Pregled bibliografske jedinice broj: 1034906
Brain‐resident memory CD8+ T cells induced by congenital CMV infection prevent brain pathology and virus reactivation
Brain‐resident memory CD8+ T cells induced by congenital CMV infection prevent brain pathology and virus reactivation // European journal of immunology, 48 (2018), 6; 950-964 doi:10.1002/eji.201847526 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1034906 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Brain‐resident memory CD8+ T cells induced by
congenital CMV infection prevent brain pathology
and virus reactivation
Autori
Brizić Ilija ; Šušak Božo ; Arapović Maja ; Huszthy Peter C. ; Hiršl Lea ; Kveštak Daria ; Juranić Lisnić Vanda ; Golemac Mijo ; Pernjak Pugel Ester ; Tomac Jelena ; Oxenius Annette ; Britt William J. ; Arapović Jurica ; Krmpotić Astrid ; Jonjić Stipan
Izvornik
European journal of immunology (0014-2980) 48
(2018), 6;
950-964
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Brain pathology ; Congenital CMV infection ; Mouse cytomegalovirus ; Microglia ; Tissue‐resident memory T cells
Sažetak
Congenital HCMV infection is a leading infectious cause of long‐term neurodevelopmental sequelae. Infection of newborn mice with mouse cytomegalovirus (MCMV) intraperitoneally is a well‐established model of congenital human cytomegalovirus infection, which best recapitulates the hematogenous route of virus spread to brain and subsequent pathology. Here, we used this model to investigate the role, dynamics, and phenotype of CD8+ T cells in the brain following infection of newborn mice. We show that CD8+ T cells infiltrate the brain and form a pool of tissue‐resident memory T cells (TRM cells) that persist for lifetime. Adoptively transferred virus‐specific CD8+ T cells provide protection against primary MCMV infection in newborn mice, reduce brain pathology, and remain in the brain as TRM cells. Brain CD8+ TRM cells were long‐ lived, slowly proliferating cells able to respond to local challenge infection. Importantly, brain CD8+ TRM cells controlled latent MCMV and their depletion resulted in virus reactivation and enhanced inflammation in brain.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
EK-FP7-322693 - Strengthening adaptive immunity via innate immunity: enhancing the CD8 T cell response by using the NKG2D ligand expressed in a herpesvirus vector (STADVINN) (Jonjić, Stipan, EK - ERC-2012-ADG_20120314) ( CroRIS)
1RO1AI089956-01A1
KK.01.1.1.01.0006
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Daria Kveštak
(autor)
Astrid Krmpotić
(autor)
Ester Pernjak-Pugel
(autor)
Ilija Brizić
(autor)
Jelena Tomac
(autor)
Vanda Juranić Lisnić
(autor)
Jurica Arapović
(autor)
Mijo Golemac
(autor)
Maja Arapović
(autor)
Stipan Jonjić
(autor)
Citiraj 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