recent arrivals (less than five years) from high-prevalence countries
  • Injection drug users
  • Residents and employees of high-risk congregate settings (e.g., prisons, nursing homes, hospitals, homeless shelters, etc.)
  • Mycobacteriology lab personnel
  • Persons with clinical conditions that place them at high risk (e.g., diabetes, prolonged corticosteroid therapy, leukemia, end-stage renal disease, chronic malabsorption syndromes, low body weight, etc.)
  • Children less than four years of age, or children and adolescents exposed to adults in high-risk categories
• 15 mm or more is positive in
  • Persons with no known risk factors for TB

A tuberculin test conversion is defined as an increase of 10 mm or more within a two-year period, regardless of age. Alternative criteria include increases of 6, 12, 15 or 18 mm.

False positive result

TST (tuberculin skin test) positive is measured by size of induration. The size of the induration considered to be a positive result depends on risk factors. For example, a low-risk patient must have a larger induration for a positive result than a high-risk patient. High-risk groups include recent contacts, those with HIV, those with chest radiograph with fibrotic changes, organ transplant recipients, and those with immunosuppression.

According to the Ohio Department of Health and US Department of Health, the Bacillus Calmette–Guérin (BCG) vaccine does not protect against TB infection. It does, though, give 80% of children protection against tuberculous meningitis and miliary tuberculosis. Therefore, a positive TST/PPD in a person who has received BCG vaccine is interpreted as latent TB infection (LTBI). Due to the test's low specificity, most positive reactions in low-risk individuals are false positives. A false positive result may be caused by nontuberculous mycobacteria or previous administration of BCG vaccine. Vaccination with BCG may result in a false-positive result for many years after vaccination.

False positives can also occur when the injected area is touched, causing swelling and itching. If the swelling is less than 5 mm, it is possibly due to error by the healthcare personnel causing inflammation to the area.

Another source of false positive results can be allergic reaction or hypersensitivity. Although rare (about 0.08 reported reactions per million doses of tuberculin), these reactions can be dangerous and precautions should be taken by having epinephrin available.

False negative result

Reaction to the PPD or tuberculin test is suppressed by the following conditions:

• Recent TB infection (less than 8–10 weeks)
• Infectious mononucleosis
• Live virus vaccine - The test should not be carried out within 3 weeks of live virus vaccination (e. g. MMR vaccine or Sabin vaccine).
• Sarcoidosis
• Hodgkin's disease
• Corticosteroid therapy/steroid use
• Malnutrition
• Immunological compromise - Those on immuno-suppressive treatment or those with HIV and low CD4 T cell counts, frequently show negative results from the PPD test.

This is because the immune system needs to be functional to mount a response to the protein derivative injected under the skin. A false negative result may occur in a person who has been recently infected with TB, but whose immune system hasn't yet reacted to the bacteria.

• Upper respiratory virus infection

In case a second tuberculin test is necessary it should be carried out in the other arm to avoid hypersensitising the skin.

BCG vaccine and the Mantoux test

The role of Mantoux testing in people who have been vaccinated is disputed. The US recommends that tuberculin skin testing is not contraindicated for BCG-vaccinated persons, and prior BCG vaccination should not influence the interpretation of the test. The UK recommends that interferon-γ testing should be used to help interpret positive Mantoux tests of over 5 mm, and repeated tuberculin skin testing must not be done in people who have had BCG vaccinations. In general, the US recommendation may result in a larger number of people being falsely diagnosed with latent tuberculosis, while the UK approach has an increased chance of missing patients with latent tuberculosis who should be treated.

According to the US guidelines, latent tuberculosis infection diagnosis and treatment is considered for any BCG-vaccinated person whose skin test is 10 mm or greater, if any of these circumstances are present:

• Was in contact with another person with infectious TB
• Was born or has lived in a high TB prevalence country
• Is continually exposed to populations where TB prevalence is high

Anergy testing

In cases of anergy, a lack of reaction by the body's defence mechanisms when it comes into contact with foreign substances, the tuberculin reaction will occur weakly, thus compromising the value of Mantoux testing. For example, anergy is present in AIDS, a disease which strongly depresses the immune system. Therefore, anergy testing is advised in cases where there is suspicion that anergy is present. However, routine anergy skin testing is not recommended.

Two-step testing

Some people who have been infected with TB may have a negative reaction when tested years after infection, as the immune system response may gradually wane. This initial skin test, though negative, may stimulate (boost) the body's ability to react to tuberculin in future tests. Thus, a positive reaction to a subsequent test may be misinterpreted as a new infection, when in fact it is the result of the boosted reaction to an old infection.

Use of two-step testing is recommended for initial skin testing of adults who will be retested periodically (e.g., health care workers). This ensures any future positive tests can be interpreted as being caused by a new infection, rather than simply a reaction to an old infection.

• The first test is read 48–72 hours after injection.
  • If the first test is positive, consider the person infected.
  • If the first test is negative, give a second test one to three weeks after the first injection.
• The second test is read 48–72 hours after injection.
  • If the second test is positive, consider the person infected in the distant past.
  • If the second test is negative, consider the person uninfected.

A person who is diagnosed as "infected in the distant past" on two-step testing is called a "tuberculin reactor".

The US recommendation that prior BCG vaccination be ignored results in almost universal false diagnosis of tuberculosis infection in people who have had BCG (mostly foreign nationals).

The latest interpretation for Mantoux test results

According to the guidelines published by Centers for Disease Control and Prevention in 2005, the results are re-categorized into 3 parts based on their previous or baseline outcomes:

• Baseline test: ≥10 mm is positive (either first or second step); 0 to 9 mm is negative
• Serial testing without known exposure: Increase of ≥10 mm is positive
• Known exposure:
  • ≥5 mm is positive in patients with baseline of 0 mm
  • ≥10 mm is positive in patients with negative baseline or previous screening result of >0 mm

Recent developments

In addition to tuberculin skin tests such as (principally) the Mantoux test, interferon gamma release assays (IGRAs) have become common in clinical use in the 2010s. In some contexts they are used instead of TSTs, whereas in other contexts TSTs and IGRAs both continue to be useful.

The QuantiFERON-TB Gold blood test measures the patient's immune reactivity to the TB bacterium, and is useful for initial and serial testing of persons with an increased risk of latent or active tuberculosis infection. Guidelines for its use were released by the CDC in December 2005. QuantiFERON-TB Gold is FDA-approved in the United States, has CE Mark approval in Europe and has been approved by the MHLW in Japan. The interferon gamma release assay is the preferred method for patients who have had immunosuppression and are about to start biological therapies.

T-SPOT.TB is another IGRA; it uses the ELISPOT method.

Heaf test

Main article: Heaf test

The Heaf tuberculin skin test was used in the United Kingdom, but discontinued in 2005. The equivalent Mantoux test positive levels done with 10 TU (0.1 ml at 100 TU/ml, 1:1000) are

• <5 mm induration (Heaf 0–1)
• 5–15 mm induration (Heaf 2)
• >15 mm induration (Heaf 3–4)

See also

• Latent tuberculosis
• QuantiFERON
• Geronimo (alpaca)
• Shambo