NK Cell Functional Impairment after Allogeneic Hematopoietic Stem Cell Transplantation Is Associated with Reduced Levels of T-bet and Eomesodermin

NK cells play a major role in protection against tumor recurrence and infection after allogeneic hematopoietic stem cell transplantation (HSCT). It has been shown that NK cell function after HSCT is impaired, but underlying molecular mechanisms are not well-known. In this report we show that the lev...

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Vydané v:The Journal of immunology (1950) Ročník 195; číslo 10; s. 4712
Hlavní autori: Simonetta, Federico, Pradier, Amandine, Bosshard, Carine, Masouridi-Levrat, Stavroula, Chalandon, Yves, Roosnek, Eddy
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 15.11.2015
Predmet:
Adolescent
Adult
Aged
CD56 Antigen - biosynthesis
Female
Graft vs Host Disease - immunology
Hematopoietic Stem Cell Transplantation
Humans
Killer Cells, Natural - immunology
Killer Cells, Natural - metabolism
Male
Middle Aged
Perforin - biosynthesis
T-Box Domain Proteins - biosynthesis
T-Box Domain Proteins - metabolism
Transcription, Genetic
Transplantation, Homologous
Young Adult
ISSN:1550-6606, 1550-6606
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Shrnutí:NK cells play a major role in protection against tumor recurrence and infection after allogeneic hematopoietic stem cell transplantation (HSCT). It has been shown that NK cell function after HSCT is impaired, but underlying molecular mechanisms are not well-known. In this report we show that the level of T-bet and Eomesodermin (Eomes), two T-box transcription factors regulating lymphocyte effector functions, is strongly reduced in NK cells from HSCT recipients compared with healthy control subjects. Reduction of T-bet and Eomes expression appeared early and persisted for years after HSCT, affecting all peripheral blood NK cells independently of their differentiation status. Reduced T-bet levels in NK cells from allogeneic HSCT recipients significantly correlated with reduced perforin expression. Acute, but not chronic, graft-versus-host disease, as well as CMV reactivation, was associated with further downregulation of T-bet expression in NK cells. Lower levels of T-bet expression in NK cells were associated with less favorable outcome after HSCT as a result of increased nonrelapse mortality. Collectively, our results provide a possible molecular explanation for the previously reported functional exhaustion of NK cells after allogeneic HSCT and suggest an impact of the NK transcriptional machinery status on HSCT outcome.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1550-6606
1550-6606
DOI:10.4049/jimmunol.1501522