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. 2021 Jul 2;18(1):1–4. doi: 10.1080/21645515.2021.1940653

The progress of postapproval clinical studies on Sabin IPV

Li Shi a, Mingbo Sun a,b,✉
PMCID: PMC8920192  PMID: 34213408

ABSTRACT

As one of the powerful vaccines for completely eradicating all types of poliovirus in the polio endgame period, the novel IPV, which is prepared from attenuated polio Sabin strains (sIPV) and is expected to reduce the overall biosafety risk, was licensed in Japan (sIPV-containing diphtheria-tetanus-acellular pertussis combination vaccines, DTP-sIPV) and China (sIPV) in November 2012 and January 2015, respectively. Limited by the development progress and the manufactured sIPV ability, it has to date only been used in Chinese Expanded Programme on Immunization (EPI) by sequential scheduling with bOPV and in Japan with DTP-sIPV vaccination. We herein summarize postapproval clinical studies of sIPV in both full-dose schedules and sequential schedules, focusing on China, to evaluate sIPV safety and immunogenicity in large populations to provide important data for its broad application in developing countries worldwide.

KEYWORDS: sIPV, postapproval clinical studies, full-dose and sequential vaccination, safety, immunogenicity

According to the requirement of the “Polio Eradication and Endgame Strategic Plan,” at least one dose of inactivated poliomyelitis vaccine (IPV) was introduced into the routine immunization schedule worldwide in 20161. In addition to conventional IPV, which is prepared from wild polio strains (cIPV) and has been used since the 1960s, another new IPV made from attenuated polio Sabin strains (sIPV) was licensed in Japan (sIPV-containing diphtheria-tetanus-acellular pertussis combination vaccines, DTP-sIPV) and China (sIPV) in November 2012 and January 2015, respectively.2 Since sIPV is expected to reduce the overall biosafety risk, the WHO recommends implementing and using sIPV in developing counties to reach the final target of polio eradication worldwide.3 In China, sIPV has been included in the Expanded Programme on Immunization (EPI) since May 2016. The first one was licensed in January 2015 and manufactured by the Institute of Medical Biology, Chinese Academy of Medical Sciences (CAMS) and was formulated to contain 30, 32, and 45 D-antigen units (DUs) for poliovirus serotypes I, II, and III, respectively. The second one was licensed in September 2017 and manufactured by the National Vaccine & Serum Institute of China National Biotech Group (CNBG); it was formulated to contain 15, 45, and 45 DU for poliovirus serotypes I, II, and III, respectively. We summarize postapproval clinical studies of sIPV in both full-dose schedules and sequential schedules, focusing on China, to provide data for reference use in the polio endgame period.

1. Safety in sequential vaccination

Immediately after sIPV licensing, safety and immunogenicity evaluations for sequential immunization of sIPV with trivalent oral poliomyelitis vaccine (tOPV) and bivalent OPV (bOPV) were performed in several provinces in China. The primary sequential schedule included sIPV-tOPV-tOPV, sIPV-sIPV-tOPV, sIPV-bOPV-bOPV, and sIPV-sIPV-bOPV compared with 3 doses of tOPV or IPV (cIPV or sIPV) or cIPV-bOPV/tOPV at ages of 2, 3, and 4 months.4–15 These postmarket studies investigated the safety of sIPV, with no vaccine-related serious adverse events (SAEs). Most adverse reactions were mild and transient, and phase I–III clinical trials were carried out.16 In addition, the safety of sIPV was comparable to that of cIPV, though adverse reactions were higher than those of tOPV.4,6,12,15 In a post hoc analysis including two clinical trials of sIPV/cIPV-bOPV sequential vaccination using commercial sIPV in 1200 infants in Guangxi Province compared with 3 doses of tOPV vaccination, injected IPV in sequential vaccination was associated with a relatively higher incidence of adverse events.5 Shi XJ15 et al. performed active surveillance among 2313 individuals in Ningxia Province and found rates of common reactions of 2464.33 and 64.92 per 100,000 doses for sIPV and tOPV, respectively. In Adverse Events Following Immunization (AEFI) passive surveillance related to 111,906 dose sIPV vaccinations from December 2015 to December 2016, rates of common reactions and rare reactions were 51.68 and 1.67 per 100,000 doses; among 3228071 doses of tOPV vaccination from January 2008 to April 2015, rates of common reactions and rare reactions were 1.73 and 0.22 per 100,000 doses, respectively, for tOPV.15 The higher incidence of adverse events (AEs) with sequential immunization combining OPV with IPV than the full tOPV schedule may be related to the vaccination route, whereby IPV was administered by intradermal injection and OPV orally. There were no significant safety differences regarding the sequential schedule evaluation.4,5,8 For example, Huang ZY et al.8 evaluated the safety of a population-based sequential vaccination schedule using sIPV-cIPV-bOPV, cIPV-sIPV-bOPV, 2 sIPV-bOPV, and 2cIPV-bOPV in 1917 infants in Shanghai city and found no significant differences in the rate of grade 3 reactions among different groups.

2. Immunogenicity evaluation of sequential vaccination

sIPV also showed good immunogenicity in sequential vaccination. Xiao ST et al10 evaluated the immunogenicity of 2 sIPV-tOPV sequential vaccination compared with tOPV-tOPV-tOPV and 3 sIPV-sIPV-sIPV in 214 infants in Shanghai and reported that sequential immunization with IPV and tOPV induced better immune effects than 3 doses of tOPV or sIPV. Shi XJ et al11 reached the same conclusion when evaluating 180 infants in Ningxia using sIPV-tOPV-tOPV sequential vaccination and tOPV-tOPV-tOPV vaccination. When immunogenicity was evaluated in sequential vaccination of sIPV (containing 30, 32, and 45 DU for poliovirus serotype I, II, and III) and bOPV, seroconversion rates were 98.9–100% for polio type I and type III neutralizing antibodies with all sequential vaccinations; however, rates were only 79.4–95% for type II for 2 sIPV-bOPV sequential immunization and 42.5–74.6% for sIPV-2bOPV sequential immunization.4,5,7,13,14 Not only the seroconversion rate but also neutralizing antibody levels for type II were lower in sIPV-bOPV sequential vaccination than in full-dose sIPV vaccination. The geometric mean titers (GMTs) for type I and III were 2048–5309.9 and 1079–2048 with sIPV-2bOPV vaccination and 2048–7359.6 and 2048–2941.1 with 2 sIPV-bOPV vaccination, whereas GMTs for type II were only 11.7–19 and 64–73.4 with sIPV-2bOPV and 2 sIPV-bOPV vaccinations, respectively. With the higher content of type II antigens (containing 15, 45, and 45 DU for poliovirus serotype I, II, and III), GMTs for type II increased, to 38.1–41.6 and 200.4–270.4 for sIPV-2bOPV and 2 sIPV-bOPV vaccinations, respectively.6,13 Nonetheless, values were still lower than those induced by three doses of sIPV or tOPV.5,17 All these sequential vaccinations suggest that one dose of sIPV in the EPI schedule is not effective and that at least two doses of sIPV with 1 dose of bOPV should be included in a sequential schedule to improve immunity against type II poliovirus. In China, the 2IPV-bOPV primary schedule was introduced into the EPI in December 2019. Summaries of sIPV-bOPV sequential vaccination immunogenicity are shown in Table 1.

Table 1.

The sIPV immunogenicity evaluation in postmarket studies of the sIPV primary schedule and sIPV–bOPV sequential schedule in China

Vaccination schedule sIPV antigen Individuals Numbers Location Type 1
 Type 2
 Type 3
 Ref.
Seroconversion
rate % (95%CI)		 GMTs(95%CI) Seroconversion
rate % (95%CI)		 GMTs(95%CI) Seroconversion
rate %(95%CI)		 GMTs(95%CI)
sIPV-bOPV-bOPV
sIPV-sIPV-bOPV		 Type I: 30 DU Type II: 32 DU Type III: 45 DU 358 Chongqing 99.7 2896
(2586–3244)		 74.58 19(15–25) 100 1079 (972–1199) 7
Type I: 30 DU Type II: 32 DU Type III: 45 DU 158 Zhejiang 100 2048 (2048–2048) 62 12 (4–32) 100 2048 (1024–2048) 4
Type I: 30 DU Type II: 32 DU Type III: 45 DU 170 Guangxi 99.4 (96.8–100.0) 5,303.9 (4610.5–6101.5) 51.8 (44.0–59.5) 11.7 (9.8–14.0) 99.4 (96.8–100.0) 1285.7 (1124.2–1470.4) 5
Type I: 15 DU Type II: 45 DU Type III: 45 DU 69 Hebei 100 4907.8 97.6 41.6 100 1692.15 13
Type I: 15 DU Type II: 45 DU Type III: 45 DU 189 Inner Mongolia, Shanxi, and Hebei 100 (98.07–100) 5029.8 (4435.2–5704.2) 91.53 (86.62–95.08) 38.1 (32.1–45.2) 100 (98.07–100) 1406.7 (1235.6–1601.5) 6
Type I: 30 DU Type II: 32 DU Type III: 45 DU 70 Shanghai 100 840.9 (1715.6–1966.3)     100 1858.5 (1742.6–1973.5) 10
Type I: 30 DU Type II: 32 DU Type III: 45 DU 152 Zhejiang 100 2048 (2048–2048) 95 64 (32–224) 100 2048 (2048–2048) 4
Type I: 30 DU Type II: 32 DU Type III: 45 DU 180 Guangxi 98.9 (90.0–99.9) 7,359.6 (6379.2–8490.6) 79.4 (72.8–85.1) 73.4 (60.1–89.7) 99.4 (96.9–100.0) 2,941.1 (2493.7–3468.9) 5
Type I: 30 DU Type II: 32 DU Type III: 45 DU 68 Hebai 100 7175.3 100 200.4 100 2986.3 13
Type I: 15 DU Type II: 45 DU Type III: 45 DU 185 Inner Mongolia, Shanxi, and Hebei   9310.9 (8132.9–10659.5) 98.4 (95.3–99.7) 270.4 (230.1–317.8) 100 (98.03–100) 4065.4 (3483.7–4744.3) 6
sIPV-sIPV-sIPV Type I: 30 DU Type II: 32 DU Type III: 45 DU 72 Shanghai 100 1085.6 (903.9–1267.2)     98.61 644.9 (518.7–771.1) 10
Type I: 30 DU Type II: 32 DU Type III: 45 DU 163 Zhejiang 100 2048 (2048–2048) 99 256 (128–512) 100 512 (256–1024) 4
Type I: 30 DU Type II: 32 DU Type III: 45 DU 1200 Yunnan 99.83 (98.1–100) 3283.3 (3091.7, 3488.9) 98.93 (96.9–99.6) 231.1 (217.3, 245.9) 99.9 (98.5–100) 932.0 (880.6, 986.3.0) 18
Type I: 15 DU Type II: 45 DU Type III: 45 DU 195 Inner Mongolia, Shanxi, and Hebei 100
(98.1–100)		 4476.7 (3982.0–5032.7) 99.5 (97.2–100) 510.2 (438.4–593.7) 100 (98.1–100) 1091.7 (942.2–1264.8) 6
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sIPV: inactivated poliomyelitis vaccine made from Sabin strains; bOPV: bivalent oral poliomyelitis vaccine

3. Safety in large populations with the sIPV schedule

A full dose of the sIPV vaccination schedule in postmarket surveillance is important to guide sIPV use in polio endgames worldwide. He H et al4 evaluated the safety of sIPV in 163 infants and observed only temporary and mild AEs; Yan S et al6 reported that most common AEs consisted of fever and rash, and no SAEs were related to vaccines among 195 sIPV vaccinators. We evaluated the safety of sIPV in a large population of 49,702 infants in Shanghai, including 20,019 for active monitoring and 29,683 for passive monitoring, using the AEFI monitoring system of the Shanghai CDC.17 The total rate of unsolicited AEs related to vaccination was 0.19%, and no grade 3 or 4 unsolicited vaccination-related reactions and no serious AEs related to vaccination were found in activating monitoring. AE rates were even lower in passive monitoring, with an incidence of 390.80/100,000 after 84,853 doses. Rare reactions in 6 participants were reported, including 4 cases of anaphylactic rash, 1 case of urticaria and 1 case of thrombocytopenic purpura, which suggested that we should pay more attention to these developments in future EPI mass vaccination. Of note, 42% cases of AEs occurred during concomitant administration with other vaccines, especially with the first dose of DTaP and DTaP-Hib, emphasizing that the effect of coadministering another vaccine with sIPV should be considered in routine vaccination.

4. Immunogenicity of the sIPV schedule in postmarket evaluation

To date, postmarket immunogenicity evaluations of sIPV have been reported in Japan and China. In Japan, sIPV was introduced into the national immunization program in November 2012, in which 3 doses of DTP-sIPV were administered to 3- to 90-month-old children at intervals of 20–56 days as the primary vaccination, followed by the fourth dose at least 6 months later; no booster was required after 2018.18,19 Hotta C et al18 reported that seroconversion rates reached 100% for all polio types after 4 doses of sIPV, and GMTs for type I, II and III polio were 173.3, 479.8 and 245.1, respectively. Comparing the neutralizing antibody titers induced by sIPV and tOPV, the polio type I neutralizing antibody titer was lower with IPV than OPV vaccination, whereas polio type II and III neutralizing antibody titers were significantly higher in IPV.18 In contrast to the DTP-sIPV antibody response in Japan, GMTs for anti-type II polio in China were lower than those for type I and type III. In a randomized, controlled, and open-label phase IV clinical trial of 3 doses of sIPV (manufactured by CNBG) involving 195 infants in China, seroconversion rates for 3 doses of sIPV vaccination reached 100%, 99.49% and 100% for type I, II and III, and GMTs were 4476.66, 510.18 and 1091.66, respectively.6 In our phase IV clinical trial of a consistency study for three commercial batches of sIPV (manufactured by IMBCAMS) in 1200 infants in China, seroconversion rates for type I, type II and type III were 99.83%, 98.93% and 99.44%, respectively, and GMTs were 3283.3, 231.1, and 932.0, respectively.17 The sIPV antigen content and manufacturing procedure may be related to the antibody level. sIPV contents for type I, II, and III polio with DTP-sIPV were 1.5, 50, and 50 sDU, 15, 45, and 45 DU and 30, 32, and 45 per dose, respectively, as manufactured by Kaketsuken, CNBG and IMBCAMS. Thus, a homologous reference measuring the antigen content of IPV is urgently needed to evaluate the potency of sIPV in clinical and postclinical trials worldwide.

With collaborative study among different laboratories, including the WHO, national regulatory departments in different countries and sIPV manufacturers, the first World Health Organization international standard for sIPV was established in 2019.20 In addition, to guarantee a sufficient IPV supply for polio eradication using a full-dose sIPV schedule instead of a sequential schedule after bOPV withdrawal in the near future, with the exception of postapproval clinical studies of current sIPV administered intramuscularly, a clinical trial of fractional doses of sIPV administered intradermally should be performed as an appropriate vaccination route for polio endgame requirements.21

In conclusion, postapproval clinical studies of sIPV with both the full-dose sIPV schedule and sequential schedule indicate that commercial sIPV has good safety in large populations. Three doses of sIPV vaccination can induce high levels of GMTs against all three types of polio, revealing its good immunogenicity and the ability to neutralize multiple individual wild and vaccine-derived polioviruses,22 with no difference in response between male and female infants or among different populations.17 All these results indicate that sIPV is suitable for completely eradicating all types of poliovirus in the polio endgame period. In addition, with the increased manufacturing capability of sIPV, the 2sIPV-bOPV sequential schedule should be used as soon as possible instead of the present sIPV-2bOPV schedule worldwide, with transition to the full-dose sIPV schedule in the future.

Disclosure of potential conflicts of interest

No potential conflicts of interest were disclosed.

References

  • 1.World Health Organization . Polio eradication & endgame strategic plan 2013-2018. Glob Polio Erad Initiat Work Draft 2013;23:1–99. [Google Scholar]
  • 2.Shimizu H. Development and introduction of inactivated poliovirus vaccines derived from Sabin strains in Japan. Vaccine. 2016;34:1975–85. doi: 10.1016/j.vaccine.2014.11.015. [DOI] [PubMed] [Google Scholar]
  • 3.Okayasu H, Sein C, Hamidi A, Bakker WA, Sutter RW. Development of inactivated poliovirus vaccine from Sabin strains: a progress report. Biologicals. 2016;44(6):581–87. doi: 10.1016/j.biologicals.2016.08.005. [DOI] [PubMed] [Google Scholar]
  • 4.He H, Wang Y, Deng X, Yue C, Tang X, Li Y, Liu Y, Yin Z, Zhang G, Chen Z, et al. Immunogenicity of three sequential schedules with Sabin inactivated poliovirus vaccine and bivalent oral poliovirus vaccine in Zhejiang, China: an open-label, randomised, controlled trial. Lancet Infect Dis. 2020;20(9):1071–79. doi: 10.1016/S1473-3099(19)30738-8. [DOI] [PubMed] [Google Scholar]
  • 5.Zhao T, Mo Z, Ying Z, Huang T, Che Y, Li G, Yang X, Sun M, Jiang L, Shi L, et al. Post hoc analysis of two clinical trials to compare the immunogenicity and safety of different polio immunization schedules in Chinese infants. Ann Transl Med. 2021;9(3):253. doi: 10.21037/atm-20-2537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Yan S, Chen H, Zhang Z, Chang S, Xiao Y, Luo L, Zhang Z, Sun L, Chen X, Yang Y, et al. Immunogenicity and safety of different sequential schedules of Sabin strain-based inactivated poliovirus vaccination: a randomized, controlled, open-label, phase IV clinical trial in China. Vaccine. 2020;38(40):6274–79. doi: 10.1016/j.vaccine.2020.07.042. [DOI] [PubMed] [Google Scholar]
  • 7.Wang Q, Zhang Y, Xu J. [Immunogenicity of sequential polio vaccination schedules that use inactivated polio vaccine as the first dose]. Chin J Vacc Immun. 2019;25(4):378–82. [Google Scholar]
  • 8.Huang Z, Sun X, Liu J, Li Z, Ren J, Wu L, Hu JY, Zhang JN. [Observation on safety of sequential vaccination schedule of different strain inactivated poliovirus vaccines]. Zhonghua Liu Xing Bing Xue Za Zhi. 2019;40(5):565–70. doi: 10.3760/cma.j.0254-6450.2019.05.014. [DOI] [PubMed] [Google Scholar]
  • 9.Fu S, Lin L, Cao F, Tian X, Chen T, Chen C, et al. [Comparison of immunization safety of 4 kinds of polio vaccines in Jilin province]. Chin J Vacc Immun. 2017;23(4):379–82. [Google Scholar]
  • 10.Xiao S, Yang T, Fei Y, Deng P, Yang L. [Basic immune effect of sequential immunization with oral live attenuated vaccine and inactivated poliomyelitis vaccine]. Chin J Biol. 2020;33(07):809–12. [Google Scholar]
  • 11.Shi X, Liu L, Zhou L, Zhou L. [Evaluation on effect of sequential immunization with inactivated poliovirus vaccine and oral live attenuated poliomyelitis vaccine]. Chin J Biol. 2018;31(5):519–22. [Google Scholar]
  • 12.Xiao S, Liu Y, Li G, Lin L. [Immunogenicity after sequential program by Sabin strain inactivated poliovirus vaccine instead of attenuated live vaccine in Meizhou City]. Occup Health. 2018;34(14):1949–51. [Google Scholar]
  • 13.Zhang J, Zhu Y, Xu X, Liu S, Wang J, Cong Y, et al. [Immunogenicity of two sequential primary immunization schedules with inactivated poliovirus vaccine and bivalent oral poliomyelitis attenuated live vaccine]. Chin J Biol. 2020;26(3):265–68. [Google Scholar]
  • 14.Ma M, G X, Yang L. [Immunogenicity and safety of sequential schedules of Sabin inactivated poliovirus vaccine with two dosage forms of bivalent oral poliovirus vaccines]. Chin General Nursing. 2020;18(25):3341–43. [Google Scholar]
  • 15.Shi X, Zhou L, Zhou L, Liu L. [Safety of domestic Sabin strain inactivated poliovirus vaccine]. Chin J Vacc Immun. 2017;8(4):383–86. [Google Scholar]
  • 16.Liao G, Li R, Li C, Sun M, Jiang S, Li Y, Mo Z, Xia J, Xie Z, Che Y, et al. Phase 3 trial of a Sabin strain-based inactivated poliovirus vaccine. J Infect Dis. 2016;214:1728–34. doi: 10.1093/infdis/jiw433. [DOI] [PubMed] [Google Scholar]
  • 17.Jiang R, Liu X, Sun X, Wang J, Huang Z, Li C, Li Z, Zhou J, Pu Y, Ying Z, et al. Immunogenicity and safety of the inactivated poliomyelitis vaccine made from Sabin strains in a phase IV clinical trial for the vaccination of a large population. Vaccine. 2021;39(9):1463–71. doi: 10.1016/j.vaccine.2021.01.027. [DOI] [PubMed] [Google Scholar]
  • 18.Hotta C, Ogawa T, Shirasawa H. Surveillance of immunity acquired from poliovirus immunization including vaccination with the Sabin strain-derived inactivated vaccine. Hum Vaccin Immunother. 2019;15:1154–59. doi: 10.1080/21645515.2019.1572408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Satoh H, Tanaka-Taya K, Shimizu H, Goto A, Tanaka S, Nakano T, Hotta C, Okazaki T, Itamochi M, Ito M, et al. Polio vaccination coverage and seroprevalence of poliovirus antibodies after the introduction of inactivated poliovirus vaccines for routine immunization in Japan. Vaccine. 2019;37:1964–71. doi: 10.1016/j.vaccine.2019.02.034. [DOI] [PubMed] [Google Scholar]
  • 20.Crawt L, Atkinson E, Tedcastle A, Pegg E, Ipvsg M, Minor P, Cooper G, Rigsby P, Martin J. Differences in antigenic structure of inactivated polio vaccines made from sabin live-attenuated and wild-type poliovirus strains: impact on vaccine potency assays. J Infect Dis. 2020;221:544–52. doi: 10.1093/infdis/jiz076. [DOI] [PubMed] [Google Scholar]
  • 21.Zipursky S, Patel M, Farrell M, Gonzalez AR, Kachra T, Folly Y, Kurji F, Veira CL, Wootton E, Hampton LM, et al. Lessons learned from managing the planning and implementation of inactivated polio vaccine introduction in support of the polio endgame. J Infect Dis. 2017;216:S15–S23. doi: 10.1093/infdis/jix185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Sun M, Li C, Xu W, Liao G, Li R, Zhou J, Li Y, Cai W, Yan D, Che Y, et al. Immune serum from sabin inactivated poliovirus vaccine immunization neutralizes multiple individual wild and vaccine-derived polioviruses. Clin Infect Dis. 2017;64(10):1317–25. doi: 10.1093/cid/cix110. [DOI] [PubMed] [Google Scholar]

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