AI Article Synopsis

  • The study examined how follicular dendritic cells (FDC) retain immune complexes using gold particles coated with TNP-myoglobin and monoclonal anti-TNP antibodies.
  • FDC preferentially retained immune complexes containing the antibody isotypes IgG2a and IgG2b more effectively than those with IgG1, IgG3, or rarely, IgM.
  • In both in vivo and in vitro settings, FDC showed consistent patterns in retaining IgG2a and IgG2b while showing variable retention for IgG1 and IgG3, with no significant differences found between FDC from lymph nodes or the spleen.

Article Abstract

Using monoclonal anti-trinitrophenyl (TNP) antibodies complexed to TNP-myoglobin-coated gold particles, we analysed at the ultrastructural level the retention by follicular dendritic cells (FDC) of immune complexes containing various antibody isotypes. Gold-labelled immune complexes were injected subcutaneously or intravenously into naive mice and, after 24 h, germinal centres of draining lymph nodes or spleen were examined by electron microscopy. FDC generally retained complexes containing IgG2a and IgG2b better than those formed with IgG1 or IgG3. IgM was rarely retained. FDC isolated from lymph nodes or spleens were incubated in vitro with gold-labelled complexes in a serum-free medium. IgG2a and IgG2b complexes were also retained in vitro in large quantities by FDC; IgG1 and IgG3 complexes were retained in smaller quantities or in highly variable quantities compared with IgG2; IgM complexes were rarely seen on FDC. There was no difference between FDC isolated from lymph nodes or from spleen with respect to the Ig isotypes required for Fc-mediated retention of immune complexes.

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Source
http://dx.doi.org/10.1111/j.1365-3083.1986.tb02101.xDOI Listing

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