학술논문

Effectiveness and Duration of Protection of One Dose of a Meningococcal Conjugate Vaccine
Document Type
article
Source
Pediatrics. 139(2)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Pediatric
Immunization
Vaccine Related
Prevention
Rare Diseases
Biotechnology
Prevention of disease and conditions
and promotion of well-being
3.4 Vaccines
Good Health and Well Being
Adolescent
Antibodies
Bacterial
Carrier State
Case-Control Studies
Child
Female
Follow-Up Studies
Humans
Immunization
Secondary
Male
Meningococcal Infections
Meningococcal Vaccines
Population Surveillance
Treatment Outcome
United States
Young Adult
Active Bacterial Core Surveillance (ABCs) Team and MeningNet Surveillance Partners
Medical and Health Sciences
Psychology and Cognitive Sciences
Pediatrics
Biomedical and clinical sciences
Health sciences
Psychology
Language
Abstract
Meningococcal conjugate vaccines were licensed beginning in 2005 on the basis of serologic end points and recommended for use in adolescents. A single dose at age 11 to 12 years was expected to provide protection through late adolescence. We conducted a case-control evaluation of vaccine effectiveness (VE) and duration of protection of a meningococcal (groups A, C, W, and Y) polysaccharide diphtheria toxoid conjugate vaccine (MenACWY-D). Cases of culture- or polymerase chain reaction-confirmed serogroup A, C, W, and Y meningococcal disease among adolescents were identified through meningococcal disease surveillance sites in the United States from January 1, 2006, through August 31, 2013. Attempts were made to enroll 4 friend and school controls per case. VE was calculated using the generalized estimating equation, controlling for underlying medical conditions and smoking. Serogroup C accounted for 88 (49%), serogroup Y 80 (44%), and serogroup W 13 (7%) of enrolled cases. Thirty-six (20%) cases and 87 (44%) controls received MenACWY-D. The overall VE estimate 0 to 8 years postvaccination was 69% (51% to 80%); VE was 79% (49% to 91%) at