Author

Elena Bonaiti

Karolinska InstitutetORCID 0009-0004-4199-3616Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Assay:bulk RNA-seq· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:genome assembly· 1

Frequent Co-Authors

Akhirunnesa MilyiD· 2 shared Carl JornsiD· 2 shared Christian M. Constantz· 2 shared Curtis CaiiD· 2 shared Elisa J. M. RaineriiD· 2 shared Elli MouchtaridiiD· 2 shared Eoghann WhiteiD· 2 shared Jenny MjösbergiD· 2 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersImmunology

Akhirunnesa MilyORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Human lymph node CD8+ T cell memory is nested within drainage regions

Curtis Cai, YouBeen Ko, Emmy Berg, Nicole Wild, Marcus Göransson, Emma E. Ringqvist, Iva Sutevski, Rafael C. Marques, Natthaphong Kaewkam, Elena Bonaiti, Demi Brownlie, Christian M. Constantz, Sabrina S. Ferreira, Yu Gao, Jyotsana Kaushal, , Marcus Buggert

The paper shows that human CD8+ T cell memory is nested within drainage regions, with shared repertoires among nodes within a region regardless of virus specificity.

bioRxiv · Oct 23, 2026 · PreprintImmunology

MAIT cell responses to S. aureus and sensitivity to HlgAB are modulated by activation and tissue-dependent virulence effects

Elisa J. M. Raineri, Caroline Boulouis, Elli Mouchtaridi, Vera Nilsén, Curtis Cai, Tobias Kammann, Juliette Tabusse, Takuya Sekine, Nicole Wild, Christian M. Constantz, Eoghann White, Thomas R. Mu?ller, Anne Marchalot, Sabrina S. Ferreira, Jyotsana Kaushal, , Johan K. Sandberg

This study examines how MAIT cells respond to S. aureus and how their sensitivity to the toxin HlgAB varies by tissue location and activation state.

bioRxiv · Mar 19, 2026 · PreprintImmunology

Tunable DNMT1 degradation reveals cooperation of DNMT1 and DNMT3B in regulating DNA methylation dynamics and genome organization

Andrea Scelfo, Viviana Barra, Nezar A. Abdennur, George Spracklin, Florence Busato, Catalina Salinas‐Luypaert, Elena Bonaiti, Guillaume Velasco, Anna Chipont, Coralie L. Guérin, Andréa E. Tijhuis, Diana C.J. Spierings, Claire Francastel, Floris Foijer, Jörg Tost, , Daniele Fachinetti

This study uses tunable DNMT1 degradation to investigate DNA methylation dynamics and genome organization, revealing cooperative roles of DNMT1 and DNMT3B and their impact on heterochromatin and cell fitness.

bioRxiv · May 4, 2023 · PreprintMolecular Biology