What are the measles (rubeola) antibody titers in adults?

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From the Guidelines

Measles Antibody Titers in Adults

Measles titers are typically considered protective if they are greater than or equal to 1:10. Adults born before 1957 are generally considered immune to measles, while those born in 1957 or later should have documentation of 1 or more doses of MMR vaccine, unless they have a medical contraindication or laboratory evidence of immunity 1.

  • Key factors influencing measles immunity include:
    • Birth year: Adults born before 1957 are generally considered immune 1.
    • Vaccination history: Documentation of 1 or more doses of MMR vaccine is recommended for adults born in 1957 or later, unless they have a medical contraindication or laboratory evidence of immunity 1.
    • Occupational or educational exposure: Adults who work in healthcare facilities, are students in postsecondary educational institutions, or plan to travel internationally may require a second dose of MMR vaccine, administered a minimum of 28 days after the first dose 1. If an adult's measles titer is less than 1:10, or if the titer is unknown, the Centers for Disease Control and Prevention (CDC) recommends administering 2 doses of the measles, mumps, and rubella (MMR) vaccine, separated by at least 28 days, to ensure adequate immunity. Alternatively, if the adult has a medical contraindication to the MMR vaccine, they may be considered immune if they have a documented history of measles infection or have received 2 doses of the measles vaccine in the past. In cases where vaccination is not possible, immune globulin may be administered as post-exposure prophylaxis, with a dose of 0.25 mL/kg of body weight, up to a maximum of 15 mL, administered within 6 days of exposure.

From the Research

Measles Antibody Titers in Adults

  • The measles-neutralizing antibody titers in adults can vary depending on the individual's vaccination history and the presence of natural infection 2, 3, 4, 5, 6.
  • Studies have shown that adults who received one or two doses of the measles-mumps-rubella (MMR) vaccine can have a range of antibody titers, with some individuals having low or undetectable levels of neutralizing antibodies 2, 3, 5.
  • A study found that 2 years after vaccination, 45.8% of participants had a medium (121-900) or high (>900) plaque reduction neutralization (PRN) titer, while 82.2% had a seroconversion rate of measles IgGs 2.
  • Another study found that 1 year after receiving a third MMR dose, no subject was seronegative, and 10 of 617 (1.6%) had low neutralizing antibody levels 3.
  • Long-term studies have shown that vaccine-induced antibody to measles can persist for 26-33 years after vaccination, with 92% of participants having a PRN titer considered protective (>1:120) 4.
  • A study found that 11 years after receiving a third MMR dose, measles and rubella neutralizing antibody levels remained high in adults, but some individuals may become susceptible to measles infection over time despite receipt of 3 vaccine doses 5.
  • The protective titers of measles neutralizing antibody have been defined as >1,000 mIU/ml to prevent measles infection and >500 mIU/ml to prevent symptomatic infection 6.

Factors Influencing Antibody Titers

  • Vaccination history: The number of doses and timing of MMR vaccination can influence antibody titers 2, 3, 4, 5.
  • Natural infection: Individuals with a history of natural infection tend to have higher antibody titers than those who have only been vaccinated 2.
  • Time since vaccination: Antibody titers can wane over time, with some individuals becoming susceptible to measles infection despite previous vaccination 3, 5.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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