ABSTRACT
Background
Although China’s Expanded Program on Immunization (EPI) provides two doses of group A meningococcal polysaccharide vaccine (MPV-A) for children younger than 2y, more self-paying group A and group C meningococcal polysaccharide conjugate vaccine (MCV-AC) has been used as an alternative to MPV-A, to prevent Neisseria meningitidis serogroup C (Men-C) earlier. We evaluated the pattern of MPV-A and MCV-AC utilization to provide evidence for China to upgrade the national meningococcal meningitis vaccination strategy.
Methods
Children born between 2008 and 2017 registered in Hangzhou’s Immunization Information System (HZIIS) were included. Descriptive epidemiological methods were used to characterize the data. Adverse event following immunization (AEFI) was collected from Chinese national adverse event following immunization information system (CNAEFIIS) to compare the safety of MPV-A and MCV-AC.
Results
Data of 1149,027 children from HZIIS were analyzed. The average immunization rate of meningococcal meningitis vaccine (MenV) was 97.50%. Percentages of children using MPV-A-only, MCV-AC-only, and MPV-A/MCV-AC sequential schedules were 68.20%, 29.73%, and 2.07%, respectively. The vaccination rate of MCV-AC-only increased by age and it was higher in resident children than migration children. The incidence rate of AEFI of MPV-A and MCV-AC was 53.36 per 100,000 and 62.13 per 100,000, respectively.
Conclusion
Children in Hangzhou had high MenV coverage. MCV-AC-only schedule use increased by year and was higher in urban areas among locally born children. Both MPV-A and MCV-AC were safe for children, while MCV-AC could protect against Men-C more effectively. This supports the rationale to introduce MCV-AC into China’s EPI system for free instead of MPV-A.
KEYWORDS: meningococcal meningitis vaccine, vaccination, China
1. Introduction
Meningococcal meningitis is a severe acute respiratory infection caused by Neisseria meningitidis meningitis (Nm). Its classic clinical features are fever, rash, and meningitis. Besides meningitis and septicemia, meningococci occasionally cause arthritis, myocarditis, pericarditis, and endophthalmitis1. Approximately 10% to 20% of the survivors of meningococcal meningitis have permanent sequelae, such as mental retardation, deafness, epilepsy, or other neurological disorders. Meningococcal disease can progress rapidly. The case fatality rate, which was 70% to 85% before the advent of antibiotics, is now 10% to 15%.2 It has become one of the most significant public health problems in many countries. The majority of countries with high incidence rates belong to the African meningitis belt; many moderate-incidence countries locate in the European and African regions, and Australia, while low-incidence countries are from Europe and the America.3 There are 12 serogroups, but the majority of the invasive meningococcal infections are caused by organisms from the A, B, C, X, Y, or W-135 serogroups which account for 95% of meningococcal meningitis cases.4 In Asia, serogroup A and serogroup C meningococcal epidemics cause high morbidity and mortality and continue being an ongoing threat, particularly in developing countries.5,6 China has got several large-scale epidemics, such as the outbreak of serogroup A and serogroup C meningitis in some provinces from the end of 2004 to the beginning of 2005.7In China, most cases occurred in children under age of 15 and especially among infants of 6months to 2y old.8
For meningococcal meningitis prevention, chemoprophylaxis should be offered to household members and anyone in close contact. However, its effectiveness of lowering disease risk for a large population in response to outbreaks of meningococcal disease may be limited.9 Meningococcal vaccination is the most effective way for meningococcal meningitis prevention. Currently, MenV in Chinese market includes meningococcal polysaccharide vaccine (MPV) and MCV. In the 1980s, MPV-A had been widely used in China, and the incidence of meningococcal meningitis decreased significantly. In 2006, MPV-A and group A and group C meningococcal polysaccharide vaccine (MPV-AC) had been introduced to EPI in Hangzhou, China. Children aged 6–18months were given two doses of MPV-A with at least 3-month interval time between the doses, followed by two booster doses of MPV-AC at 3y and 6y old. MCV-AC was available in Hangzhou in 2009 as a self-pay vaccine, mainly replacing MPV-A in children within 2y old.
Our study is to determine the coverage rates of primary immunization of meningococcal meningitis vaccines, patterns of use of MPV-A and MCV-AC, and occurrence of AEFI of MPV-A and MCV-AC in Hangzhou between 2008 and 2017.
2. Methods
2.1. Setting
Hangzhou is a supercity in Zhejiang Province in the east of China with a population of over 10,000,000. There are 15 districts in Hangzhou, 6 of which are classified as urban areas (Shangcheng, Xiacheng, Jianggan, Gongshu, Xihu, and Xihufengjingmingsheng); 6 of which are classified as suburb area (Binjiang, Xiaoshan, Yuhang, Qiantang, Fuyang, Lin’an); the other are classified as rural areas (Tonglu, Jiande, Chun’an). There are 200 vaccination clinics in Hangzhou responsible for vaccinating all children residing in Hangzhou, regardless of whether they are residents or migrants. EPI clinicians are required to inform parents of the benefits and risks of MPV-A or MCV-AC.
Since 2005, Hangzhou Center for Disease Control and Prevention (HZCDC) has operated the Hangzhou’s Immunization Information System (HZIIS), which was a computerized information system registering immunization data for children aged <15y old and adults living in Hangzhou. Children’s demographic information and immunization history (vaccine type, dose, vaccination date) were recorded in this system. HZIIS contains a client application software deployed in every immunization clinic and a web-based management platform built in HZCDC. All children, including resident and migrant children, are registered in HZIIS during their vaccination in Hangzhou.
Chinese national adverse event following immunization information system (CNAEFIIS) is a passive surveillance system, which is the only official vaccine safety surveillance system that collects AEFI cases in mainland China. AEFI is defined as damages of body tissues, organs, and function, which are suspected to be the vaccination response occurred in the process of vaccination or after vaccination. According to the causes, they can be divided into adverse reactions (including common adverse reaction and rare adverse reaction), vaccine quality accidents, implementation error accidents, coincidences, and psychogenic reactions.
2.2. Vaccination and AEFI data
Our study included children who were born between January 1, 2008 and December 31, 2017 and registered in HZIIS. Information including district of residence, gender, birth date, dose number, vaccination time, and type was obtained. We defined children who were not born but living in Hangzhou as migrant children. Data were extracted from HZIIS on June 30, 2019. AEFI of MPV-A and MCV-AC was exported from CNAEFIIS.
2.3. Data analysis
We categorized MPV-A and MCV-AC vaccination patterns into MPV-A-only, MCV-AC-only, sequential MPV-A followed by MCV-A or MCV-AC followed by MPV-A. Coverage rate of MenV was determined by dividing the number of vaccinations administered by the number of children registered in HZIIS. We described the vaccination patterns of MenV by birth year, geographical area, and migrant status. Annual incidence of AEFI in MPV-A and MCV-AC was analyzed statistically. MenV AEFI per 100,000 populations was calculated by using the number of MenV AEFI cases divided by the number of MenV recipients. All statistical analyses and graphs were made by SPSS statistical software for Windows (version 17.0, SPSS Inc., Chicago, IL, USA). A value of P <.05 (2-sided) was considered statistically significant. The chi-square test was used to compare the proportion of children who used MCV-AC-only schedule in urban, suburb, or rural; in resident and migrant; the incidence of common adverse reaction and rare adverse reaction in MPV-A and MCV-AC. The chi-square trend test was used to compare the proportion of children using MCV-AC-only schedule year by year.
2.4. Ethical considerations
This study was determined to be exempt from ethical review by the Hangzhou CDC institutional review board. Data were safe when extracted from HZIIS and CNAEFIIS and were not linked to individual identifiers.
3. Results
3.1. MenV coverage
A total of 114,9027 infants born from 2008 to 2017 were registered in HZIIS, including 604,054 males (52.57%) and 544,973 females (47.43%); 705,281 (61.38%) resident children and 443,746 (38.62%) migrant children; 377,518 urban children (32.86%), 659,876 suburb children (57.43%), and 111,633 rural children (9.72%). There were 76,899, 79319, 95,384, 107,765, 123,967, 111,864, 141,509, 112,072, 150,983, and 149,265 children in each birth cohort. Coverage rates were 99.93% for receiving at least one dose of MenV, and 97.50% for receiving at least two doses. Across all 10 birth cohorts, the two-dose coverage rates were consistently over 95% (Table 1).
Table 1.
Coverage of MenVa among children born from 2008 to 2017, by birth cohort
≥1 Dose | ≥2 Doses | ||||
---|---|---|---|---|---|
Year of birth | No. of children | No. vaccinated | Rate (%) | No. vaccinated | Rate (%) |
2008 | 76899 | 75399 | 98.05 | 73531 | 95.62 |
2009 | 79319 | 77957 | 98.28 | 76363 | 96.27 |
2010 | 95384 | 94204 | 98.76 | 92826 | 97.32 |
2011 | 107765 | 106595 | 98.91 | 105393 | 97.8 |
2012 | 123967 | 122558 | 98.86 | 121334 | 97.88 |
2013 | 111864 | 110756 | 99.01 | 109769 | 98.13 |
2014 | 141509 | 140333 | 99.17 | 139275 | 98.42 |
2015 | 112072 | 111070 | 99.11 | 110008 | 98.16 |
2016 | 150983 | 150023 | 99.36 | 148837 | 98.58 |
2017 | 149265 | 147785 | 99.01 | 143001 | 95.8 |
Total | 1149027 | 1136680 | 98.93 | 1120337 | 97.5 |
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a: Meningococcal meningitis vaccine.
3.2. MenV vaccination pattern
Across all birth cohorts, 68.20% of children used MPV-A-only schedule; 29.73% used MCV-AC-only schedule; and 2.07% used MPV-A/MCV-AC sequential schedules. The proportion of children who used MPV-A-only schedule decreased year by year, from 96.02% in 2008 to 58.53% in 2017 (χ2=37180.58, Pfor trend<0.05). The proportion of children using MCV-AC-only schedule increased year by year, from 2.73% in 2008 to 40.01% in 2017 (χ2=40415.78, Pfor trend<0.05). Sequential schedules were seldomly used, the rate of which varies from 1.25% to 2.86% per year.
The proportion of children who used MCV-AC-only schedule was 44.10%, highest in the urban, and it was 19.28%, lowest in the suburb (χ2urban,suburb=72088.93, χ2urban,rural=50.38, χ2suburb,rural=30077.20, all P-value<0.05).The proportion was higher in resident children (33.49%) than in migrant children (23.70%) (χ2=12344.49, P <.05) (Table 2). No matter in urban, suburb, or rural, more proportion of resident children used MCV-AC-only schedule than migrant children (χ2urban=10752.31, χ2suburb=789.66, χ2rural=2356.35, all P-value<0.05) (Table 3).
Table 2.
Use of different MenVa schedules by birth year, geography, and migrant status
MPV-A-onlyb | MCV-AC-onlyc | Sequential schedules | ||||||
---|---|---|---|---|---|---|---|---|
No. vaccinated | No. | Proportion (%) | No. | Proportion (%) | No. | Proportion (%) | ||
Year of birth | 2008 | 75399 | 72400 | 96.02 | 2057 | 2.73 | 942 | 1.25 |
2009 | 77957 | 66079 | 84.76 | 9646 | 12.37 | 2232 | 2.86 | |
2010 | 94204 | 69886 | 74.19 | 21653 | 22.99 | 2665 | 2.83 | |
2011 | 106595 | 74120 | 69.53 | 29440 | 27.62 | 3035 | 2.85 | |
2012 | 122558 | 81615 | 66.59 | 38318 | 31.27 | 2625 | 2.14 | |
2013 | 110756 | 72768 | 65.7 | 36076 | 32.57 | 1912 | 1.73 | |
2014 | 140333 | 84375 | 60.12 | 53789 | 38.33 | 2169 | 1.55 | |
2015 | 111070 | 67706 | 60.96 | 41285 | 37.17 | 2079 | 1.87 | |
2016 | 150023 | 99720 | 66.47 | 46593 | 31.06 | 3710 | 2.47 | |
2017 | 147785 | 86498 | 58.53 | 59122 | 40.01 | 2165 | 1.46 | |
Area | Urban | 373396 | 197298 | 52.84 | 164672 | 44.1 | 11426 | 3.06 |
Suburb | 652579 | 517884 | 79.36 | 125819 | 19.28 | 8876 | 1.36 | |
Rural | 110705 | 59985 | 54.18 | 47488 | 42.9 | 3232 | 2.92 | |
Migrant status | Resident | 700224 | 454473 | 64.9 | 234537 | 33.49 | 11214 | 1.6 |
Migrant | 436456 | 320694 | 73.48 | 103442 | 23.7 | 12320 | 2.82 | |
Total | 1136680 | 775167 | 68.2 | 337979 | 29.73 | 23534 | 2.07 |
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a: Meningococcal meningitis vaccine.
b: Children who used group A meningococcal polysaccharide vaccine(MPV-A) only.
c: Children who used group A and group C meningococcal polysaccharide conjugate vaccine (MCV-AC) only.
Table 3.
Coverage of MCV-ACa among children born from 2008 to 2017, by geography and migrant status
Urban | Suburb | Rural | Total | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
No. of children | No. vaccinated | Rate (%) | No. of children | No. vaccinated | Rate (%) | No. of children | No. vaccinated | Rate (%) | No. of children | No. vaccinated | Rate (%) | ||
Migrant status | Resident | 227366 | 114640 | 50.42 | 387560 | 78311 | 20.21 | 90355 | 41586 | 46.03 | 705281 | 234537 | 33.25 |
Migrant | 150152 | 50032 | 33.32 | 272316 | 47508 | 17.45 | 21278 | 5902 | 27.74 | 443746 | 103442 | 23.31 | |
Total | 377518 | 164672 | 43.62 | 659876 | 125819 | 19.07 | 111633 | 47488 | 42.54 | 1149027 | 337979 | 29.41 |
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a: Group A and group C meningococcal polysaccharide conjugate vaccine.
3.3. AEFI of MPV-A and MCV-AC
For 2008 to 2017 birth cohort children, a total of 838 AEFI cases of MPV-A and 459 AEFI cases of MCV-AC were reported in CNAEFIIS. The incidence of AEFI in MPV-A and MCV-AC was 53.36 per 100,000 and 62.13 per 100,000, respectively. The incidence of common adverse reaction in MPV-A and MCV-AC, mainly the injection site erythema, injection site pain, and fever, was 49.35 per 100,000 and 54.41 per 100,000, respectively (χ2=2.53, P >.05). The incidence of rare adverse reaction in MPV-A (2.87 per 100,000) was lower than that of MCV-AC (5.14 per 100,000) (χ2=7.26, P <.05) (Table 4). Allergic rash was the main rare adverse reaction for both vaccines, and few cases of epilepsy, febrile convulsion, and angioedema were reported. There were no serious reactions or deaths.
Table 4.
AEFI incidence of MPV-Aa and MCV-ACb vaccinated from 2009 to 2018
Common adverse reaction | Rare adverse reaction | Coincidental event | Total | ||||||
---|---|---|---|---|---|---|---|---|---|
Vaccine | No. vaccinated | No. of cases | Reporting rate (/100 000 doses) | No. of cases | Reporting rate (/100 000 doses) | No. of cases | Reporting rate (/100 000 doses) | No. of cases | Reporting rate (/100 000 doses) |
A | 1570518 | 775 | 49.35 | 45 | 2.87 | 18 | 1.15 | 838 | 53.36 |
A +C | 738815 | 402 | 54.41 | 38 | 5.14 | 19 | 2.57 | 459 | 62.13 |
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a: Group A meningococcal polysaccharide vaccine.
b: Group A and group C meningococcal polysaccharide conjugate vaccine.
4. Discussion
Our study showed that children in Hangzhou had a high coverage of MenV vaccination. The pattern of MenV use changed by year, and the MCV-AC only schedule was used more and more frequently for children in different areas and migrant status. Our findings demonstrate a positive safety profile of MenV with reasonable low incidences of AEFI of MPV-A and MCV-AC.
MenV has been continuously used for many years in Hangzhou. From 2008 to 2017, the coverage rates of first and second dose of MenV were all above 95%, and they were similar to the reported coverage rates of MenV in national immunization program (NIP) in China 2014 (99.39% and 99.23%).10MenV sequential schedule was not recommended, but a small number of children used MenV sequential schedule in our study. In Hangzhou, MCV-AC vaccine was not available in a small part of vaccination clinics. If children had two doses of MenV vaccines in different clinics, they may use a sequential schedule. With the high immunization level of MenV, the incidence of meningococcal meningitis decreased. From 2006 to 2017, the morbidity and mortality of meningococcal meningitis in Zhejiang province decreased gradually by year. Since 2010, less than 10 cases a year have been reported in Zhejiang,11 especially for Hangzhou. MenV effectively prevented the occurrence of meningococcal meningitis. No meningococcal meningitis exists in the place during the past few years. In our study, the percentage of children using MCV-AC-only schedule for primary immunization has increased year by year, which replaced the MPV-A-only schedule. This is consistent with a study in Guangxi, China that the alternative rate of MCV-AC for MPV-A vaccination increased from 2.71% in 2010 to 7.48% in 2016.12 The epidemic microflora of meningococcal meningitis in China has changed from group A to group C, and the epidemic microflora of meningococcal meningitis is diversified.13 Therefore, countries should consider to introduce groups B, C, Y, W, meningococcal polysaccharide conjugate vaccine, and other related vaccines into EPI and conduct further research to explore new prevention strategies. Since serogroup C meningitis was first confirmed in Guangxi, China in 2002, it has been detected in 27 provinces in China, and the detection rate of group C Nm is increasing year by year. In 2006, group C Nm accounted for 57% of the total microflora isolated from meningococcal meningitis cases and close contacts, and group C Nm has become the dominant endemic microflora. From 2008 to 2013, more than 46% of the cases of meningococcal meningitis cluster outbreak were caused by group C Nm.14 Among the laboratory-confirmed cases of meningococcal meningitis, about 48% were meningococcal meningitis in group C, and other Nm bacteria such as group B and W135 were also detected in some areas.6
MCV is especially suitable for the current situation in China.14–16 The Nm polysaccharides in MPV are t cell-independent (TI) antigens. The level of antibodies produced by MPV-A vaccination in infants under 2y old is low and the duration of antibody is short.14 The immune effect and the coverage of the bacteria cannot adapt to the current epidemic situation of cerebral meningitis. MPV-AC or groups A, C, Y, W135 MPV (MCV-ACYW135) could not reliably induce the generation of protective antibodies in infants and young infants.14 If MPV is given to young infants, it will also cause the immune tolerance to antigens when they are vaccinated again.14 But regardless of the debate over the MPV, the effectiveness and safety of the MCV have been recognized. MCV is a combination of Nm polysaccharides and protein carriers, whose antigens are converted into T cell-dependent (TD) antigens, thus inducing the body to produce high levels of antibodies. MCV can enhance the immune memory response to infants under 2y old and increase the immunogenicity and immune persistence of antibodies.14 Serological results showed that at 16months after receiving one dose of MCV, 88% of children aged 1 to 2 still had protective antibodies, and up to 96% of adolescents aged 15 to 17 had protective antibodies. Infants receiving three doses of MCV at 2-month intervals produced high levels of protective antibodies. Practical experience in the UK showed that MCV-C had a good overall performance.17 MPV-C previously inoculated will not affect the immune response of MCV, and MCV-C will not interfere with other vaccines in the immunization program.17 In recent years, foreign studies have shown that MCV-ACYW135 also has good protection and safety.18,19 Some experts suggest replacing MPV-A with MCV-AC in China, so as to further strengthen the protection of infants and reduce the incidence of meningococcal meningitis.20 It is also consistent with the views of Chinese experts.21
Our study showed that the coverage rate of children using MCV-AC-only schedule was higher in urban area than in other areas. This is consistent with a study in Shandong province, China that the coverage rate of MCV-AC in resident was higher (24.71%) than that in migrant (21.91%).22 Economic cost is an important barrier for the accessibility of self-pay vaccination in China. Parents with high income would like to pay for self-pay vaccine.23 Another study also showed that parents in urban area had more chance to know vaccine-related knowledge than in rural areas. The parents of urban are more willing to choose self-pay vaccine for children to prevent infectious diseases.24
The incidence of AEFI in MPV-A and MCV-AC in Hangzhou was lower than in previous studies.25 Despite the incidence of rare adverse reaction in MCV-AC was higher than in MPV-A, such cases were mainly allergic rashes, urticaria, etc., which did not cause more serious damage. MPV-A and MCV-AC are relatively safe for children.
This study also has some limitations. In China, the price of MCV is higher than that of MPV. Although research by the Chinese preventive medicine association has shown that vaccination with MCV is cost-effective in countries such as the United Kingdom, the United States and Canada,26 no relevant studies have been conducted in Hangzhou. When the incidence of meningococcal meningitis is low, a cost-benefit analysis is needed to include MCV-AC or MCV-ACYW135 in EPI. MenV has more varieties in China and sequential schedules are more complicated. The effect of sequential schedules on antibody production was not investigated in Hangzhou. The AEFI data used in this paper were passively monitoring data, which may not truly reflect the occurrence of AEFI of MPV-A and MPV-AC to some extent.
Conclusions and key recommendations: To sum up, we believe that MCV has the advantages of simultaneously preventing a variety of diseases, reducing the number of injections, simplifying immunization procedures, etc., and we suggest to update the current meningococcal meningitis immunization strategy in China. It is also suggested to use MCV for primary immunization in children before 2y old and MPV for enhanced immunization in children after 3y old, which can save money and solve the problem of insufficient production.
Acknowledgments
We thank the staffs at the county level Centers for Disease Control and Prevention and in vaccination clinics in Hangzhou, for their vaccination service.
Funding Statement
Our study was funded by the Hangzhou Science and Technology Development Guide Plan [grant number: 20171226Y25].
Disclosure of potential conflict of interest
The authors declare no conflicts of interest.
Authors’ contributions
Conceived and designed the study: Yan Liu, Xinren Che, Yuyang Xu. Obtained and organized the data: Jun Wang, Xinren Che, Wenwen Gu. Analyzed the data: Yan Liu, Wei Jiang. Contributed reagents/materials/analysis tools: Jian Du, Xiaoping Zhang, Xuechao Zhang. Wrote the manuscript: Xinren Che, Yan Liu.
Ethical considerations
This study was determined to be exempt from ethical review by the Hangzhou CDC institutional review board. Data were de-identified when extracted from HZIIS and were not linked to individual identifiers.
References
- 1.Ramakrishnan M, Ulland AJ, Steinhardt LC, Moïsi JC, Were F, Levine OS.. Sequelae due to bacterial meningitis among African children: a systematic literature review. BMC Med. 2009;7(1):47. doi: 10.1186/1741-7015-7-47. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Cohn AC, MacNeil JR, Clark TA, Ortega-Sanchez IR, Briere EZ, Meer HC, Baker CJ, Messonnier NE. Centers for Disease Control and Prevention (CDC): prevention and control of meningococcal disease: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2013;62:1–28. [PubMed] [Google Scholar]
- 3.Jafri RZ, Ali A, Messonnier NE, Tevi-Benissan C, Durrheim D, Eskola J, Fermon F, Klugman KP, Ramsay M, Sow S. Global epidemiology of invasive meningococcal disease[J]. Popul Health Metr. 2013;11(1):17. doi: 10.1186/1478-7954-11-17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Stephens DS. Biology and pathogenesis of the evolutionarily successful, obligate human bacterium Neisseria meningitidis. Vaccine. 2009;27(Suppl. 2):B71–77. doi: 10.1016/j.vaccine.2009.04.070. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Vyse A, Wolter JM, Chen J, NG T, SORIANO-GABARRO M. Meningococcal disease in Asia: an under-recognized public health burden. Epidemiol Infect. 2011;139(7):967⁃985. doi: 10.1017/S0950268811000574. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Shao Z. Epidemiology and switching of meningococcal disease in China[J]. Chin J Prev Med. 2013;47:891–93. [PubMed] [Google Scholar]
- 7.Experts′ consensus on immunization with meningococcal vaccines in China[J]. Chin J Prev Med. 2019;53(2):141–45. [DOI] [PubMed] [Google Scholar]
- 8.Liu WT, Li JH, Ning GJ, Wu D, Yin ZD, Li YX. Epidemiological characteristics of Meningococcal Meningitis in China, 2012-2014[J]. Chin J Vaccine Immun. 2016;2:149⁃152,179. [Google Scholar]
- 9.Plotkin SA, Orenstein WA, Offit PA. Vaccines [M]. 7th ed. Philadelphia(PA): Elsevier; 2018. p. 622. [Google Scholar]
- 10.Cui J, Cao L, Zheng JS, Cao LS, Yuan P, Wang M, Xiao QY, Wang HQ. Analysis of reported coverage rates of vaccines in national immunization program in china,2014[J]. Chin J Vaccine Immun. 2016;22(1):34–40. [Google Scholar]
- 11.Deng X, Yao PP, He HQ, Yan R, Tang XW, Zhou Y, Fu J, Xie SY. Epidemiological characteristics of meningococcal meningitis and changing trend of serogroups of Neisseria meningitidis in Zhejiang,2006-2017[J]. Disease Surveillance. 2018;33(7):547–51. [Google Scholar]
- 12.Yang RC, Zhong G, Gan M, Li S, Du JF, Huang Y, Chen SY, Dong AH. Analysis of category vaccine application status in Guangxi Zhuang autonomous region,2010 to 2016[J]. Chin Primary Health Care. 2018;32(7):34–35,38. [Google Scholar]
- 13.Li JH, Li YX, Wu D, Ning GJ, Shao ZJ, Yin Zd. Epidemiological characteristics of meningococcal meningitis and switching trend of serogroups of neisseria meningitidis in China,2006-2014[J]. Chin J Vaccine Immun. 2015;21(5):481–85. [Google Scholar]
- 14.Wen HR, Liao Z, Zhang YX, Peng SH, Xu B. Discussion on immune strategy of meningococcal vaccines[j]. Occup and Health. 2016;32(19):2729–32. [Google Scholar]
- 15.Qin CZ, Wang HJ, Tao H, Ma FB, Ze WY. Study on immunogenicity between different doses of group A/C meningococcal polysaccharide conjugate vaccine[j]. Chin J Vaccine Immun. 2010;5:462–65. [Google Scholar]
- 16.Pan JR, Chen HH, Li SJ, Luo SY, He HQ, Chen EF. Immunogenicity of group a and group c meningococcal conjugate vaccine after primary immunization in children aged 6 months[J]. Chin J Vaccine Immun. 2015;5:511–14. [Google Scholar]
- 17.Southern J, Crowley-Luke A, Borrow R. Immunogenicity of one, two or three doses of a meningococcal C conjugate vaccine conjugated to tetanus toxoid, given as a three-dose primary vaccination course in UK infants at 2,3 and 4months of age with acellular pertussis-containing DTP/Hib vaccine[J]. Vaccine. 2006;24(2):215–19. doi: 10.1016/j.vaccine.2005.07.060. [DOI] [PubMed] [Google Scholar]
- 18.Javadekar B, Ghosh A, Kompithra RZ, Awasthi S, Perminova O, Romanenko V, Rodnikova V, Kharit S, Thollot Y, Bosch-Castells V, et al. Safety and immunogenicity of two doses of a quadrivalent meningococcal polysaccharide diphtheria toxoid conjugate vaccine in Indian and Russian children aged 9 to 17 months[J]. Indian Pediatr. 2018;55(12):1050–55. doi: 10.1007/s13312-018-1440-z. [DOI] [PubMed] [Google Scholar]
- 19.Hansen J, Zhang L, Eaton A, Baxter R, Robertson CA, Decker MD, Greenberg DP, Bassily E, Klein NP. Post-licensure safety surveillance study of routine use of quadrivalent meningococcal diphtheria toxoid conjugate vaccine (MenACWY-D) in infants and children. Vaccine. 2018;36(16):2133–38. doi: 10.1016/j.vaccine.2018.02.107. [DOI] [PubMed] [Google Scholar]
- 20.Ning X, Li JH, Li YX, Yin ZD, Ze WY, Wang XX, Wang HQ, Li L. Feasibility of meningococcal polysaccharide vaccines integrated into Chinese NIP and the foundation of immunization schedule[J]. Chin J Vaccine Immun. 2008;14(2):171–75. [Google Scholar]
- 21.Chai ZK, Li J, Shao ZJ, Li FX, Diao LD, Li L, Yin JD. Minutes of the meningococcal meningitis surveillance and immunization prevention seminar[J]. Modern Prev Med. 2015;16(12):901–03. [Google Scholar]
- 22.Zhang WY, Zhang YJ, Liu SN, Zeng Z, Xu Q, Li Z, Xiao ZK, Song LZ. Analysis of the current status of category vaccination among children aged 1-5 in Shangdong province[J]. Modern Prev Med. 2016;43(10):1886–89. [Google Scholar]
- 23.Chang J, Hou ZY, Yue DH, Wu Q, Fang H, Meng QY. Factors related to self-paid vaccination and its related factors among children aged 0-3years in China[J]. Chin J Public Health. 2014;30(5):579–82. [Google Scholar]
- 24.Qingchun L. Investigation of cognitive status of residents in varicella vaccine in Linqing[J]. Henan J Prev Med. 2016;7:524–525,528. [Google Scholar]
- 25.Che XR, Xu EP, Pan JR, Liu Y, Xi Y, Peng J, Zhu JH, Fang T, Qian CY. Observation on the adverse effects following immunization of group A meningococcal polysaccharide vaccine and group A and group C meningococcal conjugate vaccine[J]. Zhejiang Prev Med. 2013;25(11):51–53. [Google Scholar]
- 26.Chinese preventive medicine association . Efficacy, safety, and cost-effectiveness of meningococcal vaccines[J]. Chin J Vaccine Immun. 2019;25(1):102–108,114. [DOI] [PubMed] [Google Scholar]