1972
DOI: 10.1016/s0022-3476(72)80007-6
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IgG subclasses: Development of the serum concentrations in “normal” infants and children

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Cited by 134 publications
(63 citation statements)
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“…The staggered production of different subclasses merely demonstrates the complexity of neonatal development; IgG3 and IgG1 appear before IgG4 and IgG2. 22,23 These results are supported by in vitro studies that investigated IgG subclass production in normal children of various ages. 3 Previous studies clearly indicated that the in vitro induction of IgG subclass is markedly affected by the specific stimulus used, including PWM, [24][25][26] SAC, 25,27 LPS, 25,28 EBV, 25 CD3 antibody, 15 phorbol myristate acetate (PMA) with mouse thymoma cell lines (EL4), 29 and CD40 antibody.…”
Section: Introductionmentioning
confidence: 66%
“…The staggered production of different subclasses merely demonstrates the complexity of neonatal development; IgG3 and IgG1 appear before IgG4 and IgG2. 22,23 These results are supported by in vitro studies that investigated IgG subclass production in normal children of various ages. 3 Previous studies clearly indicated that the in vitro induction of IgG subclass is markedly affected by the specific stimulus used, including PWM, [24][25][26] SAC, 25,27 LPS, 25,28 EBV, 25 CD3 antibody, 15 phorbol myristate acetate (PMA) with mouse thymoma cell lines (EL4), 29 and CD40 antibody.…”
Section: Introductionmentioning
confidence: 66%
“…We speculated that the need to lower the cutoff level might have been due to the fact that the children were 10 years of age, while the patients were adults. It was, however, uncertain whether 10 years of age would still necessitate an agecorrelated cutoff level, since at that age children have reached adult IgG concentrations (9).…”
Section: Discussionmentioning
confidence: 99%
“…28 Previous studies of maternal-infant IgG subclasses to various pathogens demonstrated higher levels of IgG1, lower levels of IgG2, and equivalent levels of IgG3 and IgG4 in maternal sera compared with that of their infants. [29][30][31][32][33][34][35][36] These differences may partly explain the susceptibility of newborns to various pathogens or antigens, such as anti-tetanus toxoid and anti-streptococcal carbohydrate, which bind predominantly to IgG1 and IgG2, respectively. 37,38 In this study, transfer of dengue-specific IgG1 and IgG2 was found to be more efficient than that of IgG3 and IgG4; however, only IgG3 was shown to be significantly higher in the maternal sera than in the cord sera.…”
Section: Discussionmentioning
confidence: 99%