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妊娠:自然的实验系统。儿童免疫性疾病的短暂表现。

Pregnancy: Nature's experimental system. Transient manifestation of immunological diseases in the child.

作者信息

Scott J S

出版信息

Lancet. 1976 Jan 10;1(7950):78-81. doi: 10.1016/s0140-6736(76)90166-5.

DOI:10.1016/s0140-6736(76)90166-5
PMID:54595
Abstract

Major advances in knowledge of immunological diseases have resulted from observation of transient effects on children borne by women with such diseases. The discoveries that in Graves' disease and myasthenia gravis there are IgG antibodies directed against receptors sites are examples of such developments, while "ikiopathic" thrombocytopenic purpura is now accepted as immunological owing to its behaviour during pregnancy. In some instances observations of transient neonatal forms do not correspond with the disease manifestations in the mother. These discrepancies may be due to surgical removal of an organ vital to the disease process; inactivating damage by the disease to such an organ; presence of a blocking antibody of a molecular type not transferred across the placenta; differing tissue-antigen specificity or differing lymphocyte cooperation based on genetic variation. At present there are unexplained observations of fetal/neonatal effects in relation to diabetes mellitus and systemic lupus erythematosus which suggest that study of immunological parameters might be profitable. Determination of the HLA status of mother/fetus pairs may give rewarding clues. In the elucidation of the diseases now proven as antibody-mediated in the antibodies first discovered often turned out to be irrelevant red herrings.

摘要

对患有免疫性疾病的女性所生育子女的短暂影响进行观察,从而在免疫性疾病知识方面取得了重大进展。在格雷夫斯病和重症肌无力中发现存在针对受体部位的IgG抗体就是这类进展的例子,而“特发性”血小板减少性紫癜因其在孕期的表现,现在也被认为是免疫性疾病。在某些情况下,对短暂新生儿形式的观察结果与母亲的疾病表现并不相符。这些差异可能是由于手术切除了对疾病进程至关重要的器官;疾病对该器官造成的失活损伤;存在未通过胎盘转移的分子类型的封闭抗体;基于基因变异的不同组织抗原特异性或不同淋巴细胞协同作用。目前,关于糖尿病和系统性红斑狼疮存在一些无法解释的胎儿/新生儿影响观察结果,这表明对免疫参数的研究可能会有所收获。确定母婴对的HLA状态可能会提供有价值的线索。在阐明目前已被证明是抗体介导的疾病时,最初发现的抗体往往是无关紧要的干扰因素。

相似文献

1
Pregnancy: Nature's experimental system. Transient manifestation of immunological diseases in the child.妊娠:自然的实验系统。儿童免疫性疾病的短暂表现。
Lancet. 1976 Jan 10;1(7950):78-81. doi: 10.1016/s0140-6736(76)90166-5.
2
Tissue-specific autoimmune diseases in pregnancy.妊娠期组织特异性自身免疫性疾病。
Clin Obstet Gynaecol. 1979 Dec;6(3):473-91.
3
Antibody-mediated perinatal diseases.
Clin Lab Med. 1981 Jun;1(2):239-63.
4
Human pregnancy--an experimental model for the study of immunological disease.人类妊娠——用于免疫性疾病研究的实验模型。
Aust N Z J Obstet Gynaecol. 1971 Aug;11(3):164-9. doi: 10.1111/j.1479-828x.1971.tb00471.x.
5
Immunological diseases in pregnancy.妊娠期免疫性疾病
Prog Allergy. 1977;23:321-66.
6
[Autoimmune diseases in perinatal medicine].
An Esp Pediatr. 1985 Aug;23(2):83-9.
7
Pregnancy as an experimental system for the study of immunological diseases.妊娠作为研究免疫性疾病的实验系统。
J Reprod Fertil Suppl. 1968 Apr;3:Suppl 3:41-8.
8
[Autoimmune syndromes in human clinical cases].[人类临床病例中的自身免疫综合征]
Ann Inst Pasteur (Paris). 1970 Apr;118(4):485-512.
9
[Immunoreactive diseases in pregnancy].[妊娠期免疫反应性疾病]
Zentralbl Gynakol. 1986;108(16):961-73.
10
Maternal autoimmune disease and the fetus.母体自身免疫性疾病与胎儿
Arch Dis Child. 1985 Sep;60(9):794-7. doi: 10.1136/adc.60.9.794.

引用本文的文献

1
Congenital AV-block: role of anti-Ro and anti-La antibodies.先天性房室传导阻滞:抗Ro和抗La抗体的作用
Springer Semin Immunopathol. 1989;11(4):397-408. doi: 10.1007/BF00201878.
2
Transplacental induction of membranous nephropathy in a neonate.新生儿经胎盘诱导的膜性肾病
Pediatr Nephrol. 1990 Mar;4(2):111-6. doi: 10.1007/BF00858820.
3
Congenital discoid lupus in the newborn.新生儿先天性盘状红斑狼疮。
J Med Genet. 1977 Aug;14(4):283-6. doi: 10.1136/jmg.14.4.283.
4
Congenital heart block and maternal systemic lupus erythematosus.先天性心脏传导阻滞与母亲的系统性红斑狼疮
Br Med J. 1979 May 12;1(6173):1235-8. doi: 10.1136/bmj.1.6173.1235.
5
Immunological aspects of chronic heart block: a review.慢性心脏传导阻滞的免疫学方面:综述
Proc R Soc Med. 1977 May;70(5):327-9. doi: 10.1177/003591577707000508.
6
Immunological studies in the neonate of a mother with Addison's disease and diabetes mellitus.对患有艾迪生病和糖尿病的母亲的新生儿进行的免疫学研究。
Clin Exp Immunol. 1977 Apr;28(1):192-5.