-
Je něco špatně v tomto záznamu ?
Lymphocyte profile in peripheral blood of patients with multiple myeloma
T. Dekojová, H. Gmucová, D. Macečková, R. Klieber, P. Ostašov, M. Leba, T. Vlas, A. Jungová, VS. Caputo, M. Čedíková, D. Lysák, P. Jindra, M. Holubová
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články
Grantová podpora
FNPl, 00669806
Ministerstvo Zdravotnictví Ceské Republiky
SVV 260 561
Charles University
Cooperatio, research area ONCO
Charles University
NLK
ProQuest Central
od 1997-03-01
Medline Complete (EBSCOhost)
od 2000-01-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest)
od 1997-03-01
Health & Medicine (ProQuest)
od 1997-03-01
Springer Nature OA/Free Journals
od 1955-03-01
- MeSH
- B-lymfocyty imunologie MeSH
- buňky NK imunologie MeSH
- cytokiny krev MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mnohočetný myelom * krev imunologie terapie MeSH
- NKT buňky imunologie MeSH
- podskupiny lymfocytů imunologie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Multiple myeloma (MM) is a disease which remains incurable. One of the main reasons is a weakened immune system that allows MM cells to survive. Therefore, the current research is focused on the study of immune system imbalance in MM to find the most effective immunotherapy strategies. Aiming to identify the key points of immune failure in MM patients, we analysed peripheral lymphocytes subsets from MM patients (n = 57) at various stages of the disease course and healthy individuals (HI, n = 15) focusing on T, NK, iNKT, B cells and NK-cell cytokines. Our analysis revealed that MM patients exhibited immune alterations in all studied immune subsets. Compared to HI, MM patients had a significantly lower proportion of CD4 + T cells (19.55% vs. 40.85%; p < 0.001) and CD4 + iNKT cells (18.8% vs. 40%; p < 0.001), within B cells an increased proportion of CD21LCD38L subset (4.5% vs. 0.4%; p < 0.01) and decreased level of memory cells (unswitched 6.1% vs. 14.7%; p < 0.001 and switched 7.8% vs. 11.2%; NS), NK cells displaying signs of activation and exhaustion characterised by a more than 2-fold increase in SLAMF7 MFI (p < 0.001), decreased expression of NKG2D (MFI) and NKp46 (%) on CD16 + 56 + and CD16 + 56- subset respectively (p < 0.05), Effective immunotherapy needs to consider these immune defects and monitoring of the immune status of MM patients is essential to define better interventions in the future.
Department of Haematology and Oncology University Hospital Pilsen Pilsen 323 00 Czech Republic
Faculty of Applied Science University of West Bohemia Pilsen 301 00 Czech Republic
Institute of Allergology and Immunology University Hospital Pilsen Pilsen 323 00 Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25010587
- 003
- CZ-PrNML
- 005
- 20250429134505.0
- 007
- ta
- 008
- 250415s2024 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s00277-024-05820-x $2 doi
- 035 __
- $a (PubMed)38832999
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Dekojová, Tereza $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic $u Department of Histology and Embryology, Faculty of Medicine in Pilsen, Charles University, Pilsen, 323 00, Czech Republic $u Laboratory of Tumor Biology and Immunotherapy, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, Pilsen, 323 00, Czech Republic
- 245 10
- $a Lymphocyte profile in peripheral blood of patients with multiple myeloma / $c T. Dekojová, H. Gmucová, D. Macečková, R. Klieber, P. Ostašov, M. Leba, T. Vlas, A. Jungová, VS. Caputo, M. Čedíková, D. Lysák, P. Jindra, M. Holubová
- 520 9_
- $a Multiple myeloma (MM) is a disease which remains incurable. One of the main reasons is a weakened immune system that allows MM cells to survive. Therefore, the current research is focused on the study of immune system imbalance in MM to find the most effective immunotherapy strategies. Aiming to identify the key points of immune failure in MM patients, we analysed peripheral lymphocytes subsets from MM patients (n = 57) at various stages of the disease course and healthy individuals (HI, n = 15) focusing on T, NK, iNKT, B cells and NK-cell cytokines. Our analysis revealed that MM patients exhibited immune alterations in all studied immune subsets. Compared to HI, MM patients had a significantly lower proportion of CD4 + T cells (19.55% vs. 40.85%; p < 0.001) and CD4 + iNKT cells (18.8% vs. 40%; p < 0.001), within B cells an increased proportion of CD21LCD38L subset (4.5% vs. 0.4%; p < 0.01) and decreased level of memory cells (unswitched 6.1% vs. 14.7%; p < 0.001 and switched 7.8% vs. 11.2%; NS), NK cells displaying signs of activation and exhaustion characterised by a more than 2-fold increase in SLAMF7 MFI (p < 0.001), decreased expression of NKG2D (MFI) and NKp46 (%) on CD16 + 56 + and CD16 + 56- subset respectively (p < 0.05), Effective immunotherapy needs to consider these immune defects and monitoring of the immune status of MM patients is essential to define better interventions in the future.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a mnohočetný myelom $x krev $x imunologie $x terapie $7 D009101
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a buňky NK $x imunologie $7 D007694
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a podskupiny lymfocytů $x imunologie $7 D016131
- 650 _2
- $a cytokiny $x krev $7 D016207
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a B-lymfocyty $x imunologie $7 D001402
- 650 _2
- $a NKT buňky $x imunologie $7 D055611
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Gmucová, Hana $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Macečková, Diana $u Department of Histology and Embryology, Faculty of Medicine in Pilsen, Charles University, Pilsen, 323 00, Czech Republic $u Laboratory of Tumor Biology and Immunotherapy, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Klieber, Robin $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic $u Laboratory of Tumor Biology and Immunotherapy, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Ostašov, Pavel $u Department of Histology and Embryology, Faculty of Medicine in Pilsen, Charles University, Pilsen, 323 00, Czech Republic $u Laboratory of Tumor Biology and Immunotherapy, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Leba, Martin $u Faculty of Applied Science, University of West Bohemia, Pilsen, 301 00, Czech Republic
- 700 1_
- $a Vlas, Tomáš $u Institute of Allergology and Immunology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Jungová, Alexandra $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Caputo, Valentina S $u Cancer Biology and Therapy laboratory, School of Applied Sciences, London South Bank University, London, UK
- 700 1_
- $a Čedíková, Miroslava $u Laboratory of Tumor Biology and Immunotherapy, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Lysák, Daniel $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Jindra, Pavel $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic
- 700 1_
- $a Holubová, Monika $u Department of Haematology and Oncology, University Hospital Pilsen, Pilsen, 323 00, Czech Republic. monika.holubova@lfp.cuni.cz $u Laboratory of Tumor Biology and Immunotherapy, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, Pilsen, 323 00, Czech Republic. monika.holubova@lfp.cuni.cz
- 773 0_
- $w MED00000424 $t Annals of hematology $x 1432-0584 $g Roč. 103, č. 12 (2024), s. 5615-5625
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/38832999 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250415 $b ABA008
- 991 __
- $a 20250429134500 $b ABA008
- 999 __
- $a ok $b bmc $g 2311767 $s 1247668
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 103 $c 12 $d 5615-5625 $e 20240604 $i 1432-0584 $m Annals of hematology $n Ann Hematol $x MED00000424
- GRA __
- $a FNPl, 00669806 $p Ministerstvo Zdravotnictví Ceské Republiky
- GRA __
- $a SVV 260 561 $p Charles University
- GRA __
- $a Cooperatio, research area ONCO $p Charles University
- LZP __
- $a Pubmed-20250415