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position paper

Indian Pediatr 2014;51: 719-722

IAP Perspectives on Measles and Rubella Elimination Strategies

Vipin M Vashishtha, Vijay N Yewale, CP Bansal and Pravin J Mehta

For the Indian Academy of Pediatrics, Advisory Committee on Vaccines and Immunization Practices (ACVIP)

Correspondence to: Dr Vipin M Vashishtha, Convener, IAP Advisory Committee on Vaccines & Immunization Practices, Mangla Hospital and Research Center, Shakti Chowk, Bijnor, Uttar Pradesh, 246 701, India.
Email: [email protected]
 


The Academy’s Expert group on Immunization has discussed various issues pertaining to rubella vaccine introduction in to the Universal Immunization Program. Though the move to introduce rubella vaccine in to the UIP is laudable, the decision to overlook mumps seems inexplicable and illogical. Logistics also support the use of measles-mump and rubella (MMR) vaccine instead of measles-rubella (MR) vaccine. Regarding the timing of administration of MMR/MR vaccine, the academy recommends that the vaccine should be given early to have much higher coverage than introducing it late at the time of 1st booster of DPT. According to available evidence, both these vaccines (MMR/MR) can be given safely at different ages including at 9 months of age. The second dose should also be of the same antigen (MMR/MR) and be given along with 1st DPT booster at 16-24 months of age.

Keywords: Measles mumps rubella vaccine, Prevention, Universal immunization program.


T
he Academy reviewed the recently circulated ICMR Expert Group Recommendations on Rubella vaccine [1] which includes: (i) Introduction of rubella vaccine as Measles-Rubella (MR) vaccine at the time of first DPT booster at 16-24 months of age in States having achieved more than 80% coverage of first dose of measles vaccine; (ii) a onetime catch up campaign of adolescent girls with rubella vaccine to offset potential increase in susceptible women in reproductive age group if children alone are vaccinated; and (iii) sentinel surveillance for congenital rubella syndrome (CRS) should be included in Measles-Rubella surveillance program [1].

The Indian Academy of Pediatrics Advisory Committee on Vaccines and Immunization Practices discussed various issues pertaining to rubella vaccine introduction in National Immunization Program (NIP). Key points that emerged after deliberations are discussed in this communication.

Objective of the Initiative

Indian Academy of Pediatrics – based on their members’ clinical experience and inputs – strongly supports elimination of not only measles and rubella, but also of mumps. The Academy believes that it is unethical to employ stand-alone measles vaccine today, when effective MR and MMR vaccines are available at an affordable price.

The Academy welcomes the Government of India, (GoI) decision of taking on at least two key infectious diseases, measles and rubella, simultaneously; though it would have been ideal had mumps also been included in this initiative. The Academy also agrees with the GoI that the major concern is not rubella disease in childhood, but Congenital rubella syndrome (CRS) in infants born to mothers who catch rubella during pregnancy. Though cost and other logistics issues, and global focus may be hindrance to take on three instead of two significant illnesses right now, the ultimate need of the country is to target for elimination/control of all the three diseases instead of the two. Already the program managers have missed the opportunity of using at least a combined MR vaccine in previous special immunization activities conducted earlier in many states.

The Disease Burden and the Country’s Need

The Academy believes that the burden of CRS and mumps is significant. Though exact community burden of CRS is lacking, a systematic review documented 17% susceptibility rate among pregnant women [2].

The burden of mumps is less specified and only sporadic outbreaks are reported [3-8]. However, based on the inputs and acceptance of mumps vaccination by our members, and the available data captured through the academy’s own IDSurv portal [9], the Academy is confident that mumps also poses a significant burden. Hence, both CRS and mumps are eligible as targets for elimination and control. At the same time, the Academy urges the GoI/ICMR to take initiatives to strengthen ongoing rubella surveillance, initiate efforts to measure community burden of CRS, and invest in starting mumps surveillance all over the country.

Why Is Mumps Important?

The Academy considers mumps to be as significant in terms of morbidity as rubella. complications of mumps are many, and can be profound – aseptic meningitis, encephalitis, orchitis, oophoritis, pancreatitis, deafness, transverse myelitis, facial palsy, ascending polyradi-culitis and cerebellar ataxia. Like rubella, mumps in pregnancy can also give rise to fetal damage in the form of aqueductal stenosis leading to congenital hydrocephalus [10]. Incidence of serious complications has become more common in recent years [11]. Four Union Territories (Delhi, Goa, Pudduchury and Sikkim) are already using MMR in their UIP program. The coverage of MMR vaccine has been reported as 42%, 30% and 5% from Delhi, Chandigarh and Goa, respectively [12]. Kerala has become the latest entrant to start universal MMR vaccination in the state from 2014. By 2012, 132 of 194 WHO member states have introduced Rubella containing vaccine (RCV) in their National immunization programs, either as MR or MMR. Of these, 117 have RCV included in both routinely administered doses of measles-containing vaccine [13]. Logistics also support the use of MMR vaccine instead of MR because with the same effort, money and manpower, three common infectious diseases could be eliminated simultaneously – instead of two. Availability of an indigenous producer and supplier should also bolster our efforts to launch large scale vaccination drives against these diseases. While single dose of rubella/rubella containing vaccines is sufficient to provide almost 100% protection against the disease, two or more doses of measles and mumps vaccines are needed to accord adequate protection [14].

Timing of The First Dose of Rubella Containing Vaccine

The Academy supports that at least 80% coverage must be achieved to offset any presumed epidemiological shift of rubella (and mumps), and consequently higher incidence of congenital complications. Regarding the timing of administration of MMR/MR vaccine, the Academy believes the vaccine should be given early to have much higher coverage than introducing it late at the time of first booster of DTP. This is to be noted that the measles vaccine coverage at 9 months is 74.1% and the coverage of DPT booster at 18 months is 41.4% only – according to UNICEF’s Coverage Evaluation Survey of 2009. According to available evidence, both MMR and MR vaccines can be given safely at 9 months of age (Table I) [15-21]. Most important thing is to achieve minimum 80% coverage of childhood vaccination which will not allow virus to circulate freely and infect women of child bearing age thus avoiding any inadvertent epidemiological shift. Hence, it is of paramount importance to provide first dose of the vaccine (MMR/MR) at 9 month of age in place of measles vaccine to attain high coverage. The second dose should also be of the same antigens, (MMR or MR) and be given along with first DPT booster at 16-24 months of age. These recommendations also confirm to the SAGE guidelines [13] which include (i) for countries introducing or using rubella vaccine, it is strongly recommended that this be given in combination with the first dose of measles containing vaccine (MCV) (as MR or MMR); (ii) in countries using RCV and a two-dose schedule of MCV, both doses should be of the same formulation [13].

TABLE I

Summary of Studies Evaluating Seroconversion After Measles, Mumps and Rubella Vaccines Administered at Different Ages 
Place, Year Ages/age groups (mo)  Seroconversions at different age groups
Measles Mumps Rubella
South Africa, 1990 [15] 9, 15 Better at 9 mo
groups groups
Similar in both Similar in both
Italy, 1993 [16] 10-12,15-24 Similar, but lower Similar, but lower Similar,  
GMTs  at 9-12 mo GMTs at 9-12 mo  
Vellore,  1994  [17] 9, 12, 15 Lower at 9 mo (80%) Lower at 9 mo (75%) Similar (92%) at all
than at 12 & 15 mo
(95%)
than at 12 & 15 mo
(92%)
the three age groups
Brazil, 1997  [18] 9,15 Similar in both groups Similar in both
groups
GMTs higher in
15 mo age group
Germany, 2000  [19] 9-11, 12-14 or 15-17 Lower seroconversion
in 1 & 3 groups only
(84.8%, 100%)
Similar in all the
groups
Similar in all the groups
New Delhi, 2003  [20] 9-10,15-18 Similar  (92%) in
each group)
Similar
(100% vs. 96%)
Similar (98% vs. 94%)
Singapore, 2007 [21] 9,12 Similar (>92%) 
in each group)
Similar Similar 
GMT: Geometric mean titers; *Seroconversion of varicella along with measles, mumps and rubella was also studied.

Operational Issues

The Academy believes that though minimum is 80%, we must aim at achieving a very high coverage (>95%) with MMR/MR vaccine in the NIP. The target age should be based on our ultimate objective, "Control" vs. "Elimination". At the time of introduction of vaccine, one time campaign to vaccinate adolescent girls with rubella vaccine is a proven strategy, but we need to explore all avenues to cover the whole susceptible pediatric population. There is a need to have large special immunization activities to cover young children, school children (at entry) and adolescents. No doubt, this will pose unprecedented burden on health infrastructure and machinery, but we must remain positive and avoid speculating about the low quality/low coverage. Our past experience with measles catch-up campaigns has shown that it is possible to achieve very high coverage of more than 80% in states.

For control, the target age groups should be from 9 months to 15 years (following introduction in NIP). Further decision to expand shall be guided by the epidemiology of the disease (age distribution, seropre-valence data, age-specific fertility rates, susceptibility data of women of child bearing age, and maternal age distribution of CRS. For elimination, we must target all the above age groups along with expansion of target age of coverage beyond 15 years. They should include special immunization activities targeting adults (up to 40 yrs of age). Further age groups for inclusion in target age for these activities will depend on sero-epidemiology data. Here, both the sexes, must be included for vaccination.

Regarding coverage of adolescent girls and children in other age groups who are not covered with these antigens, school-based vaccination programs, could also be a good modality. Many adolescent girls’ oriented activities are now being introduced through ICDS, including iron folic acid and nutrition programs. MR/MMR vaccine can also be introduced through that system.

In conclusion, the Academy thinks that reaching all children with measles vaccine gives us an opportunity to also reach them with rubella and mumps, in a combined vaccine. Congenital rubella syndrome can be prevented, and the Academy fully supports efforts to prevent infant and childhood disability and the associated health, social and economic costs. By preventing measles, rubella and mumps together we produce significant savings for our country and communities.

Funding: None; Competing interests: None stated.

References

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8. Vaidya SR, Chowdhury DT, Kumbhar NS, Tomar R, Kamble MB, Kazi MI. Circulation of two mumps virus genotypes in an unimmunized population in India. J Med Virol. 2013;85:1426-32.

9. IDsurv. Infectious Disease Surveillance Project. Available from: www.idsurv.org

10. WHO Position Paper, Mumps Virus Vaccines. Wkly Epidemiol Rec. 2007;82:49-60.

11. Wang W, Zhu Y, Wu H, Jiao Y, Van Halm-Lutterodt N, Li W. IL-6 and IFNa are elevated in severe mumps cases: A study of 960 mumps patients in China. J Infect Dev Ctries. 2014;8:208-14.

12. Background material for NTAGI Standing Technical Sub-Committee (STSC) Meeting on "Potential Strategies for the Control of Rubella and CRS Burden in India." February 26, 2014; Indian Council of Medical Research, New Delhi.

13. Status Report on Progress towards Measles and Rubella Elimination. SAGE Working Group on Measles and Rubella (17 October 2013) Available from: http://www. who.int/immunization/sage/meetings/2013/november/Status_Report_Measles_Rubella21Oct2013_FINAL.pdf Accessed on May 19, 2014.

14. Measles, Mumps and Rubella Vaccines. In: Vashishtha VM, Choudhury P, Bansal CP, Yewale VN, Agarwal R. editors. IAP Guidebook on Immunization 2013-2014. National Publication House, Indian Academy of Pediatrics, Gwalior, 2014.

15. Schoub BD, Johnson S, McAnerney JM, Wagstaff LA, Matsie W, Reinach SG, et al . Measles, mumps, and rubella immunization at nine months in a developing country. Pediatr Infect Dis J. 1990; 9:263-7.

16. Giammanco G1, Li Volti S, Salemi I, Giammanco Bilancia G, Mauro L. Immune response to simultaneous administration of a combined measles, mumps and rubella vaccine with booster doses of diphtheria-tetanus and poliovirus vaccine. Eur J Epidemiol. 1993; 9:199-202.

17. Singh R, John TJ, Cherian T, Raghupathy P. Immune response to measles, mumps and rubella vaccine at 9, 12 and 15 months of age. Indian J Med Res.1994; 100:155-9.

18. Forleo-Neto E, Carvalho ES, Fuentes IC, Precivale MS, Forleo LH, Farhat CK. Seroconversion of a trivalent measles, mumps, and rubella vaccine in children aged 9, 12 and 15 months. Vaccine. 1997;15:1898-901.

19. Klinge J1, Lugauer S, Korn K, Heininger U, Stehr K. Comparison of immunogenicity and reactogenicity of a measles, mumps and rubella (MMR) vaccine in German children vaccinated at 9-11, 12-14 or 15-17 months of age. Vaccine. 2000;18:3134-40.

20. Yadav S, Thukral R, Chakarvarti A. Comparative evaluation of measles, mumps & rubella vaccine at 9 & 15 months of age. Indian J Med Res. 2003;118:183-6.

21. Goh P, Lim FS, Han HH, Willems P. Safety and immunogenicity of early vaccination with two doses of tetravalent measles-mumps-rubella (MMRV) vaccine in healthy children from 9 months of age. Infection 2007;35:326-33.

 

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