Paper # 880 
Persistence of Protective Antibody to Hepatitis B, Japanese Encephalitis, Measles, Mumps, and Rubella up to 3 Years after Revaccination in HIV-infected Children with Immune Recovery a
Linda Aurpibul*1, T Sujaridruk2, M Lao-araya2, T Puthanakit1, T Sirisanthana1, and V Sirisanthana1
1Res Inst for Hlth Sci, Chiang Mai Univ, Thailand and 2Faculty of Med, Chiang Mai Univ, Thailand
Background: Revaccination with childhood vaccines
among HIV-infected children after immune recovery has resulted in high response
rate. However, there is a concern of the rapid waning of antibody over time. To
determine the protective antibodies to Hepatitis B(HBV), Japanese
encephalitis(JE), measles, mumps, and rubella at 3 years after revaccination in
HIV-infected children receiving antiretroviral therapy(ART).
Methods: HIV-infected children who had no protective
antibody levels were revaccinated with HBV, JE or MMR vaccines while receiving
ART and had had immune recovery. The levels of protective antibodies were
measured at 3 years and compared to those at 6 months after revaccination. Children
with antiHBs ≥10 mIU/mL, JE Neutralizing antibody ≥1:10, measles
IgG ≥ 320 mIU/mL, mumps IgG ≥ 1:500, and rubella IgG ≥10
IU/mL were defined as having protective antibodies.
Results: Enrolled were 75 HIV+ children
with a mean age of 9.7 years (SD2.1) at the time of revaccination. Their mean
CD4 percentage at nadir was 5.5 (SD4.7). At the time of revaccination they have
had immune recovery (CD4 ≥15%) for a median of 20 months (IQR 16 to 27).
The current CD4 percentage was 30.5 (SD6.1). Viral suppression was documented
in 97% of children. The protective antibodies were shown in Table 1. There was
significantly dropped in proportion of children with protective antibody to HBV
at 3 years comparing to 6 months after revaccination (71% vs 96%, P <0.01).
Those who had anti-HBV below protective level at year 3 had significant lower
antibody titer at month 6 comparing to those with persistent protective
antibody [89 (95%CI 49 to 130) vs 5617 (95%CI 3496 to 7738), P<0.01],
while age at the time of revaccination, gender, baseline CD4, baseline HIV RNA
level, or duration from immune recovery to time of revaccination were not a
predictor for antibody loss.
Table 1 Seroprevalence of
protective antibodies in HIV-infected children after revaccination
|
Disease
|
Time after re-vaccination
|
|
|
Number of cases
|
6 months
|
3 years
|
p-value
|
|
Hepatitis B
|
69
|
66 (96)
|
49 (71)
|
<0.01
|
|
Japanese encephalitis
|
43
|
38 (88)
|
35 (81)
|
0.37
|
|
Measles
|
34
|
29 (85)
|
29 (85)
|
1.00
|
|
Mumps
|
38
|
25 (66)
|
23 (61)
|
0.63
|
|
Rubella
|
38
|
34 (90)
|
30 (79)
|
0.34
|
Conclusions: There were high rate of protective
antibodies up to 3 years after revaccination of childhood vaccines in
HIV-infected children after received ART. Revaccination program for those
children after immune recovery should be considered to ensure protection of
common diseases.
|