KinnunenLab
@KinnunenLab
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Research group of Tuure Kinnunen at @UniEastFinland. All things immunology, with a particular interest in T cells and autoimmunity
Kuopio, Finland
Joined April 2020
New science out from our group, this time looking at the specificities of autoantibodies in patients with juvenile idiopathic arthritis #JIA.
Plasma samples from untreated patients with active JIA were analyzed for ANA specificities. Results showed chromatin was the main target of autoantibody reactivity in JIA, and 20% of JIA patients had reactivity to dsDNA-nucleosome complexes A&R https://t.co/wV176y9Bom
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🌍 QuantumScale training sessions happening across continents! Same commitment everywhere: Your breakthrough = our success Real support. Real results. Real partnership. https://t.co/HOdLtPpK9J
#GlobalScience #SingleCellRNA #ScaleBio
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Interesting observation: turns out mouse PD-1 is less inhibitory than human PD-1, so many observations in mouse cancer immunotherapy models may not hold true in humans. Another fine example why we need more human studies and/or more humanized rodent models.
Thrilled to share our @SciImmunology paper! Rodent PD-1 is weaker than human PD-1 (reduced ligand binding & signaling) & lacks a conserved vertebrate motif. Humanizing mouse PD-1 disrupts T cell anti-tumor responses, raising many questions. Kudos to @MasubuchiTakeya for leading
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An exciting advance in Type 1 diabetes First person to receive her own stem cells, reprogrammed with transcription factors, to reverse it! @CellCellPress
https://t.co/NzhTO6tZrg
@Nature
https://t.co/zbNNtLCrot
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Huge congratulations @SchAnnMari for brilliantly defending your thesis today! And many thanks @lettipitko for acting as the opponent and leading the inspiring discussions.
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Doctoral defence of Anna-Mari Schroderus, MSc, 13 Dec 2024: Alterations in T-cell landscape observed at different stages of type 1 diabetes progression. @ClinmedUef @UEFMetabolicRC
uef.fi
The findings of the dissertation provide timely insight into the T-cell landscape at different stages of T1D progression.
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T-solupopulaatioissa tapahtuu tyypin 1 diabeteksen kehittymisen eri vaiheissa muutoksia, joista voisi ehkä tulla biomarkkereita hoitoon, havaitsi FM Anna-Mari Schroderus väitöstutkimuksessaan. Väitös Kuopiossa 13.12.2024. @ClinmedUef @UEFMetabolicRC
uef.fi
Tutkimuksen tulokset tarjoavat ajankohtaista tietoa T-solupopulaatioiden biologiasta tyypin 1 diabeteksen kehittymisen eri vaiheissa.
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Interesting early success by CAR-T therapies to treat (highly selected!) patients with severe autoimmune diseases, like lupus.
How engineered T cells are changing the face of autoimmune diseases via B cell depletion https://t.co/yREY9OSeyY
@ScienceMagazine @NewsfromScience @jcouzin open-access
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New paper out @Nature - why are males more vulnerable to severe infections (ex acute #COVID), while females suffer more from autoimmunity (SLE, MS etc and also #LongCovid)? sex chromosomes or hormones? Here we studied adaptation of human immune systems to gender-affirming
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Ok, so this is the future I guess. Someone made an AI-generated 30 sec highlight of our research paper. Looks and sounds very convincing on the surface, but on a closer look the pictures and texts in the animation are complete gibberish…
An early CMV infection can reprogram your immune system's 'software' for years, like a computer update that sticks around. @KinnunenLab @ClinmedUef @helsinkiuni @UniTurku @UniOulu
https://t.co/xPzsbuRNur
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5/ Thanks again to all the collaborators at @ClinmedUef @helsinkiuni @UniTurku @UniOulu, and of course the funding sources @SuomenAkatemia @SigridJuselius
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4/ The mechanism is completely speculative, but recently there have been some evidence for a protective effect on autoimmunity for certain subsets of highly differentiated CD8+ T cell subsets, such as the CD8+KLRG1+TIGIT cells, we recently studied in #T1D:
diabetesjournals.org
CD8+ T cells are perceived to play a major role in the pathogenesis of type 1 diabetes (T1D). In this study, we characterized the function and phenotype of
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3/ So, what does this have to do with autoimmunity? Not necessarily anything, but there are some signals that early life CMV infection may protect from autoimmunity, such as our earlier study some years ago:
onlinelibrary.wiley.com
Aims/Hypothesis Evidence of the role of cytomegalovirus (CMV) infection in the pathogenesis of type 1 diabetes (T1D) has remained inconclusive. Our aim was to elucidate the possible role of CMV...
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3/ As expected based on earlier research, increased frequencies of memory T cells with an ”advanced differentiation” phenotype were observed early after infection, and the increase in the most highly differentiated memory T cells persisted into the latent phase (6 years of age).
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1/ Check out our recent translational research on the effect of early life CMV infection on T cell memory in children! https://t.co/2DyInckWhk
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Verenkierron CD8-positiivisissa T-soluissa tapahtuu erityyppisiä muutoksia tyypin 1 diabeteksen kehittymisen eri vaiheissa, osoittaa Itä-Suomen yliopiston tutkimus. Tieto voi auttaa tyypin 1 diabeteksen kehittymisen ennustamisessa. @KinnunenLab @SchAnnMari
uef.fi
Verenkierron CD8-positiivisissa T-soluissa havaittiin erilaisia muutoksia juuri tyypin 1 diabetekseen sairastuneilla lapsilla verrattuna sairastumisriskissä oleviin lapsiin, jotka myöhemmin sairast...
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Two distinct signatures were detected in a subset of circulating, highly differentiated CD8-positive T cells in children at different stages of type 1 diabetes development. The study was led by prof. Tuure Kinnunen at the #UEF. @KinnunenLab @SchAnnMari
https://t.co/cGiiWA4mHA
uef.fi
A study conducted at the UEF found distinct signatures in CD8-positive T cells in blood samples from children with newly diagnosed type 1 diabetes and in autoantibody-positive children who later...
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6/ I wish to thank all our collaborators at @ClinmedUef @Pshyvinvointi @helsinkiuni @UniTurku, and especially my brilliant student @SchAnnMari, who spearheaded the project! Special thanks also to the funders: @SuomenAkatemia @SigridJuselius
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5/ Therefore, it can be speculated that in at-risk individuals there is an ongoing immune process aiming to restrict autoimmunity, which is reflected by increased blood CD8+KLRG1+TIGIT+ cells, and this could potentially be enhanced by immunotherapy to prevent the onset of T1D
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