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人FcγRI触发单核吞噬细胞呼吸爆发。

Human Fc gamma RI triggering of the mononuclear phagocyte respiratory burst.

作者信息

Pound J D, Lund J, Jefferis R

机构信息

Immunology Department, The Medical School, Edgbaston, Birmingham, U.K.

出版信息

Mol Immunol. 1993 Apr;30(5):469-78. doi: 10.1016/0161-5890(93)90115-r.

Abstract

This study investigates the role played by Fc gamma RI and Fc gamma RII in triggering the respiratory burst induced in human monocyte-like U937 cells by monoclonal chimaeric anti-NIP antibodies expressing the human IgG subclass and mouse IgG2b heavy chains. Respiratory burst activity was measured as superoxide generation. Four separate lines of evidence indicate a predominant role for Fc gamma RI in triggering superoxide generation induced by erythrocytes sensitized with up to the maximum of 100,000 IgG molecules per cell. Firstly, erythrocytes sensitized with mouse IgG2b anti-NIP antibodies which are not recognized by human Fc gamma RI, did not induce a response but when residue Glu-235 was replaced by Leu to give the lower hinge sequence of mouse IgG2a which is recognized by Fc gamma RI, the mutant bound to Fc gamma RI and induced a response equal to 80% of that given by chimaeric human IgG3. Chimaeric human IgG3 antibodies with amino acid substitutions in the lower hinge showed reduced activity and the greatest reductions (< 32% of wild type antibody activity) were associated with changes at Leu-235 which is critical for recognition by Fc gamma RI. Secondly, chimaeric human IgG4 antibodies which are not recognized by Fc gamma RII, were able to induce superoxide generation. The rank order of abilities of chimaeric human IgG subclass antibodies to induce responses was IgG3 > IgG1 > IgG4 > > IgG2. Thirdly, responses induced by chimaeric human IgG were inhibited by concns of monomeric human IgG3 in the nM range. Finally, chimaeric human IgG3 induced responses were inhibited by anti-Fc gamma RI, but not anti-Fc gamma RII monoclonal antibodies. Consistent with a major role for Fc gamma RI in triggering the responses of U937 cells, erythrocytes sensitized with chimaeric human IgG3 did not induce superoxide generation by neutrophils which express Fc gamma RII and Fc gamma RIII, or eosinophils which express Fc gamma RII, but neither of which expresses Fc gamma RI.

摘要

本研究调查了FcγRI和FcγRII在触发人单核细胞样U937细胞中由表达人IgG亚类和小鼠IgG2b重链的单克隆嵌合抗NIP抗体诱导的呼吸爆发中所起的作用。呼吸爆发活性以超氧化物生成量来衡量。四条独立的证据表明,FcγRI在触发由每个细胞最多100,000个IgG分子致敏的红细胞诱导的超氧化物生成中起主要作用。首先,用不被人FcγRI识别的小鼠IgG2b抗NIP抗体致敏的红细胞不诱导反应,但当残基Glu-235被Leu取代以产生被FcγRI识别的小鼠IgG2a的较低铰链序列时,该突变体与FcγRI结合并诱导的反应相当于嵌合人IgG3诱导反应的80%。在较低铰链区有氨基酸取代的嵌合人IgG3抗体活性降低,最大降低(<野生型抗体活性的32%)与Leu-235的变化有关,Leu-235对FcγRI的识别至关重要。其次,不被FcγRII识别的嵌合人IgG4抗体能够诱导超氧化物生成。嵌合人IgG亚类抗体诱导反应的能力排序为IgG3 > IgG1 > IgG4 >> IgG2。第三,嵌合人IgG诱导的反应被纳摩尔范围内的单体人IgG3浓度所抑制。最后,嵌合人IgG3诱导的反应被抗FcγRI单克隆抗体抑制,但不被抗FcγRII单克隆抗体抑制。与FcγRI在触发U937细胞反应中起主要作用一致,用嵌合人IgG3致敏的红细胞不会诱导表达FcγRII和FcγRIII的中性粒细胞或表达FcγRII但不表达FcγRI的嗜酸性粒细胞产生超氧化物。

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