To investigate the antibody titer necessary to prevent hepatitis A virus infection, either 15 or 7.5 mg/kg of immune serum globulin was injected into 10 antihepatitis A virus negative volunteers and their serum antihepatitis A virus titers were observed for 28 wk. In addition, antibody titers were o
Hepatitis A antibody titres after infection and immunization: implications for passive and active immunization
✍ Scribed by H. L. Zaaijer; A. Leentvaar-Kuijpers; H. Rotman; P. N. Lelie
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 560 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
Abstract
Titres of antibodies against hepatitis A virus (HAV) were determined in patients, in donors, and in volunteers after active, passive, and combined immunization. Highest titres were found in recently infected persons: in 109 IgM anti‐HAV positive persons, the geometric mean titre (GMT) was 15,400 mlU/ml. The GMT in 265 anti‐HAV positive blood donors was 10,700 mlU/ml. The anti‐HAV seroprevalence in 19,746 donors increases with age: at the age of 40 years, 50% have antibodies. Titres after active, passive, and combined immunization were studied in three groups: 51 persons received inactivated HAV vaccine at months 0, 1, and 6. The GMT after the booster was 3,400 mlU/ml at month 7. All persons produced more than 100 mlU/ml anti‐HAV. Forty‐nine persons received both 5 ml immunoglobulin and three vaccinations, yielding a GMT of 1,300 mlU/ml at month 7. One person in this group produced less than 100 mlU/ml anti‐HAV. Forty‐nine persons received 5 ml immunoglobulin intramuscularly. At day 5 the GMT was 96 mlU/ml. The estimated minimum protective level (10 mlU/ml) was reached in 3 months. Hepatitis A vaccination may supersede the use of immunoglobulin as prophylaxis for travellers to endemic areas. Passive immunization remains necessary for protection during outbreaks. The dosage regimen for passive immunization is based on old studies using preparations with unknown anti‐HAV content. Concern regarding the antibody levels in immunoglobulin preparations is justified; the prevalence of HAV antibodies in developed countries continues to fall. Our results indicate that dosage regimens should be reconsidered. Dosage should be deduced logically from the anti‐HAV antibody content of the immunoglobulin preparation. © 1993 Wiley‐Liss, Inc.
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