Immunoglobulins

Immunoglobulins—also called antibodies—are proteins your immune system makes to fight infections and remember past exposures. Measuring them in blood helps explain frequent infections, verify immune competence, and provide context for conditions such as allergyautoimmunity, and plasma-cell disorders.

A proactive work-up starts with total IgG, IgA, and IgM, then adds IgE (allergy context), IgG subclasses (1–4), and functional antibody testing (e.g., pneumococcal serotype responses) when needed. If protein levels are unusually high or low, your clinician may add serum protein electrophoresis (SPEP)immunofixation (IFE), and serum free light chains to screen for monoclonal gammopathies (MGUS, myeloma) or to clarify patterns. These tests support screeningdiagnostic triage, and monitoring, but they do not replace a clinician’s evaluation or urgent care for severe illness.

Signs, Symptoms & Related Situations

  • Frequent or severe infections: ≥4 ear/sinus infections per year, recurrent bronchitis/pneumonia, unusual or hard-to-treat infections

  • Poor vaccine responses: illness despite full vaccination; clinician may check pre-/post-vaccine titers (e.g., pneumococcal)

  • Allergy & atopy context: asthma, eczema, allergic rhinitis—IgE may be informative

  • Autoimmunity/inflammation clues: joint pain, rashes, swollen glands, fevers of unknown origin

  • Protein abnormalities: high total protein or globulin gap, anemia, bone pain, kidney issues (consider SPEP/IFE and free light chains)

  • Malabsorption or loss: chronic diarrhea, weight loss, protein-losing enteropathynephrotic syndrome

  • Medication/therapy effects: immunosuppressants, rituximab, or recent IVIG/SCIG (can elevate IgG and affect antibody tests)
    Seek urgent care now for trouble breathing, high fever with confusion, severe dehydration, chest pain, or rapidly worsening symptoms.

Why These Tests Matter

What testing can do

  • Screen immune function with IgG/IgA/IgM and CBC with differential

  • Identify selective deficiencies (e.g., IgA deficiency) and IgG subclass patterns in people with recurrent infections

  • Assess functional antibody production using pneumococcal serotype IgG before/after vaccination

  • Flag monoclonal or polyclonal patterns with SPEP/IFE and serum free light chains for clinician review

What testing cannot do

  • Diagnose a specific immune disorder from one result—patterns and clinical history are essential

  • Guarantee protection; antibody levels correlate with protection differently across diseases

  • Replace vaccines/boosters or clinical judgment on prevention and treatment

What These Tests Measure (at a glance)

  • Total Immunoglobulins:

    • IgG: main long-term antibody; low in many primary/secondary immunodeficiencies; high in chronic infection/autoimmunity.

    • IgA: mucosal defense; selective IgA deficiency is common and affects interpretation of celiac IgA tests.

    • IgM: early response antibody; rises in acute infection; very low in some immune defects.

  • IgE: allergy/atopy context; markedly high levels occur in allergic disease and some rare syndromes.

  • IgG Subclasses (1–4): supportive when total IgG is normal but infections persist; interpret with vaccine response tests.

  • Specific Antibody Responses: Pneumococcal serotype IgG (pre- and ~4–6 weeks post-vaccination) to test functional antibody production.

  • SPEP/IFE: separates proteins and detects monoclonal bands; used with clinical context to evaluate MGUS/myeloma.

  • Serum Free Light Chains (κ, λ, ratio): sensitive screen for light-chain monoclonal disease; interpret with SPEP/IFE.

  • Contextual adds: CBC with differentialcomplements (C3/C4/CH50)CRP/ESR for inflammation, basic metabolic panel for kidney status.

Collection notes: Fasting is not required. Recent infections, IVIG/SCIG, and some medicines can shift results—list them on your order.

Quick Build Guide

Clinical goal Start with Add if needed
Recurrent sinus/chest infections IgG/IgA/IgM • CBC with differential IgG Subclasses • Pneumococcal serotype IgG (pre/post)
Allergy/atopy context IgE CBC eosinophils • Specific allergen testing(separate category)
Abnormal total protein/globulin gap SPEP • IFE Serum Free Light Chains • CBC • CMP
Suspected IgA deficiency IgA Use celiac IgG-based tests if evaluating celiac disease (clinician-directed)
Immune status screen IgG/IgA/IgM • CBC with diff Complement (C3/C4/CH50) • CRP/ESR
Post-therapy monitoring (e.g., rituximab/IVIG) IgG (± IgA/IgM) Specific antibody responses if clinically indicated

How the Testing Process Works

  1. Choose your starting panel: begin with IgG/IgA/IgM and CBC with differential for a broad screen.

  2. Layer functional tests: add IgG subclasses and pneumococcal serotype IgG pre/post vaccination if infections persist.

  3. Assess protein patterns: order SPEP/IFE and free light chains if total protein is high, the globulin gap is wide, or anemia/kidney findings raise concern.

  4. Get your draw: simple blood draw at a nearby patient service center; results post securely.

  5. Review & plan: interpret results with your clinician; next steps may include vaccines, specialist referral, or targeted follow-up testing.

Interpreting Results (General Guidance)

  • Low IgG/IgA/IgM: consider primary immunodeficiency, medication effects, protein loss, or malnutrition; confirm functional antibody responses.

  • Selective IgA deficiency: common and often silent; affects IgA-based tests (e.g., celiac).

  • High polyclonal immunoglobulins: seen in chronic infection, inflammation, liver disease, or autoimmune conditions.

  • Monoclonal spike on SPEP/IFE or abnormal κ/λ ratio: needs clinician evaluation for MGUS/myeloma context.

  • IgG subclass results: interpret only with clinical history and vaccine responses—isolated subclass “lows” are often nonspecific.
    Always interpret results with a qualified healthcare professional; patterns over time matter more than a single value.

Choosing Panels vs. Individual Tests

  • Basic screen (most adults with recurrent infections): IgG/IgA/IgM + CBC with differential

  • Functional assessment: Pneumococcal serotype IgG (pre/post) ± IgG subclasses

  • Protein evaluation: SPEP/IFE + Serum Free Light Chains (± β-2 microglobulin per clinician)

  • Allergy emphasis: IgE (allergen testing is a separate category)

  • Inflammation/complement context: CRP/ESR • C3/C4/CH50

FAQs

Do I need to fast for immunoglobulin testing?
No. Fasting is not required.

Can a recent infection change my levels?
Yes. IgM and IgG can rise after infection. Tell your clinician about recent illnesses.

Does IVIG/SCIG therapy affect results?
Yes. It raises IgG and can blur vaccine antibody interpretation for weeks. Share infusion dates.

What’s the difference between total IgG and IgG subclasses?
Total IgG measures overall antibody; subclasses (1–4) look for patterns. Subclass results are most useful with infection history and vaccine response testing.

If my IgA is low, can I do celiac testing?
Yes—clinicians use IgG-based celiac assays in IgA deficiency.

When are SPEP/IFE and free light chains needed?
When protein levels are high, anemia or kidney problems exist, or a monoclonal process is suspected.

Can these tests prove I’m protected from infections?
They show capacity and history, but protection varies by disease. Your clinician may pair them with specific antibodytiters.

Related Categories & Key Tests

  • Immunity & Titer Tests Hub

  • Vaccine Titers • COVID-19 Antibody Tests • Autoimmune & Rheumatologic Tests • Inflammation (CRP/ESR) • Hematology (SPEP/IFE) • Lymphocyte Subsets

  • Key Tests: IgG • IgA • IgM • IgE • IgG Subclasses (1–4) • Pneumococcal Serotype IgG (pre/post)• SPEP • IFE • Serum Free Light Chains (κ, λ, ratio) • CBC with Differential • Complement (C3/C4/CH50) • CRP/ESR

References

  • American Academy of Allergy, Asthma & Immunology (AAAAI) — Practice parameters for primary immunodeficiency evaluation.
  • Infectious Diseases Society of America — Guidance on assessment of antibody responses to vaccines.
  • European Society for Immunodeficiencies — Diagnostic criteria and evaluation pathways for humoral immunodeficiencies.
  • International Myeloma Working Group — Criteria for monoclonal gammopathies, SPEP/IFE, and free light chains.
  • Centers for Disease Control and Prevention — Vaccine immunogenicity and serologic evidence of immunity.
  • Clinical and Laboratory Standards Institute (CLSI) — Best practices in immunology and protein electrophoresis.

Available Tests & Panels

Your Immunoglobulins menu is pre-populated in the Ulta Lab Tests system. Start with IgG/IgA/IgM and CBC with differential, add IgEIgG subclasses, and pneumococcal serotype IgG if infections persist, and use SPEP/IFE with serum free light chains when protein patterns raise concern. Review timing (recent infections, IVIG dates) and discuss results with your clinician to plan next steps.

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Blood
Blood Draw

The Total Immunoglobulins Panel measures IgA, IgG, and IgM levels to evaluate immune system function. Abnormal results may indicate immune deficiency, chronic infections, autoimmune disorders, or certain blood cancers. IgA helps protect mucous membranes, IgG provides long-term defense, and IgM is the body’s first response to infection. Doctors use this blood test to diagnose, monitor, and manage immune-related conditions and overall immune health.

Blood
Blood Draw

Most Popular

The Immunoglobulin A (IgA) Test measures IgA antibody levels in blood to evaluate immune system health and mucosal defense in the respiratory and digestive tracts. Low IgA may indicate immune deficiency, celiac disease, or recurrent infections, while high levels may suggest autoimmune disorders, liver disease, or chronic inflammation. Doctors use this test to assess unexplained illness or immune imbalance. Results provide key insight into antibody function and overall immunity.

Blood
Blood Draw
Also Known As: Immunoglobulin A Test, Immunoglobulin A Antibody Test, IgA Antibody Test

The IgA Subclasses Panel evaluates IgA1 and IgA2 subclasses, which are critical for mucosal defense and immune balance. Deficiencies may increase susceptibility to sinus, lung, or digestive infections and may also be linked to autoimmune disease. This test supports assessment of antibody function, systemic health, and conditions tied to mucosal immunity and immune dysregulation.

Blood
Blood Draw

Most Popular

The Immunoglobulin E (IgE) Test measures IgE antibody levels in blood to evaluate allergic reactions, asthma, and immune response. Elevated IgE may indicate allergies to food, pollen, or other triggers, as well as eczema or parasitic infections. Doctors order this test to investigate symptoms like hives, sneezing, or wheezing and to guide allergy treatment. Results provide vital insight into immune health, allergic sensitivity, and overall diagnostic care.

Blood
Blood Draw
Also Known As: Immunoglobulin E Test, Immunoglobulin E Antibody Test, IgE Antibody Test

The IgE Antibody (Anti-IgE IgG) test detects functional IgG autoantibodies against IgE or the high-affinity FcεRI receptor, a marker found in many cases of autoimmune chronic urticaria. These antibodies trigger mast cell and basophil degranulation, producing wheals, itching, and redness. Designed via immunoassay, the test uses serum (red-top tube), with preferred overnight fasting; results under ~168 ng/mL are considered within typical reference range.

Blood
Blood Draw
Also Known As: Anti-IgE IgG Test

Most Popular

The Immunoglobulin G (IgG) Test measures IgG antibody levels in blood to assess immune system function and long-term response to infections. Low IgG may indicate immune deficiencies or recurrent infections, while high levels may signal chronic inflammation, autoimmune disease, or certain infections. Doctors use this test to evaluate unexplained illness, monitor immune disorders, or assess overall immunity. Results provide vital insight into immune health and disease management.

Blood
Blood Draw
Also Known As: Immunoglobulin G Test, Immunoglobulin G Antibody Test, IgG Antibody Test

The IgG Subclasses Panel measures four IgG antibody subclasses (IgG1, IgG2, IgG3, IgG4) to assess immune system function. Abnormal levels may indicate primary immunodeficiency, recurrent infections, autoimmune disease, or allergic conditions. Doctors order this test for patients with chronic sinus, lung, or ear infections or suspected immune imbalance. Results provide key insight into antibody response, guiding diagnosis, treatment, and long-term immune monitoring.

Blood
Blood Draw
Also Known As: IgG Subclasses Test

Most Popular

The Immunoglobulin M (IgM) Test measures IgM antibody levels in blood to evaluate immune response and early defense against infections. High IgM may indicate recent or acute infections, autoimmune disease, or certain blood disorders, while low levels may suggest immune deficiency. Doctors order this test to investigate recurrent infections, unexplained inflammation, or suspected immune problems. Results provide vital insight into antibody health, immune status, and diagnostic care.

Blood
Blood Draw
Also Known As: Immunoglobulin M Test, Immunoglobulin M Antibody Test, IgM Antibody Test

The Immunofixation Serum Test identifies abnormal proteins in the blood called monoclonal immunoglobulins, often linked to multiple myeloma, Waldenström macroglobulinemia, or other plasma cell disorders. Physicians use this test to detect, classify, and monitor abnormal antibody production. Results help confirm suspected conditions, assess disease progression, and guide ongoing management of disorders affecting immune system function.

Blood
Blood Draw

The Immunofixation (IFE) Urine test detects and characterizes monoclonal proteins (free light chains/M-proteins) excreted in urine to evaluate plasma cell and lymphoproliferative disorders. It supports workup of light-chain disease, multiple myeloma, Waldenström macroglobulinemia, and amyloidosis, and helps distinguish monoclonal from polyclonal free light chains seen with glomerular leak, infection, or inflammation.

Urine
Urine Collection
Also Known As: IFE Urine Test

The Kappa/Lambda Light Chains Free with Ratio and Reflex to Immunofixation Test measures free light chains in blood and calculates the kappa/lambda ratio to evaluate plasma cell disorders. Abnormal levels can indicate multiple myeloma, light chain amyloidosis, or related monoclonal gammopathies. Reflex immunofixation confirms monoclonal proteins, supporting diagnosis and monitoring of plasma cell dyscrasias.

Blood
Blood Draw

Blood
Blood Draw

Immunoglobulins are also known as Igs, antibodies, immune globulins, gamma globulins, and immune serum globulins.

There are two standard definitions of Immunoglobulins:

1.  A solution sourced from human blood plasma, which has concentrated levels of antibodies that offer protection from certain diseases.

For instance, someone could have short-term protection from particular infections or even Rh sensitization while they’re pregnant. These solutions can be created using human blood plasma that is pooled and processed from sources of blood donations before undergoing purification.

2.  Special proteins made inside the human body as a response to foreign elements like viruses and bacteria. Plasma cells in lymphoid tissues and bone marrow make five different classes of immunoglobulins that bind to foreign substances and then neutralize them: A, D, E, G, and M.

This overview will concentrate on definition #2.

Immunoglobulin A (or IgA) is one of the more common immunoglobulins. It’s mostly present in bodily secretions. It’s also the primary antibody in saliva, tears, and the mucous membranes of the respiratory and gastrointestinal tracts.

Immunoglobulin D (or IgD) is found in small volumes in blood serum and considered functional in response to particular allergies.

Immunoglobulin E (or IgE) is often found in the mucous membranes and skin. It is thought to serve some capacity in allergic reactions and in response to environmental antigens.

Immunoglobulin G (or IgG) is widely prevalent throughout the body, offering long-term defense against antigens and most bacterial invasions.

Immunoglobulin M (or IgM) is a relatively big molecule and is found in the human bloodstream where it fights blood infections. It’s the initial or primary immunoglobulin to be produced after antigen exposure.

Immunoglobulins A, G, and M

Why Should You Get Tested?

Testing helps analyze the status of your immune system. It can also detect and/or monitor deficiency or excess in different classes of immunoglobulins.

When Should You Get Tested?

If you have chronic diarrhea or recurring infections, you should get tested. Also, it’s good to get tested if your doctor thinks there might be an excess or deficiency in a certain immunoglobulin. Routine testing is also useful in tracking circumstances that might impact immunoglobulin levels, be they genetic, like selective IgA deficiency, or acquired, as would be in the cases of HIV, AIDS, and multiple myeloma.

What Exactly Gets Tested?

Immunoglobulins serve a crucial function in the overall immune system of the human body. They are proteins created by certain immune cells known as plasma cells and are a response to viruses, bacteria, and a variety of other microorganisms. They can also be a response to exposures to numerous other substances that the body determines to be harmful antigens that aren’t part of the body. This testing measures immunoglobulin amounts for A, G, and M in your blood. In some cases, it also tests for them in your saliva or cerebrospinal fluid, also known as CSF.

When you are first exposed or infected with an antigen or foreign substance, your immune system is likely to recognize that the substance or microorganism as ‘non-self’ material that shouldn’t be there. In response, plasma cells are instigated to make particular immunoglobulin antibodies intended to bind to the threat and then neutralize it. If any recurring exposures happen, your immune system can ‘remember’ previously encountered antigens, which means additional antibodies are created quickly. In the event of subsequent exposure to microorganisms encountered before, this can help you avoid re-infection.

Immunoglobulins are classified into five distinct classes, with a number of subclasses. Every class categorizes a different collection of antibodies, and they all have minor variations in the functions they perform. Immunoglobulin classes include:

IgM (or Immunoglobulin M) antibodies are the first thing the human body makes when responding to any new infection or ‘non-self’ antigen. Providing a short duration of protection, these IgM antibodies are likely to increase for a few weeks before declining in favor of IgG production.

IgG (or Immunoglobulin G) constitutes 70 to 80 percent of all the immunoglobulins in your blood. Certain IgG antibodies are produced in the first case of exposure to an antigen or infection, growing in volume for several weeks before coming back down to a stable level. The human body keeps an inventory of IgG antibodies, which can see prompt reproduction if exposure to the same antigen happens again. It’s IgG antibodies that allow humans to enjoy long-running defense against the many microorganisms in nature. For individuals with typical immune systems, re-infection is frequently prevented with enough IgG production. Vaccinations take advantage of this particular process so that initial infections can be avoided, while the inventory of IgG antibodies is grown. This happens by exposing people to either antigens that stimulate microorganism identification or to a live-but-weakened microorganism. IgG is the one immunoglobulin capable of passing through a placenta. Thus, the IgG antibodies of the mother protect her fetus throughout pregnancy, as well as the first several months of a baby’s life after delivery. IgG has four subclasses, known as IcG1, IgG2, IgG3, as well as IgG4.

IgA (or Immunoglobulin A) makes up approximately 15 percent of all the immunoglobulins in a person’s blood. However, it’s also located in gastric secretions, respiratory secretions, tears, saliva, and even breast milk. IgA offers protection from infections in the body’s mucosal areas. These areas include the gastrointestinal tract, where the intestines and stomach are, as well as the respiratory tract, which includes the lungs and sinuses. As this immunoglobin can pass through breast milk from a mother to a child, it offers an infant gastrointestinal tract protection and benefits. Human babies don’t start producing substantial volumes of IgA until after six months after birth, which means any IgA the baby has in their blood before that is a result of mother’s milk they were fed.  IgA has two subclasses known as IgA1 and also IgA2.

IgD (or Immunoglobulin D) is a class of immunoglobulin where the function isn’t entirely understood, nor is it measured frequently.

IgE (or Immunoglobulin E) is associated with conditions like parasitic infections, allergies, and allergic diseases. Usually measured as a component of allergy testing blood panels, IgE is not normally incorporated into quantitative immunoglobulin testing.

Immunoglobulin testing is designed to measure the overall volume of major immunoglobulin classes without distinguishing between subclasses. Additional testing can measure the subclasses or look for particular antibodies.

Various conditions might increase or decrease immunoglobulin production. An increase is known as hypergammaglobulinemia, and a decrease is referred to as hypogammaglobulinemia. Some conditions can affect every class of immunoglobulins, while in other circumstances, only one class might be impacted. Some of these conditions are acquired, whereas others are inherited from a previous.

How Is This Used?

Testing is utilized to look for a deficiency or excess in the three primary immunoglobulin classes of IgM, IgG, and IgA. This testing provides valuable data about how healthy the immune system of the person being tested is. It can also assist in the diagnosis of different diseases and conditions that impact Ig levels in one or more of the three classes.

Typically, immunoglobulin disorders might be categorized as follows:

  • Immunoglobulin Excess
  • Monoclonal excess is where the extra immunoglobulins come from the clones of a single plasma cell
  • Polyclonal excess is where the extra immunoglobulins come from many different immune plasma cells
  • Immunoglobulin Deficiency
  • Primary (inherited) deficiencies are rare disorders where the human body can’t produce one or more immunoglobulin classes
  • Secondary (acquired) deficiencies are the most common deficiencies and are caused by an underlying factor or condition

This test can be ordered in conjunction with other tests, like a urine and/or serum protein electrophoresis, to diagnose and track conditions related to excessive or abnormal immunoglobulin production. In cases like these, urine samples might also be collected.

If the amount of one of the main immunoglobulin classes is excessive, then additional testing via immunofixation can be performed to ascertain whether or not the immunoglobulin comes from clones of an abnormal plasma cell (monoclonal gammopathy). Monoclonal gammopathies are present with cases of multiple myeloma, which is a malignancy of the plasma cells. A serum-free light chain test may also be conducted.

When Is This Ordered?

Doctors order the Immunoglobulins (IgA, IgG, IgM) test for patients with symptoms of deficient immunoglobulins, like chronic diarrhea or recurring infections of the digestive or respiratory tracts.

Additionally, immunoglobulins testing may get ordered if a person shows signs of chronic infection or inflammation, or just when a doctor thinks that immunoglobulin production might be abnormal or excessive. The Igs test may be ordered routinely to track the course of someone’s condition over time.

This test might also be performed on cerebrospinal fluid (or CSF) anytime a doctor thinks that a particular condition that’s impacting the patient’s central nervous system could be related to excess production of immunoglobulins.

What Do the Test Results Actually Mean?

The test results for IgM, IgA, and IgG levels are typically analyzed as a group. Abnormal test results frequently suggest that the immune system is being impacted by something, thus indicating the need for more testing. Immunoglobulin testing isn’t diagnostic on its own, but it does prove to be a rather robust indicator of some a condition or disease. Various conditions are known to be associated with decreases or increases in immunoglobulins.

Higher Levels

Higher levels of polyclonal immunoglobulins might occur in conjunction with numerous different conditions.

Monoclonal immunoglobulins can be seen in blood cell tumors involving plasma cells or lymphocytes. In such disorders, it’s common to see a definitive increase in one immunoglobulin class with a decrease happening in the remaining classes. Even though impacted people might have higher levels of immunoglobulins overall, they are, in actuality, immunocompromised since most of their immunoglobulin production is categorized as abnormal and doesn’t support the body’s immune response.

Here are particular instances of conditions which might result in increased levels of immunoglobulins.

A polyclonal increase in any or all of the three classes (A, G, M) may be associated with the following conditions:

  • Chronic inflammation
  • Inflammatory disorders
  • Autoimmune disorders (rheumatoid arthritis, systemic lupus erythematosus, scleroderma)
  • Hyperimmunization reactions
  • Cirrhosis
  • Wiskott-Aldrich syndrome
  • Acute and chronic infections

In a newborn: infection during pregnancy (CMV, rubella, toxoplasmosis, or congenital syphilis).

A monoclonal increase in a single class, either with or without corresponding decreases in the remaining two classes, may be associated with the following conditions:            

  • CLL (or chronic lymphocytic leukemia)
  • Multiple myelomas
  • Lymphoma
  • MGUS (or monoclonal gammopathy of undetermined significance)

             In the case of IgM: Waldenstrom’s macroglobulinemia

Low Levels

The most frequent reasons for a decrease in immunoglobulins are acquired underlying (secondary) conditions, which either impact the capacity of the body to make immunoglobulins or that just increase protein loss in the body.  Deficiencies can also result from corticosteroids, immunosuppressants, phenytoin, and carbamazepine, or due to toxins.

Here are certain instances of conditions which might result in decreased levels of immunoglobulins.

Conditions/factors that affect immunoglobulin production may be associated with the following conditions:

  • Drugs like immunosuppressants, phenytoin, and carbamazepine
  • Complications resulting from conditions like diabetes or kidney failure
  • Transient production delay in newborns, especially in premature infants (or transient hypogammaglobulinemia of infancy)

Conditions causing abnormal protein loss may be associated with the following conditions:

  • Nephrotic syndrome (a particular kidney disease where protein gets lost through the urine stream
  • Burns
  • Protein-losing enteropathy (any condition impacting the gastrointestinal tract and thus affecting protein absorption and/or digestion

Inherited immune deficiencies tend to be rare, and they’re frequently called primary immunodeficiencies. They might impact all immunoglobulin production, just one class, or various subclasses. These various disorders can include hyper-IgM syndrome, SCID (or severe combined immunodeficiency), Wiskott-Aldrich syndrome, ataxia-telangiectasia, x-linked agammaglobulinemia, agammaglobulinemia, and CVID (or common variable immunodeficiency).

In CSF, immunoglobulins typically are present in very low concentrations. 

Increased levels may be associated with conditions including inflammatory conditions:

  • Multiple sclerosis
  • Central nervous system infections like encephalitis and meningitis
  • A decrease in the level of salivary IgA might happen in patients with recurring infections of the respiratory tract

Why Did My Newborn Have an IgM Test?

Sometimes, this test is used to see if a newborn acquired an infection before birth.  Since IgM antibodies are too big to pass through a placenta from the mother to the baby in the womb, the presence of IgM antibodies indicates the infection began during pregnancy.

What Else Should I Be Aware Of?

Those with conditions resulting in lower immunoglobulin levels don’t enjoy robust immune responses to things like vaccinations. Their bodies might not make enough antibodies to result in appropriate protection. They also might not be able to receive live vaccines, like the ones used for measles or polio.

Quite a few lab tests can measure the levels of antibodies in a person’s blood, but anyone with immunoglobulin deficiencies might get false-negative results in their testing. Celiac disease is one thing that can get missed in standard testing, meaning that further testing might be suggested – for example, a celiac disease test for the IgA class of anti-tissue transglutaminase antibody (or anti-tTG).

When IgA or IgG concentrations are lower, or a subclass deficiency is suspected, then subclass testing can help identify the deficiency with more precision. Subclass deficiencies can happen even when class concentrations are within normal ranges.

Some patients who have IgA deficiencies can even develop anti-IgA antibodies. If a person who has anti-IgA receives a blood component transfusion which contains IgA, they may have a severe anaphylactic transfusion reaction.