Assessment of safety and immunogenicity of two different lots of diphtheria, tetanus, pertussis, hepatitis B and Haemophilus influenzae type b vaccine manufactured using small and large scale manufacturing process

被引:12
作者
Sharma, Hitt J. [1 ]
Patil, Vishwanath D. [2 ]
Lalwani, Sanjay K. [3 ]
Manglani, Mamta V. [4 ]
Ravichandran, Latha [5 ]
Kapre, Subhash V. [1 ]
Jadhav, Suresh S. [1 ]
Parekh, Sameer S. [1 ]
Ashtagi, Girija [2 ]
Malshe, Nandini [3 ]
Palkar, Sonali [3 ]
Wade, Minal [4 ]
Arunprasath, T. K. [5 ]
Kumar, Dinesh [5 ]
Shewale, Sunil D. [1 ]
机构
[1] Serum Inst India Ltd, Pune 411028, Maharashtra, India
[2] Jawaharlal Nehru Med Coll & Hosp, Belgaum, Karnataka, India
[3] Bharati Vidyapeeth Univ Med Coll & Hosp, Pune, Maharashtra, India
[4] Lokmanya Tilak Municipal Med Coll & Gen Hosp, Bombay, Maharashtra, India
[5] Sri Ramchandra Univ Med Coll & Hosp, Madras, Tamil Nadu, India
关键词
Pentavalent vaccine; Haemophilus influenzae type b vaccine; Large scale; Immunogenicity; Safety; India; EVENT FOLLOWING IMMUNIZATION; CASE-DEFINITION; DATA-COLLECTION; INJECTION SITE; GUIDELINES; INFANTS; BURDEN;
D O I
10.1016/j.vaccine.2011.11.067
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Hib vaccine can be easily incorporated in EPI vaccination schedule as the immunization schedule of Hib is similar to that of DTP vaccine. To meet the global demand of Hib vaccine, SIIL scaled up the Hib conjugate manufacturing process. This study was conducted in Indian infants to assess and compare the immunogenicity and safety of DTwP-HB+ Hib (Pentavac (R)) vaccine of SIIL manufactured at large scale with the 'same vaccine' manufactured at a smaller scale. Methods: 720 infants aged 6-8 weeks were randomized (2:1 ratio) to receive 0.5 ml of Pentavac (R) vaccine from two different lots one produced at scaled up process and the other at a small scale process. Serum samples obtained before and at one month after the 3rd dose of vaccine from both the groups were tested for IgG antibody response by ELISA and compared to assess non-inferiority. Results: Neither immunological interference nor increased reactogenicity was observed in either of the vaccine groups. All infants developed protective antibody titres to diphtheria, tetanus and Hib disease. For hepatitis B antigen, one child from each group remained sero-negative. The response to pertussis was 88% in large scale group vis-a-vis 87% in small scale group. Non-inferiority was concluded for all five components of the vaccine. No serious adverse event was reported in the study. Conclusions: The scale up vaccine achieved comparable response in terms of the safety and immunogenicity to small scale vaccine and therefore can be easily incorporated in the routine childhood vaccination programme. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:510 / 516
页数:7
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