Comparing the kinetics of NK cells, CD4, and CD8 T cells in murine cytomegalovirus infection Journal Article


Authors: Schlub, T. E.; Sun, J. C.; Walton, S. M.; Robbins, S. H.; Pinto, A. K.; Munks, M. W.; Hill, A. B.; Brossay, L.; Oxenius, A.; Davenport, M. P.
Article Title: Comparing the kinetics of NK cells, CD4, and CD8 T cells in murine cytomegalovirus infection
Abstract: NK cells recognize virus-infected cells with germline-encoded activating and inhibitory receptors that do not undergo genetic recombination or mutation. Accordingly, NK cells are often considered part of the innate immune response. The innate response comprises rapid early defenders that do not form immune memory. However, there is increasing evidence that experienced NK cells provide increased protection to secondary infection, a hallmark of the adaptive response. In this study, we compare the dynamics of the innate and adaptive immune responses by examining the kinetic profiles of the NK and T cell response to murine CMV infection. We find that, unexpectedly, the kinetics of NK cell proliferation is neither earlier nor faster than the CD4 or CD8 T cell response. Furthermore, early NK cell contraction after the peak of the response is slower than that of T cells. Finally, unlike T cells, experienced NK cells do not experience biphasic decay after the response peak, a trait associated with memory formation. Rather, NK cell contraction is continuous, constant, and returns to below endogenous preinfection levels. This indicates that the reason why Ag-experienced NK cells remain detectable for a prolonged period after adoptive transfer and infection is in part due to the high precursor frequency, slow decay rate, and low background levels of Ly49H+ NK cells in recipient DAP12-deficient mice. Thus, the quantitative contribution of Ag-experienced NK cells in an endogenous secondary response, with higher background levels of Ly49H+ NK cells, may be not be as robust as the secondary response observed in T cells. Copyright © 2011 by The American Association of Immunologists, Inc.
Keywords: controlled study; nonhuman; cd8+ t lymphocyte; cell proliferation; animal cell; mouse; cell growth; animal experiment; animal model; cd4+ t lymphocyte; natural killer cell; adoptive transfer; innate immunity; adaptive immunity; cytomegalovirus infection; cytomegalovirus; immunological memory; cell kinetics; murine cytomegalovirus
Journal Title: Journal of Immunology
Volume: 187
Issue: 3
ISSN: 0022-1767
Publisher: The American Association of Immunologists, Inc  
Date Published: 2011-08-01
Start Page: 1385
End Page: 1392
Language: English
DOI: 10.4049/jimmunol.1100416
PROVIDER: scopus
PUBMED: 21697462
PMCID: PMC3771860
DOI/URL:
Notes: --- - "Export Date: 3 October 2011" - "CODEN: JOIMA" - "Source: Scopus"
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  1. Joseph C Sun
    131 Sun