Pregled bibliografske jedinice broj: 678128
NKG2D signaling on CD8+ T cells represses T-bet and rescues CD4-unhelped CD8+ T cell memory recall but not effector responses
NKG2D signaling on CD8+ T cells represses T-bet and rescues CD4-unhelped CD8+ T cell memory recall but not effector responses // Nature medicine, 18 (2012), 3; 422-428 doi:10.1038/nm.2683 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 678128 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
NKG2D signaling on CD8+ T cells represses T-bet and rescues CD4-unhelped CD8+ T cell memory recall but not effector responses
Autori
Zloza, Andrew ; Kohlap, Frederick J. ; Lyons, Gretchen E. ; Scehnkel, Jason M. ; Moore, Tamson V. ; Lacek, Andrew T. ; O'Sullivan, Jeremy A. ; Varanasi, Vineeth ; Williams, Jesse W. ; Jagoda, Michael C. ; Bellavance, Emily C. ; Marzo, Amanda L. ; Thomas, Paul G. ; Zafirova, Biljana ; Polić, Bojan ; Al-Harthi, Lena ; Sperling, Anne I. ; Guevara-Patiño, José A.
Izvornik
Nature medicine (1078-8956) 18
(2012), 3;
422-428
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
NKG2D; CD8 T cell memory; vacine
Sažetak
CD4-unhelped CD8+ T cells are functionally defective T cells primed in the absence of CD4+ T cell help. Given the co-stimulatory role of natural-killer group 2, member D protein (NKG2D) on CD8+ T cells, we investigated its ability to rescue these immunologically impotent cells. We demonstrate that augmented co-stimulation through NKG2D during priming paradoxically rescues memory, but not effector, CD8+ T cell responses. NKG2D-mediated rescue is characterized by reversal of elevated transcription factor T-box expressed in T cells (T-bet) expression and recovery of interleukin-2 and interferon-g production and cytolytic responses. Rescue is abrogated in CD8+ T cells lacking NKG2D. Augmented co-stimulation through NKG2D confers a high rate of survival to mice lacking CD4+ T cells in a CD4-dependent influenza model and rescues HIV-specific CD8+ T cell responses from CD4-deficient HIV-positive donors. These findings demonstrate that augmented co-stimulation through NKG2D is effective in rescuing CD4-unhelped CD8+ T cells from their pathophysiological fate and may provide therapeutic benefits.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
062-0621261-1271 - Uloga NKG2D u razvoju, homeostazi i efektorskim funkcijama imunološkog sustava (Polić, Bojan, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi www.ncbi.nlm.nih.gov www.nature.comCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE