HIV
Positive People May Need Triple Dose of Hepatitis A Vaccine
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SUMMARY:
People with HIV require 3 doses of hepatitis A virus (HAV)
vaccine to achieve the same level of antibody protection that
HIV negative people can get with 2 doses, according to a study
presented at the 50th Interscience Conference on Antimicrobial
Agents and Chemotherapy (ICAAC 2010)
last month in Boston. HAV antibody response was particularly
weak among HIV positive men with a CD4 count below 200, all
of whom needed the third vaccine booster dose. |
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By
Liz Highleyman
Hepatitis
A is spread through contaminated food and water, as well as household
contact and some types of sexual activity. It can cause flu-like symptoms
and jaundice, but it resolves without treatment; unlike hepatitis
B and C, it does not cause liver
fibrosis or lead to cirrhosis or liver cancer.
Hepatitis
A immunization (vaccine)
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Studies
have shown that men who have sex with men (MSM) are at increased risk
for hepatitis A, and the Centers for Disease Control and Prevention
(CDC) recommends that HIV positive MSM should be screened for HAV and
vaccinated if not previously infected.
Yu-Tzu Tseng from Taipei City Hospital and colleagues conducted a study
to determine optimal hepatitis A vaccine dose schedules for HIV positive
gay/bisexual men in the era of highly
active antiretroviral therapy. People with seriously compromised
immune systems -- as indicated by a low CD4 cell count -- may not be
able to produce enough antibodies in response to a vaccine, but outcomes
in HIV positive people with well-preserved
immune function have not been well studied.
The present analysis included HIV positive and HIV negative MSM under
40 years of age enrolled between June 2009 and April 2010 at HIV clinics
and counseling and testing sites in Taiwan.
Participants were first screened for hepatitis A IgG antibodies. Men
found to be HAV seronegative were given 2 doses (administered at baseline
and 6 months) or 3 doses (at baseline, 1 month, and 6 months) of hepatitis
A vaccine. Among participants who consented to vaccination, 140 HIV
positive men and all HIV negative men received 2 doses, while 178 HIV
positive men received 3 doses.
Anti-HAV antibodies titres were measured at 6 months (just before the
final vaccine dose was administered) and again after 12 months.
Results
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At
baseline, hepatitis A virus seroprevalence was more than twice as
high among HIV positive men as among HIV negative men, 15% vs 7%,
respectively. |
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At
6 months, before the final vaccine dose, HIV positive men who received
1 previous dose were less likely to have mounted an antibody response
than either HIV positive men who received 2 prior doses or HIV negative
men: |
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HIV
positive, 1 dose: 38% HAV seroconversion; |
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HIV
positive, 2 doses: 63% seroconversion; |
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HIV
negative, 1 dose: 57% seroconversion. |
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HAV
seroconversion rates were significantly higher among HIV positive
men with CD4 cell counts > 200 cells/mm3 compared to those with
lower counts: |
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2-dose
group at 6 months: 40%; |
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2-dose
group at 12 months: 70%; |
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3-dose
group at 6 months: 50%; |
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3-dose
group at 12 months: 90%. |
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In
contrast, none of the HIV positive men with CD4 counts < 200
cells/mm3 achieved an HAV antibody response at 6 or 12 months with
only 2 vaccine doses. |
At 6 months
after starting the vaccination process, "HIV-infected MSM receiving
2 [more] doses of HAV vaccine achieved similar serologic responses to
HIV-uninfected MSM receiving 1 [more] dose," the researchers concluded.
"The response rates of these two groups were much higher than that
of the HIV-infected MSM who received 1 [more] dose of HAV vaccine."
Investigator affiliations: Taipei City Hospital, Taipei, Taiwan;
National Taiwan University Hospital, Taipei, Taiwan.
10/26/10
Reference
Y Tseng, W Liu, C Lu, and others. Comparisons of serologic responses
to hepatitis A vaccination between HIV-infected and HIV-uninfected men
who have sex with men in the era of highly active antiretroviral therapy.
50th Interscience Conference on Antimicrobial Agents and Chemotherapy
(ICAAC 2010). Boston, September 12-15, 2010. Abstract
H-217.