对婴儿喂养与儿童癌症之间关联证据的回顾。

M K Davis
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摘要

为了评估婴儿喂养与儿童癌症之间的关系,对9项已发表的病例对照研究进行了定性回顾。综合结果表明,从未母乳喂养或短期母乳喂养的儿童比母乳喂养>或= 6个月的儿童患霍奇金病(HD)的风险更高,但非霍奇金淋巴瘤或急性淋巴细胞白血病的风险较低。HD具有复杂的细胞免疫紊乱和慢性感染的特点。母乳含有广泛的抗微生物活性,似乎可以刺激婴儿免疫系统的早期发育。人工喂养的婴儿在没有这种免疫武器的情况下接触传染因子,并且在抵抗感染方面不如母乳喂养的婴儿。因此,母乳可以通过调节感染因子与发育中的婴儿免疫系统之间的相互作用,或通过直接影响婴儿免疫系统的长期发育,使母乳喂养的婴儿更好地应对未来的致癌损害。进一步的研究应试图在大规模、基于人群的病例对照研究中证实婴儿喂养与HD之间的联系。如果未来的研究要提高我们对这种关联的理解,就必须解决婴儿喂养的改进测量。此外,应在母乳喂养和非母乳喂养的幼儿群体中研究免疫的具体措施,特别是细胞免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Review of the evidence for an association between infant feeding and childhood cancer.

To assess the association between infant feeding and childhood cancer, a qualitative review of 9 published case-control studies was undertaken. The results of this synthesis suggest that children who are never breast-fed or are breast-fed short-term have a higher risk than those breast-fed for > or = 6 months of developing Hodgkin's disease (HD), but not non-Hodgkin's lymphoma or acute lymphoblastic leukemia. HD has features of a complex cellular immune disorder and of chronic infection. Human milk contains an extensive array of anti-microbial activity and appears to stimulate early development of the infant immune system. Artificially fed infants negotiate exposure to infectious agents without the benefits of this immunologic armament and do not do as well as breast-fed infants in resisting infection. Thus, human milk may make the breast-fed infant better able to negotiate future carcinogenic insults by modulating the interaction between infectious agents and the developing infant immune system or by directly affecting the long-term development of the infant immune system. Further research should attempt to confirm the association between infant feeding and HD in large, population-based, case-control studies. Improved measurement of infant feeding must be addressed if future studies are to advance our understanding of this association. In addition, studies of specific measures of immunity, particularly of cellular immune responses, should be conducted in populations of breast-fed and non-breast-fed young children.

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