TY - JOUR
T1 - Novel Mouse Model of Murine Cytomegalovirus-Induced Adaptive NK Cells
AU - Jensen, Isaac J.
AU - Martin, Matthew D.
AU - Tripathy, Sandeep K.
AU - Badovinac, Vladimir P.
N1 - Publisher Copyright:
© 2022 American Association of Immunologists. All rights reserved.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - NK cells are important mediators of viral control with the capacity to form adaptive immune features following infection. However, studies of infection-induced adaptive NK cells require adoptive cell transfer to lower the precursor frequency of .Ag-specific. NK cells, potentially limiting the diversity of the NK cell response. In seeking an unmanipulated model to probe the adaptive NK cells, we interrogated a wide range of Collaborative Cross (CC) inbred mice, inbred mouse strains that exhibit broad genetic diversity across strains. Our assessment identified and validated a putative .ideal. CC strain, CC006, which does not require manipulation to generate and maintain adaptive NK cells. Critically, CC006 mice, in contrast to C57BL/6 mice, are capable of developing enhanced NK cell-mediated protective responses to murine CMV infection following m157-mediated vaccination. This work both furthers our understanding of adaptive NK cells and demonstrates the utility of CC mice in the development and interrogation of immunologic models.
AB - NK cells are important mediators of viral control with the capacity to form adaptive immune features following infection. However, studies of infection-induced adaptive NK cells require adoptive cell transfer to lower the precursor frequency of .Ag-specific. NK cells, potentially limiting the diversity of the NK cell response. In seeking an unmanipulated model to probe the adaptive NK cells, we interrogated a wide range of Collaborative Cross (CC) inbred mice, inbred mouse strains that exhibit broad genetic diversity across strains. Our assessment identified and validated a putative .ideal. CC strain, CC006, which does not require manipulation to generate and maintain adaptive NK cells. Critically, CC006 mice, in contrast to C57BL/6 mice, are capable of developing enhanced NK cell-mediated protective responses to murine CMV infection following m157-mediated vaccination. This work both furthers our understanding of adaptive NK cells and demonstrates the utility of CC mice in the development and interrogation of immunologic models.
UR - http://www.scopus.com/inward/record.url?scp=85129532312&partnerID=8YFLogxK
U2 - 10.4049/immunohorizons.2100113
DO - 10.4049/immunohorizons.2100113
M3 - Article
C2 - 35031582
AN - SCOPUS:85129532312
SN - 2573-7732
VL - 6
SP - 8
EP - 15
JO - ImmunoHorizons
JF - ImmunoHorizons
IS - 1
ER -