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Adaptive NK cell reconstitution is associated with better clinical outcomes
Frank Cichocki, Emily Taras, Flavia Chiuppesi, John E. Wagner, Bruce R. Blazar, Claudio Brunstein, Xianghua Luo, Don J. Diamond, Sarah Cooley, Daniel J. Weisdorf, Jeffrey S. Miller
Frank Cichocki, Emily Taras, Flavia Chiuppesi, John E. Wagner, Bruce R. Blazar, Claudio Brunstein, Xianghua Luo, Don J. Diamond, Sarah Cooley, Daniel J. Weisdorf, Jeffrey S. Miller
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Clinical Research and Public Health Immunology Transplantation

Adaptive NK cell reconstitution is associated with better clinical outcomes

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Abstract

BACKGROUND. Human cytomegalovirus (CMV) reactivation is a common occurrence early after transplant and is associated with heterogeneous NK cell subset expansion. These adaptive NK cell expansions are highly variable between recipients, with respect to magnitude and relative frequencies of adaptive NK cell subsets. METHODS. To gain insight into the factors that influence adaptive NK cell expansion from a CMV naive graft source, we performed a high-resolution NK cell and CD8+ T cell phenotypic analysis of 215 patients with hematological malignancies that were transplanted with 2 partially HLA matched CMV negative umbilical cord blood units. RESULTS. We found that adaptive NK cells were significantly higher in recipients who received nonmyeloablative conditioning (NMAC) relative to myeloablative conditioning (MAC), and high CMV neutralizing antibody titers correlated with the degree of adaptive NK cell expansion. The frequencies of adaptive NK cell subsets (defined by NKG2C, FcεRγ, EAT-2, and SYK expression) that reconstitute from donor hematopoietic progenitor cells largely matched the frequencies observed in the NK cell compartment of the recipient prior to conditioning, suggesting that host — as well as viral reactivation factors — may determine the phenotypic diversification after transplant. Additionally, multivariable analyses show that higher adaptive NK cell expansion associated with better disease-free survival. CONCLUSIONS. Our findings provide important insights into adaptive NK cell reconstitution after transplant and support a role for adaptive NK cells in promoting better clinical outcomes. FUNDING. The NIH and the National Marrow Donor Program.

Authors

Frank Cichocki, Emily Taras, Flavia Chiuppesi, John E. Wagner, Bruce R. Blazar, Claudio Brunstein, Xianghua Luo, Don J. Diamond, Sarah Cooley, Daniel J. Weisdorf, Jeffrey S. Miller

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Figure 5

Frequencies of adaptive NK cell subsets within the recipient CD3–CD56dim NK cell compartment before transplant compared with donor-derived NK cells after transplant.

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Frequencies of adaptive NK cell subsets within the recipient CD3–CD56dim...
The percentages of adaptive NK cell subsets, defined by expression of CD57 and either NKG2C, FcεRγ, EAT-2, or SYK, in recipient NK cells before transplant and donor-derived NK cells at various time points after transplant were plotted for CMV seropositive NMAC HCT recipients who experienced viral reactivation. (A) Three representative individuals who displayed low (<5%) frequencies of all adaptive NK cell subsets in the recipient pretransplant. (B) Three representative individuals who displayed high (>5%) frequencies of at least 1 adaptive NK cell subset in the recipient pretransplant. (C) Cumulative (transplants 1–18) percentages of adaptive NK cell subsets before transplant and 1 year after transplant stratified by pretransplant frequency (<5% or >5%). Statistical significance was determined using unpaired t tests. *P < 0.05, **P < 0.01, ***P < 0.001. Box and whisker plots show means, along with minimum and maximum values.

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