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免疫原性在对氨基苯胂酸偶联物诱导耐受性中的作用。

The role of immunogenicity in the induction of tolerance with conjugates of arsanilic acid.

作者信息

Collotti C, Leskowitz S

出版信息

J Exp Med. 1970 Mar 1;131(3):571-82. doi: 10.1084/jem.131.3.571.

DOI:10.1084/jem.131.3.571
PMID:5413329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2138824/
Abstract

A number of azobenzenearsonate (ABA) conjugates have been prepared and tested for ability to react with antibody, to sensitize for hapten-specific delayed hypersensitivity and to induce hapten-specific unresponsiveness. All conjugates tested by in vitro or in vivo methods show a capacity to react with preformed antibody. Conjugates of L-amino acid polymers are immunogenic and induce tolerance. Conjugates of D-amino acid polymers or conjugates with high density of ABA groups are nonimmunogenic and fail to induce tolerance. Since paired D- and L-polymer conjugates react comparably with preformed antibody but differ markedly in tolerance induction, it is argued that combination with an antibody-like receptor molecule on the surface of an immune-competent cell is not a sufficient condition for tolerance. The lack of effectiveness of sterically crowded conjugates as well as D-polymer conjugates argues for a preliminary biologic "processing" of antigen necessary for induction of immunity or tolerance. Such a processing event might well involve enzymatic attack on the antigen.

摘要

已经制备了多种偶氮苯砷酸盐(ABA)缀合物,并测试了它们与抗体反应、使半抗原特异性迟发型超敏反应致敏以及诱导半抗原特异性无反应性的能力。通过体外或体内方法测试的所有缀合物都显示出与预先形成的抗体反应的能力。L-氨基酸聚合物的缀合物具有免疫原性并诱导耐受性。D-氨基酸聚合物的缀合物或具有高密度ABA基团的缀合物无免疫原性,不能诱导耐受性。由于成对的D-和L-聚合物缀合物与预先形成的抗体反应相当,但在耐受性诱导方面有显著差异,因此有人认为与免疫活性细胞表面的抗体样受体分子结合不是诱导耐受性的充分条件。空间拥挤的缀合物以及D-聚合物缀合物缺乏有效性,这表明诱导免疫或耐受性所需的抗原需要进行初步的生物学“加工”。这样的加工事件很可能涉及对抗原的酶促攻击。

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本文引用的文献

1
Studies on the immunologic mechanism of anaphylaxis. I. Antibody-hapten interactions studied by passive cutaneous anaphylaxis in the guinea pig.过敏反应的免疫机制研究。I. 通过豚鼠被动皮肤过敏反应研究抗体-半抗原相互作用。
J Immunol. 1960 Apr;84:409-15.
2
Affinity labeling-a general method for labeling the active sites of antibody and enzyme molecules.亲和标记——一种标记抗体和酶分子活性位点的通用方法。
Biochemistry. 1962 Nov;1:1031-9. doi: 10.1021/bi00912a013.
3
Quantitative micro-complement fixation and its use in the study of antigenic structure by specific antigen-antibody inhibition.定量微量补体结合及其在通过特异性抗原-抗体抑制研究抗原结构中的应用。
J Immunol. 1961 Sep;87:290-5.
4
Studies on hypersensitivity. IV. The relationship between contact and delayed sensitivity: a study of the specificity of cellular immune reactions.超敏反应研究。IV. 接触性超敏反应与迟发型超敏反应之间的关系:细胞免疫反应特异性的研究
J Exp Med. 1961 Mar 1;113(3):571-85. doi: 10.1084/jem.113.3.571.
5
Azoproteins. I. Spectrophotometric studies of amino acid azo derivatives.偶氮蛋白。I. 氨基酸偶氮衍生物的分光光度研究。
J Biol Chem. 1959 Jul;234(7):1726-30.
6
Production of hapten-specific unresponsiveness in adult guinea-pigs by prior injection of monovalent conjugates.通过预先注射单价结合物在成年豚鼠中产生半抗原特异性无反应性。
Immunology. 1967 Jul;13(1):9-17.
7
Formation and isolation of rabbit antibodies to a synthetic antigen of low molecular weight.兔抗低分子量合成抗原抗体的形成与分离
J Immunol. 1967 Apr;98(4):739-44.
8
Mechanism of delayed reactions.迟发反应的机制
Science. 1967 Jan 20;155(3760):350-2. doi: 10.1126/science.155.3760.350.
9
Immunochemical studies on the antigenic determinants required to elicit delayed and immediate hypersensitivity reactions.关于引发迟发型和速发型超敏反应所需抗原决定簇的免疫化学研究。
J Exp Med. 1966 Jun 1;123(6):1083-95. doi: 10.1084/jem.123.6.1083.
10
Immunochemical study of antigenic specificity in delayed hypersensitivity. V. Immunization with monovalent low molecular weight conjugates.迟发型超敏反应中抗原特异性的免疫化学研究。V. 单价低分子量缀合物免疫接种
J Exp Med. 1966 Feb 1;123(2):229-37. doi: 10.1084/jem.123.2.229.