Epstein Barr virus/complement C3d receptor is an interferon alpha receptor
- PMID: 1849076
- PMCID: PMC452735
- DOI: 10.1002/j.1460-2075.1991.tb08025.x
Epstein Barr virus/complement C3d receptor is an interferon alpha receptor
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.
Similar articles
-
Structural requirements for C3d,g/Epstein-Barr virus receptor (CR2/CD21) ligand binding, internalization, and viral infection.J Biol Chem. 1990 Jul 25;265(21):12293-9. J Biol Chem. 1990. PMID: 1695627
-
Identification of gp350 as the viral glycoprotein mediating attachment of Epstein-Barr virus (EBV) to the EBV/C3d receptor of B cells: sequence homology of gp350 and C3 complement fragment C3d.J Virol. 1987 May;61(5):1416-20. doi: 10.1128/JVI.61.5.1416-1420.1987. J Virol. 1987. PMID: 3033269 Free PMC article.
-
Epstein-Barr virus/complement fragment C3d receptor (CR2) reacts with p53, a cellular antioncogene-encoded membrane phosphoprotein: detection by polyclonal anti-idiotypic anti-CR2 antibodies.Proc Natl Acad Sci U S A. 1989 Dec;86(24):10054-8. doi: 10.1073/pnas.86.24.10054. Proc Natl Acad Sci U S A. 1989. PMID: 2557614 Free PMC article.
-
Structure and function of the complement receptors, CR1 (CD35) and CR2 (CD21).Adv Immunol. 1989;46:183-219. doi: 10.1016/s0065-2776(08)60654-9. Adv Immunol. 1989. PMID: 2551147 Review. No abstract available.
-
CR2 complement receptor.J Invest Dermatol. 1990 Jun;94(6 Suppl):112S-117S. doi: 10.1111/1523-1747.ep12876069. J Invest Dermatol. 1990. PMID: 2161885 Review.
Cited by
-
Targeting pathogenic postischemic self-recognition by natural IgM to protect against posttransplantation cardiac reperfusion injury.Circulation. 2015 Mar 31;131(13):1171-80. doi: 10.1161/CIRCULATIONAHA.114.010482. Epub 2015 Feb 17. Circulation. 2015. PMID: 25825397 Free PMC article.
-
Maternal antibodies: clinical significance, mechanism of interference with immune responses, and possible vaccination strategies.Front Immunol. 2014 Sep 16;5:446. doi: 10.3389/fimmu.2014.00446. eCollection 2014. Front Immunol. 2014. PMID: 25278941 Free PMC article. Review.
-
Lupus-associated innate receptors drive extrafollicular evolution of autoreactive B cells.bioRxiv [Preprint]. 2024 Jan 9:2024.01.09.574739. doi: 10.1101/2024.01.09.574739. bioRxiv. 2024. PMID: 38260501 Free PMC article. Preprint.
-
Association of four antigens of the tetraspans family (CD37, CD53, TAPA-1, and R2/C33) with MHC class II glycoproteins.Immunogenetics. 1994;39(4):249-56. doi: 10.1007/BF00188787. Immunogenetics. 1994. PMID: 8119731
-
Analysis of Epstein-Barr virus (EBV) receptor CD21 on peripheral B lymphocytes of long-term EBV- adults.Clin Exp Immunol. 1999 Jun;116(3):468-73. doi: 10.1046/j.1365-2249.1999.00912.x. Clin Exp Immunol. 1999. PMID: 10361236 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases