Lagos Rosanna, Munoz Alma, Dumas Rafaele, Pichon Sylvie, Zambrano Betzana, Levine Myron, Vidor Emmanuel
Centro para la Vacunas en Desarollo-Chile, Hospital Roberto del Rio, Santiago, Chile.
Vaccine. 2003 Sep 8;21(25-26):3730-3. doi: 10.1016/s0264-410x(03)00385-2.
In hepatitis A virus (HAV)-seronegative infants, inactivated hepatitis A vaccines are highly immunogenic. On the contrary, in infants who are HAV-seropositive before vaccination, the interfering effect of passively-transferred maternal anti-HAV antibodies leads to lower post-primary immunization anti-HAV levels, as compared to those achieved by seronegative infants. One possible way to overcome this drawback is to delay hepatitis A vaccination later during the first year of life. The objective of the study was to document the immunogenicity of an inactivated hepatitis A vaccine in 6 months old HAV-seropositive infants, given as two dose regimen consisting of a single primary immunization at 6 months of age, followed by a booster dose 6 months later.
The immunogenicity of one hepatitis A vaccine (Avaxim pediatric, Aventis Pasteur) was documented in 108 6 months old, HAV-seropositive infants randomly assigned to receive one priming dose of hepatitis A vaccine either concomitantly with (Group 2) or 2 weeks after the third dose of routine diphteria-tetanus-whole cell pertussis reconstituting lyophilized tetanus conjugated Haemophilus influenzae type b (DTwcP//PRP approximately T) vaccine and oral poliomyelitis vaccine (OPV) (Group 1). A booster dose was given 6 months later, concomitantly with MMR vaccine.
The 91 infants who were HAV-seropositive (ELISA titer >20 mIU/ml) at the moment of primo vaccination remained seropositive 1 month later. Geometric mean titers (GMT) decreased from 292 and 278 mIU/ml 1 month after the first dose, to 77.6 and 76.0 mIU/ml 6 months after, in Groups 1 and 2, respectively. Post-booster titers increased markedly in both groups, with GMTs of 1731 and 1866 mIU/ml and geometric mean post/pre-immunization titer ratios of 22.3 and 24.6, respectively.
These results suggest that immunological priming induced by a single dose of Avaxim pediatric administered to 6 or 6.5 months old, HAV-seropositive infants is present and should not preclude the use of this vaccine in such populations.
在甲型肝炎病毒(HAV)血清学阴性的婴儿中,灭活甲型肝炎疫苗具有高度免疫原性。相反,在接种疫苗前HAV血清学阳性的婴儿中,被动转移的母体抗HAV抗体的干扰作用导致初次免疫后抗HAV水平低于血清学阴性婴儿。克服这一缺点的一种可能方法是在生命的第一年后期延迟接种甲型肝炎疫苗。本研究的目的是记录灭活甲型肝炎疫苗在6个月大的HAV血清学阳性婴儿中的免疫原性,接种方案为两剂,6个月龄时进行单次初次免疫,6个月后进行加强剂量接种。
在108名6个月大的HAV血清学阳性婴儿中记录了一种甲型肝炎疫苗(Avaxim pediatric,赛诺菲巴斯德公司)的免疫原性,这些婴儿被随机分配,一组(第2组)在接种第三剂常规白喉-破伤风-全细胞百日咳重组冻干破伤风结合b型流感嗜血杆菌(DTwcP//PRP - T)疫苗和口服脊髓灰质炎疫苗(OPV)时同时接种一剂甲型肝炎疫苗,另一组(第1组)在接种第三剂常规白喉-破伤风-全细胞百日咳重组冻干破伤风结合b型流感嗜血杆菌(DTwcP//PRP - T)疫苗和口服脊髓灰质炎疫苗(OPV)两周后接种一剂甲型肝炎疫苗。6个月后与麻疹-腮腺炎-风疹疫苗同时接种加强剂量。
初次接种时HAV血清学阳性(ELISA滴度>20 mIU/ml)的91名婴儿在1个月后仍为血清学阳性。第1组和第2组的几何平均滴度(GMT)从第一剂接种后1个月的292和278 mIU/ml,分别降至6个月后的77.6和76.0 mIU/ml。两组加强接种后的滴度均显著升高,GMT分别为1731和1866 mIU/ml,免疫后几何平均滴度与免疫前几何平均滴度之比分别为22.3和24.6。
这些结果表明,给6或6.5个月大的HAV血清学阳性婴儿接种一剂Avaxim pediatric可诱导免疫启动,且不应排除在此类人群中使用该疫苗。