Literature DB >> 3733160

CH2 and CH3 domain deleted IgG1 paraproteins inhibit differently Fc receptor mediated binding and cytolysis.

G Sármay, R Jefferis, J Gergely.   

Abstract

Domain deleted paraproteins are suitable tools to study the interaction between IgG domains and Fc receptor (FcR) binding sites. The effect of the C gamma 2 or C gamma 3 domain deleted paraproteins was compared on antibody dependent cellular cytotoxicity (ADCC) and on FcR mediated rosette formation. The C gamma 2 domain deleted paraprotein (TIM) had no significant effect on lymphocyte or monocyte mediated ADCC, while the C gamma 3 domain deleted paraprotein (SIZ) inhibited both types of cytotoxicity. FcR dependent rosette formation was also inhibited by SIZ but TIM was ineffective. The data further confirm our previous results suggesting a significant role of C gamma 2 domain in the transfer of killing signal in ADCC and that of C gamma 3 domain in the high affinity binding to lymphocyte FcR.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3733160     DOI: 10.1016/0165-2478(86)90035-0

Source DB:  PubMed          Journal:  Immunol Lett        ISSN: 0165-2478            Impact factor:   3.685


  3 in total

1.  Distinctive role of IgG1 and IgG3 isotypes in Fc gamma R-mediated functions.

Authors:  Z Rozsnyay; G Sármay; M Walker; K Maslanka; Z Valasek; R Jefferis; J Gergely
Journal:  Immunology       Date:  1989-04       Impact factor: 7.397

2.  Activation of effector functions by immune complexes of mouse IgG2a with isotype-specific autoantibodies.

Authors:  E Rajnavölgyi; G Fazekas; J Lund; M Daeron; J L Teillaud; R Jefferis; W H Fridman; J Gergely
Journal:  Immunology       Date:  1995-04       Impact factor: 7.397

3.  Aglycosylation of human IgG1 and IgG3 monoclonal antibodies can eliminate recognition by human cells expressing Fc gamma RI and/or Fc gamma RII receptors.

Authors:  M R Walker; J Lund; K M Thompson; R Jefferis
Journal:  Biochem J       Date:  1989-04-15       Impact factor: 3.857

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.