Literature DB >> 2685909

Measles active and passive immunity in a worldwide perspective.

F L Black.   

Abstract

'The simplest of all virus disease is measles' said Kenneth Maxy 40 years ago in a chapter on epidemiology. I hope that the data set out here provide the reader with a sufficiently complete and clear picture of the factors that determine measles epidemiology, that he or she will agree with Maxy's prescient words. Measles is an antigenically complex virus, but few components of the immune response to this virus are epidemiologically relevant. The relevant components are durable for a lifetime. They can be conveniently measured by serological tests, and the results of these tests correlate well with measles immunity. The tests show that measles is an extremely infectious disease, and that very high antibody prevalence rates are needed for herd protection. The currently available measles vaccine is capable of yielding adequate antibody prevalence rates for herd immunity, but to achieve this, immunization procedural flaws and faulty records must be kept to very low levels. The greatest obstacle to worldwide control of measles is a failure of vaccination programs to produce adequate herd immunity levels in less-developed countries. There, vaccine must be given promptly after passive immunity wanes, because the level of endemicity is so high. It is difficult to determine just what age is optimal, because it varies from one country to another. Premature vaccination not only fails to immunize, but also interferes with subsequent re-immunization. Because we now know this, further direct tests of vaccine effectiveness in very young children are ethically undesirable, and methods that use determination of passively acquired antibody are to be preferred. The levels of antibody that mothers have to pass to their children vary considerably. These differences are important in comparisons of South Asian countries with others, but not elsewhere. Differences in efficiency of transport of antibody across the placenta also play a role, but usually a minor one. Most important seems to be variation in antibody durability in the infant. Where families are poor, the children acquire many infections at an early age, and passively acquired antibody is swept out. These children who are least able to withstand the effects of measles infection, are hit at the earliest age. To provide protection for them, the vaccine must be given at a carefully determined age, specific for each community. Only when this is done can we hope to reduce measles worldwide to a sufficiently low level that it will be removed as a threat to persons in the United States, or anywhere else.

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Year:  1989        PMID: 2685909

Source DB:  PubMed          Journal:  Prog Med Virol        ISSN: 0079-645X


  11 in total

1.  Molecular detection of measles virus from children during a sporadic outbreak in two semi-urban areas in Nigeria.

Authors:  B A Olusola; J A Adeniji
Journal:  Afr J Infect Dis       Date:  2014

2.  Immunosorbent assay based on recombinant hemagglutinin protein produced in a high-efficiency mammalian expression system for surveillance of measles immunity.

Authors:  F Bouche; W Ammerlaan; F Berthet; S Houard; F Schneider; C P Muller
Journal:  J Clin Microbiol       Date:  1998-03       Impact factor: 5.948

3.  Facebook and Twitter vaccine sentiment in response to measles outbreaks.

Authors:  Michael S Deiner; Cherie Fathy; Jessica Kim; Katherine Niemeyer; David Ramirez; Sarah F Ackley; Fengchen Liu; Thomas M Lietman; Travis C Porco
Journal:  Health Informatics J       Date:  2017-11-17       Impact factor: 2.681

4.  Measles vaccine efficacy during an outbreak in a highly vaccinated population: incremental increase in protection with age at vaccination up to 18 months.

Authors:  G De Serres; N Boulianne; F Meyer; B J Ward
Journal:  Epidemiol Infect       Date:  1995-10       Impact factor: 2.451

5.  Immunity to measles in young adults in Israel.

Authors:  Y Lerman; S Riskin-Mashiach; D Cohen; R Slepon; T Shohat; H Harari; M Wiener; Y L Danon
Journal:  Infection       Date:  1993 May-Jun       Impact factor: 3.553

6.  Performance and reliability of the Enzygnost measles enzyme-linked immuno-sorbent assay for detection of measles virus-specific immunoglobulin M antibody during a large measles epidemic.

Authors:  G Ozanne; M A d'Halewyn
Journal:  J Clin Microbiol       Date:  1992-03       Impact factor: 5.948

7.  A chimeric alphavirus replicon particle vaccine expressing the hemagglutinin and fusion proteins protects juvenile and infant rhesus macaques from measles.

Authors:  Chien-Hsiung Pan; Catherine E Greer; Debra Hauer; Harold S Legg; Eun-Young Lee; M Jeff Bergen; Brandyn Lau; Robert J Adams; John M Polo; Diane E Griffin
Journal:  J Virol       Date:  2010-02-03       Impact factor: 5.103

8.  Dose-dependent protection against or exacerbation of disease by a polylactide glycolide microparticle-adsorbed, alphavirus-based measles virus DNA vaccine in rhesus macaques.

Authors:  Chien-Hsiung Pan; Nitya Nair; Robert J Adams; M Christine Zink; Eun-Young Lee; Fernando P Polack; Manmohan Singh; Derek T O'Hagan; Diane E Griffin
Journal:  Clin Vaccine Immunol       Date:  2008-02-20

9.  Use of Vaxfectin adjuvant with DNA vaccine encoding the measles virus hemagglutinin and fusion proteins protects juvenile and infant rhesus macaques against measles virus.

Authors:  Chien-Hsiung Pan; Gretchen S Jimenez; Nitya Nair; Qun Wei; Robert J Adams; Fernando P Polack; Alain Rolland; Adrián Vilalta; Diane E Griffin
Journal:  Clin Vaccine Immunol       Date:  2008-06-04

10.  Age-appropriate vaccination against measles and DPT-3 in India - closing the gaps.

Authors:  Niyi Awofeso; Anu Rammohan; Kazi Iqbal
Journal:  BMC Public Health       Date:  2013-04-17       Impact factor: 3.295

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