Freeze-dried live attenuated smallpox vaccine prepared in cell culture "LC16-KAKETSUKEN": Post-marketing surveillance study on safety and efficacy compliant with Good Clinical Practice

被引:26
作者
Nishiyama, Yasumasa [1 ]
Fujii, Tatsuya [1 ]
Kanatani, Yasuhiro [2 ]
Shinmura, Yasuhiko [3 ]
Yokote, Hiroyuki [3 ]
Hashizume, So [4 ]
机构
[1] Japan Self Def Forces Cent Hosp, Hlth Care Ctr, Setagaya Ku, Tokyo 1548232, Japan
[2] Natl Inst Publ Hlth, Wako, Saitama 3510197, Japan
[3] Chemoserotherapeut Res Inst Kaketsuken, Kita Ku, Kumamoto, Kumamoto 8608568, Japan
[4] Chiba Univ, Chiba, Chiba 2638522, Japan
关键词
Attenuated smallpox vaccine; LC16m8; LC16-KAKETSUKEN; Postmarketing surveillance study; Safety; Efficacy; LC16M8; PROTECTION; IMMUNOGENICITY; MONKEYPOX; MICE;
D O I
10.1016/j.vaccine.2015.09.067
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: In Japan, production of smallpox vaccine LC16m8 (named LC16-KAKETSUKEN) was restarted and was determined to be maintained as a national stockpile in March 2002. Objective: To conduct a post-marketing surveillance study of the vaccination of freeze-dried live attenuated smallpox vaccine prepared in cell culture LC16-KAKETSUKEN using attenuated vaccinia strain LC16m8. The study complied with Good Clinical Practice, focusing on a comparison between primary vaccinees and re-vaccinees. Method: 268 personnel (261 males and 7 females) of the Japan Ground Self-Defense Force were inoculated with LC16-KAKETSUKEN and thereafter adverse events and efficacy were evaluated. Results: Among 268 vaccinee participants, the following vaccinees showed adverse events, none serious: 53 of 196 primary vaccinees (without previous smallpox vaccination), 4 of 71 re-vaccinees (with previous smallpox vaccination) and 1 vaccinee with unknown previous vaccination history. A breakdown of adverse events observed in this study (total 268 vaccinees) showed the following minor or mild adverse events: 52(19.4%) swelling of axillary lymph node, 4(1.5%) fever, 2(0.7%) fatigue, 1(0.4%) of rash, 14 (5.2%) erythema at the inoculation site, 1(0.4%) swelling at the inoculation site and 1(0.4%) autoinoculation. The incidence of adverse events for primary vaccinees (53/196; 27.0%) was significantly higher than for re-vaccinees (4/71; 5.6%). However, the proportion of vaccine take was significantly higher for primary vaccinees (185/196; 94.4%) than for re-vaccinees (58/71; 81.7%). Although the proportion of vaccine take of re-vaccinees was significantly lower than for primary vaccinees due to preexisting immunity by previous vaccination, no significant difference was found in neutralizing antibody titers between primary vaccinees and re-vaccinees at 1,4 and 7 months after LC16-KAKETSUKEN vaccination. Conclusion: The present post-marketing surveillance study compliant with Good Clinical Practice demonstrated the efficacy and safety of the smallpox vaccine LC16-KAKETSUKEN in an adult population. LC16-KAKETSUKEN is the sole currently available licensed smallpox vaccine for both adult and pediatric populations. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:6120 / 6127
页数:8
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