[Note: to read the full text of this article free, click HERE.]
Background: Xenotropic Murine Leukemia Virus-related Virus (XMRV) is a human gammaretrovirus recently identified in prostate cancer tissue and in lymphocytes of patients with chronic fatigue syndrome.
To establish the etiologic role of XMRV infection in human disease requires large scale epidemiologic studies. Development of assays to detect XMRV-specific antibodies would greatly facilitate such studies.
However, the nature and kinetics of the antibody response to XMRV infection have yet to be determined.
Results: Three rhesus macaques were infected with XMRV to determine the dynamics of the antibody responses elicited by infection with XMRV.
All macaques developed antibodies to XMRV during the second week of infection, and the predominant responses were to the envelope protein gp70, transmembrane protein p15E and capsid protein p30.
In general, antibody responses to gp70 and p15E appeared early with higher titers than to p30, especially in the early period of seroconversion.
Antibodies to gp70, p15E and p30 persisted to 158 days and were substantially boosted by re-infection, thus, were identified as useful serologic markers.
Three high-throughput prototype assays were developed using recombinant proteins to detect antibodies to these viral proteins. Both gp70 and p15E prototype assays demonstrated 100% sensitivity by detecting all Western Blot (WB) positive serial bleeds from the XMRV-infected macaques and good specificity (99.5-99.9%) with blood donors.
Seroconversion sensitivity and specificity of the p30 prototype assay was 92% and 99.4% respectively.
Conclusions: This study provides the first demonstration of seroconversion patterns elicited by XMRV infection.
• The nature and kinetics of antibody responses to XMRV in primates were fully characterized.
• Moreover, key serologic markers useful for detection of XMRV infection were identified.
• Three prototype immunoassays were developed to detect XMRV-specific antibodies.
• These assays demonstrated good sensitivity and specificity; thus will facilitate large scale epidemiologic studies of XMRV infection in humans.
Source: Retrovirology, Aug 17, 2010. doi:10.1186/1742-4690-7-68 by Qiu X, Swanson P, Luk K, Tu B, Villinger F, Das Gupta J, Silverman RH, Klein EA, Devare s, Schochetman g, Hackett J Jr. Abbott Diagnostics, Abbott Park, Illinois; Department of Pathology, Emory University School of Medicine/Yerkes National Primate Research Center, Atlanta, Georgia; Department of Cancer Biology, Lerner Research Institute, and Glick Urological and Kidney Institute and LRI, Cleveland Clinic Foundation, Cleveland, Ohio, USA. [See also “Characterization of XMRV in prostate cancer,” March 2010.]