Epstein Barr virus/complement C3d receptor is an interferon alpha receptor.

  • Delcayre A
  • Salas F
  • Mathur S
  • et al.
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Abstract

Interferon alpha contains a sequence motif similar to the complement receptor type two (CR2/CD21) binding site on complement fragment C3d. Antibodies against a peptide with the CR2 binding sequence on C3d react with a peptide carrying the IFN alpha CR2 binding motif (residues 92-99) and with recombinant IFN alpha. The IFN alpha-derived peptide, as well as recombinant IFN alpha, inhibits C3bi/C3d interaction with CR2 on the Burkitt lymphoma Raji. The direct interaction of IFN alpha and CR2 is inhibited by polyclonal anti-IFN alpha, anti-CR2 and anti-C3d peptide antibodies as well as by C3bi/C3d, EBV coat protein gp350/220 and IFN but not by IFN gamma. [125I]IFN alpha binding to Raji cells is inhibited by polyclonal anti-IFN alpha and anti-CR2 antibodies, by peptides with the CR2 binding motif and partially by C3bi/C3d. Monoclonal anti-CR2 antibody HB5, but not OKB-7, blocks IFN alpha binding to Raji cells. CR2 or CR2-like molecules may therefore be the major IFN alpha receptors on B lymphocytes.

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Delcayre, A. X., Salas, F., Mathur, S., Kovats, K., Lotz, M., & Lernhardt, W. (1991). Epstein Barr virus/complement C3d receptor is an interferon alpha receptor. The EMBO Journal, 10(4), 919–926. https://doi.org/10.1002/j.1460-2075.1991.tb08025.x

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