A role for complement in feedback enhancement of antibody responses by IgG3

被引:46
作者
de Ståhl, TD
Dahlström, J
Carroll, MC
Heyman, B [1 ]
机构
[1] Uppsala Univ, Dept Genet & Pathol, Rudbeck Lab, SE-75185 Uppsala, Sweden
[2] Harvard Univ, Sch Med, Ctr Blood Res, Boston, MA 02115 USA
关键词
rodents; Fc receptors; cellular activation; transgenic/knockout;
D O I
10.1084/jem.20022232
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IgG1, IgG2a, and IgG2b, passively administered with soluble Ags, enhance specific Ab responses. The effect of IgG3 in this type of feedback regulation has not been studied previously. We immunized mice with trinitrophenyl (TNP)-coupled carrier proteins (bovine serum albumin [BSA] or ovalbumin [OVA]) alone or complexed to monoclonal TNP-specific IgG3. The carrier-specific Ab responses were enhanced by several hundred-fold by IgG3. Enhancement was significantly impaired in mice depleted of complement factor C3 and in mice lacking complement receptors 1 and 2 (Cr2(-/-)). In contrast, mice lacking the common Fc-receptor gamma chain (FcRgamma(-/-)), resulting in reduced expression of FcgammaRI and lack of FcgammaRIII, and mice lacking FcgammaRIIB (FcgammaRIIB(-/-)), responded equally well to immunization with IgG3-complexed Ag as wild-type controls. These findings demonstrate that IgG3 can induce feedback enhancement and that IgG3, in analogy with IgM, uses the complement system for this function.
引用
收藏
页码:1183 / 1190
页数:8
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