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Independence of Granzyme B Secretion and Interferon-γ Production during Acute Simian Immunodeficiency Virus Infection
Sandra A. Calarota, Miguel Otero, Tara M. Robinson, Anlan Dai, Mark G. Lewis, Jean D. Boyer and David B. Weiner
The Journal of Infectious Diseases
Vol. 193, No. 10 (May 15, 2006), pp. 1441-1450
Published by: Oxford University Press
Stable URL: http://www.jstor.org/stable/30086569
Page Count: 10
You can always find the topics here!Topics: Infections, T lymphocytes, Viral load, Secretion, Blood plasma, RNA, Simian immunodeficiency virus, HIV 1, Quantification, Viruses
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Background. Quantification of interferon (IFN)-γ by enzyme-linked immunospot (ELISPOT) assay is currently used as a surrogate measurement of cytotoxic T lumphocyte (CTL) activity in nonhuman primates, particularly in simian immunodeficiency virus (SIV) models. Given that noncytotoxic cells and natural killer cells can also release IFN-γ, quantification of granzyme B (GrB), a molecule secreted predominantly by activated $CD8^+$ cells, may represent an additional surrogate measurement of CTL activity. Methods. We evaluated, by ELISPOT assay, GrB activity in response to 3 overlapping SIV Gag peptide pools in 18 rhesus macaques with acute $SIV_mac251$ infection and analyzed its correlation with IFN-γ ELISPOT responses and plasma viral load. Results. SIV Gag-specific GrB activity increased from 3.9- to 14.4-fold after infection, compared with that observed before infection. GrB secretion did not correlate directly with IFN-γ production. Importantly, SIV Gag specific IFN-γ production was negatively correlated with plasma viral load, whereas GrB activity was not. However, the peak of GrB activity coincided with the lowest plasma viral load detected after infection, whereas the magnitude of IFN-γ production was 1.8-fold lower than the GrB response; these results illustrate that the responses differ. Conclusion. Our data support the concept the GrB and IFN-γ ELISPOT assays measure immune responses in different immune-cell populations with unique specificities.
The Journal of Infectious Diseases © 2006 Oxford University Press