Laboratorio Sperimentale Oncoematologia Pediatrica, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
Int J Immunopathol Pharmacol. 2010 Jan-Mar;23(1):247-54. doi: 10.1177/039463201002300122.
In the present study we evaluated B-cell subsets and their functional development in 74 newborns from birth to 6 months of life. Moreover, we evaluated natural antibody production in vitro. The results documented a predominance of naive B-lymphocytes at all time-points evaluated, decreasing from birth to 6 months (p=0.009). The percentages of CD27+IgD+ and CD27+IgDneg memory B-cells were very low at birth and significantly increased only at 6 months (p=0.02 and p less than 0.001, respectively). We found a significant increase only in in vitro stimulated IgG production at 6 months as compared to birth (p less than 0.001). Moreover, a lower secretion of anti-Pn IgM antibodies up to 6 months of age, as compared to controls was observed. Our results underline that the susceptibility and severe course of infection in the neonate can be attributed, at least in part, to the lack of pre-existing immunological memory and competent adaptive immunity.
在本研究中,我们评估了 74 名新生儿从出生到 6 个月的 B 细胞亚群及其功能发育情况。此外,我们还评估了体外天然抗体的产生情况。结果表明,在所有评估的时间点,幼稚 B 淋巴细胞均占优势,从出生到 6 个月逐渐减少(p=0.009)。出生时 CD27+IgD+和 CD27+IgDneg 记忆 B 细胞的百分比非常低,仅在 6 个月时显著增加(p=0.02 和 p 小于 0.001)。与出生时相比,我们仅发现 6 个月时体外刺激 IgG 产生显著增加(p 小于 0.001)。此外,与对照组相比,我们观察到新生儿在 6 个月龄时抗肺炎球菌 IgM 抗体的分泌水平较低。我们的研究结果表明,新生儿易感染且感染过程严重的原因,至少部分是由于缺乏预先存在的免疫记忆和成熟的适应性免疫。