Solubilization of immune precipitates by complement in the absence of properdin or factor D

FEBS Lett. 1988 Jul 4;234(1):131-4. doi: 10.1016/0014-5793(88)81318-8.

Abstract

Various experiments have demonstrated that immune precipitates (IPs) are not solubilized by complement in the absence of alternative pathway function. To determine whether the characteristics of the IPs were responsible for these observations, we studied the solubilization (Sol) of IPs formed by bovine serum albumin (BSA)-rabbit antiBSA and tetanus toxoid (TT)-human antiTT. Sera deficient in properdin solubilized a fraction of BSA-antiBSA precipitates, although only when the IPs were formed in antibody excess. The same sera solubilized TT-antiTT precipitates with some delay but almost as efficiently as normal serum. Factor D-depleted serum solubilized a fraction of TT-antiTT precipitates too, indicating that Sol may proceed through activation of the classical pathway only. Thus, the requirements for complement-mediated Sol depend on the characteristics of the IPs and do not necessarily include alternative pathway function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / immunology
  • Antigen-Antibody Complex*
  • Complement Activating Enzymes / physiology*
  • Complement Activation
  • Complement C3 / physiology
  • Complement C3b / metabolism
  • Complement Factor D / physiology*
  • Erythrocytes / immunology
  • Humans
  • Properdin / physiology*
  • Receptors, Complement / metabolism
  • Receptors, Complement 3b
  • Serum Albumin, Bovine / immunology*
  • Solubility
  • Tetanus Toxoid / immunology*

Substances

  • Antibodies
  • Antigen-Antibody Complex
  • Complement C3
  • Receptors, Complement
  • Receptors, Complement 3b
  • Tetanus Toxoid
  • Properdin
  • Serum Albumin, Bovine
  • Complement C3b
  • Complement Activating Enzymes
  • CFD protein, human
  • Complement Factor D