Evidence map›Paper›PMID 33765968›Full record

ArticleBMC infectious diseases2021

Measles and rubella serosusceptibity among population vaccinated with different schedules: the potential impact on measles-rubella elimination in Iran.

Hana Saffar, Maryam Khalifeloo, Mohammad-Jafar Saffar, Alireza Abdollahi, Mohammad-Reza Parsaei, Gholam-Reza Ghorbani, Samaneh Salarvand, Mohsen Aarabi

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In one paragraph

Article in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Hana SaffarDepartment of Pathology, School of medicine, IKHC, Teheran University of Medical Sciences, Tehran, Iran. hana_saffar283@yahoo.com.
Maryam KhalifelooDepartment of Pathology, School of medicine, IKHC, Teheran University of Medical Sciences, Tehran, Iran.
Mohammad-Jafar SaffarPediatric Infectious Diseases Research Center, communicable Diseases Institute, and Department of Pediatric Infectious Diseases, Bu-Ali Sina Hospital, Mazandaran University of Medical Sciences, Pasdaran Bolv, Sari, Iran.ORCID http://orcid.org/0000-0002-9335-6262
Alireza AbdollahiDepartment of Pathology, School of medicine, IKHC, Teheran University of Medical Sciences, Tehran, Iran.
Mohammad-Reza ParsaeiDeputy of Health, Mazandaran University of Medical Sciences, Sari, Iran.
Gholam-Reza GhorbaniDeputy of Health, Mazandaran University of Medical Sciences, Sari, Iran.
Samaneh SalarvandDepartment of Pathology, School of medicine, IKHC, Teheran University of Medical Sciences, Tehran, Iran.
Mohsen AarabiDeputy of Health, Mazandaran University of Medical Sciences, Sari, Iran.
Mazandaran University of Medical Sciences · IRIran University of Medical Sciences · IRSina Hospital · IR

Funding

Mazandaran University of Medical Sciences IR.MAZUMS. Rec.1396.3074Tehran University of Medical Sciences IR.TUMS.IKHC.Rec.1399.075
6 · The paper itself

Abstract

backgroundIranian children were vaccinated with the scheduled two doses of monovalent measles vaccine (mMV) from 1984. In December 2003, a nationwide campaign of measles-rubella (MR) immunization was established to vaccinate 5-25 year- old individuals. In 2004, the mMV was replaced with measles- mumps- rubella (MMR) vaccine. Despite the high vaccination coverage, the outbreaks of measles still occur in the country. In this Study, the MR immunity status of various age groups, vaccinated with different schedules was investigated, and the immunologic response of seronegative subjects to revaccination was examined.

methodsThis cross-sectional study was conducted among 7-33-year-old healthy individuals with a documented history of measles vaccination from November 2017 to June 2018. The subjects were categorized as follows: group A, including 20-33 year-old individuals; vaccinated with 1-2 doses of mMV at ages 9 and 15 months, and revaccinated with MR, group B, including 15-19-year-old individuals, vaccinated with two doses of mMV at 9 and 15 months of age, and received additional dose of MMR upon school entrance, group C, including 11-14 year-old individuals, vaccinated with two-doses of MMR at the ages of 15 months and 6 years, and group D, including 7-10 year-old individuals vaccinated with two-doses of MMR vaccine at the ages 12 and 18 months, respectively. Levels of antimeasles- antirubella IgG antibodies in the collected sera were measured. Also antimeasles- antirubella IgM and IgG of seronegative individuals were reexamined at 4-6 weeks after MMR revaccination. The collected data were analyzed using descriptive statistical methods.

resultsA total of 635 individuals were investigated in this study. Group A, 98; group B, 295; group C, 139; and group D, 103 persons. Overall, 12.3 and 18.4% of the population were seronegative for measles and rubella antibodies. This rate varied greatly between the 4 groups: group A, 0/0-2%; group B,15.2-25.0%; group C,11.5-17.2%; and groupD,14.6-18.4%. After revaccination, 92 and 94.9% of seronegative individuals showed IgG response to measles and rubella vaccines, respectively.

conclusionDespite the high coverage rate of M-R containing vaccines, a significant number of vaccinated subjects were seronegative for measles and rubella, possibly because of secondary vaccine failure; this may negatively affect measles-rubella elimination targets in the country. If these findings are confirmed in similar future studies, a more robust regional/national supplementary immunization activity will be considered.

Indexed as

AdolescentAdultAntibodies, ViralChildChild, PreschoolCross-Sectional StudiesFemaleHumansImmunization ScheduleImmunization, SecondaryImmunoglobulin GIranMaleMeaslesMeasles-Mumps-Rubella VaccineRubellaAntibodies, ViralImmunoglobulin GMeasles-Mumps-Rubella VaccineCongenial rubella syndrome. IranMeaslesMeasles eliminationMMRRubella

Identifiers

PMID33765968
PMCPMC7995582
OpenAlexW3120789982

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.