Molecular mimicry of hepatitis B surface antigen by an anti-idiotype-derived synthetic peptide.

Michael W. Pride(Roswell Park Comprehensive Cancer Center), Huaxiu Shi(Roswell Park Comprehensive Cancer Center), Jerry M. Anchin(Roswell Park Comprehensive Cancer Center), D. Scott Linthicum(Roswell Park Comprehensive Cancer Center), Philip T. LoVerde(Roswell Park Comprehensive Cancer Center), Aditya Thakur(Roswell Park Comprehensive Cancer Center), Yasmin Thanavala(Roswell Park Comprehensive Cancer Center)
Proceedings of the National Academy of Sciences
December 15, 1992
Cited by 63Open Access

Abstract

Monoclonal antibody 2F10 is an "internal-image" anti-idiotype (anti-id) antibody capable of mimicking the group-specific "a" determinant of human hepatitis B surface antigen (HBsAg). By mRNA sequencing and computer-assisted molecular modeling of monoclonal antibody 2F10, we identified a 15-amino acid region of the heavy-chain hypervariable region that has partial residue homology with sequences of the "a" determinant epitopes of HBsAg. We have established that a linear 15-mer peptide from a contiguous region on the anti-id antibody can (i) generate anti-HBsAg-specific antibodies when injected into mice, (ii) prime murine lymph node cells for in vitro HBsAg-specific T-cell proliferative responses, and (iii) stimulate in vitro human CD4+ T cells that were primed in vivo to HBsAg by natural infection with hepatitis B virus or vaccination with a commercially available HBsAg vaccine. Significantly, this peptide could also stimulate CD4+ T cells of human hepatitis B virus carriers. We conclude that a 15-mer peptide derived from the anti-id sequence can duplicate the B- and T-cell stimulatory activity of the intact anti-id antibody and the antigen that is mimicked, HBsAg.


Related Papers

No related papers found

Powered by citation graph analysis