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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1993-4-8
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pubmed:abstractText |
Pre- and postexposure prophylaxis against hepatitis A virus (HAV) infection with immune serum globulin (Ig) is only effective for 4-6 months. We compared the safety, tolerability and immunogenicity of a single i.m. injection of Ig with a single and booster dose of an inactivated hepatitis A virus vaccine (iHAV) in adults. Healthy volunteers (18-50 years) received a single Ig i.m. injection (n = 30), or iHAV i.m. (n = 15) at 0 and 24 weeks, or placebo (n = 4) at the same intervals. Anti-HAV seroconversion was measured by radioimmunoassay (RIA) and neutralizing antibodies by an antigen reduction assay. After Ig injection (0.06 ml/kg), anti-HAV seroconversion occurred in 100% of recipients at week 1, declining to 10% at week 12 and 0% by week 20. In contrast, after a single 25 ng dose, RIA seropositivity in iHAV vaccinees was 80% by week 2, reaching 100% by week 5 and persisted up to week 24, at which time anti-HAV geometric mean titres (GMT) were two fold higher than those seen at week 1 after Ig. Postbooster anti-HAV titres in iHAV recipients rose within 4 weeks to 73-fold greater than the peak GMT seen one week after Ig, and 400-fold higher than GMT at 12 weeks after Ig. Neutralizing antibody titres after iHAV followed a similar pattern, as observed for anti-HAV. iHAV was well tolerated; placebo and vaccine tolerability were indistinguishable, with no serious adverse experiences observed. In conclusion, active vaccination with a single iHAV dose may eventually replace Ig for pre-exposure prophylaxis.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Hepatitis A Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Hepatitis A Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/Hepatitis Antibodies,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulins,
http://linkedlifedata.com/resource/pubmed/chemical/Vaccines, Inactivated,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Hepatitis Vaccines
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pubmed:status |
MEDLINE
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pubmed:issn |
0264-410X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11 Suppl 1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
S9-14
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8383390-Adolescent,
pubmed-meshheading:8383390-Adult,
pubmed-meshheading:8383390-Female,
pubmed-meshheading:8383390-Hepatitis A,
pubmed-meshheading:8383390-Hepatitis A Antibodies,
pubmed-meshheading:8383390-Hepatitis A Vaccines,
pubmed-meshheading:8383390-Hepatitis Antibodies,
pubmed-meshheading:8383390-Hepatovirus,
pubmed-meshheading:8383390-Humans,
pubmed-meshheading:8383390-Immunization, Secondary,
pubmed-meshheading:8383390-Immunoglobulins,
pubmed-meshheading:8383390-Male,
pubmed-meshheading:8383390-Middle Aged,
pubmed-meshheading:8383390-Safety,
pubmed-meshheading:8383390-Vaccines, Inactivated,
pubmed-meshheading:8383390-Viral Hepatitis Vaccines
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pubmed:year |
1993
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pubmed:articleTitle |
Single and booster dose responses to an inactivated hepatitis A virus vaccine: comparison with immune serum globulin prophylaxis.
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pubmed:affiliation |
Liver Unit, Hadassah University Hospital, Jerusalem, Israel.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Controlled Clinical Trial,
Research Support, Non-U.S. Gov't
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