Potential Crossreactivity of Human Immune Responses Against HCMV Glycoprotein B

Author(s): Guglielmo Lucchese, Darja Kanduc

Journal Name: Current Drug Discovery Technologies

Volume 13 , Issue 1 , 2016

Become EABM
Become Reviewer


Antigens of infectious agents share amino acid sequences with human proteins. Such a peptide matching may lead to autoimmunity through crossreactivity phenomena following pathogen infection and/or immunotherapeutic approaches. In this framework, we analyzed as a model the primary sequence of human cytomegalovirus (HCMV) glycoprotein B (gB) protein and searched for viral peptide sequences shared with human proteins. We show that the HCMV antigen has a high peptide identity with a large number of human proteins at the penta-, hexa-, and heptapeptide level, with the viral versus human peptide overlap involving host proteins implicated in crucial processes such as embryonic development, spermatogenesis, spatial learning, and hippocampal plasticity, inter alia. This study might help understand the etiology of the pathologic sequela associated with HCMV (re)activation and, in addition, address scientific and clinical research toward the definition of antiviral therapeutics based on non-crossreactive viral sequences.

Keywords: Anti-HCMV immune response, autoimmune diseases, crossreactivity, HCMV glycoprotein B, human proteins, peptide sharing.

promotion: free to download

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2016
Page: [16 - 24]
Pages: 9
DOI: 10.2174/1568009616666160129100621

Article Metrics

PDF: 34