| Innate Immunity | |
| Distinct TLR-mediated cytokine production and immunoglobulin secretion in human newborn naïve B cells: | |
| Matthew APettengill1  | |
| 关键词: B lymphocyte; TLR; cytokine; neonatal; class-switch recombination; | |
| DOI : 10.1177/1753425916651985 | |
| 学科分类:生物科学(综合) | |
| 来源: Sage Journals | |
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【 摘 要 】
Neonatal innate immunity is distinct from that of adults, which may contribute to increased susceptibility to infection and limit vaccine responses. B cells play critical roles in protection from infection and detect PAMPs via TLRs, that, when co-activated with CD40, can drive B-cell proliferation and Ab production. We characterized the expression of TLRs in circulating B cells from newborns and adults, and evaluated TLR- and CD40-mediated naïve B-cell class-switch recombination (CSR) and cytokine production. Gene expression levels of most TLRs was similar between newborn and adult B cells, except that newborn naïve B cells expressed more TLR9 than adult naïve B cells. Neonatal naïve B cells demonstrated impaired TLR2- and TLR7- but enhanced TLR9-mediated cytokine production. Significantly fewer newborn naïve B cells underwent CSR to produce IgG, an impairment also noted with IL-21 stimulation. Additionally, co-stimulation via CD40 and TLRs induced greater cytokine production in adult B cells. Thus, while...
【 授权许可】
CC BY
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201904028409288ZK.pdf | 592KB |
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