Detailed Information on Publication Record
2022
CMV-reactive Vdelta1 gd T cells are equally cytotoxic to CMV-specific ab T cells in HLA-A*02 healthy donors
TOLOCHOVA, Petra, Martin PISKÁČEK, Renata HÉŽOVÁ, Elleni MICHU, Ondřej SLABÝ et. al.Basic information
Original name
CMV-reactive Vdelta1 gd T cells are equally cytotoxic to CMV-specific ab T cells in HLA-A*02 healthy donors
Authors
TOLOCHOVA, Petra, Martin PISKÁČEK (40 Austria, belonging to the institution), Renata HÉŽOVÁ (203 Czech Republic), Elleni MICHU (203 Czech Republic, belonging to the institution), Ondřej SLABÝ (203 Czech Republic, belonging to the institution) and Andrea KNIGHT (203 Czech Republic, belonging to the institution)
Edition
8th International Congenital CMV Conference & 18th International CMV Workshop, 28th March-1st April 2022 Cambridge, 2022
Other information
Language
English
Type of outcome
Konferenční abstrakt
Field of Study
30102 Immunology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
RIV identification code
RIV/00216224:14110/22:00129661
Organization unit
Faculty of Medicine
Keywords in English
CMV-reactive Vdelta1 gd T cells
Tags
Tags
International impact
Změněno: 24/4/2023 16:08, Mgr. Tereza Miškechová
Abstract
V originále
Cytomegalovirus (CMV) infection is responsible for significant morbidity and mortality in immunocompromised patients, namely haematopoietic cell transplant recipients (HCT) despite prophylaxis and pre-emptive treatment. Earlier, we demonstrated the role of Vdelta1 gamma-delta (gd) T cells in the reconstitution of CMV immunity post-transplant. Here, we analysed CMV+ healthy donors with five most commonly presented alleles including HLA-A*02 (n=23), HLA-A*01 (n=17), HLA-A*24 (n=10), HLA-B*07 (n=5) and HLA-B*35 (n=10) for frequencies and phenotypes of Vd1+ gd T cells and CMV-specific alpha-beta (ab) T cells in the same donors. Multicolour flow cytometry was used to directly compare Vd1 gd T cells with donor paired CMV-specific ab T cells that have been identified by CMV-specific MHC Pentamers (ProImmune Limited, UK) for HLA-A*0201 (NLV), HLA-A*0101 (YSE), HLA-A*2402 (VYA), HLA-B*0702 (TPR) and HLA-B*3501 (IPS) alleles. Second, we determined the cytotoxic reactivity of ab and gd T cells against CMV-infected MRC-5 fibroblasts in HLA-A*02 donors in 4h flow cytometric killing assays. Both, ab CMV-specific T cells and pair-matched freshly isolated or ex-vivo cultured Vd1 gd T cells were highly lytic to CMV-infected targets at 10:1 E:T ratio with no significant differences in specific lysis observed between the ab and gd T cells (p>0.05). Next, we compared the microRNA (miRNA) expression profiles for Vd1 gd T cells and ab T cells isolated from the same HLA-A*02 and HLA-A*01 donors. We identified 20 miRNAs differentially expressed (P<0.001) for HLA-A*02 and 10 miRNAs for HLA-A*01 allele (P<0.05) known to be associated with suppression of tumour cell proliferation, invasion and metastasis in addition to regulating inflammation in multiple cancers predicting patient prognosis and disease outcome. In summary, we provide further evidence for CMV reactive Vd1 gd T cells implicated in CMV chronic infection that could be used in adoptive transfer in HCT recipients regardless of HLA status.
Links
NV19-05-00410, research and development project |
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