Age-dependent differences in IgG isotype and avidity induced by measles vaccine received during the first year of life

被引:55
作者
Nair, Nitya
Gans, Hayley
Lew-Yasukawa, Linda
Long-Wagar, Andrea C.
Arvin, Ann
Griffin, Diane E.
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, W Harry Feinstone Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] Stanford Univ, Med Ctr, Sch Med, Dept Pediat, Stanford, CA 94305 USA
关键词
D O I
10.1086/522519
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Measles remains an important cause of death worldwide, and vaccinating individuals at an earlier age could lead to better control of the disease. However, persistence of maternal antibody and young age affect the quantity of vaccine-induced neutralizing antibody and may also affect antibody quality. Methods. Enzyme immunoassay was used to analyze measles virus-specific IgG levels, avidity maturation, and isotype changes, using serum samples from infants who received measles vaccine at 6 months of age and measles-mumps-rubella (MMR)-II at 12 months of age (n = 26), measles vaccine at 9 months of age and measles-mumps-rubella (MMR)-II at 12 months of age (n = 48), or only MMR-II at 12 months of age (n = 27). Results. The median IgG level was lower among infants with maternal antibody than among those without maternal antibody. Compared with median avidity indices for infants aged 12 months, median values were lower for 6-month-old infants with maternal antibody (P = .0001), 6-month-old infants without maternal antibody (P = .001), 9-month-old infants with maternal antibody (P = .03), and 9-month-old infants without maternal antibody (P = .006). The median IgG3 level was highest at 6 months of age. IgG1 was predominant at 12 months. Low avidity responses at 6 or 9 months of age did not hinder higher avidity responses or the switch to IgG1 after secondary vaccination. The 2-dose regimen did not augment the response, compared with the response in infants who received 1 dose at 12 months of age. Conclusions. Avidity and isotype maturation of measles vaccine-induced antibody are affected by age, providing insight into the ontogeny of the immune response to measles vaccine.
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页码:1339 / 1345
页数:7
相关论文
共 36 条
[1]   The sequence of vaccinations and increased female mortality after high-titre measles vaccine: Trials from rural Sudan and Kinshasa [J].
Aaby, P ;
Ibrahim, SA ;
Libman, MD ;
Jensen, H .
VACCINE, 2006, 24 (15) :2764-2771
[2]   Differences in female-male mortality after high-titre measles vaccine and association with subsequent vaccination with diphtheria-tetanus-pertussis and inactivated poliovirus: reanalysis of West African studies [J].
Aaby, P ;
Jensen, H ;
Samb, B ;
Cisse, B ;
Sodemann, M ;
Jakobsen, M ;
Poulsen, A ;
Rodrigues, A ;
Lisse, IM ;
Simondon, F ;
Whittle, H .
LANCET, 2003, 361 (9376) :2183-2188
[3]   Neutralizing B cell response in measles [J].
Bouche, FB ;
Ertl, OT ;
Muller, CP .
VIRAL IMMUNOLOGY, 2002, 15 (03) :451-471
[4]  
CHARGELEGUE D, 1995, CLIN EXP IMMUNOL, V99, P175, DOI 10.1111/j.1365-2249.1995.tb05529.x
[5]   IMMUNOGENICITY OF HIGH-TITER AIK-C OR EDMONSTON-ZAGREB VACCINES IN 3.5-MONTH-OLD INFANTS, AND OF MEDIUM-TITER OR HIGH-TITER EDMONSTON-ZAGREB VACCINE IN 6-MONTH-OLD INFANTS, IN KINSHASA, ZAIRE [J].
CUTTS, FT ;
NYANDU, B ;
MARKOWITZ, LE ;
FORSEY, T ;
ZELL, ER ;
OTHEPA, O ;
WILKINS, K .
VACCINE, 1994, 12 (14) :1311-1316
[6]   Measles elimination:: progress and challenges [J].
Cutts, FT ;
Henao-Restrepo, AM ;
Olivé, JM .
VACCINE, 1999, 17 :S47-S52
[7]  
deSouza VAUF, 1997, J MED VIROL, V52, P275
[8]  
DEVEY ME, 1984, IMMUNOLOGY, V52, P377
[9]   Measles virus protein-specific IgM, IgA, and IgG subclass responses during the acute and convalescent phase of infection [J].
El Mubarak, HS ;
Ibrahim, SA ;
Vos, HW ;
Mukhtar, MM ;
Mustafa, OA ;
Wild, TF ;
Osterhaus, ADME ;
de Swart, RL .
JOURNAL OF MEDICAL VIROLOGY, 2004, 72 (02) :290-298
[10]   Measles and mumps vaccination as a model to investigate the developing immune system: passive and active immunity during the first year of life [J].
Gans, H ;
DeHovitz, R ;
Forghani, B ;
Beeler, J ;
Maldonado, Y ;
Arvin, AM .
VACCINE, 2003, 21 (24) :3398-3405