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Brief report: immunoglobulin A deficiency in a subset of autistic subjects.

作者信息

Warren R P, Odell J D, Warren W L, Burger R A, Maciulis A, Daniels W W, Torres A R

机构信息

Utah State University, Logan 84322, USA.

出版信息

J Autism Dev Disord. 1997 Apr;27(2):187-92. doi: 10.1023/a:1025895925178.

DOI:10.1023/a:1025895925178
PMID:9105969
Abstract
摘要

相似文献

1
Brief report: immunoglobulin A deficiency in a subset of autistic subjects.
J Autism Dev Disord. 1997 Apr;27(2):187-92. doi: 10.1023/a:1025895925178.
2
Increased frequency of the null allele at the complement C4b locus in autism.自闭症患者中补体C4b基因座无效等位基因的频率增加。
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3
Immunogenetic studies in autism and related disorders.
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4
Decreased plasma concentrations of the C4B complement protein in autism.自闭症患者血浆中C4B补体蛋白浓度降低。
Arch Pediatr Adolesc Med. 1994 Feb;148(2):180-3. doi: 10.1001/archpedi.1994.02170020066011.
5
The link of C4B null allele to autism and to a family history of autoimmunity in Egyptian autistic children.C4B 无功能等位基因与自闭症以及埃及自闭症儿童自身免疫家族史的关联。
J Neuroimmunol. 2010 Jun;223(1-2):115-9. doi: 10.1016/j.jneuroim.2010.03.025. Epub 2010 May 10.
6
Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.
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7
Dysregulated immune system in children with autism: beneficial effects of intravenous immune globulin on autistic characteristics.自闭症儿童免疫系统失调:静脉注射免疫球蛋白对自闭症特征的有益影响。
J Autism Dev Disord. 1996 Aug;26(4):439-52. doi: 10.1007/BF02172828.
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Confirmation of the association of the C4B null allelle in autism.
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C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism.C4B无效等位基因与自闭症中相邻基因CYP21A2的基因多态性无关。
BMC Med Genet. 2008 Jan 7;9:1. doi: 10.1186/1471-2350-9-1.
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Polymorphism of the human complement component C4.人类补体成分C4的多态性
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A Proteomics Investigation of Salivary Profiles as Potential Biomarkers for Autism Spectrum Disorder (ASD).

本文引用的文献

1
Decreased plasma concentrations of the C4B complement protein in autism.自闭症患者血浆中C4B补体蛋白浓度降低。
Arch Pediatr Adolesc Med. 1994 Feb;148(2):180-3. doi: 10.1001/archpedi.1994.02170020066011.
2
Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.扩展的HLA/补体等位基因单倍型:人类中T/t样复合体的证据。
Proc Natl Acad Sci U S A. 1983 Jan;80(1):259-63. doi: 10.1073/pnas.80.1.259.
3
Family studies of IgA deficiency.IgA缺乏症的家族研究。
基于蛋白质组学的唾液特征分析作为自闭症谱系障碍(ASD)生物标志物的研究。
Protein J. 2023 Oct;42(5):607-620. doi: 10.1007/s10930-023-10146-0. Epub 2023 Aug 11.
4
The Alteration of Salivary Immunoglobulin A in Autism Spectrum Disorders.自闭症谱系障碍患者唾液免疫球蛋白A的改变
Front Psychiatry. 2021 May 21;12:669193. doi: 10.3389/fpsyt.2021.669193. eCollection 2021.
5
Immunoglobulin A-specific deficiency induces spontaneous inflammation specifically in the ileum.免疫球蛋白 A 特异性缺乏会导致自发性炎症,这种炎症主要发生在回肠。
Gut. 2022 Mar;71(3):487-496. doi: 10.1136/gutjnl-2020-322873. Epub 2021 May 7.
6
Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders.免疫功能障碍和自身免疫作为自闭症谱系障碍的病理机制
Front Cell Neurosci. 2018 Nov 13;12:405. doi: 10.3389/fncel.2018.00405. eCollection 2018.
7
Immune Abnormalities in Autism Spectrum Disorder-Could They Hold Promise for Causative Treatment?自闭症谱系障碍中的免疫异常——它们能为病因治疗带来希望吗?
Mol Neurobiol. 2018 Aug;55(8):6387-6435. doi: 10.1007/s12035-017-0822-x. Epub 2018 Jan 6.
8
Serum proteomic analysis identifies sex-specific differences in lipid metabolism and inflammation profiles in adults diagnosed with Asperger syndrome.血清蛋白质组学分析鉴定出被诊断为阿斯伯格综合征的成年人在脂质代谢和炎症特征方面的性别特异性差异。
Mol Autism. 2014 Jan 27;5(1):4. doi: 10.1186/2040-2392-5-4.
9
Low serum IgA and increased expression of CD23 on B lymphocytes in peripheral blood in children with regressive autism aged 3-6 years old.3-6 岁退行性自闭症儿童外周血血清 IgA 水平降低,B 淋巴细胞表面 CD23 表达增加。
Arch Med Sci. 2012 May 9;8(2):324-31. doi: 10.5114/aoms.2012.28561.
10
Above genetics: lessons from cerebral development in autism.超越遗传学:自闭症大脑发育的启示
Transl Neurosci. 2011 Jun 1;2(2):106-120. doi: 10.2478/s13380-011-0016-3. Epub 2011 Jun 26.
Immunogenetics. 1985;21(4):333-42. doi: 10.1007/BF00430799.
4
Reduced natural killer cell activity in autism.自闭症患者自然杀伤细胞活性降低。
J Am Acad Child Adolesc Psychiatry. 1987 May;26(3):333-5. doi: 10.1097/00004583-198705000-00008.
5
Covalent binding properties of the C4A and C4B isotypes of the fourth component of human complement on several C1-bearing cell surfaces.人类补体第四成分的C4A和C4B同种型在几种携带C1的细胞表面上的共价结合特性。
J Immunol. 1986 Apr 1;136(7):2542-50.
6
HLA antigens in IgA deficient paediatric patients.IgA 缺乏的儿科患者中的 HLA 抗原
Tissue Antigens. 1988 Oct;32(4):218-23. doi: 10.1111/j.1399-0039.1988.tb01659.x.
7
Immune abnormalities in patients with autism.自闭症患者的免疫异常。
J Autism Dev Disord. 1986 Jun;16(2):189-97. doi: 10.1007/BF01531729.
8
Association of homozygous C4B deficiency with bacterial meningitis.
J Infect Dis. 1989 Sep;160(3):448-51. doi: 10.1093/infdis/160.3.448.
9
Complotypes and extended haplotypes in laboratory medicine.检验医学中的复合单倍型和扩展单倍型
Complement Inflamm. 1989;6(1):8-18. doi: 10.1159/000463067.
10
Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes.患有IgA缺乏症和常见可变免疫缺陷的个体共享主要组织相容性复合体III类基因的多态性。
Proc Natl Acad Sci U S A. 1989 Oct;86(20):8015-9. doi: 10.1073/pnas.86.20.8015.